Reactive metal boride nanoparticles trap lipopolysaccharide and peptidoglycan for bacteria-infected wound healing

Meng, Yun; Chen, Lijie; Chen, Yang; Shi, Jieyun; Zhang, Zheng; Wang, Yiwen; Wu, Fan; Jiang, Xingwu; Yang, Wei; Zhang, Li; Wang, Chaochao; Meng, Xianfu; Wu, Yelin; Bu, Wenbo

doi:10.1038/s41467-022-35050-6

Download PDF

Article
Open access
Published: 29 November 2022

Reactive metal boride nanoparticles trap lipopolysaccharide and peptidoglycan for bacteria-infected wound healing

Yun Meng^1,2^na1,
Lijie Chen²^na1,
Yang Chen^1,3^na1,
Jieyun Shi¹,
Zheng Zhang⁴,
Yiwen Wang⁴,
Fan Wu²,
Xingwu Jiang²,
Wei Yang¹,
Li Zhang¹,
Chaochao Wang¹,
Xianfu Meng¹,
Yelin Wu ORCID: orcid.org/0000-0002-0746-8541¹ &
…
Wenbo Bu ORCID: orcid.org/0000-0001-6664-3453^1,2

Nature Communications volume 13, Article number: 7353 (2022) Cite this article

8901 Accesses
37 Citations
14 Altmetric
Metrics details

Subjects

Abstract

Bacteria and excessive inflammation are two main factors causing non-healing wounds. However, current studies have mainly focused on the inhibition of bacteria survival for wound healing while ignoring the excessive inflammation induced by dead bacteria-released lipopolysaccharide (LPS) or peptidoglycan (PGN). Herein, a boron-trapping strategy has been proposed to prevent both infection and excessive inflammation by synthesizing a class of reactive metal boride nanoparticles (MB NPs). Our results show that the MB NPs are gradually hydrolyzed to generate boron dihydroxy groups and metal cations while generating a local alkaline microenvironment. This microenvironment greatly enhances boron dihydroxy groups to trap LPS or PGN through an esterification reaction, which not only enhances metal cation-induced bacterial death but also inhibits dead bacteria-induced excessive inflammation both in vitro and in vivo, finally accelerating wound healing. Taken together, this boron-trapping strategy provides an approach to the treatment of bacterial infection and the accompanying inflammation.

Pseudomonas aeruginosa: pathogenesis, virulence factors, antibiotic resistance, interaction with host, technology advances and emerging therapeutics

Article Open access 25 June 2022

Multimodal nanoimmunotherapy engages neutrophils to eliminate Staphylococcus aureus infections

Article 17 April 2024

Multiscale architecture design of 3D printed biodegradable Zn-based porous scaffolds for immunomodulatory osteogenesis

Article Open access 11 April 2024

Introduction

Impaired wound healing is a growing global concern driven by aging populations and the increasing prevalence of chronic conditions, such as diabetes and obesity. It affects ∼20 million individuals worldwide and over $31 billion has been spent annually on their treatment and management¹. Infection is a major factor that delays wound healing, which can lead to sepsis and multiorgan failure, and even cause death in severe cases^2,3. Currently, antibiotics are the main strategies to reduce the bacterial burden for wound healing and lower the mortality rates after severe infection. However, over-prescription and misuse of antibiotics have contributed to the emergence of antibiotic-resistant organisms, limiting the treatment efficacy of wound healing⁴. Moreover, the dead bacteria accumulating at the site of infection could induce undesirable tissue inflammation^5,6. One of the most important reasons is that the dead bacteria can release massive amounts of endotoxin (lipopolysaccharide (LPS) in Gram-negative bacteria and peptidoglycan (PGN) in Gram-positive bacteria) that can activate immune cells to induce excessive inflammation, leading to impaired wound healing, systemic inflammation, intravascular coagulation, and organ dysfunction^7,8,9. This is a leading cause of death in the US alone, with over 700,000 cases estimated every year, and the mortality rate ranges from 28% to 60%¹⁰. Therefore, developing strategies to simultaneously inhibit the survival of live bacteria and dead bacteria-induced excessive inflammation to heal infected wounds is urgently needed.

Certain components of pathogens are crucial for their structure and function, ensuring pathogen survival and pathogenicity. LPS and PGN are typically the key components of Gram-negative and Gram-positive bacteria, respectively¹¹. On one hand, LPS/PGN is a structural component of the bacteria cell wall, which maintains the integrity of the bacteria and protects the bacteria against antibacterial treatments¹². On the other hand, LPS/PGN is the main functional component of the endotoxin, which is released from the bacterial surface upon bacteria die or lyse. These free LPS/PGN can induce excessive inflammation and toxicity to the host^13,14. Therefore, targeting the key component of bacteria would structurally inhibit bacterial survival and functionally suppress dead bacteria-induced excessive inflammation and toxicity. Currently, LPS-binding peptides have been reported to react with LPS, resulting in antibacterial activity or the inhibition of LPS/PGN-induced immune cell activation^10,15,16, however, the precise mechanism by which these peptides perform their biological activities remains elusive. Furthermore, the poor bioavailability and the proteolytic stability of peptides limit their application in clinic¹⁷. Therefore, targeting the key component of bacteria (LPS/PGN) to simultaneously inhibit bacterial survival and dead bacteria-induced excessive inflammation for wound healing is still facing serious challenges.

LPS/PGN is mainly composed of many different sugars such as hexose or pentose, which contains many 1,2 or 1,3-dial dihydroxyl groups^18,19. Studies have shown that borate materials can produce dynamic borate ester bonds through an esterification reaction with the dihydroxyl groups²⁰. This dynamic covalent bond has been widely used to identify substances such as blood, glucose, and ATP^21,22,23. Considering that bacterial LPS/PGN contains structures of 1,2-diol or 1,3-diol and that borate derivatives are prone to react with diol-containing compounds to form borate-diol esters^24,25, materials possessing boron dihydroxyl functional groups may react with LPS/PGN to inhibit bacterial survival and simultaneously reduce dead bacteria-induced inflammation. However, such dynamic covalent bonds easily dissociate under acidic and inflammatory conditions. Hence, it is necessary to design an antibacterial reagent that efficiently forms stable borate ester bonds with the key component of bacterial LPS/PGN, finally promoting wound healing.

Reactive metal borides (MB NPs) have rich bonding characteristics, among which the strength of B–M ion bond is relatively weak. Therefore, MB NPs undergo the ion exchange reactions with protons during hydrolysis, and the breaking of boron–metal ion bonds, leading to the release of hydroxide, cation ions, and the formation of boron hydride (BH) nanosheets²⁶. In addition, BH nanosheets can be further hydrolyzed to generate boron dihydroxyl groups. Meanwhile, the hydroxides released by the MB NPs can regulate the configuration transition of boron atom, which is helpful for the complexation of the boron dihydroxyl groups with LPS/PGN to form more stable O–B–O bonds. Therefore, MB NPs are the ideal material system to trap LPS/PGN. Moreover, the strength of B–M ion bond of the corresponding MB NPs varies greatly with the selection of different raw metal materials. Taking Mg, Al, and Be as examples, after the reaction of these small-sized, low-charge metal elements with boron, the corresponding B–M bonds are significantly reduced²⁷, which effectively improve the hydrolysis ability of the MB NPs, accelerating the generation of boron dihydroxyl groups, and facilitating the complex reaction of such material system with LPS/PGN. Since metal cations such as silver²³, magnesium²⁸, aluminum²⁹, bismuth^30,31, cobalt³², among others^33,34,35 are often responsible for antibacterial activities and the B–M bond energy can be affected by the metal cations, the selection of metal components is very important to regulate the hydrolysis ability of this material system. Therefore, we hypothesized that MB NPs (M = Mg, Al, and Be) could form stable borate ester bonds with LPS/PGN, the key component of bacteria, consequently inhibiting bacterial survival and decreasing dead bacteria-induced excessive inflammation for wound healing.

Herein, we proposed a boron-trapping strategy and synthesized a class of nanoscale MB NPs (M = Mg, Al, and Be), using Nano-MgB₂ as a representative example to elucidate the mechanism and function of MB NPs in promoting infected wound healing (Fig. 1). The Nano-MgB₂ could gradually hydrolyze to generate boron dihydroxy groups and metal cations while generating a local alkaline/low reactive oxygen species (ROS) microenvironment. The alkaline microenvironment could promote the Nano-MgB₂ to trap much more LPS/PGN through the esterification reaction between the boron dihydroxyl group and diol of LPS/PGN. This process could not only induce a high focal concentration of Mg²⁺ on the bacterial membrane, enhancing the ability of Mg²⁺ to disrupt the membrane structure of living bacteria, but also trap dead bacteria-released LPS/PGN from escaping, resulting in the inhibition of LPS/PGN-induced excessive inflammation. The suppression of both bacterial growth and excessive inflammation could significantly promote wound healing. This boron-trapping strategy can be used to develop methods for promoting the healing of infected wounds.

**Fig. 1: Boron-trapping strategy for bacteria-infected wound healing.**

Results

Synthesis and characterization of Nano-MgB₂

As proof of concept, MB NPs, a series of boron-trapping materials, were synthesized using an improved self-propagating high-temperature synthesis (SHS) approach³⁶. As seen in Supplementary Fig. 1 as well as Fig. 2e, the X-ray diffraction (XRD) results demonstrated that Nano-MgB₂ can be indexed to the hexagonal phase of MgB₂ (JCPDS: 38-1369), Nano-AlB₂ can be indexed to the hexagonal phase of AlB₂ (JCPDS: 39-1483), and Nano-BeB_x can be ascribed to the mixture of the tetragonal phase of BeB₆ (JCPDS: 13-0361) and hexagonal phase of BeB₁₂ (JCPDS: 19-0152). Dynamic light scattering (DLS) results revealed that the mean diameter of MB NPs was about 150–250 nm (Supplementary Fig. 2). We hypothesized that these three MB NPs had antibacterial effects. Therefore, we incubated different concentrations of MB NPs with Pseudomonas aeruginosa, the most common Gram-negative bacteria in the chronic wounds⁵, to screen the most effective antibacterial MB NP. As shown in Supplementary Fig. 3, all MB NPs exhibited significant antibacterial effects, however, Nano-MgB₂ showed a stronger antibacterial effect compared to AlB₂ and BeB_x. Therefore, we used Nano-MgB₂ as a representative example to evaluate the synthesis, characterization, and function of MB NPs.

**Fig. 2: Morphology and characterization of Nano-MgB₂.**

As shown in Fig. 2a, b, scanning electron microscopic (SEM) and transmission electron microscopic (TEM) images indicated that the obtained Nano-MgB₂ was well dispersed in H₂O. High-resolution TEM (HRTEM) analysis clearly revealed the lattice fringes of Nano-MgB₂ with d-spacing of 2.11 Å, corresponding to the crystalline face (101) of Nano-MgB₂ (Fig. 2c). Moreover, the images obtained using low-magnification high-angle annular dark-field scanning TEM (HAADF-STEM) as well as the elemental mapping indicated that this nanoplatform was mainly composed of Mg, B, and O (Fig. 2d). Because of the layered properties of Nano-MgB₂, it formed 2D-like nanostructures after hydrolysis (Fig. 2f, g). Moreover, atomic force microscopy (AFM) indicated that the thickness of Nano-MgB₂ decreased from 60–100 nm before hydrolysis to 7–8 nm after hydrolysis (Fig. 2h, i) further demonstrating that the morphology of Nano-MgB₂ changed from nanoparticles to 2D nanosheets. All these data demonstrated that the designed nanoparticles were successfully synthesized.

Functional characterization of Nano-MgB₂

To determine the functional characterization of Nano-MgB₂, we first evaluated its ability to generate a weakly alkaline microenvironment, Mg²⁺, and boron hydroxyl groups. As shown in Fig. 3a, the pH rapidly increased within 30 min and became nearly stable at around 200 min (pH stabilized at 9.5 in a buffer solution of pH = 7.5 and at 8.5 in a buffer solution of pH = 5.5). As shown in FTIR spectrum (Fig. 3b), the characteristic peak of boron hydroxyl groups (broad peak at 3000–3500 cm⁻¹) began to appear after about 20 min of Nano-MgB₂ hydrolysis, which suggested that Nano-MgB₂ can exhibit an instant therapeutic effect on the minute scale and the produced boron hydroxyl groups can exist stably for at least 15 days (Supplementary Fig. 4). Furthermore, as shown in Fig. 3c, d, buffer solution with a lower pH led to a faster hydrolysis rate of Nano-MgB₂. These data demonstrate that the hydrolysis of MB NPs leads to the generation of an alkaline microenvironment with metal ions and boron hydroxyl groups. To determine whether boron hydroxyl groups act as a boron-trapping agent to trap LPS/PGN, the key components of Gram-negative and -positive bacteria, Nano-MgB₂ was incubated with LPS, PGN, or dead P. aeruginosa (HIB, heat-inhibited bacteria). As shown in Fig. 3e, the characteristic peak at 1072 cm⁻¹ demonstrated that the hydrolysate of Nano-MgB₂ reacted with LPS, PGN, and HIB to form boronic ester (O–B–O) bonds. Besides Nano-MgB₂, Nano-AlB₂ and Nano-BeB_x can also react with LPS and PGN to form O–B–O bonds, suggesting that members of this class of nanoscale MB NPs have similar boron-trapping functions (Supplementary Fig. 5). Furthermore, we compared the LPS/PGN binding activity of Nano-MgB₂ with that of H₃BO₃ which contains boron hydroxyl groups. As shown in SEM images equipped with elemental mapping, a much larger amount of B element was enriched on the bacteria in the Nano-MgB₂-incubated group than that in the H₃BO₃-incubated group (Fig. 3f and Supplementary Fig. 6). To analyze this phenomenon, the borate ester bonds formed by the complexation of H₃BO₃ and hydrolysate of nano-MgB₂ with the bacterial polysaccharide fraction were calculated based on density functional theory (DFT). Taking LPS as an example, its polysaccharide component is composed of a unique bicyclic monosaccharide structure, and each sugar motif has two binding sites (3, 4-o-hydroxyl or 4, 5-o-hydroxyl) that can complex with boron dihydroxyl groups. For the binding site of 3, 4-o-hydroxyl (Supplementary Figs. 7–8), the C–O bond lengths of the borate ester bond formed by H₃BO₃ (1.451 Å/1.451 Å) are longer than that of nano-MgB₂ hydrolysate (1.431 Å/1.439 Å), indicating that the C–O bond formed by the former is easier to break. Moreover, we used crystal orbital Hamilton population (COHP) analysis to reflect the strength of C–O bonding. The values of ICOHP of the C–O bonds formed by nano-MgB₂ hydrolysate (−8.853 eV/−9.071 eV) are much negative compared to H₃BO₃ (−8.592 eV/−8.655 eV), which directly proves the enhancement of the C–O bonds. For the binding site of 4, 5-o-hydroxyl, we obtained similar theoretical calculation results (Supplementary Figs. 9–10). The above data indicate that Nano-MgB₂ forms more stable borate ester bonds with LPS when compared to H₃BO₃.

In addition, X-ray photoelectron spectroscopy (XPS) was performed to analyze the metal components of MB NPs (Supplementary Figs. 11–13). According to the survey XPS spectra, O and corresponding metal signals can be clearly observed. Specifically, the Mg 2p signal of the Nano-MgB₂ consisted of Mg²⁺ (50.5 eV) alone, the Al 2p signal of the Nano-AlB₂ consisted of Al³⁺ (74.3 eV) alone, and the Be 1s signal of the Nano-BeB_xconsisted of Be²⁺ (113.5 eV) alone. XPS was also utilized to characterize the hydrolysis process of MB NPs. Take Nano-MgB₂ as an example (Fig. 3g, h), the sample was characterized by the disappearance of the characteristic peak for the negatively charged boron species (B-Mg bond, 185.8 eV) and the appearance of the characteristic peak for the positively charged boron species (190.9 eV for B–OH bond and 192.7 eV for HO–B–OH bond, respectively) after hydrolysis. Therefore, the hydrolysis of Nano-MgB₂ involved oxidation of boron elements. Considering the oxidative stress microenvironment of the bacteria-infected wound, we further examined the ROS-scavenging ability of Nano-MgB₂. Nano-MgB₂ exhibited high reactivity towards broad-spectrum ROS (Fig. 3i), reactive nitrogen species (RNS) (Supplementary Fig. 14), and the direct •OH scavenging ability of Nano-MgB₂ (Supplementary Fig. 15). Thus, the designed MB NPs are gradually hydrolyzed to generate boron dihydroxy groups and metal cations while generating a local alkaline/low ROS microenvironment, which promoted the esterification reaction between boron hydroxyl groups and LPS/PGN.

Nano-MgB₂ disrupted the structure of bacteria in vitro

As the experiments described above demonstrated that Nano-MgB₂ can react with LPS to form O–B–O bonds, the antibacterial activity of Nano-MgB₂ was further evaluated. As shown in Fig. 4a, b, Nano-MgB₂ exhibited excellent antibacterial activity at a low concentration at around 12.5 μg/mL, whereas H₃BO₃ + Mg²⁺ group exhibited little or no antibacterial effect against P. aeruginosa at the same concentration. This antibacterial effect of our synthesized Nano-MgB₂ was dramatically stronger than that of commercial MgB₂ powders³⁷, and was comparable to the effects of gentamicin, amikacin, ciprofloxacin, levofloxacin, and better than imipenem, meropenem, ceftazidime, cefepime, ampicillin+sulbactam, aztreonam (Supplementary Fig. 16a). Furthermore, as shown in Supplementary Fig. 17a, b, Nano-MgB₂ also showed a significant antibacterial effect against S. aureus. We also compared the antibacterial activity of Nano-MgB₂ with three kinds of antibiotics for S. aureus. As shown in Supplementary Fig. 16b, the antibacterial effect of Nano-MgB₂ was better than that of cephalexin, but not that of erythromycin and mupirocin. Taken together, all these data demonstrate that Nano-MgB₂ has an excellent antimicrobial function which is comparable to the effects of certain kinds of antibiotics.

**Fig. 4: Nano-MgB₂ reacted with LPS to disrupt bacterial cell membrane.**

To further investigate Nano-MgB₂ trapping LPS is required for the antibacterial effect of Nano-MgB₂, different concentrations of LPS were added to block the reaction between Nano-MgB₂ and LPS. Nano-MgB₂ (6.25 μg/mL) significantly inhibited the growth of P. aeruginosa, however, this inhibition effect was rescued by adding LPS, demonstrating that the O–B–O bond between Nano-MgB₂ and LPS is involved in Nano-MgB₂-induced bacterial death (Fig. 4c). Furthermore, as shown in the result of SEM of P. aeruginosa and S. aureus, the bacteria typically had a rod-shaped morphology with a smooth and intact cell wall in the blank and H₃BO₃ + Mg²⁺ groups, whereas those treated with Nano-MgB₂ became wrinkled and shrunk (Fig. 4d and Supplementary Fig. 17c). TEM analysis revealed that the cytoplasm of bacteria was lost in the Nano-MgB₂-treated group compared with that in the blank and H₃BO₃ + Mg²⁺ groups, indicating that degradation of the cytoplasm components or cell membrane leakage occurred after Nano-MgB₂ treatment (Fig. 4e and Supplementary Fig. 17d). These data demonstrate that Nano-MgB₂ triggers damage to the bacterial membrane.

Metal cations are often responsible for disrupting the bacterial membrane by altering the membrane potential and permeability. The reaction between MB and LPS on the cell wall not only produces a focal source of metal ions but also narrows the distance between metal cations and cell membrane³⁸. Therefore, we first measured the change of the membrane potential in bacteria treated with Nano-MgB₂ and H₃BO₃ + Mg²⁺ using the fluorophore dye DiSC₃(5) (a cyanine dye that shows increased fluorescence upon dissipation of the membrane potential)³⁹. As shown in Fig. 4f, Nano-MgB₂ significantly changed the membrane potential compared to the blank and H₃BO₃ + Mg²⁺ groups, indicating that a focal source of Mg²⁺ from Nano-MgB₂ damages the cell membrane by changing the membrane potential. Next, we detected the permeability of bacterial membranes after Nano-MgB₂ treatment. P. aeruginosa and S. aureus treated with H₃BO₃ + Mg²⁺ and Nano-MgB₂ were stained with SYTO9 and propidium iodide (PI). SYTO9 is a green-fluorescent dye that freely permeates cell membranes and shows a large increase in fluorescence upon binding to nucleic acids. PI is a red-fluorescent dye that can specifically bind to DNA or RNA to enhance fluorescence but cannot pass through the intact membranes of viable cells³⁹. As shown in Fig. 4g and Supplementary Fig. 17e, Nano-MgB₂-treated group exhibited a large number of bacteria with red fluorescence (PI staining), compared with the blank and H₃BO₃ + Mg²⁺ groups, suggesting that Nano-MgB₂ significantly increased the membrane permeability of bacteria. Next, we stained the bacteria with PI and performed fluorescence-activated cell sorting (FACS) to further quantify permeability changes in bacteria in the presence of Nano-MgB₂. As shown in Fig. 4h and Supplementary Fig. 17f, Nano-MgB₂ induced a dramatical change in membrane permeability (96.8% in P. aeruginosa and 89.0% in S. aureus) than that of H₃BO₃ + Mg²⁺ (14.9% in P. aeruginosa and 5.91% in S. aureus). Taken together, these data suggest that Nano-MgB₂ induces cell membrane damage by altering the membrane potential and permeability.

To further investigate the molecular mechanism by which Nano-MgB₂ induces bacteria death, RNA-seq was performed to screen for changes in gene expression in Nano-MgB₂-treated P. aeruginosa. As shown in Supplementary Fig. 18, Nano-MgB₂ down-regulated 1984 genes and upregulated 1918 genes. Furthermore, Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis of known Nano-MgB₂-related genes was performed. Numerous important pathways such as ‘ribosome’, ‘aminoacyl-tRNA biosynthesis’, and ‘Protein export’ were enriched, and most genes in these pathways were upregulated in Nano-MgB₂-treated P. aeruginosa, suggesting that Nano-MgB₂ induced a stress response (Fig. 4i). Interestingly, the RNA degradation pathway was enriched, and 14 of the 16 related genes were upregulated after Nano-MgB₂ treatment (Fig. 4j). Accordingly, we verified the expression of these 16 genes in P. aeruginosa treated with Nano-MgB₂ using QPCR. As shown in Fig. 4k, l, Nano-MgB₂ significantly promoted the expression of these 16 RNA degradation-related genes, consistent with the results of RNA-seq. These data suggest that Nano-MgB₂ kills bacteria by promoting RNA degradation. Indeed, previous studies showed that RNA was degraded in response to changes in membrane permeability^40,41. Thus, these data demonstrate that Nano-MgB₂ reacts with LPS in the cell wall continuously releasing Mg²⁺ at the cell membrane, which disrupts the bacterial membrane, leading to RNA degradation and bacterial death (Fig. 4m).

Nano-MgB₂ suppressed dead bacteria- and LPS-induced inflammation in vitro

To further investigate whether Nano-MgB₂ inhibits inflammation induced by dead bacteria or dead bacteria-released endotoxin (LPS), we first assessed the toxicity of Nano-MgB₂ towards human cell lines, including skin keratinocytes (HaCat cells) and immunocytes (Raw264.7 macrophages) using cell counting kit-8 (CCK-8). As shown in Supplementary Fig. 19, Nano-MgB₂ was not toxic to skin keratinocytes and immunocytes after incubation for 24 h, and the components released from Nano-MgB₂ such as Mg²⁺ and H₃BO₃ showed no toxicity towards keratinocytes. Next, we treated macrophage cells with LPS or dead bacteria (HIB, heat-inhibited bacteria) in the presence or absence of Nano-MgB₂. As shown in Fig. 5a, b, LPS and HIB dramatically induced the expression of inflammation-related molecules such as tumor necrosis factor α (TNF-α), interleukin 6 (IL-6), and interleukin 1beta (IL-1β), which were significantly inhibited after treatment with Nano-MgB₂. These results indicate that dead bacteria and dead bacteria-released endotoxin (LPS) can significantly induce a strong inflammatory response in immune cells and Nano-MgB₂ can interact with LPS to block the inflammatory response. As previously reported, LPS can activate Toll-like receptor 4 and induce the production of inflammatory factors by regulating the mitogen-activated protein kinase (MAPK) signaling pathway^42,43. As shown in Fig. 5c–e, LPS-induced phosphorylation of MAPK such as p38, Erk, and JNK were significantly inhibited by Nano-MgB₂ treatment, suggesting that Nano-MgB₂ blocks HIB/endotoxin (LPS)-induced inflammation by regulating MAPK signaling pathway (Fig. 5f).

**Fig. 5: Nano-MgB₂ inhibited LPS- and dead bacteria-induced inflammation in Macrophage.**

Nano-MgB₂ inhibited bacterial survival in vivo

To evaluate the in vivo antibacterial efficacy of Nano-MgB₂, a P. aeruginosa-infected skin infection model was constructed. As shown in Fig. 6a, the P. aeruginosa infection-induced lesion area was significantly inhibited by Nano-MgB₂ treatment. Consistently, the number of bacteria in the lesions was also decreased (Fig. 6b). As bacterial infections can progress from a local to systemic state, the number of bacteria in the spleen was also decreased by Nano-MgB₂ treatment (Fig. 6c). To further investigate the effect of Nano-MgB₂ on P. aeruginosa-infected skin tissue, the skin lesion areas were dissected using hematoxylin and eosin (H&E) staining. As shown in Fig. 6d, the bacteria-infected skin showed severely destroyed epithelia cells in the epidermis and increased lipogenesis and hematoxylin-positive cells in the dermis. After Nano-MgB₂ treatment, the epidermal epithelialization was accelerated, and the lipogenesis and hematoxylin-positive cells were dramatically decreased in the dermis, indicating the decrease of inflammation. Furthermore, the granulation tissues were transferred into the scar tissue with more fibroblasts, demonstrating that the infected skin was repaired after Nano-MgB₂ treatment. To determine whether the increased hematoxylin-positive cells were inflammatory cells, we performed immunofluorescence staining with the neutrophil cell marker myeloperoxidase (MPO)^44,45 and macrophage cell marker F4/80^46,47. As shown in Fig. 6e, Nano-MgB₂ treatment significantly decreased the number of P. aeruginosa-induced neutrophils and macrophages, indicating decreased skin infection after Nano-MgB₂ treatment. Consistently, inflammatory factors such as IL-6, TNF-α, and monocyte chemoattractant protein (MCP)-1 were inhibited after Nano-MgB₂ treatment (Fig. 6f). Similar results were observed in mice infected with S. aureus in the presence of Nano-MgB₂. Nano-MgB₂ significantly inhibited the increase of lesional size in the S. aureus-infected skin (Supplementary Fig. 20a, b) and bacteria numbers in the skin and spleen (Supplementary Fig. 20c–f). Furthermore, inflammatory factors such as IL-6, TNF-α, and MCP-1 were significantly inhibited (Supplementary Fig. 20g, h). These data demonstrate that Nano-MgB₂ can inhibit bacteria growth and decrease bacteria-induced inflammation in vivo.

**Fig. 6: Nano-MgB₂ inhibited skin infection in vivo.**

Nano-MgB₂ suppressed dead bacteria-induced skin inflammation in vivo

Beside bacteria infection, the dead bacteria also induce excessive inflammation in the skin. For example, LPS can be released from the bacterial surface upon bacteria die or lyse. This free LPS, called endotoxin, can induce excessive inflammation and toxicity to the host. As shown in Fig. 7a, dead bacteria significantly cause the redness and swelling of the skin, and this phenomenon was dramatically inhibited after Nano-MgB₂ treatment. To further investigate the inflammatory conditions and histopathological within the skin, the skin lesional areas were dissected for H&E and immunofluorescence staining. As shown in the H&E staining images, no obvious pathological changes in the epidermis were observed in the HIB-treated skin. Comparatively the lipogenesis and hematoxylin-positive cells were dramatically increased in the dermis, and these phenomena were dose-dependently inhibited by the Nano-MgB₂, indicating that Nano-MgB₂ may inhibit dead bacteria-induced inflammatory response (Fig. 7b). Consistent result was showed in immunofluorescence staining that Nano-MgB₂ significantly decreased the number of neutrophils (MPO-positive cells) and macrophages (F4/80-positive cells) induced by dead bacteria (Fig. 7c, d). Furthermore, the inflammatory factors such as IL-6, TNF-α, and MCP-1 were also significantly inhibited after Nano-MgB₂ treatment (Fig. 7e). All these data demonstrate that even dead bacteria can induce serious skin inflammation, and Nano-MgB₂ can inhibit dead bacteria-induced inflammation.

**Fig. 7: Nano-MgB₂ inhibited dead bacteria-induced skin inflammation in vivo.**

Nano-MgB₂ promoted infected-wound healing in vivo

Because of the excellent antibacterial and anti-inflammatory activities of Nano-MgB₂ both in vitro and in vivo, we next investigated the function of Nano-MgB₂ in P. aeruginosa-infected skin wound healing. As shown in Fig. 8a, b, 50 µg of Nano-MgB₂ clearly accelerated the healing rate of P. aeruginosa-infected wound. Furthermore, the number of P. aeruginosa in the skin and spleen was significantly reduced after Nano-MgB₂ treatment (Fig. 8c). To further investigate the histopathological alterations within the wound, the wounds were collected on day 12 and the section was cut for H&E staining. As shown in Fig. 8d, the epidermal layer in the infected wound is still incomplete. Necrotic cells along with a large number of hematoxylin-positive cells were seen in the wound area in the infected wound. However, in the Nano-MgB₂ treatment group, the epithelization was complete, and the wound was covered by a full layer of epidermal. Furthermore, the number of necrotic cells and the hematoxylin-positive cells was dramatically decreased, when compared with that of infected wounds. In addition, the results of immunofluorescence staining showed that Nano-MgB₂ treatment significantly reduced the number of neutrophils (MPO-positive cells) and macrophages (F4/80-positive cells), indicating decreased bacterial infection and inflammation after Nano-MgB₂ treatment (Fig. 8e). Moreover, inflammatory factors such as TNF-α and IL-6 were dramatically decreased after Nano-MgB₂ treatment, further demonstrating decreased bacterial infection and inflammation in Nano-MgB₂-treated wounds (Fig. 8f). These results are consistent with those observed in S. aureus-infected skin wounds treated with Nano-MgB₂. Nano-MgB₂ significantly promoted S. aureus-infected skin wound healing (Supplementary Fig. 21a, b) and inhibited bacterial growth in the skin (Supplementary Fig. 21c, d). Furthermore, hematoxylin-positive cells and inflammatory factors such as TNF-α, IL-6, and MCP-1 were significantly inhibited (Supplementary Fig. 21e, f). In addition, the mRNA expression level of the oxidative stress gene Hmox1 was dramatically decreased in Nano-MgB₂-treated wounds, when compared with the untreated group, suggesting that Nano-MgB₂ decreases oxidative stress through its ROS-scavenging activity (Supplementary Fig. 22). These data demonstrate that Nano-MgB₂ promotes wound healing by inhibiting bacterial growth, bacteria-induced excessive inflammation, and oxidative stress.

**Fig. 8: Nano-MgB₂ enhanced infected-wound healing.**

Discussion

Bacteria and bacteria-induced excessive inflammation are involved in the healing of infected wounds. Wound treatment strategies that simultaneously inhibit both bacterial infection and dead-bacteria-induced excessive inflammation are urgently needed in the clinic. LPS/PGN is the key structural and functional component of bacteria that is crucial for ensuring bacterial survival and pathogenicity. Therefore, targeting LPS/PGN is a promising strategy for simultaneously inhibiting live bacterial infection and dead bacteria-induced excessive inflammation, leading to bacteria-infected wound healing. In this study, we proposed a boron-trapping strategy to trap LPS/PGN from escaping or moving by forming stable borate ester bonds between MB NPs and diol of LPS/PGN, resulting in excellent antibacterial and anti-inflammatory effects, finally promoting infected wound healing.

Currently, LPS-binding peptides have been reported to react with LPS or LPS-related receptors, exhibiting antibacterial or anti-inflammatory effects. For example, HVF18 (HVFRLKKWIQKVIDQFGE), a Thrombin-derived C-terminal peptide, can bind to LPS. The binding of the HVF18 to LPS competitively blocks CD14–LPS interaction, thus interfering with TLR4 dimerization and the downstream inflammatory responses¹⁰. However, this peptide has no antibacterial activity. In addition, antimicrobial peptides, such as cathelicidins, are able to bind to LPS, suppressing LPS-induced pro-inflammatory responses¹⁷. However, the proteolytic stability of peptides limits their application. Therefore, compared with LPS-binding peptides, MB NPs can consistently and stably trap LPS/PGN, exerting its excellent antibacterial and anti-inflammatory effects.

Recently, advances in nanotechnology have led to the development of metal nanomaterials and 2D materials, which exhibit antimicrobial properties. Metals such as silver and magnesium oxide have been utilized for their antimicrobial properties for thousands of years. The mechanisms responsible for the metal nanomaterials were derived from the production of ROS and the metal cations. Two-dimensional (2D) materials such as nanosheets and nanoplatelets have been reported as potential antimicrobials. The general antimicrobial mechanisms include cell membrane damage, charge transfer, ROS production, and oxidative stress. Compared with metal nanomaterials and 2D antibacterial materials, MB NPs possess the unique hydrolytic two-dimensionalization characterization and biological activity (Supplementary information Table 1). MB NPs belong to the interstitial compound, which is composed of intralayer boron-boron (B–B) covalent bonds and interlayer boron–metal (B–M) ion bonds⁴⁸. During the hydrolysis process, the interlayer B–M bonds are preferentially broken to form boron–hydrogen (B–H) bonds, at the same time, metal ions, as well as hydroxides are released, and the morphology of MB NPs gradually becomes two-dimensional²⁶. The specific surface area of MB NPs gradually increased during the hydrolysis process, which realized the continuous provision of the boron dihydroxyl groups, ensuring a long-time interaction between MB NPs and LPS/PGN. Furthermore, the gradually released hydroxides from MB NPs hydrolysis can regulate the configuration of boron atom, which is helpful to form stable borate ester bonds between MB NPs and LPS/PGN. This gradually provided boron dihydroxyl groups and the released hydroxides during the hydrolysis of MB NPs significantly improved the ability of MB NPs to trap LPS/PGN, which not only effectively enhanced the local cation concentration, destroying the bacterial cell membrane and achieving a strong antibacterial effect, but also complexed dead bacteria-released LPS and PGN to inhibit excessive inflammation, finally promoting wound healing. Taken together, the hydrolytic two-dimensional feature of MB NPs significantly enhances the biological function of MB NPs, which is distinct from other traditional metal nanomaterials and 2D antimicrobial materials, both in terms of material structure and biological mechanism.

In this study, MB NPs were synthesized using improved Self-propagating high-temperature synthesis as previously reported by our group³⁶. The SHS process utilizes the exothermic heat of the reaction to synthesize materials, and its spontaneous-sustaining, fast-propagating nature endows this technique with the ability for the large-scale synthesis of MB NPs^49,50. In addition, we can change the reaction conditions, such as gas atmosphere, or heating/cooling rate⁵¹, to realize the crystallization of synthetic materials in nanoscale. Therefore, these MB NPs have the prospect of clinical transformation.

In this study, MB NPs exhibited higher LPS/PGN-trapping activities than other materials containing boron dihydroxyl groups. This is because the local alkaline microenvironment generated by hydrolysis of MB NPs could enhance the stability of borate ester bonds to effectively improve the binding ability of MB NPs to bacterial polysaccharides. Boron dihydroxyl groups interact with 1,2- or 1,3-diols of polysaccharides to form cyclic esters. If the boron atom is in a planar trigonal configuration (sp² hybridized), the corresponding boronic ester bond is affected by the relatively large ring strain, which is prone to bond breakage. If the boron atom is in a tetrahedral configuration (sp³ hybridized), the ring tension of the O–B–O bond can be effectively relieved, making the overall structure of the boronate eater bond more stable⁴². Because MB NPs can be hydrolyzed to release hydroxides, this unique feature makes the configuration of the boron atom of its hydrolyzed product change from sp² to sp³ configuration. Furthermore, the DFT calculations show that the strength of the borate ester bonds formed by the hydrolysate of MB NPs is stronger than that of H₃BO₃. Therefore, MB NPs formed more stable boronic ester bonds than sp²-hybridized H₃BO₃.

The inhibition efficacy of Nano-MgB₂ against Gram-positive bacteria was lower than that against Gram-negative bacteria. This is because the LPS of P. aeruginosa contains much more 1,2-diol or 1,3-diol compared to PGN of S. aureus, thus much more Nano-MgB₂ reacted with LPS than with PGN, supporting the importance of generating borate ester bonds to achieve antibacterial and anti-inflammatory activities. In addition to the bacteria, this strategy may also be suitable for the treatment of virus infection. Trapping the key component of the virus, such as the spike glycoprotein of SARS-CoV-2, which is the shell protein of the virus and mediates the fusion of the virus membrane with the host cell membrane¹⁷, may provide a therapeutic method for virus infection.

Another interesting finding is that all three types of MB NPs (MgB₂, AlB₂, and BeB_x) showed antibacterial activity but exhibited variable activities against P. aeruginosa, indicating that different ions in the NPs have different antibacterial roles. It is generally accepted that metal cations often disrupt the bacterial membrane. Consistently, our study confirmed that Nano-MgB₂ disrupted bacterial membranes through altering the membrane potential and permeability. However, the cause of the varied antibacterial activity among these metal cations requires further investigation.

In conclusion, we introduced a boron-trapping strategy for inhibiting the survival and pathogenicity of a pathogen by trapping the key component of the pathogen. Specifically, we designed and synthesized a series of MB NPs to trap LPS/PGN, the key component of Gram-negative bacteria and Gram-positive bacteria, respectively. Both in vitro and in vivo data demonstrated that the formation of a stable borate ester bond between MB NPs and LPS/PGN not only inhibited bacterial survival but also decreased the excessive inflammation induced by dead bacteria. These effects ultimately promoted the healing of infected wounds. Our findings provide a strategy of trapping the key component of a pathogen to promote the pathogen-infected wound healing.

Methods

Chemical reagents

All the chemical reagents were of analytical grade and used directly without further purification. Magnesium powder (Mg, 99.9%, AR), Aluminum (Al, 99.9%, AR), Beryllium (Be, 99.9%, AR), and Boron (B, 99.9%, AR) powder were purchased from Aladdin. Anhydrous ethanol was purchased from Sigma-Aldrich. The ultrapure water used throughout the experiment was prepared by the ELGA PURELAB classic water purification system.

Material characterization

Transmission electron microscope (TEM) images and corresponding element mapping were obtained with Thermo Fisher Scientific Tecnai G2 F30. Scanning electron microscope (SEM) images were acquired by HITACHI S-480. X-ray diffraction (XRD) data were acquired from a Rigaku D/MAX 2250 V diffractometer with a scanning rate of 5° min⁻¹ in the 2θ range of 10–80°. Atomic force microscopy (AFM) images were obtained on a Dimension Fast Scan (Bruker) under ScanAsyst mode. The hydrodynamic size distribution was measured via dynamic light scattering (DLS) in Microtrac Nanotrac wave II. Fourier transform infrared spectroscopy (FTIR) spectra were obtained with a BRUKER TENSOR II using KBr pellets. The variation in pH of the hydrolysate of Nano-MgB₂ nanoparticles (MB NPs) was acquired by using a pH meter (FE28, METTLER TOLEDO). Element concentration was obtained with inductively coupled plasma optical emission spectrometry (ICP-OES) by Agilent Technologies. The X-ray photoelectron spectroscopy (XPS) plots were conducted with a Thermo Fisher Scientific Escalab 250Xi, and the accurate binding energies were determined by taking the position of C 1s peak at 284.8 eV as the calibration reference. Electron spin resonance (ESR) spectra were acquired from the JEOL FA200 electron paramagnetic resonance spectrometer. The ultraviolet-visible absorption spectra (UV-vis) were recorded on the Shimadzu UV-3600 Plus spectrophotometer.

Synthesis of MB NPs

The MB NPs (Nano-MgB₂, Nano-AlB₂, and Nano-BeB_x) were synthesized by a self-propagating high-temperature synthesis (SHS) approach. Typically, 30 mM of metal powder (Mg, Al, or Be) and 40 mM of boron powder were fully ground and placed in a 15 mL corundum crucible. The mixture reacted at 800 °C under an Ar (5% O₂) atmosphere for 3 h with a heating rate of 10 °C/min. Then the resultant products were dispersed in 200 mL anhydrous ethanol and centrifuged at 2775 × g for 5 min to remove large particles. Subsequently, the NPs were collected by centrifugation at 18,759 × g for 15 min and then washed several times with ethanol.

The temporal variation in the pH and of Nano-MgB₂ hydrolysate

1 mL Nano-MgB₂ solution (1 M Nano-MgB₂) was sealed in a dialytic bag (cutoff molecular weight: 5000 Dalton). Then the dialytic bag was placed in a beaker containing 100 mL citric acid-sodium citrate buffer solutions of various pH values (7.5, 6.5, and 4.5) and processed in a shaker at 37 °C for 24 h (shaking speed: 100 rpm). At regular intervals, the pH value was detected by a pH meter. 1 mL solution was collected to determine the release concentration of Mg and B elements by using ICP-OES, and 1 mL fresh buffer solution was returned.

Theoretical simulation

The DFT calculations were conducted based on the Vienna Ab-inito Simulation Package (VASP). The projector-augmented wave (PAW) method and the Perdew-Burke-Ernzerhof (PBE) exchange-correlation functional supplied with the VASP package were employed for B (s2p1 06Sep2000), O (s2p4 08Apr2002), H (ultrasoft test 15Jun2001), and C (s2p2 08Apr2002). For structural optimization including Boron ring, the positions of Boron were fixed when the others were fully relaxed. The kinetic energy cutoff of the plane wave basis set was chosen to be 520 eV and the Brillouin zone integration is performed with only Gamma point due to large enough cell parameters. An energy tolerance of 1.0 × 10⁻⁵eV and a maximum displacement of 1.0 × 10⁻²Å were considered. The COHP was calculated using a lobster package.

Verification of scavenging effect of Nano-MgB₂ on hydroxyl radical (•OH)

Using 5,5-Dimethyl-1-pyrroline N-oxide (DMPO) as the spin trap, electron spin resonance (ESR) spectroscopy was used to confirm the •OH scavenging effect of Nano-MgB₂. 100 μL citric acid-sodium citrate buffer solution was prepared (pH = 6.5, 20 μM FeSO₄), and Nano-MgB₂ NPs were added to the experimental group (100 μg/mL, without Nano-MgB₂ in the control group), then 20 μL of the mixed solution was added (5 mM H₂O₂ and 100 mM DMPO) after 15 min. The obtained mixture solution was detected by an ESR spectrometer at room temperature.

Verification of scavenging effect of Nano-MgB₂ on ROS and RNS

The ability of Nano-MgB₂ to scavenge ROS and RNS was demonstrated by PTIO• and DPPH• scavenging experiments, respectively. PTIO• radicals were dissolved with pH = 7.5 phosphate buffer at a concentration of 25 μg/mL (DPPH• radicals were dissolved in anhydrous ethanol at a concentration of 20 μg/mL), then various concentrations of Nano-MgB₂ (from 0 to 400 μg/mL) were added. The total volume of the reaction mixture remains the same by the addition of the corresponding reagent. The mixed solution was incubated at 37 °C for 2 h in a water bath under dark conditions, the absorbance was measured at 557 nm (519 nm for DPPH•) by UV-vis absorption spectra.

Bacterial culture and antibacterial activity test

Staphylococcus aureus (ST398) and Pseudomonas aeruginosa (PA-14) were from Jiang’s lab at East China Normal University. S. aureus were cultured in Trypticase Soy Broth (TSB) and P. aeruginosa were grown in Luria-Broth medium (LB). One day before the experiment, bacteria were incubated overnight in a culture medium at 37 °C (220 rpm shaking), and a small aliquot of cells (4%) was re-inoculated into a fresh culture medium and then grew to logarithmic phase S. aureus, OD = 0.6–0.8, about 10⁸ bacteria; P. aeruginosa, OD = 0.5, about 10⁹ bacteria. The P. aeruginosa were diluted to 10⁸/mL colony-forming units, and the S. aureus were diluted to 10⁷/mL colony-forming units. Ten microliters of live bacteria were incubated with different concentrations of Nano-MgB₂ at 37 °C for 6 h, The bacteria from the mixture were diluted and plated on TSB or LB agar for 24 h at 37 °C, respectively. Finally, the number of colonies were counted. For antibacterial activities of the antibiotics, ten microliters of live bacteria were incubated with Nano-MgB₂ (12.5 μg/mL for P. aeruginosa, 1 mg/mL for S. aureus) and different kinds of antibiotics (Thermo Fisher Scientific Cat GN4F, 16 μg/mL) for 6 h and 24 h. Antibiotics for P. aeruginosa infection include aminoglycosides (gentamicin, amikacin), carbapenems (imipenem, meropenem), cephalosporins (ceftazidime, cefepime), fluoroquinolones (ciprofloxacin, levofloxacin), penicillin with β-lactamase inhibitors (BLI) (ampicillin/sulbactam), monobactams (aztreonam); Antibiotics for S. aureus include cephalexin (Sangon Biotech (A600280-0005), erythromycin (Sangon Biotech A600192-0025), and mupirocin (Sangon Biotech A606674-0500).

Live/dead fluorescent staining and Flow cytometry

P. aeruginosa (10⁸/mL) treated with 272 μM Nano-MgB₂ (12.5 μg/mL) or 544 μM H₃BO₃ + Mg²⁺ for 3 h were stained with SYTO9 (Thermo Fisher Scientific Cat 2266591 6 μM) and Propidium iodide (Beyotime Cat ST511, 15 μM) for 15 min at room temperature in the dark. For S. aureus, S. aureus (1 × 10⁸) were incubated with 10.88 mM Nano-MgB₂ (500 μg/mL) or 21.76 mM H₃BO₃ + Mg²⁺ for 3 h. The live and dead cells were visualized with confocal laser microscopy (Nikon A1 + R-980). For the Flow cytometry assay, bacteria treated with Nano-MgB₂ and H₃BO₃ + Mg²⁺ for 3 h were added with 15 μM Propidium iodide and incubated for 30 min in the dark. Flow cytometry was performed using FACScan (BD LSRFortessa X-20). The gating strategy for the Flow cytometry was listd as follows. First, using Forward Scatter Area (FSA) and Side Scatter Area (SSA) to find the main group of bacteria; second, using SSA and SSH(Side Scatter High) to remove adherent bacterial populations; last, using SSA and PE to display the positive cell population of dead bacteria (Supplementary Fig. 23).

Preparation of bacterial samples for SEM/TEM

Bacteria (1 × 10⁹) were collected and treated with 272 μM Nano-MgB₂ (12.5 μg/mL) and 544 μM H₃BO₃ + Mg²⁺ for 3 h, and then washed with PBS and fixed in 2.5% glutaraldehyde solution. After being washed with PBS and dehydrated by ethanol, bacteria were analyzed with SEM (ZEISS) Gemini300 and elemental mapping (OXFORD Xplore). For TEM analysis. Bacteria were fixed with 2.5% glutaraldehyde at 4 °C and post-fixed with 1% OsO₄. The materials were then washed three times with PBS (15 min each) and dehydrated in a graded series of ethanol (15 min for each concentration). After penetration with 100% acetone, the materials were embedded with Epon 812 and successively polymerized at 37 °C for 18 h, 48 °C for 24 h, and at 60 °C for 48 h. The embedded samples were finally ultrathin-sectioned for 70 nm and stained with uranyl acetate and lead citrate for transmission electron microscopic (JEM2100, JEOL, Japan) observation and photography. For the C and B elemental mapping, 1 × 10⁹P. aeruginosa were incubated with 272 μM Nano-MgB₂ (12.5 μg/mL) or 544 μM H₃BO₃ + Mg²⁺ for 3 h; and 1 × 10⁸S. aureus were incubated with 10.88 mM Nano-MgB₂ (500 μg/mL) or 21.76 mM H₃BO₃ + Mg²⁺ for 3 h, respectively. Took 2 mL samples directly to the conductive glue and sprayed gold for 45 sec using Oxford-Quorum-SC7620. Photograph the morphology and elemental of the sample using a scanning electron microscope(GeminiSEM-300/TESCAN-MIRA-LMS).

Cytoplasmic membrane depolarization assay

The ability of Nano-MgB₂ to alter the cytoplasmic membrane electrical potential was determined using the membrane potential-sensitive dye DiSC3(5) (3,3’-Dipropylthiadicarbocyanine Iodide; MKBio). Bacteria grown at 37 °C in LB medium to mid-logarithmic phase (OD600 = 0.5) were harvested, washed once with PBS, and resuspended by a final concentration of 2 μM DiSC3(5). The mixture was then incubated for 30 min at room temperature to enable dye uptake and fluorescence quenching. The change in fluorescence was measured immediately after the addition of 272 μM Nano-MgB₂ and 544 μM H₃BO₃ + Mg²⁺ using FACScan (Beckman Coulter) for detection. The gating strategy for Flow cytometry was the same as in Live/dead fluorescent staining.

RNA isolation and QPCR

RNA isolation procedure for cells

Raw264.7 cells in a 24-well plate were washed with PBS and lysed with TRIzol (Life Technologies, Cat15596026). The total RNA was separated with chloroform, precipitated by isopropanol and washed with 75% ethanol in DEPC-treated H₂O. For tissue, the only difference from the procedure in cells is the first step. The tissue was cut into 2 mm pieces and pulverized in 1 mL TRIzol with a homogenizer at 4 °C for a total of 2 × 60 s. For bacteria, 1 mL of bacteria were collected and lysed with 100 μL lysozyme (0.4 mg/mL) for 3–5 min. After that, an Eastep Super RNA isolation kit (Shanghai Promega, LS1040) was used for RNA isolation. DNase was used to clean the genome DNA as described by the instructions.

Reverse transcription of RNA and QPCR

Each sample of RNA (1–5 μg) was reversed to cDNA using Hifair® III 1st Strand cDNA Synthesis SuperMix for QPCR (YESEN, CHINA 11141ES60) as described by the instructions. Finally, the cDNA was analyzed by Quantitative PCR using Hieff® QPCR SYBR® Green Master Mix (YESEN, CHINA, 11202ES03) on ABI real-time instruments (ABI 7500) as described by the instructions. The primers were synthetized by Tsingke Cp. Ltd (China) and listed in Supplementary information Table 2.

RNA-seq data analysis and QPCR

Total RNA was extracted using a QIAGEN RNeasy kit (catalog no. 74104) following the manufacturer’s instructions. Ribosomal RNA removal, cDNA library construction, and paired-end sequencing with NovaSeq 6000 platform (Illumina) were completed by Nanjing Personal Biotechnology Cp. Ltd (China). Gene expression values were computed from fragments per kilo bases per million fragments (FPKM) values produced by addition of a pseudocount of 1 and log2 transformation of the results. These FPKM values were used for drawing the heatmap with the pheatmap R package. Paired differential gene expression analyses were performed with DEseq R package by addition of fold change > 2 and p-value <0.05. Volcano plots of these differential genes were drawing with ggplots2 R package. KEGG enrichment analyses of differential genes were performed using clusterprofiler version 3.16.1. QPCR primers for Pseudomonas aeruginosa were synthetized by Tsingke Cp. Ltd and listed in Supplementary information Table 3.

Western blot

Protein from cells. Cells in 6-well plate were lysed with 100 μL RIPA lysis buffer on ice for 20 min (RIPA buffer: 150 mM NaCl, 1% IGEPAL CA-630, 0.5% sodium deoxycholate, 0.1% SDS, 50 mM Tris-HCl, pH 8.0 and protease inhibitors). Protein was collected from the supernatant by centrifuging at 10,625 × g at 4 °C for 20 min in a microcentrifuge. Protein from tissues. Equal amounts of lesional skins (infected skin (0.2 g), wounded skin (0.1 g)) were collected and cut into small pieces. The samples were added with ice-cold lysis buffer (RIPA, infected skin (1 mL), wounded skin (0.5 mL)) and homogenized with an electric homogenizer at 4 °C for a total of 2 × 60 s. Protein was collected from the supernatant by centrifuging at 10,625 × g at 4 °C for 20 min in a microcentrifuge.

The protocol for western blot was performed as follows⁵². Equal amounts of protein (20-30 μg) were reduced and denatured with 5×laemmli sample buffer, separated by SDS-PAGE gel, and transferred to the nitrocellulose membrane. After that, the membrane was blocked by 5% milk, incubated with the first antibody and second antibody as described by the manufacturer’s instructions. Finally, the membranes were developed by the Odyssey LI-COR instrument. The antibodies from Abways technology (China Inc.) were listed as follows: P38 antibody (Cat:CY5488, 1:1000); Pp38 antibody (Cat:CY6391, 1:1000; ERK1/2 antibody (Cat:CY5487, 1:1000); pErk1/2 antibody (Cat:CY5277, 1:1000); JNK1/2/3 antibody (Cat:CY5490, 1:1000); pJNK1/2/3 antibody (Cat:CY5541, 1:1000); GAPDH (Cat: AB0037, 1:5000). All antibodies were diluented by Antibody Diluent (Cat:P0023A, Beyotime (China Inc.). All the uncropped blots were supplied in the Source data file.

H&E and IF

The samples from the skin wound were dissected and fixed in 4% paraformaldehyde. After dehydrated in gradient alcohol, the samples were embedded in paraffin. Five micrometers of tissue sections were cut and mounted on glass slides. For H&E staining, the sections were dewaxed in xylene, rehydrated in gradient alcohol, washed briefly in distilled H₂O, stained in Harris hematoxylin solution, differentiated with 0.3% acid alcohol, and stained with eosin. After dehydrating in gradient alcohol again, the sections were cleared in xylene and mounted with a xylene-based mounting medium. For immunofluorescence assays, the sections were pretreated with antigen retrieval solution (pH = 9.0 EDTA solution) after dewaxed in xylene, stained with indicated first antibodies (MPO (Abcam ab208670, 1:100); mF4/80(Santacruz (BM8), sc-52664, 1:500) and second antibodies Alexa Fluor 594 donkey anti-rabbit, Alexa Fluor 488 donkey anti-rat according to the manufacturer’s introduction, and then mounted with DAPI-contained mounting solution. The images were scanned by 3DHISTECH CaseViewer 2.4.

Inflammation cytokine detection

Protein was collected as mentioned above. TNF-α, IL-6, and MCP-1 concentrations were detected by BD cytometric bead array (CBA) mouse inflammation kit (Catalog No. 552364) using BD FACSCalibur. The samples were prepared as follows: added 50 µL the mixed Capture Beads and 50 μL of sample to assay tubes, then added 50 µL the Mouse Inflammation PE Detection Reagent to each tube. Incubated for 2 h at room temperature in the dark. Added 1 mL wash buffer and centrifuged at 200 × g for 5 min. Resuspended in 300 μL wash buffer. Detected by flow cytometry and analyzed by FCAP Array software.

Animals

Balb/c mice (7–8 weeks) were purchased from Charles River (CHINA Inc). All the experiments were bred separately and housed in the specific pathogen-free (SPF) animal facilities in the East China Normal University (light/dark cycle 10 h:14 h, temperature 20–26 °C, humidity 40–70%). All mouse experiments performence were approved by the East China Normal University Animal Care and Use Committee, and the ethics number is m20170215. All the surgeries were performed under a general anesthetic condition to minimize suffering. All the mice used in the experimental groups were randomly assigned.

Cutaneous bacteria and heat-inhibited bacteria (HIB) infection in mice

The dorsal of mice were shaved and hair was removed by using chemical depilation (VEET, CHINA). For bacteria infection⁵³, bacteria in the logarithmic phase (S. aureus, OD = 0.6–0.8, about 10⁸ bacteria; P. aeruginosa, OD = 0.5, about 10⁹ bacteria) were collected and 10⁶ S. aureus or 10⁷P. aeruginosa were intradermally injected into mouse dorsal skin and then intradermally treated with indicated concentrations of Nano-MgB₂; For heat-inhibited bacteria infection⁵⁴, 2 × 10⁹ CFU/mL P. aeruginosa were washed with PBS and killed at 70 °C for 1 h in 1 mL PBS. The bacteria were diluted and plated on TSB or LB agar to make sure all the bacteria were totally killed. 2 × 10⁸ CFU heat-inhibited P. aeruginosa in 100 μL PBS with or without Nano-MgB₂ were intradermally injected into mouse dorsal skin. The lesions were photographed and measured by Image J software. Mice were euthanized on day 3 and the lesional skins were collected and homogenized to determine the survival number of bacteria. In some experiments, the lesional skins were collected for H&E staining, QPCR, and inflammation cytokine detection.

Cutaneous-infected wound in mice

Mouse skins were shaved as mentioned above. Excisional dorsal skin wounds were made with an 8 mm sterile biopsy punch as previous report and then infected with 10⁶ S. aureus or 10⁷P. aeruginosa in the presence or absence of Nano-MgB₂⁵⁵. The wounds were finally covered with a special kind of plastic sticker (Tegaderm Film, 3M, XH003801525), the wound areas were photographed at the indicated times and calculated by Image J. The mice were euthanized and the skin surrounding the wound edges was collected for H&E staining, QPCR, and Elisa. In some experiments, the whole lesional skins were collected and homogenized to determine the survival number of bacteria.

Statistical analysis and reproducibility

The GraphPad Prism 8.0 was used for statistical analysis. All data are representative of at least three independent experiments with similar results, and the data are presented as means ± SEM. A two-tailed t-test was used to determine the significance between the two groups. One-way or two-way ANOVA with Bonferroni post test was used to analyze multiple groups. For all the statistical tests, P values <0.05 were considered to be statistically significant.

Reporting summary

Further information on research design is available in the Nature Portfolio Reporting Summary linked to this article.

Data availability

The main data supporting the results in this study are available within the paper and its Supplementary Information. All data generated in this study are available from the corresponding authors. The RNA-seq data are deposited in the Gene Expression Omnibus (GEO) database under the identification number GSE218031. These data can be accessed by https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE218031. The source data of linear graph and column diagram are provided as a Source data file 1. The source data of uncropped scans of Western blots in the figures are provided as a Source data file 2. Source data are provided with this paper.

References

Li, S., Renick, P., Senkowsky, J., Nair, A. & Tang, L. Diagnostics for wound infections. Adv. Wound Care 10, 317–327 (2021).
Article Google Scholar
Xue, M., Zhao, R., Lin, H. & Jackson, C. Delivery systems of current biologicals for the treatment of chronic cutaneous wounds and severe burns. Adv. Drug Deliv. Rev. 129, 219–241 (2018).
Article CAS PubMed Google Scholar
Chin, J. S., Madden, L., Chew, S. Y. & Becker, D. L. Drug therapies and delivery mechanisms to treat perturbed skin wound healing. Adv. Drug Deliv. Rev. 149-150, 2–18 (2019).
Article CAS PubMed Google Scholar
Shaw, Z. L. et al. Antipathogenic properties and applications of low-dimensional materials. Nat. Commun. 12, 3897 (2021).
Article CAS PubMed PubMed Central Google Scholar
Ovington, L. Bacterial toxins and wound healing. Ostomy Wound Manag. 49, 8–12 (2003).
Google Scholar
Haidari, H. et al. Multifunctional ultrasmall AgNP hydrogel accelerates healing of S. aureus infected wounds. Acta Biomater. 128, 420–434 (2021).
Article CAS PubMed Google Scholar
Sang, Y. et al. Construction of nanozyme‐hydrogel for enhanced capture and elimination of bacteria. Adv. Func. Mater. 29, 1900518 (2019).
Article Google Scholar
Kohanski, M. A., Dwyer, D. J. & Collins, J. J. How antibiotics kill bacteria: from targets to networks. Nat. Rev. Microbiol. 8, 423–435 (2010).
Article CAS PubMed PubMed Central Google Scholar
Rippon, M. G., Westgate, S. & Rogers, A. A. Implications of endotoxins in wound healing: a narrative review. J. Wound Care 31, 380–392 (2022).
Article PubMed Google Scholar
Saravanan, R. et al. Structural basis for endotoxin neutralisation and anti-inflammatory activity of thrombin-derived C-terminal peptides. Nat. Commun. 9, 2762 (2018).
Article PubMed PubMed Central Google Scholar
Gjodsbol, K. et al. Multiple bacterial species reside in chronic wounds: a longitudinal study. Int. Wound J. 3, 225–231 (2006).
Article PubMed PubMed Central Google Scholar
Wrighton, K. H. Bacterial physiology: bridging the gap for lipopolysaccharides. Nat. Rev. Microbiol. 16, 184–185 (2018).
Article CAS PubMed Google Scholar
Yang, X. et al. Bacterial endotoxin activates the coagulation cascade through gasdermin D-dependent phosphatidylserine exposure. Immunity 51, 983–996 (2019).
Article CAS PubMed Google Scholar
Deng, M. et al. The endotoxin delivery protein HMGB1 mediates caspase-11-dependent lethality in sepsis. Immunity 49, 740–753 (2018).
Article CAS PubMed PubMed Central Google Scholar
Shibusawa, K., Murakami, T., Yomogida, S., Tamura, H. & Nagaoka, I. Antimicrobial cathelicidin peptide CAP11 suppresses HMGB1 release from lipopolysaccharide-stimulated mononuclear phagocytes via the prevention of necrotic cell death. Int. J. Mol. Med. 23, 341–346 (2009).
CAS PubMed Google Scholar
Rosenfeld, Y., Papo, N. & Shai, Y. Endotoxin (lipopolysaccharide) neutralization by innate immunity host-defense peptides. Peptide properties and plausible modes of action. J. Biol. Chem. 281, 1636–1643 (2006).
Article CAS PubMed Google Scholar
Giuliani, A., Pirri, G. & Rinaldi, A. C. Antimicrobial peptides: the LPS connection. Methods Mol. Biol. 618, 137–154 (2010).
Article CAS PubMed Google Scholar
Sampath, V. Bacterial endotoxin-lipopolysaccharide; structure, function and its role in immunity in vertebrates and invertebrates. Agric. Nat. Resour. 52, 115–120 (2018).
Google Scholar
Dong, H. et al. Structural basis for outer membrane lipopolysaccharide insertion. Nature 511, 52–56 (2014).
Article CAS PubMed Google Scholar
Chen, W., Zhen, X., Wu, W. & Jiang, X. Responsive boron biomaterials and their biomedical applications. Sci. China.: Chem. 63, 648–664 (2020).
Article CAS Google Scholar
Ni, N. et al. Probing the general time scale question of boronic acid binding with sugars in aqueous solution at physiological pH. Bioorg. Med. Chem. 20, 2957–2961 (2012).
Article CAS PubMed PubMed Central Google Scholar
Yuanyuan, M., Hanting, L., Jinghong, M. & Jinghua, G. Glucose-responsive hydrogels based on phenylboronic acid. Mater. Sci. Forum 913, 714–721 (2018).
Article Google Scholar
Marco-Dufort, B. & Tibbitt, M. W. Design of moldable hydrogels for biomedical applications using dynamic covalent boronic esters. Mater. Today Chem. 12, 16–33 (2019).
Article CAS Google Scholar
Peters, J. A. Interactions between boric acid derivatives and saccharides in aqueous media: structures and stabilities of resulting esters. Coord. Chem. Rev. 268, 1–22 (2014).
Article CAS Google Scholar
Wang GSaB. A detailed examination of boronic acid-diol complexation. Tetrahedron 58, 5291–5300 (2002).
Article Google Scholar
Nishino, H. et al. Formation mechanism of boron-based nanosheet through the reaction of MgB₂ with water. J. Phys. Chem. C. 121, 10587–10593 (2017).
Article CAS Google Scholar
Kadri, M. T., Derradji, N. E. & Belkhir, H. Elastic and electronic properties of fluorite-like boride Be2B and its ternary compounds XBeB (X= Na, Mg, Al) from first principles. Inorg. Chem. Front. 247, 41–47 (2010).
CAS Google Scholar
Ikram, M. et al. Doping of Mg on ZnO nanorods demonstrated improved photocatalytic degradation and antimicrobial potential with molecular docking analysis. Nanoscale Res. Lett. 16, 78 (2021).
Article CAS PubMed PubMed Central Google Scholar
Greg, S. & Binghe, W. A detailed examination of boronic acid–diol complexation. Tetrahedron 58, 5291–5300 (2002).
Article Google Scholar
Ikram, M. et al. Impact of Bi doping into boron nitride nanosheets on electronic and optical properties using theoretical calculations and experiments. Nanoscale Res. Lett. 16, 82 (2021).
Article CAS PubMed PubMed Central Google Scholar
Qumar, U. et al. Synergistic effect of Bi-doped exfoliated MoS₂ nanosheets on their bactericidal and dye degradation potential. Dalton Trans. 49, 5362–5377 (2020).
Article CAS PubMed Google Scholar
Hassan, J. et al. h-BN nanosheets doped with transition metals for environmental remediation; a DFT approach and molecular docking analysis. Mater. Sci. Eng., B 272, 115365–115379 (2021).
Article CAS Google Scholar
Ikram, M. et al. Bactericidal behavior of chemically exfoliated boron nitride nanosheets doped with zirconium. Appl. Nanosci. 10, 2339–2349 (2020).
Article CAS PubMed PubMed Central Google Scholar
Raza, A. et al. Liquid-phase exfoliated MoS₂ nanosheets doped with p-type transition metals: a comparative analysis of photocatalytic and antimicrobial potential combined with density functional theory. Dalton Trans. 50, 6598–6619 (2021).
Article CAS PubMed Google Scholar
Raza, A. et al. Molecular docking and DFT analyses of magnetic cobalt doped MoS₂ and BN nanocomposites for catalytic and antimicrobial explorations. Surf. Interfaces 27, 101571–101587 (2021).
Article CAS Google Scholar
Chen, Z. D. N., Yanyan, L., Heliang, Y., Wenbo, B. & Jianlin, S. Magnesium silicide nanoparticles as a deoxygenation agent for cancer starvation therapy. Nat. Nanotechnol. 121, 378–386 (2017).
Google Scholar
Badica, P. et al. Antibacterial composite coatings of MgB₂ powders embedded in PVP matrix. Sci. Rep. 11, 9591 (2021).
Article CAS PubMed PubMed Central Google Scholar
Slavin, Y. N., Asnis, J., Hafeli, U. O. & Bach, H. Metal nanoparticles: understanding the mechanisms behind antibacterial activity. J. Nanobiotechnol. 15, 65 (2017).
Article Google Scholar
Sun, Y. et al. CCN1 promotes IL-1beta production in keratinocytes by activating p38 MAPK signaling in psoriasis. Sci. Rep. 7, 43310 (2017).
Article PubMed PubMed Central Google Scholar
Deutscher, M. P. Degradation of RNA in bacteria: comparison of mRNA and stable RNA. Nucleic Acid Res. 34, 659–666 (2006).
Article CAS PubMed PubMed Central Google Scholar
Surwade, P., Luxton, T., Clar, J., Xin, F. & Shah, V. Impact of the changes in bacterial outer membrane structure on the anti-bacterial activity of zinc oxide nanoparticles. J. Nanopart. Res. 22, 43–51 (2020).
Article CAS Google Scholar
Frazier, W. J., Xue, J., Luce, W. A. & Liu, Y. MAPK signaling drives inflammation in LPS-stimulated cardiomyocytes: the route of crosstalk to G-protein-coupled receptors. PLoS ONE 7, e50071 (2012).
Article CAS PubMed PubMed Central Google Scholar
Wang, W. et al. Neoagaro-oligosaccharide monomers inhibit inflammation in LPS-stimulated macrophages through suppression of MAPK and NF-kappaB pathways. Sci. Rep. 7, 44252 (2017).
Article PubMed PubMed Central Google Scholar
Amanzada, A. et al. Myeloperoxidase and elastase are only expressed by neutrophils in normal and in inflamed liver. Histochem. Cell Biol. 135, 305–315 (2011).
Article CAS PubMed PubMed Central Google Scholar
Pulli, B. et al. Measuring myeloperoxidase activity in biological samples. PLoS ONE 8, e67976 (2013).
Article CAS PubMed PubMed Central Google Scholar
Khazen, W. et al. Expression of macrophage-selective markers in human and rodent adipocytes. FEBS Lett. 579, 5631–5634 (2005).
Article CAS PubMed Google Scholar
Dos Anjos Cassado, A. F4/80 as a major macrophage marker: the case of the peritoneum and spleen. Results Probl. Cell. Differ. 62, 161–179 (2017).
Article PubMed Google Scholar
Chen, H. & Zou, X. Intermetallic borides: structures, synthesis and applications in electrocatalysis. Inorg. Chem. Front. 7, 2248–2264 (2020).
Article CAS Google Scholar
Radev, D. D., Marinov, M., Tumbalev, V., Radev, I. & Konstantinov, L. Mechanically activated self-propagated high-temperature synthesis of nanometer-structured MgB₂. Phys. C. 418, 53–58 (2005).
Article CAS Google Scholar
Su, X. et al. Self-propagating high-temperature synthesis for compound thermoelectrics and new criterion for combustion processing. Nat. Commun. 5, 4908 (2014).
Article CAS PubMed Google Scholar
He, Z., Zhang, K., Xue, J., Zhao, W. & Zhang, H. Self-propagating chemical furnace synthesis of nanograin Gd2Zr2O7 ceramic and its aqueous durability. J. Nucl. Mater. 512, 385–390 (2018).
Article CAS Google Scholar
Wu, Y. et al. Hyperglycaemia inhibits REG3A expression to exacerbate TLR3-mediated skin inflammation in diabetes. Nat. Commun. 7, 13393 (2016).
Article CAS PubMed PubMed Central Google Scholar
Li, C. et al. Interleukin-33 increases antibacterial defense by activation of inducible nitric oxide synthase in skin. PLoS Pathog. 10, e1003918 (2014).
Article PubMed PubMed Central Google Scholar
Lai, Y. et al. Commensal bacteria regulate Toll-like receptor 3-dependent inflammation after skin injury. Nat. Med 15, 1377–1382 (2009).
Article CAS PubMed PubMed Central Google Scholar
Guo, G. et al. Self‐amplification immunomodulatory strategy for tissue regeneration in diabetes based on cytokine‐ZIFs system. Adv. Funct. Mater. 31, 2100795–2100808 (2021).
Article CAS Google Scholar

Download references

Acknowledgements

The authors thank ECNU Multifunctional Platform for Innovation (004) for technology support. The authors would greatly acknowledge the financial support by the National Funds for Distinguished Young Scientists (Grant No. 51725202 to W.B.), the Key Project of Shanghai Science and Technology Commission (Grant No. 19JC1412000 to W.B), and the National Natural Science Foundation of China (Grant No. 51872094 to W.B., 82172091 to Y.W.). National Science Foundation for the Young Scientists of China (Grant No. 32000948 to Y.C.).

Author information

These authors contributed equally: Yun Meng, Lijie Chen, Yang Chen.

Authors and Affiliations

Tongji University Cancer Center, Shanghai Tenth People’s Hospital, Tongji University School of Medicine, Shanghai, 200072, P. R. China
Yun Meng, Yang Chen, Jieyun Shi, Wei Yang, Li Zhang, Chaochao Wang, Xianfu Meng, Yelin Wu & Wenbo Bu
Department of Materials Science and State Key Laboratory of Molecular Engineering of Polymers, Fudan University, Shanghai, 200433, P. R. China
Yun Meng, Lijie Chen, Fan Wu, Xingwu Jiang & Wenbo Bu
School of Life Sciences and Technology, Tongji University, Shanghai, 200092, P. R. China
Yang Chen
School of Life Science, East China Normal University, Shanghai, 200241, P. R. China
Zheng Zhang & Yiwen Wang

Authors

Yun Meng
View author publications
You can also search for this author in PubMed Google Scholar
Lijie Chen
View author publications
You can also search for this author in PubMed Google Scholar
Yang Chen
View author publications
You can also search for this author in PubMed Google Scholar
Jieyun Shi
View author publications
You can also search for this author in PubMed Google Scholar
Zheng Zhang
View author publications
You can also search for this author in PubMed Google Scholar
Yiwen Wang
View author publications
You can also search for this author in PubMed Google Scholar
Fan Wu
View author publications
You can also search for this author in PubMed Google Scholar
Xingwu Jiang
View author publications
You can also search for this author in PubMed Google Scholar
Wei Yang
View author publications
You can also search for this author in PubMed Google Scholar
Li Zhang
View author publications
You can also search for this author in PubMed Google Scholar
Chaochao Wang
View author publications
You can also search for this author in PubMed Google Scholar
Xianfu Meng
View author publications
You can also search for this author in PubMed Google Scholar
Yelin Wu
View author publications
You can also search for this author in PubMed Google Scholar
Wenbo Bu
View author publications
You can also search for this author in PubMed Google Scholar

Contributions

W.B. and Y.W. conceived and supervised the study. Y.M., L.C., and Y.C. designed and performed the experiments. J.S., Z.Z., X.C., and W.Y. prepared and characterized the nanomaterials. Y.M., F.W., and X.J. performed most cell biological and animal experiments. W.Y., L.Z., and C.W. assisted with cell biological and animal experiments. L.C., X.M., and Y.C. analyzed the data. W.B. and Y.W. wrote the manuscript. All authors contributed to the review, revision, and finalization of the manuscript.

Corresponding authors

Correspondence to Yelin Wu or Wenbo Bu.

Ethics declarations

Competing interests

The authors declare no competing interests.

Peer review

Peer review information

Nature Communications thanks Fei Guo, Aaron Elbourne and the other, anonymous, reviewer(s) for their contribution to the peer review of this work.

Additional information

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Supplementary Information

Reporting Summary

Source data

Source Data

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and permissions

About this article

Cite this article

Meng, Y., Chen, L., Chen, Y. et al. Reactive metal boride nanoparticles trap lipopolysaccharide and peptidoglycan for bacteria-infected wound healing. Nat Commun 13, 7353 (2022). https://doi.org/10.1038/s41467-022-35050-6

Download citation

Received: 22 April 2022
Accepted: 17 November 2022
Published: 29 November 2022
DOI: https://doi.org/10.1038/s41467-022-35050-6

This article is cited by

Nanotechnology’s frontier in combatting infectious and inflammatory diseases: prevention and treatment
- Yujing Huang
- Xiaohan Guo
- Guobo Shen
Signal Transduction and Targeted Therapy (2024)
Tetrahedral framework nucleic acids/hyaluronic acid-methacrylic anhydride hybrid hydrogel with antimicrobial and anti-inflammatory properties for infected wound healing
- Cai Qi
- Qiang Sun
- Yunfeng Lin
International Journal of Oral Science (2024)
A pH/enzyme dual responsive PMB spatiotemporal release hydrogel promoting chronic wound repair
- Lanlan Dong
- Can Huang
- Gaoxing Luo
Journal of Nanobiotechnology (2023)
Stretchable graphene–hydrogel interfaces for wearable and implantable bioelectronics
- Yuyao Lu
- Geng Yang
- Kaichen Xu
Nature Electronics (2023)

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.