Rapidly photocurable silk fibroin sealant for clinical applications

Sealants are useful as agents that can prevent the leakage of gas or nonclotting fluids from damaged tissues and of blood from the vascular system following injury or repair. Various formulations for sealants have been developed and applied clinically, but problems still remain in terms of biocompatibility issues, long crosslinking times and low adhesive properties. Herein, to address these issues, we report a methacrylated silk fibroin sealant (Sil-MAS) with rapidly crosslinkable, highly adhesive and biocompatible properties and demonstrate its versatility as a medical glue. The excellent physical properties of Sil-MAS are revealed via in vitro mechanical tests and ex vivo aorta pressure tests. In addition, in in vivo biological tests on the skin, liver, and blood vessels of rats, Sil-MAS showed a superb hemostatic and adhesive ability, with high biocompatibility. Specifically, Sil-MAS strongly contributed to faster wound healing than commercially available materials. Furthermore, we showed a successful proof of concept that Sil-MAS could serve as an ideal photocuring laparoscopic medical glue in a laceration rabbit model of liver and stomach serosa using a homemade endoscopic device. These findings on the applicability of rapidly photocurable silk fibroin indicate that Sil-MAS is a suitable material to supplant existing sealants, adhesives, or hemostatic agents. An efficient, fast-acting and biocompatible glue for sealing damaged body tissue has been developed by scientists in South Korea and the USA. The ability to stop bleeding is crucial in surgery. One solution is to use medical glues that can seal tissue and blood vessels. These glues need to be biocompatible, fast-acting, long-lasting and low cost. Many such sealants are now clinically available, but most do not meet all these requirements. Chan Hum Park from Hallym University in Chuncheon, South Korea, and co-workers developed a fast-acting, highly adhesive and biocompatible medical glue using a material derived from a silk protein. The team tested their methacrylated silk fibroin sealant on rat skin, liver and blood vessels and observed faster wound healing than that obtained using commercially available materials. We report methacrylated silk fibroin sealant (Sil-MAS) with rapid crosslinkable, highly adhesive and biocompatible properties and demonstrate its versatility as medical glue. The excellence for physical properties of Sil-MAS is revealed via in vitro mechanical tests and ex vivo aorta pressure test. In in vivo biological tests on skin, liver, and blood vessels of rat, Sil-MAS showed a superb hemostatic and adhesive ability with high biocompatibility. Specifically, Sil-MAS strongly contributed to fast wound healing. Furthermore, we showed that Sil-MAS could be an ideal photocuring laparoscopic medical glue in laceration rabbit model of liver and stomach serosa using self-made endoscopic device.


Introduction
To stop bleeding, sealing tissues and gluing vessels together have become increasingly important, especially with the expansion of minimally invasive surgery. Medical glues including hemostatic agents, sealants and adhesives have therefore become more critical in surgical practice 1 . The ideal medical glues should be safe, easy to use, low cost and able to meet regulatory requirements in addition to efficacy 1 . Although various products fulfill some of these criteria, issues remain with each of them. Many hemostatic agents are available as powders, sponges, thin films or sheets for surface wounds when pressure must be applied or for covering large areas of profusely bleeding wounds that have regular shapes. What is needed, however, is a medical glue that could be applied to wounds of various shapes, repair soft tissue and have the capability of being crosslinked once in place. Among the various medical glues, fibrin sealant is the only commercially available material applicable for all three functions, as a hemostatic agent, sealant and adhesive, but the risks of virus transmission and poor adhesion under wet conditions need to be addressed 2 .
Silk fibroin (SF) has been studied extensively due to its high biocompatibility in wound dressings 3 , enzyme immobilization matrixes 4 , tympanic membranes 5 , ridge preservation grafts 6 , and vascular prosthesis and structural implants 7,8 . Additionally, SF has already been developed as a medical glue including SF blended with polyvinyl alcohol and hyaluronic acid 9 , SF hybridized with duck's feet collagen 10 , and RGD peptide-fused recombinant mussel adhesive protein 11 . In this manner, to be applied to medical glue, SF has been fabricated as a solid material (e.g., powder, sponge, or mesh) to provide a mechanical tamponade, which limits its application to irregular or large areas. SF-based medical glues have also been developed as colloidal-type glues in a few studies, for example, SF blended with chemically active polyethylene glycol (PEG) 12 and catechol-functionalized SF containing PEG 13 . In these studies, SF has been shown to be effective by supporting other materials; in combination, SF can increase the hydrophobicity or mechanical strength or alter the degradability. More recently, tannic acidintroduced SF 14 has also been developed; however, this method has a long gelation time. To our knowledge, rapidly crosslinkable colloidal medical glues composed of SF alone have never been studied. Recently, temporally and spatially controlling the physical properties of SF has become available through the photopolymerization of SF methacryloyl 15 . The functionality of SF was improved with SF methacryloyl for fast crosslinking, ease of use (e.g., bioink), and consistent rheological and mechanical properties while maintaining its excellent biocompatibility; therefore, we can now extend the application of SF methacryloyl beyond existing biomedical applications of SF. Herein, we report the applicability of SF methacryloyl as a versatile medical glue that can be applied as a hemostatic agent, sealant, or adhesive. To do so, we systematically evaluated the adhesive properties of SF methacryloyl under various conditions in vitro and its sealing/hemostasis properties via adhesion on skin, liver, and vascular structures in vivo or ex vivo. Finally, laparoscopic surgery was performed with a homemade endoscopic device consisting of SF methacryloyl and a light source in a rabbit liver/stomach laceration model.

Preparation of the silk fibroin sealant (Sil-MAS)
Sil-MAS was synthesized according to our established protocol 15 . Bombyx mori (B. mori) cocoons were provided by the Rural Development Administration (Jeonju, Korea). Each silkworm cocoon was sliced into four pieces. Forty grams of sliced cocoons were boiled in 1 L of 0.05 M Na 2 CO 3 solution for 30 min at 100°C to remove sericins from the silk and then were washed with distilled water (DW) several times. The degummed silk was dried at room temperature, and 20 g of it was dissolved in 100 mL of 9.3 M lithium bromide solution (in DW) at 60°C for 1 h to make regenerated SF solutions. Then, 6 mL (424 mM) of GMA was slowly added to the mixture with stirring at 300 rpm and 60°C for 3 h. Next, the resulting solution was filtered through a rayon-polyester membrane (Miracloth, Calbiochem ® , San Diego, CA, USA) and dialyzed against DW using 12-14 kDa cutoff dialysis tubes for 7 days. Finally, this methacrylated SF solution was frozen at −80°C for 12 h and freeze-dried for 48 h. The lyophilized methacrylated SF (d-Sil-MAS) was stored at −80°C for further use.
d-Sil-MAS was dissolved in DW at a concentration of 25% (w/v). Then, LAP filtered through a cellulose acetate syringe filter (0.2 µm, GVS Filter Technology Inc., Findlay, OH, USA) was added into the solution at a concentration of 0.3% (w/v) and mixed until fully dissolved using a planetary vacuum mixer (ARV-310, Thinky Corp., Tokyo, Japan). This solution was then strained through a nylon mesh cell strainer (40 µm, SPL Co., Pocheon, Korea) and finally pasteurized at 60°C for 30 min. For in vitro and ex vivo testing, the sterilization process was skipped. The final solution was called liquid (l)-Sil-MAS. After stabilization at room temperature for 30 min, the l-Sil-MAS was irradiated with ultraviolet (UV) light for 10-30 s at a distance of 5 cm using a UV spot-curing machine (SP-LED-1, ARC UV Corp., Yongin, Korea) equipped with a filter of 365 nm. The spot diameter was 1.5 cm, and the light intensity was measured at 6 mW/cm 2 by a UV meter. This crosslinked material was called c-Sil-MAS.
c-Sil-MAS samples for the mechanical test and in vivo biocompatibility test were 3D printed by a digital light processing (DLP) printer that was customized by professional manufacturers (NBRTech. Ltd, Chuncheon, Korea) 15 . Samples were designed by CADian3D (Intelli-Korea, Seoul, Korea) depending on the test conditions. The following printing parameters were used: printing thickness, 50 μm; number of base layers, 3; curing time of base layer, 4 s; number of buffer layers, 1; and curing time of buffer layers, 3 s. Prints were carried out by repeating the process of projecting an image into the hydrogel followed by raising the Z-stage in an aseptic environment. After printing, the printed objects were rinsed with saline to remove uncrosslinked l-Sil-MAS surrounding the c-Sil-MAS before testing.

Characterization of Sil-MAS
To determine the successful synthesis of the sealant prepolymer, d-Sil-MAS was examined through proton nuclear magnetic resonance ( 1 H NMR) spectroscopy at a frequency of 400 MHz using a Bruker DPX FT-NMR Spectrometer (9.4 T, Bruker Analytik GmbH, Karlsruhe, Germany). First, 5 mg of d-Sil-MAS was dissolved in 700 μL of deuterium oxide (D 2 O, Sigma-Aldrich) and then filtered using a nylon syringe filter (0.45 μm) before analysis. 1 H NMR spectra were recorded for unsubstituted SF and GMA with 1:1 mol unsubstituted amines on SF: mol GMA.
Samples were prepared by a 3D printer for the rheological properties test (a disk with 2.5 cm diameter and 0.2 cm height), for the compression test (a disk with 1.12 cm diameter and 1 cm height), for the tensile test (a dumbbell shape sample of a concave column with 1.6 cm (w) × 0.7 cm (d) × 0.2 cm (h)), for the swelling rate (a disk with 2.5 cm diameter and 0.2 cm height) and for the in vitro degradation study (a square sample with 1 cm (w) × 1 cm (d) × 0.2 cm (h)). The rheological properties of l-Sil-MAS and c-Sil-MAS were measured at 25°C using an Anton Paar MCR 302 (Anton Paar, Zofingen, Switzerland) rheometer. The mechanical strength of the hydrogel was obtained by a universal testing machine (UTM; QM100S, QMESYS, Gunpo, Korea) that was equipped with a 10 kgf load cell in an unconfined environment. The mechanical force was loaded at a rate of 5 mm/min until the hydrogel broke. For the swelling property of c-Sil-MAS, the hydrogels were immersed in DW or PBS, and then, the swelling ratio was estimated by measuring the length of the X and Y axes based on the initial status immediately after printing.
In vitro degradation 16 of 3D-printed c-Sil-MAS was measured for 30 days using protease XIV (from Streptomyces griseus) (Pronase E ® , Merck, Darmstadt, Germany) with an activity of 2 U/mL. Samples were immersed in 2 mL of PBS (pH 7.4) containing 2 U/mL protease enzyme and incubated at 37°C. The enzyme solution was exchanged with freshly prepared solution every 3 days. The three samples were dried and weighed at predetermined time points. The degradation rate was calculated by the following formula: where Wi is the initial dry weight of the construct and Wt is the final weight after 0, 3, 6, 9, 12, 15, 18, and 30 days of incubation.

Adhesive mechanical tests 17
The common treatment for all adhesive tests was as follows: All tests were conducted according to the ASTM guidelines modified in terms of the size of the specimen, strain rate, or area of sample treatment. The three mechanical tests relative to adhesion of Sil-MAS (n = 3) were performed using a UTM that was equipped with a 3 kgf load cell in an unconfined environment. MLB (n = 3) was used as a control. Fresh shaved rat skin from male SD rats (180-220 g) was prepared as a substrate tissue. This rat skin tissue was kept in PBS, and the moisture was wiped immediately before use. To attach rat skin tissue on glass slides and steel fixtures, instantaneous adhesives (LOCTITE401, Henkel, Rocky Hill, CN, USA) were used. Different quantities of sealants (l-Sil-MAS and MLB) and UV treatment times for each test were used for the experiments. All tests of physical properties were performed in a room under strictly controlled conditions (80% humidification, room temperature) to prevent drying out.
(1) In vitro lap shear test: The strength properties of sealants in lap shear by tension loading were analyzed according to the ASTM F2255-05 standard. Rat skin (2.5 cm × 2.5 cm) was attached on the edge of the short side of two glass slides (9 cm × 2.5 cm). Next, 300 µL of each sealant was uniformly placed on the skin. Then, the other tissue-coated slide was symmetrically covered with sealants. The Sil-MAS group was irradiated with UV light (20 s) from every direction, and the MLB group was allowed to dry at room temperature. These assembled slides were loaded in a UTM for shear testing by tensile loading with a strain rate of 2 mm/min. The point of detachment was fixed as the maximum load. Shear strength (kPa) was the maximum load (N) divided by the bonding area (0.5 cm 2 ). To visualize the adhesive strength of Sil-MAS, 300 µL of l-Sil-MAS (2.5 cm × 2.5 cm) was applied between a 0.9 kg wrench and a plastic ruler, and after UV crosslinking (20 s), the ruler was lifted for 2 h.
(2) Pull-off adhesion strength: The strength properties of sealants in tension were quantified according to the ASTM F2258-05 standard. The test aims to measure the adhesive tensile strength of Sil-MAS in conjunction with the skin tissue and the force necessary to separate this bond. Two rat skin tissues (2 cm × 2 cm) were attached on the steel fixtures with 2 cm in each dimension. Then, 300 µL of each sealant was uniformly placed on the skin on the bottom side of the steel fixture. The gap between the fixtures was set at 2 mm. The Sil-MAS group was irradiated with UV light (20 s) from every direction, and the MLB group was allowed to dry at room temperature. A transient tensile test at a constant transducer speed of 5 mm/min was performed until complete sealant-skin substrate seal failure. The adhesion strength of sealants was determined by dividing the maximum load detected in the pull-off curve by the bonding area (4 cm 2 ).
(3) In vitro wound closure strength: The wound closure strength of the sealants was tested according to the ASTM F2458-05 standard, which is specifically focused on determining the wound closure strength of medical glue. The rat skin was cut into rectangular shapes 2.5 cm × 2.5 cm in size. The tissues were fixed onto two glass slides (9 cm × 2.5 cm) with 1.5 mm spaces between the slides. The center of the tissue was cut using a razor blade to mimic wound injury. Then, 400 µL of each sealant was uniformly applied onto the cut area (0.5 cm × 0.5 cm), and UV light was applied to crosslink the sealant from every direction. These assembled slides were placed carefully into the UTM by tensile loading with a strain rate of 5 mm/min. The point of tearing was defined as the wound closure strength (kPa).

Ex vivo porcine aorta burst pressure test
The burst pressure testing of Sil-MAS (n = 3) was conducted using a modified setup for determining vessel seal burst strength 18 . Briefly, fresh porcine aortas (diameter 1.8 cm) from a local slaughterhouse (Hongcheon, Korea) were immersed in saline, and the experiment was carried out within 10 h after the aorta harvest. The aorta was cut into 15 cm segments, and an infusion catheter (diameter 2 cm) was fitted in one opened side of the aorta. The orifice diameter of the tube was larger than that of the aorta so that the aorta covered the tube very tightly. The other opened side of the aorta was gripped by a curved mosquito clamp. The catheter was connected to a syringe pump (PILOT Anaesthesia 2, Fresenius Vial Corp., Brezins, France), which was connected to a patient monitor (MP1000NT PLUS, MEK Corp., Giheung, Korea) to verify the intraluminal pressure. Then, a small incision (3 and 9 mm length) was made by scalpel (#15) in the middle of the aorta, and 200 µL of l-Sil-MAS was placed onto the sectioned area and photocrosslinked by UV light (20 s).
Next, to test the subsidiary effect of Sil-MAS on suturing, the porcine aorta was cut in half using a scalpel. An aorta end-to-end anastomosis was performed using interrupted polyamide sutures (Blue Nylon, Ailee Corp., Busan, Korea). One milliliter of l-Sil-MAS was then applied to the anastomotic site and treated with UV light (20 s). The aorta sutured without sealant was used as a control. The above aortas were filled with PBS using a syringe pump through the other opened side of the aorta until the aorta was swelled by its diameter or leakage occurred at the suture site, and this point was set to zero mmHg. Then, additional PBS was injected into the aorta using the syringe pump to increase the infusion pressure. The aorta was swollen under continuous PBS injection, and the burst pressure (kPa) of Sil-MAS was recorded at the point of material burst, detachment or tissue burst.

Animal study
In vivo study using a rat model Common treatment for all rat tests: The animal studies were carried out in accordance with guidelines and approval of the Institutional Animal Care and Use Committee (IACUC) of Hallym University in Korea (# Hallym 2018-11). Healthy male Sprague-Dawley (SD) rats each weighing 180-220 g were used (Samtako, Osan, Korea). After being raised under experimental conditions for 1 week, the rats were randomly divided into 1-3 groups depending on the analysis. Anesthesia was induced with 3% isoflurane in a 75:25 mixture of nitrous oxide and oxygen in a standard induction chamber with a gas vaporizer (Harvard Apparatus, South Natick, MA, USA) and maintained at 2%, administered via a small rodent respirator. Each group was tested in triplicate. For animal sacrifices, the rats were euthanized with a lethal dose of thiopental urethane.
(1) Wound closure animal study: To evaluate the adhesive property of Sil-MAS, the backs of rats (n = 3) were shaved. After disinfection, skin incisions 1.5 cm long and partial-skin thickness deep were made on the backs of rats by a surgical blade (#10). l-Sil-MAS (200 µL) was quickly applied to the wound, with fingers used to slightly hold both ends of the incision, and then crosslinked with UV light for 10 s. Next, sealing by Sil-MAS was confirmed by gently pulling the sealed site in the opposite direction of incision with two fingers.
(2) Hemostasis and wound healing in an in vivo partialthickness skin wound model: The rats were divided into three groups: the Sil-MAS group (n = 3), the Avitene™ group (n = 3) and the gauze group (n = 3). Commercial artificial dermis Avitene™ and standard gauze as controls were cut into 1 cm × 1 cm square shapes. After shaving and disinfection of the backs of rats, in the rostral-to caudal direction, three 1 cm (w) × 1 cm (d) × 0.3 cm (h) partial-thickness skin defects per animal were cut out with a homemade tool. Through this procedure, the epidermis and partial dermis were removed. One of the three wounds was covered with Avitene™, and another was covered with gauze. The other wound was sequentially treated with l-Sil-MAS (200 µL) and UV light (25 s). To secure the treatment, Surgifix ® (BSN medical, Victoria, Australia) was wrapped around the animal from below the forelimbs to above the hindlimbs. The wound site was photographed on the 0, 3rd, 7th, 14th, and 21st days, and the remaining wound area was measured and converted to a percentage based on the initial wound area. After photography, rats were sacrificed, and full-thickness skin tissue was harvested at the initial wound size and divided into two equal portions for western blotting and histology analysis.
(3) Femoral artery hemorrhage: The hair of rats (n = 3) was removed over the right inguinal region. After disinfection, the skin and subcutaneous tissues were cut to expose the femoral vein and artery. Bleeding was produced by incision of the femoral artery and vein using a sterilized scalpel. After free bleeding was observed for 5 s, the damaged area was pressed gently with gauze for 3 s. The gauze was removed, and immediately, l-Sil-MAS (50 µL) and UV light (20 s) were sequentially applied to the wound.
(4) Subcutaneous implantation: For in vivo degradation tests and biocompatibility tests, samples (1.5 cm (w) × 1.5 cm (d) × 0.2 cm (h)) were printed out by a 3D DLP printer. The backs of rats were shaved and disinfected. Two incisions 1 cm long were created on the rostral side and caudal side on the dorsal midline of the backs of the rats. The separated subcutaneous pockets were made using Metzenbaum scissors. Printed c-Sil-MAS samples were placed in the subcutaneous pockets. At 2, 4, 10, and 16 weeks after implantation, the rats were euthanized, and the implanted c-Sil-MAS samples were harvested with the surrounding tissue. Explanted samples were washed with DW. For the degradation test (n = 3), excess tissue surrounding the samples was carefully removed. In vivo degradation was measured based on the sample size before and after implantation using a stereomicroscope (SMZ25, Nikon Co., Tokyo, Japan).
(5) Liver hemorrhage: For liver hemostasis surgery, rats were divided into two groups: the Sil-MAS group and the fibrin glue group. An abdominal midline incision was made after local disinfection. The liver was exposed and separated from the surrounding tissues by a retractor. Two of the three lobes of the liver were scraped out (0.5 cm deep and 0.5 cm diameter) using tissue forceps and a scalpel after punching with a tissue punch (diameter 0.5 cm). After free bleeding for 5 s, the damaged area was pressed gently with gauze for 3 s. Then, l-Sil-MAS (200 µL) and UV light (20 s) were sequentially applied to the wound immediately after removal of gauze. The fibrin sealant was prepared and applied to the wound according to the manufacturer's instructions. At 1, 2, 4, or 8 weeks after surgery, the rats were euthanized, and the sealanttreated region, including peri-implant tissue, was resected from the rats for further histological analysis.

Laparoscopic surgery in a rabbit laceration model of liver and stomach serosa
Laparoscopic surgery was performed in a female New Zealand white rabbits weighing 2.8 kg. Anesthesia was induced with intramuscular ketamine (250 mg/5 mL, Huons, Seongnam, Korea) and Rompun injection (23.32 mg/mL, Bayer Korea, Seoul, Korea) and maintained with inhalational sevoflurane (2%) and oxygen mixed with room air (1.5 L/min) using a ventilator (Veterinary anesthesia ventilator, Solar Medical Tech, Taipei, Taiwan). The study was approved by the IACUC of Hallym University in Korea. A rabbit was secured to the table in the supine position. The CO 2 insufflator and camera system with a 4 mm 0°endoscope (Karl Storz, Tuttlingen, Germany) was combined with the complete laparoscopic unit (MGB, Berlin, Germany). Three 5 mm laparoscopic trocars (Laport, Sejong Medical, Paju, Korea) were introduced into the abdominal cavity, and the insufflation pressure was established as 8-12 mmHg CO 2 gas. The instruments used were endoscopic scissors, forceps, a suction-irrigation probe, a homemade endoscopic sealant device with fiber optics and a microsyringe pump. Multiple superficial or deep liver laceration wounds were made by endoscopic scissors. Bleeding liver laceration lesions were briefly pressed with gauze, and l-Sil-MAS (1 mL) and UV light (20 s) were applied by a homemade endoscopic sealant device. Rebleeding or leakage of blood at the lesions was checked using an endoscopic camera and forceps. In the same way, through laparoscopic operation, laceration of stomach serosa, Sil-MAS treatment, and checking the result were performed.

Western blotting
Twenty milligrams of frozen tissue (frozen with liquid nitrogen) was mixed with 1 mL of ice-cold RIPA buffer (with protease, dephosphorylase inhibitor cocktail) and homogenized using a hand homogenizer (Super Fast Prep-2 TM , MP Biomedicals, Santa Ana, CA, USA). Then, the mixture was incubated at 4°C for 2 h with agitation, and the supernatants were collected by centrifugation for 20 min. The protein concentration in the supernatants was measured using a Bradford assay (Bio-Rad, Hercules, CA, USA). The same amount of denatured protein sample was then loaded and separated on an SDS-polyacrylamide gel and transferred to a PVDF membrane (Millipore, Billerica, MA, USA). Nonspecific binding was blocked using 10% skim milk for 2 h at room temperature. Then, the membrane was incubated with primary antibodies (1:1000) overnight at 4°C. Primary antibodies for vimentin, fibronectin, VEGF, and cyclin D1 were purchased from Abcam (Cambridge, UK). β-Actin antibody was supplied by Sigma-Aldrich and used at 1:5000. Afterward, the membrane was incubated at room temperature for 1 h with species-matched secondary antibodies (goat anti-rabbit and goat anti-mouse IgG) (Enzo Life Sciences, Farmingdale, NY, USA). Finally, bands were detected by a chemiluminescence system (Fusion FX, Vilber Lourmat). Experiments were conducted using tissue samples from three different rats.

Histology
The harvested samples were fixed with 4% paraformaldehyde for 24 h, dehydrated in graded alcohols and xylene and then embedded in paraffin. Tissue samples five microns thick were prepared and stained with hematoxylin and eosin (HE) to analyze the re-epithelialization and inflammatory response and Masson's trichrome (MT) to detect collagen production. Furthermore, to check tissue compatibility, samples harvested from liver and subcutaneous tissue at each time point were immunostained with anti-CD68 (Abcam, Cambridge, MA, USA) and anti-CD31 (Novus Biologicals, Centennial, CO, USA) primary antibodies and then with DyLight ® 550-conjugated (Bethyl Laboratories, Montgomery, TX, USA) and FITCconjugated secondary antibodies, respectively. The slides were mounted by Vectashield antifade mounting medium with DAPI (Vector Laboratories, Burlingame, CA, USA). Stained sections were analyzed under a fluorescence microscope (Eclipse 80i, Nikon Co.).

Cytocompatibility assay and cell migration assay
To test the cytotoxicity of Sil-MAS depending on the UV treatment time and wound healing effect of Sil-MAS in vitro, the elution test method was applied. Two milliliters of l-Sil-MAS was prepared in 6-well plates, and UV treatment was administered for 10, 20, and 30 s. Then, 10 mL of a growth medium consisting of Dulbecco's modified Eagle medium (DMEM) with 10% (v/v) fetal bovine serum and 1% (v/v) penicillin-streptomycin was added and incubated in a 5% CO 2 incubator at 37°C for 72 h. This medium (Sil-MAS conditioned medium) was extracted and sterilely filtered with a cellulose acetate syringe filter (0.2 µm) to preserve all living cells. NIH/3T3 mouse fibroblast cells (Koram Biotech, ATCC distributor, Seoul, Korea) were cultured in the above growth medium. All cultures were maintained in a 5% CO 2 incubator at 37°C with the medium changed every three days. Cells were detached using trypsin-EDTA 0.25%, and 5,000 cells/well were plated in 24-well plates. After stabilization of cell attachment, the culture medium was replaced with 200 µL of the filtered Sil-MAS conditioned medium and cultured for 3 days without medium changes. The cell viability depending on culture time was examined by CCK-8 assay (Dojindo Molecular Technology, Rockville, MD, USA) according to the manufacturer's protocol. As a positive control group, 200 µL of SF solution prepared at a concentration of 25% (w/v) in the growth medium was added to cells.
For the wound healing assay in vitro, NIH/3T3 cells were cultured until the confluence reached approximately 80-90%. A scratch was created using 200 µL micropipette tips. Immediately after the scratch, floating cells were removed by PBS washing, and 200 µL of Sil-MAS conditioned medium and growth medium (control) was added to each well. While cells were being cultured, images were captured at 3 h intervals for 15 h with a digital camera (EOS 100D, Canon, Tokyo, Japan) through an optical microscope (Eclipse 80i, Nikon Co.). The rate of migration was quantified through the total distance that the NIH3T3 cells moved toward the center of the wound from the edge of the wound within 15 h.

Statistical analysis
Samples for each group were assessed in triplicate to analyze the statistical data. The data are presented as the mean value ± standard deviation (s.d.) (*p < 0.05, **p < 0.01, ***p < 0.001, and **** p < 0.0001). Curve fitting was performed using Prism, version 6.0 software (GraphPad, San Diego, CA, USA), and one-way ANOVA followed by the Tukey multiple comparisons test was used to assess significant differences among multiple groups.

Results and discussion
Fabrication of Sil-MAS Figure 1a presents a schematic diagram illustrating the synthetic process of the prepolymer for Sil-MAS, which relies on the reaction of GMA with SF, as well as the chemical structure of Sil-MAS according to the conditions. In the synthesis, the photoreactive vinyl groups of GMA responsible for UV crosslinking were mainly conjugated to the primary amine groups of SF after epoxide ring opening, resulting in secondary or tertiary amines with hydroxyl groups. The modification of SF by GMA was confirmed through NMR spectroscopy (Fig. S1). Creation of l-Sil-MAS was completed by the addition of LAP as a photoinitiator to the Sil-MA solution immediately before use. Finally, l-Sil-MAS was photocrosslinked (c-Sil-MAS) on the target by UV irradiation at 365 nm. LAP produces free radicals following light treatment, causing l-Sil-MAS to become crosslinked via free radical vinyl polymerization. In this study, Sil-MAS was tested for various external and internal uses; Fig. 1b depicts a schematic drawing of the applications of Sil-MAS such as the treatment of damaged skin, liver, blood vessels, and stomach.

Adhesion properties of Sil-MAS
The detailed physical properties of Sil-MAS, such as the mechanical, rheological and degradable properties, are presented in the Supporting Information (Table S1, Fig.  S2-S4). l-Sil-MAS shows a suitable viscosity for handling, a proper mechanical strength for internal organs, a low swelling ratio to avoid affecting surrounding organs, and a slow degradation rate (slower than that of commercial sealants 2 ) suitable for long-term sealing effects on targets.
Adhesion tests to measure the lap shear strength, tensile adhesion strength and wound closure strength of sealants were performed (Fig. 2). Medifoam ® Liquid bandage (MLB, Mundipharma), which is a commercially available active sealant in Korea, was used as a control. A lap shear test was applied based on the ASTM F2255-05 standard to determine the shear strength of sealants (Fig. 2a). In addition to performing the skin test, we carried out the test on steel without tissue because the biological membranes themselves have inconsistent surface properties and vary by sample. On both surfaces, Sil-MAS showed higher shear strain and shear stress at break than MLB. Reflecting the high resistance to shear, the adhesive strength of Sil-MAS was strong enough to lift and hold a wrench (0.9 kg) for prolonged time periods (Fig. 2b, Video S1). To test the strength properties of sealants in tension, a pull-off adhesion test was performed using modified ASTM F2258-05 (Fig. 2c). Similar to the results of the lap-shear test, Sil-MAS produced higher tensile strength and higher elongation at break than MLB. The wound closure strength of sealants was assessed using modified ASTM F2458-05 (Fig. 2d). Both the highest adhesive strength and elongation of Sil-MAS were shown to be higher than those of MLB. In addition, Sil-MAS was superior to MLB at both the breaking stress and breaking strain points, which means that Sil-MAS has higher ductile properties, lower brittleness, and greater toughness. To test the effectiveness of Sil-MAS for in vivo sealing without any surgical methods, a rat model of skin incision was used (Fig. 2e, Video S2). Skin incisions 1.5 cm   in length and partial skin thickness in depth were successfully sealed via crosslinking of l-Sil-MAS. The sealed site was not torn when pulled gently with fingers.

Biocompatibility of Sil-MAS in vitro and in vivo
The biocompatibility of Sil-MAS was tested both in vitro and in vivo. Sil-MAS showed high cell viability regardless of UV treatment time (10-30 s) on Sil-MAS (Fig. 3a). The longer the sealant was crosslinked by UV light, the higher the cell viability and the better the proliferation. However, there was no significant difference among the groups, and even the result for the Sil-MAS group treated by UV for only 10 s was similar to that of treated pure SF. The tissue response following subcutaneous implantation of c-Sil-MAS in rats was histologically examined through HE staining and immunohistochemistry (IHC) for CD68 over the subsequent 16 weeks (Fig. 3b). An increase in the number of vascular structures and the formation of collagenous tissue accompanied by a decrease in the number of macrophages with time were observed, which reflects the biocompatibility of Sil-MAS.

Hemostasis and wound healing effect of Sil-MAS in an in vivo partial-thickness skin wound model
We evaluated the hemostasis and healing properties of Sil-MAS in an acute partial-thickness wound rat model (Fig. S5, Video S3). In the partial-thickness wound, bleeding substantially stopped following application of l-Sil-MAS and completely stopped following UV curing. The advantages of the application of Sil-MAS were not limited to hemostasis following abrasion. It was hypothesized that wound healing can progress naturally without removal of the Sil-MAS covering because c-Sil-MAS has high viscoelasticity and SF possesses good biocompatibility and an intrinsic wound healing effect 3 . Photographic records were generated to analyze the macroscopic wound closure at days 0, 3, 7, 14, and 21 after treatment with Sil-MAS, Avitene™ (control group 1) and gauze (control group 2) on rat partial-thickness wounds (Fig. S6). The Sil-MAS covering on the wound peeled off as the skin was repaired. Moreover, it was confirmed that the wound site in the Sil-MAS treatment group had a smooth and hairy surface without wrinkles from the third day. This result proves that Sil-MAS administered on the wound does not need to be replaced because it adheres well to the injured tissue without sticking, absorbs exudate, promotes wound healing and peels off spontaneously as the wound heals 3 . Quantitatively, the wound area in the Sil-MAS group decreased the fastest among the groups (Fig. 4a). To further confirm whether Sil-MAS promotes skin regeneration, the protein expression levels of wound healing-related factors were assessed using western blot analysis (Fig. 4Bi). Vascular endothelial growth factor (VEGF) promotes wound healing by several mechanisms such as collagen deposition, angiogenesis and epithelization 19 . Fibronectin is an adhesive molecule that contributes to wound healing, including extracellular matrix formation and reepithelialization 20 . Vimentin has been shown to be involved in tissue repair and regeneration including cell migration, proliferation, differentiation, angiogenesis, extracellular matrix remodeling and immune responses 21 . Finally, cycle regulatory protein (cyclin D1) is associated with cell proliferation and wound healing 22 . Western blot analysis showed that in all groups, there were increased levels of VEGF, fibronectin, vimentin, and cyclin D1 in the wound tissue at days 3 and 7 compared with immediately after wounding. Of note, in the Sil-MAS group at day 3, all proteins were found to be expressed the most among all of the groups tested, and the expression levels also reached their peaks during the test period (Fig. 4Bii). This result indicated that Sil-MAS promoted the wound healing process through upregulation of these proteins, which is in agreement with our previous studies that SF solution increased the cell migration of primary human dermal fibroblasts and induced the expression of the same proteins in vivo 22 . These studies demonstrate that the major component SF within Sil-MAS could affect the wound healing process.
We assessed the histological features of wound healing in rats, including the re-epithelialization, inflammatory response, deposition of collagen and regeneration of adnexal structures, through HE and MT staining (Fig. 4c). Briefly, overall, Avitene™ and Sil-MAS showed quick and stable healing based on rapid regrowth of epithelium, well-arranged and dense collagen, large numbers of fibroblasts, and a rich reconstitution of adnexal structures. However, the Avitene™ group retained a few agglomerations of Avitene™ until 7 days posttreatment. The gauze group showed the slowest healing among groups, exhibiting late, irregular and immature re-epithelization, fewer fibroblasts, less vascular structure and more loosely packed collagen. The wound healing effect of Sil-MAS was doubly evaluated in vitro using a wound scratch assay (Fig. 4d). The scratched gap of NIH3T3 cells in the Sil-MAS group narrowed more rapidly than that in the medium-treated group. In light of these results, Sil-MAS Fig. 4 In vivo wound healing effect of Sil-MAS using a rat partial-thickness skin wound model. a Remaining wound area over time after dressing treatments. The wound area was measured and converted to a percentage based on the initial wound area. Gauze and Avitene™ were used as controls. b Expression level analysis of wound healing-related proteins in skin tissue harvested from the wound area. (i) Western blot analysis and (ii) quantification of western blots shown (i). The Sil-MAS group showed the strongest expression at day 3. Data are reported as the means ± SD (**p < 0.01, ***p < 0.001, and ****p < 0.0001; n = 3), G: gauze, S: Sil-MAS, and A: Avitene™. c Histological evaluation via HE and MT staining. Among the groups, the Sil-MAS group showed a quick and stable healing process (see Supporting Information for more details). G: gauze remaining on the wound, A: continued agglomeration of Avitene™ on the wound, E: regenerated epidermis, C: densely packed and regularly arranged collagen fibers, could serve as an improved occlusive dressing for healing following skin abrasion or split-thickness donor site healing.

Vascular closure effect and hemostatic effect of Sil-MAS on wet surfaces
Vascular injury is one of the main causes of death and disability, and hemostatic control from damaged arteries is essential for successful surgery. To evaluate the efficacy of Sil-MAS on vascular hemostasis and vascular sealing, burst pressure testing ex vivo was performed (Fig. 5a). The burst pressure after Sil-MAS treatment was within the range of physiological systolic arterial pressure in humans (90-140 mmHg) (Fig. 5b, Video S4). We further confirmed a potential burst pressure improvement by Sil-MAS after aorta end-to-end anastomosis made with interrupted sutures (Fig. 5c). The joining strength provided by Sil-MAS was superior (1.5 times) to that provided by nylon suture only. However, the use of Sil-MAS would be limited to repairing veins or capillaries  or combined with direct arterial suture repair because arterial blood pressure can exceed 200 mmHg during vascular surgery. Figure 5d shows snapshots from the rat femoral artery hemorrhage experiment. In the rat vascular incision model, the bleeding completely stopped after treatment with Sil-MAS (Video S5). Finally, Sil-MAS was applied to a rat liver using a parenchymal injury model as a potential clinical application to determine its effect on hemostasis, wound healing and biocompatibility. The bleeding was easily stopped by sequential treatment with l-Sil-MAS and UV light (Fig. 5e, Video S6). Fibrin glue also stopped the bleeding after thrombin crosslinking; however, it required a longer polymerization time (<60 s) than Sil-MAS (<30 s). This additional time led to dispersal of the fibrin glue and increased the risk of fibrin sealant liquid pooling 2 . The fibrin glue almost disappeared completely at 4weeks posttreatment (Fig. 5f). On the other hand, the Sil-MAS group showed a glistening appearance of c-Sil-MAS at 4 weeks, which progressively decreased over time.

Wound healing effect and inflammatory response of Sil-MAS in a liver punch biopsy model
To identify the wound healing and in vivo response surrounding the implants, we harvested wound beds from the rat livers at 1, 2, 4, and 8 weeks after surgery and performed histological examination. Tissue remodeling via wound healing and material degradation were analyzed following HE staining (Fig. 6a). In both the Sil-MAS and fibrin glue groups, stable collagenous tissue and normal liver tissue were found with prolonged time. Vascular structures in the newly formed tissue and cell infiltration into the materials and material absorption were found to be more abundant and to occur earlier in the fibrin glue group than in the Sil-MAS group over a period of 8 weeks.
Since endothelial cells and macrophages play a critical role in the inflammatory and healing process 23 , the presence of CD31 and CD68 was verified by double immunofluorescent staining (Fig. 6b). Both CD31 and CD68 were detected in greater numbers and earlier in the fibrin glue group than in the Sil-MAS group, reflecting more rapid material absorption during the test. The level of endothelial cells and macrophages in the Sil-MAS group was consistent with a mild inflammatory response. These long-term histological findings indicate that Sil-MAS forms natural and stable collagen and does not induce a chronic inflammatory response in vivo except for a mild inflammatory response consistent with normal healing. Such slight differences between fibrin glue and Sil-MAS might result from their different degradation rates.
Laparoscopic surgery using a homemade laparoscopic Sil-MAS device in a rabbit laceration model of liver and stomach serosa Endoscopic or laparoscopic surgery is the preferred surgical approach for patients due to less postoperative pain, better cosmetic results, a shorter duration of hospital stay, and earlier return to work than those of other approaches 24 . Even though this surgical procedure is currently frequently performed, it has numerous complications such as bleeding from the operation site 25 . In this evaluation, we present a proof of concept that Sil-MAS could be a suitable photocuring laparoscopic medical glue via laparoscopic surgery. Therefore, we fabricated an endoscopic device specially designed for laparoscopic surgery, which consists of l-Sil-MAS and a light source (Fig. 7a). This device is designed for easy manipulation and rapid gelation with minimal blood loss inside the body. Last, we applied this system to a rabbit laceration model of liver and stomach serosa through laparoscopic surgery. l-Sil-MAS was easily administered via the laparoscopic surgery device and successfully achieved gelation, adhesion, and hemocoagulation on wet liver tissue via UV treatment (Fig. 7b, Video S7). Likewise, Sil-MAS performed adequately in the laceration model of stomach serosa, which affords the possibility of application to all intestinal lesions through fast and strong adhesive effects (Fig. 7c, Video S8). These results proved that Sil-MAS represents an ideal surgical glue and a viable option to improve the efficiency of laparoscopic operation. In addition, the developed laparoscopic surgery device of an all-in-one sealant/light source would be invaluable to deliver photocurable sealants including Sil-MAS.
As noted above, Sil-MAS was applied well to tissues both externally (skin) and internally (vascular structures, liver, and stomach) with rapid photocrosslinking (within 30 s). The rapid gelation created a physical barrier to protect the wound site, contributed to successful hemostasis, and produced a strong bridge between torn tissues, even for wet tissue such as the liver. We believe that this material's strong adhesive properties result from a combination of mechanical interlocking 17 by  In both groups, stable collagenous tissue (marked by C) and liver tissue (marked by L) were found. Vascular structures (black arrowheads) in the newly formed tissue and cell infiltration (empty arrowheads) into the materials and material absorption were found to be more abundant and to appear earlier in the fibrin glue group than in the Sil-MAS group over a period of 8 weeks. (F: remaining fibrin gel, and S: remaining c-Sil-MAS; see Supporting Information for more details). b Double immunofluorescence analysis for CD31 (endothelial cell, red) and CD68 (macrophage, green) according to the healing process at 1, 2, and 4 weeks. Macrophages and endothelial cells were detected in greater numbers and earlier in the fibrin glue group than in the Sil-MAS group, reflecting more rapid material absorption. The levels of endothelial cells and macrophages were consistent with a mild inflammatory response. This result indicates a normal healing and tissue integration process (see Supporting Information for more details). Scale bars = 100 μm.
penetration of l-Sil-MAS into the irregular tissue surfaces and covalent bonding of the radicals generated during the photopolymerization process 26 . Additionally, the hydrophobic/hydrophilic interactions and electrostatic interactions between the tissue surface and l-Sil-MAS would increase adhesion. The adhesion mechanism of Sil-MAS needs to be further studied to improve our understanding.
The international commission on nonionizing radiation protection (ICNIRP) guidelines recommend limiting UV exposure at 365 nm to 27 J/cm 2 for the eyes and skin 27 . Accordingly, our condition (0.18 J/cm 2 at 365 nm) is well within this limit. It has been reported that LAP, a type I photoinitiator, minimizes cytotoxicity compared with Irgacure 2959 28 . In addition, in contrast to Irgacure 2959, which has a low water solubility (<0.5%) and a molar extinction coefficient of 4 M −1 cm −1 at 365 nm 28 , LAP possesses higher water solubility (<8.5%) and faster polymerization rates due to its higher molar extinction coefficient (218 M −1 cm −1 at 365 nm). If slowed gelation is acceptable, LAP also enables work in the safe visible light region (>400 nm) because of LAP's visible light absorption tail. Free radicals formed during photopolymerization can be more cytotoxic than the photoinitiator itself 29 ; however, it is known that the lifetime of free radicals is shorter than a second and may be promptly quenched following light exposure 29 . Nevertheless, safety evaluations of longer periods of Sil-MAS treatment should be further conducted.
Many sealants are derived from living sources. Animalderived products such as collagen or gelatin involve high costs and the risk of pathogen transmission. Fibrin glue use in surgical procedures has gained popularity in recent years, and its efficacy in hemostasis is well known. However, fibrin glue has poor adhesive functions, difficulties of gelation control, and weak mechanical properties on wet tissues. Additionally, human-derived products risk transmitting viral infections (hepatitis or AIDS) or potentially prion disease. Recombinant products such as MeTro 30 eliminate the risk of infectious transmission; however, they may cause allergic reactions secondary to the hamster or snake proteins used during processing. In contrast, SF is a superior biocompatible material that is nontoxic, biodegradable, and approved by the FDA 4,12,15 . Using published market data, the price per milligram (online search in 2018) of the starting materials for the various sealants is as follows: bovine type I collagen ($1.6/mg), human recombinant tropoelastin ($333/mg), human serum albumin ($175/mg), and fibrinogen from human plasma ($1.1/mg). For SF, the cost is only $0.29/mg. Given all of these advantages, assuming FDA approval and competitive pricing of SF, we would expect Sil-MAS to be rapidly adopted for clinical practice, with low barriers to switching for surgeons.

Conclusions
We present, for the first time, the applicability of a photocurable SF sealant on both wet and dry soft tissue. Sil-MAS provided strong and long-lasting sealing through its excellent adhesive properties, hemostatic effects, and wound healing effect in vitro and in vivo. In addition, Sil-MAS showed biocompatibility and an adequate degradation time, which eliminated the need for retreat or removal of Sil-MAS from the wound site. In particular, the proof-of-concept studies using Sil-MAS and a developed laparoscopic tool suggest application prospects in the field of robotic surgery. Overall, our study suggests that Sil-MAS could be a versatile medical glue worth being applied in clinical use.