Zinc oxide nanoparticles using plant Lawsonia inermis and their mosquitocidal, antimicrobial, anticancer applications showing moderate side effects

Microbes or parasites spread vector-borne diseases by mosquitoes without being affected themselves. Insecticides used in vector control produce a substantial problem for human health. This study synthesized zinc oxide nanoparticles (ZnO NPs) using Lawsonia inermis L. and were characterized by UV–vis, FT-IR, SEM with EDX, and XRD analysis. Green synthesized ZnO NPs were highly toxic against Anopheles stephensi, whose lethal concentrations values ranged from 5.494 ppm (I instar), 6.801 ppm (II instar), 9.336 ppm (III instar), 10.736 ppm (IV instar), and 12.710 ppm (pupae) in contrast to L. inermis treatment. The predation efficiency of the teleost fish Gambusia affinis and the copepod Mesocyclops aspericornis against A. stephensi was not affected by exposure at sublethal doses of ZnO NPs. The predatory potency for G. affinis was 45 (I) and 25.83% (IV), copepod M. aspericornis was 40.66 (I) and 10.8% (IV) while in an ZnO NPs contaminated environment, the predation by the fish G. affinis was boosted to 71.33 and 34.25%, and predation of the copepod M. aspericornis was 60.35 and 16.75%, respectively. ZnO NPs inhibited the growth of several microbial pathogens including the bacteria (Escherichia coli and Bacillus subtilis) and the fungi (Alternaria alternate and Aspergillus flavus), respectively. ZnO NPs decreased the cell viability of Hep-G2 with IC50 value of 21.63 µg/mL (R2 = 0.942; P < 0.001) while the concentration increased from 1.88 to 30 µg/mL. These outcomes support the use of L. inermis mediated ZnO NPs for mosquito control and drug development.

Globally, mosquitoes (Diptera: Culicidae) are threatening human individual and public health as vectors of parasites and pathogens 1 . Mosquitoes provide a substantial threat when compared to other disease-transmitting insects as they spread disease causing pathogens. Anopheles stephensi is a vector which transmits the globally most threatful contagious disease malaria 2 . The most serious health problem caused by malaria affects 214 million cases in 2015 3,4 . The appearance of multi-drug resistance of the disease causing protists belonging to Plasmodium spp. possess a major obstacle to successful chemoprophylaxis and chemotherapy of this disease 5 .
Then exposure to acoustic vibrations within determined frequency bands leads to dorsal tracheal trunk (DTT) wall rupture in mosquitoes, resulting in the discharge of gases into the body cavity, that block larval development, increase mortality rates or rendering adult mosquitoes flightless. Phyto-constituents that are naturally Scientific Reports | (2021) 11:8837 | https://doi.org/10.1038/s41598-021-88164-0 www.nature.com/scientificreports/ synthesized by medicinal plants can be utilized for ecofriendly applications in vector control 6,7 . Nanocomplexes using phyto-and microorganisms will minimize the side effects caused by synthetic drugs and also the toxicity to target organisms 8 in an environmentally friendly manner 9 . Drug resistance provides the main drawback in executing chemotherapy in cancer 10 . The development of efficient versatile drugs against both mosquito-borne diseases and cancer were highlighted 11 . In spite of increasing evidence for the outstanding mosquitocidal potency of phyto-synthesized nanocompounds and their toxicity against natural predators of mosquitoes, their effects have rarely been studied with respect to sub-lethal doses on predation 12 . Water predators, including juvenile instars of dragon flies, tadpoles, beetles, fishes, and crustaceans 13 . The impact of predatory animals on water bodies is important because such predators were introduced throughout many warm regions of the world for mosquito control 14 . Metabolites with functional groups such as carbonyl, hydroxyl and functional groups of amines, especially the OH-group of flavonoids that react with metal ions lead to a reduced size of metal ions that can be used for nanoparticle synthesis 12 . Zinc oxide nanoparticles can show several morphological varieties such as nanoflowers, nanosheets and even nanorods which were shown to successfully inhibit the growth and development of the bacteria Escherichia coli, Staphylococcus aureus, and Klebsiella pneumonia. Plant derived nanomaterials exhibit various shapes and sizes when compared to nanoparticles produced by other organisms such as algae, fungi, and bacteria 13 . There is no published report that evaluates zincoxide nanocomplex toxicity against the non-target predatory efficiency of Mesocyclops aspericornis. Traditional medicine records the plant Lawsonia inermis L. as a potential natural dye with numerous medicinal applications. Nanoparticles that are synthesized from the plant materials showed several applications in fields such as medicine, agriculture and the food industry 14 . ZnO NPs (zinc oxide nanoparticles which exhibit remarkable properties such as binding energy (large) and band gap (wide). Wahab et al. 15 demonstrated applications of multi-dimensional (0D, 1D, 2D) nanostructures for the cytological evaluation of cancer cells and their bacterial responses. These were the properties which made zinc oxide nanoparticles biocompatible, safe, and non-toxic 15 . Zinc oxide nanoparticles are known to have different applications, such as in medical and biological industries, optoelectronics, as antiplatelet agents, anti-inflammatory, anti-angiogenesis, especially as auspicious anti-cancer agents, providing catalytic and semiconductor properties 16 . Zincoxide nanoparticles are known to show insecticidal properties 7 . ZnO NPs were synthesized from L. inermis in the present study are also used to resolve the following issues: (a) the lethal effect against the A. stephensi malaria vector, to find out the larvicidal and pupicidal effect; (b) the predatory efficiency of the Gambussia affinis fishes and small crustacean Mesocyclops aspericornis against younger instars of Anopheles larvae in ZnO NPs contaminated water environments; (c) antimicrobial potential of nano-formulations against pathogenic microorganism and; (d) invitro cytotoxicity against the cancer Hep-G2 cells.

Materials and methods
This study was carried out in compliance with the ARRIVE guidelines (http:// www. nc3rs. org. uk/ page. asp? id= 1357).
Several aspects of below materials and methods are similar to and detailed by our earlier paper Jaganathan et al. 17 . All methods were performed in accordance with the relevant guidelines and regulations of international law and the IAECC of Bharathiar University (see below statement).
Anopheles stephensi cultivation. Details are provided in our earlier paper by Jaganathan et al. 17 Anopheles stephensi eggs were collected from a local breeding habitat, a fresh water tank in Kalveerampalaiyam, Coimbatore (Tamil Nadu, India) and laboratory reared for egg hatching (80% relative humidity and 27 °C and a photoperiod of 14:10 h (L/D). Emerging larvae and pupae were used for toxicological testing as outlined below.
Leave collection and processing. Plant samples (Lawsonia inermis) were collected on a private farm at Maruthamalai hill, Coimbatore, Tamil Nadu, India) with the consent of the farmer. No further legal requirements were necessary for the leave collection of this commercially available plant. The collection of this plant material complied with the relevant institutional (Bharathiar University), national, and international guidelines and legislation. It was authenticated at the Botanical Survey of India, whose voucher specimens number was BSI/ SRC/5/23/2019/Tech and deposited at the Department Zoology, BharathiarUniversity. The leaves were rinsed by tap water and dried at room temperature (28 ± 2 °C), and finely powdered. Powdered leave material (10 g) were boiled with 100 mL of double distilled water for further nanocomposite preparation.
Synthesis of ZnO NPs. The leaf extract was combined with 1-mM ZnNO 3 (Sigma-Aldrich, India) solution and was stirred at room temperature (35 ± 2 °C) for 1 h. A brown-yellowish precipitate was heated under stirring at 60 °C for 4 h and further, the solution was continuously stirred at room temperature for 24 h 18 . The precipitate was dried at 100 °C. The obtained sample was ground gently using a pestle and mortar and finally, the sample was calcined at 400 °C for 3 h.
Characterization. The synthesized ZnO NPs samples were analyzed by a UV-vis diffuse reflectance spectroscopy (UV-vis DRS) at a wavelength range of 200-700 nm, using a UV-vis spectrophotometer (Shimadzu-UV 2600, Tokyo, Japan) 19 . Fourier transform infrared spectroscopy (FT-IR) analysis was carried out using a spectrum 65 FT-IR spectrometer (PerkinElmer Co., Ltd., Massachusetts, USA). ZnO NPs were used for scanning electron microscopy (FEI QUANTA-200; SEM), energy-dispersive X-ray spectroscopy (EDX) 18 . XRD pattern were recorded using Cu Kα radiation at a wavelength of 1.54060 Å, with a nickel monochromator in the 2θ range from 10° to 80° using an analytical X-PERT PRO, diffractometer. Predation assays under standard laboratory conditions. Details are provided in our earlier paper Jaganathan et al. 17 . Here, predation efficiency of G. affinis adults was assessed against A. stephensi (I-IV) instar larvae. In each trial mosquitoes, n = 200 larvae were introduced with one G. affinis adult in a 2-L glass arena filled with dechlorinated water and five replicates were conducted. Control arenas contained dechlorinated water only. All arenas were checked every 24 h for 5 days and the number of prey missing that were assumed to be eaten by mosquito fish was recorded. After each check, the missing mosquito larvae were replaced with new ones. Predation efficiency was calculated by (Eq. 2).
We confirm that the experimental protocol was approved by the here named institutional committee: Institutional Animal Ethical Clearance Certificate (IAEC) of the Bharathiar University, Coimbatore-641046 (see appended original document signed by IAEC Chairman Prof. V. Vijaya Padma).

Predatory efficiency of G. affinis species after treatment with synthesized ZnO NPs. Details
are provided in our earlier paper Jaganathan et al. 17 . Predation assays in contaminated aquatic environments: the predation efficiency of G. affinis adults was assessed against I-IV instar larvae of A. stephensi, after a mosquitocidal treatment with standard and green-synthesized ZnO NPs. For both mosquito species, n = 200 I-IV instar larvae were introduced with one G. affinis adult in a 2 L glass tank filled with dechlorinated water plus 1 mL of the desired concentration of NPs (i.e. 5 ppm of ZnO NPs, 1/3 of the LC 50 calculated against I instar mosquito larvae) 20 . For each mosquito species, three replicates were used. Control was dechlorinated water only. All experimental tanks were checked every 24 h at day and night time and the number of prey eaten by mosquito fishes was recorded. After each checking, the predated mosquito larvae were replaced by new ones. Predation efficiency was calculated using the above-mentioned formula (Eq. 2).
Predation of Mesocyclops aspericornis against malaria mosquitoes. Details are provided in our earlier paper Jaganathan et al. 17 . In this experiment, the predation efficiency of Mesocyclops aspericornis adults was assessed against A. stephensi larvae. For each instar, n = 100 mosquitoes were introduced, with 10 copepods, in a 500-mL glass beaker containing 250 mL of dechlorinated water. Mosquito larvae were replaced daily by new ones. For each mosquito instar, five replicates were conducted. Control was 250 mL of dechlorinated water without copepods. All beakers were checked after 1, 2, 3, 4 and 5 days and the number of prey consumed by copepods was recorded. Predatory efficiency was calculated using the following formula (Eq. 2): Predation of M. aspericornis against malaria mosquitoe post-treatment with ZnO NPs. Here, we evaluated the predation efficiency of M. aspericornis adults against A. stephensi larvae, after a mosquitocidal treatment with synthesized ZnO NPs. For each instar, n = 100 mosquitoes were introduced with 10 copepods in a 500-mL glass beaker filled with dechlorinated water treated with synthesized ZnO NPs (i.e. for both species, 1/3 of the LC 50 calculated against first instar larvae). Mosquito larvae were replaced daily with new ones. For each mosquito instar, five replicates were conducted. Consumed by copepods was recorded. Predatory efficiency was calculated using the above-mentioned formula (Eq. 2). Control was dechlorinated water without copepods. All beakers were checked after 1, 2, 3, 4 and 5 days and the number of prey consumed by copepods was recorded.

Antimicrobial inhibitory assay. All were provided by the Microbial Type Culture Collection and Gene
Bank Institute of Microbial Technology Sector 39-A, Chandigarh-160,036 (India). Antimicrobial activity of Li-ZnO NPs was tested against the selected bacteria (Escherichia coli and Bacillus subtilis) and the fungal strains (Alternaria alternate and Aspergillus flavus) using the disk diffusion method 21 . The standard inoculum suspension (10 6 CFU/mL) was streaked over the surface of the media using a sterile cotton swab to ensure confluent www.nature.com/scientificreports/ growth of the organisms. 10 μL of synthesized ZnO NPs was diluted with two volumes of 5% dimethyl sulfoxide (DMSO), impregnated on filter paper disks that were placed on the surface of the agar plates. Petri plates were kept for incubation at room temperature (27 °C ± 2) for 24 h. Inhibition was measured in millimeters using a photomicroscope (Leica ES2, Leipzig, Germany) and compared with standard positive controls, i.e. tetracycline (for bacteria) and fluconazole (for fungi).

Cytotoxicity on liver cancer cell lines. Human liver cancer cell line (Hep-G2) was obtained from
National Centre for Cell Science (NCCS), Pune and grown in Eagles Minimum Essential Medium containing 10% fetal bovine serum (FBS) 22 . The cell lines were cultured and incubated according to the procedure given and used for further toxicity studies.
MTT assay. After 48 h of incubation, 15 μL of MTT (5 mg/ mL) in phosphate buffered saline (PBS) was added to each well and incubated at 37 °C for 4 h. The medium with MTT was then flicked off and the formed formazan crystals were solubilized in 100 μL of DMSO and then measured at 570 nm using a microplate reader 23 . Following the below mentioned formula the cell viability will be calculated (Eq. 3): Data analysis. SPSS 16.0 version was used for all analyses. The average larval and pupal mortality data were subjected to probit analysis for calculating LC 50 , LC 90 , and other statistics at 95% confidence limits, and chisquare values were calculated using the SPSS Statistical software package 13.0 version. Results with P < 0.05 were considered as statistically significant.

Results
As shown in Fig. 1, the absorption spectra obtained for biosynthesized ZnO NP were at 364 nm when investigated under UV-spectroscopy. This absorption was confirmed by the formation ZnO NPs. When L. inermis extract was analyzed by FTIR, its spectrum showed several vibration peaks at 3575, 3272, 2073, 1636 and 489 cm −1 . Thereafter, synthesized ZnO NPs spectrum showed vibration peaks at 1473, 878, 668, and 575 cm −1 (Fig. 2). The nanostructure of synthesized ZnO NPs was seen in SEM which acquired 5 nm given in Fig. 3. EDX analysis of synthesized ZnO NPs showed dual peaks which were situated between 1.2 and 8.6 keV, where it is for zinc characteristic lines K and L shell, as shown in Fig. 4 Percentage cell viability (%) = (Mean experimental call absorbance (A620)/(Mean control call absorbance (A620)) × 100  (Table 4). Antimicrobial effects of synthesized ZnO NPs against selected pathogens like E. coli and B. subtilis (bacteria) and fungal species like Alternaria alternate, and Aspergillus flavus were evaluated in the present investigation. Synthesized ZnO NPs were highly effective in inhibiting the growth of E. coli (13.3 mm) which were then followed by B. subtilis (8.4 mm) respectively given in Table 5 and Fig. 6. Similarly, a maximum zone of inhibition was achieved for the fungus Alternaria alternate (11.5 mm), followed by Aspergillus flavus (7.8 mm). Synthesized ZnO NPs treated with Hep-G2 cell lines were tested to ensure its cell viability after 24 h. The cytotoxicity on Hep-G2 cell lines mediated by ZnO NPs exhibited a dose-dependent relationship as shown in Fig. 7. In the present study IC 50 values were found to be 21.63 µg/mL (R 2 = 0.942; P < 0.001), respectively, and its morphology and cell inhibition was shown in Fig. 8.
ROS results provided a gradual increase of DCF-Fluorescence from 25 to 100 ug/mL ZnO-NPs concentration (Fig. 9). ROS results provided a gradual increase of DCF-Fluorescence from 25 to 100 ug/mL ZnO-NPs concentration Zinc oxide nanoparticles (ZnO NPs) are well known for their anti-cancer effect due to reactive oxygen species (ROS) generation 57,58 . Therefore, their release into the environment is expected to raise major concern towards ecotoxicity. ZnO nanoparticles have the unique ability to induce oxidative stress in cancer cells, which has been found to be one of the mechanisms of cytotoxicity of ZnO nanoparticles towards cancer cells. This property is due to the semiconductor nature of ZnO. ZnO NPs induces ROS generation, leading to oxidative          www.nature.com/scientificreports/ stress and eventually cell death when the anti-oxidative capacity of the cell is exceeded 59,60 . In the present work apoptotic induction potential of synthesized ZnO NPs were concentrations dependently, when the concentration increases the ROS production also increased and leading to cancer cell death (Fig. 9).

Discussion
As shown in Fig. 1, a UV-vis DRS analysis of synthesized ZnO NPs showed an absorption peak at 364 nm, revealing a blue shift at a band gap value of 3.40 eV. The direct band gap of the synthesized ZnO NPs was evaluated using Eq. (4); where Eg provides the band gap (eV) and λ max is the wavelength (nm) of the absorption edge within the spectrum. As a red shift indicates an increase in particle size and a blue shift indicates a decrease in particle size. Generally, green synthesized ZnO NPs show an absorption peak at 375 nm and a band gap at 3.30 eV. The higher band gap ZnO NPs was suitable for biological application, which highly promoted the generation of ROS in NPs 17 (see  www.nature.com/scientificreports/ Fig. 9). In this study, synthesized ZnO NPs exhibited a blue shift of an absorption peak at 364 nm higher ban gap value at 3.31 eV. The same trend was observed with previous reports [24][25][26] . FT-IR spectrum of L. inermis extract exhibited various stretching and transmittance peaks corresponding to various functional groups including alkyl halides, amine, alkynes, and alcohols. Here, peptide bonds of proteins correspond to N-H and C=O stretching frequencies exhibiting a peak at 3575 cm -1 . A similar banding pattern at 3402 cm -1 was reported by Natarajan et al. 27 and or alcohols and/or phenols, as well as aliphatic amines support the presence of polyphenols at 1027 ~ 1092 cm −1 for C-N vibration 28 . The peaks at 802 cm −1 , stay for the C-H stretching frequencies within the free catechins in the aromatic ring 29 . The plant extract consists of bioactive molecules which help in the nucleation process and the formation of Zn (OH) 2 . After calcining at 400 0 C, the sample changed from Zn (OH) 2 into ZnO NPs 23 . The synthesized ZnO NPs spectrum reveal several characteristic peaks at 1473, 878, and 668 & 575 cm −1 respectively, being similar in the vibration modes of the functional chemical bonds of C=O symmetric stretching, C-H bending, and weak Zn-O stretching. Evaluating the surface morphology of synthesized ZnO NPs, our results indicate them as spherical structures of an average of 5 nm in size. Typically, the green synthesized ZnO NPs using phytoconstituents and its products attain morphologies like cubic, rod, triangular, spherical, or sometimes they are flat round of sizes ranging between 5 to 35 nm 30 . Different size and shape of ZnO NPs was related to plant species and bioactive compounds 31,32 . EDX spectra indicates O and Zn elements having energy levels of 0.5, 1.2, and 8.6 keV, respectively. Moreover, two additional peaks of Cl and Ag were found as well. The major peak of the sample represented Ag, which was due to the sputter coating process with silver (Ag). XRD analysis of synthesized ZnO NPs demonstrated a well-crystallized structure. The three distinctly high diffraction peaks at 2θ = 31.75°, 34.40°, and 36.25° corresponded to the planes of (100), (002), and (101) [33][34][35] . This was confirmed by the hexagonal structure of ZnO. This was also matching well with the JCPDS card no. 36-1451.
The toxicity on larval and pupal stages of A. stephensi caused by ZnO NPs might be due to the reduction of nanoparticles caused by the plant extract. The tiny NP spheres penetrate cells and interfere with physiological processes such as molting 36 . The present study corroborates with the findings of Gandhi and Madhusudhan 37 , who postulated the efficiency of Momordica charantia leaves reducing ZnO NPs against C. quinquefasciatus and A. stephensi. Murugan et al. 38 found that Sargassum wightii-synthesized ZnO NPs were highly effective in killing the larvae and pupae of the malaria vector A. stephensi. In contrast, silver nanoparticles were found to be efficient at lower doses against the malarial vector A. stephensi-however, only against its larval instars. Equally high toxic effects against larvae and pupae of A. stephensi. were provided by leaf extracts from both S. occidentalis and Ocimum basilicum. A dose dependent effect was in agreement with previous evidences from other plant extracts 39 . Our results clearly indicate that ZnO NPs affect pathogen growth by cell wall disruption. ZnO NPs may reduce surface hydrophobicity of bacterial cells and its oxidative stress-resistance genes were downregulated, causing finally degradation and the death of cells 40 . ZnO NPs has freshly achieved individual notices concerning possible electronic applications due to its unique optical, electrical, and chemical properties 41 . Its heterogeneous catalytic property might be the cause for bacterial growth inhibition through different mechanisms as known from conventional antibiotics 42,43 . Previous reports of 70-74 postulates higher MIC of ZnO NPs against E. coli, Listeria monocytogenes, Salmonella typhi, and S. aureus provide supportive evidence for the present microbial evaluation. Most of the fungal strains like F. solani, A. alternate, and A. flavus had shown antifungal drug resistance 44 . Hence it was in need to formulate nanoparticles with potent chemical and structural nature to overcome such drug resistance 45 .
Similarly, Chobu et al. 46 demonstrated that Anopheles gambiae was less efficiently predated upon by the mosquitofish G. affinis. Murugan et al. 47 noted that the teleost guppy fish, P. reticulata actively predates on the larvae of A. stephensi. Subramaniam et al. 48 mentioned another study showing that green synthesized Ag NPs with Mimusops elengi did not affect predation rates of the mosquitofish G. affinis on the mosquitoes A. albopictus and A. stephensi. In a paper by Murugan et al. 49 the predatory efficiency of a single copepod species belonging to M. aspericornis was 8.0, 6.3, 0.8, and 0.2 larvae (instar I, II, III, and IV, respectively) per day after a post-treatment with seaweed-synthesized silver nanoparticles. Mahesh Kumar et al. 50 studied the predatory efficiency of a single adult copepod of M. thermocyclopoides being 6.5, 4.6, 0.76, and 0.14 C. quinquefasciatus larvae per day (instar I, II, III, and IV, respectively). The predatory efficiency was enhanced to 8.7, 5.9, 1.2, and 0.36 larvae day (instar I, II, III, and IV, respectively) after treatment with Solanum xanthocarpum fruit extract. Khooshe-Bast et al. 51 insecticidal effects of zinc oxide nanoparticles made with Beauveria bassiana TS11 on the hemipteran insect Trialeurodes vaporariorum.
Several tracemetal based NPs showed effect against different cancer cell lines. Generally, were quantum dot approaches shown as being effective among others in cancer treatment. Ahmad et al. (2020) 52 could demonstrate cytotoxicity and cell death induced by engineered nanostructures (quantum dots and nanoparticles) in human cell lines. Gold quantum dots shown to impair the tumorigenic potential of glioma stem-like cells via β-catenin downregulation. Zinc oxide quantum dots were demonstrated as Multifunctional candidates for arresting C2C12 cancer cells and their role towards caspase 3 and 7 genes 53 . ZnO NPs also acted as anticancer agents with minimum dosage as confirmed by the IC 50 values. In the later study the anti cervical cancer effect of ZnONPs against SiHa cancer cells was evaluated using MTT and apoptosis was evaluated. ZnONPs indicated a suppression of SiHa cells with no cytotoxic effect on normal PBMC cells. Results of cytological staining suggested that ZnONPs induced apoptosis through DNA damage and activation of mitochondria mediated intrinsic pathways. Microwave plasma-assisted silicon nanoparticles were shown to be cytotoxic and to have molecular and numerical responses against cancer cells 54 . Silver nanoparticles and earthworm combinations mediated anti-proliferative activity at increasing concentration as revealed by DNA analysis of Hep-G2 cells 55,56 . In accordance to our present findings were Amorphophallus paeoniifolius peels ZnO NP inducing cancer cell apoptosis at higher concentrations 57  www.nature.com/scientificreports/ Depending on their reactivity and localization, ROS are involved in physiological (termed oxidative eustress) and pathophysiological processes (termed oxidative stress). One major source of increased cellular ROS levels is dysfunctional mitochondria. However, increased ROS levels and, in consequence, an altered redox status of the cell provide a specific vulnerability of cancer cells, which can be used for therapeutic approaches. Recently, two opposing redox status modulating therapies have been tested in clinical trials. In the first approach, antioxidants are used to lower the content of ROS in tumor cells upon treatment of ZnO NPs, subsequently inducing cell cycle arrest and, lastly, apoptosis. The other pro oxidative concept aims to increase the ROS level of cancer cells to an extent that exceeds their survival strategies, and in the end results in an increased apoptotic rate as well 57 . Normally, the imbalance of the pro oxidative and antioxidative systems towards higher ROS levels in cancer cells is still maintained below a cytotoxic threshold. Impairment of the cellular antioxidant system or treatment with exogenous ROS generating agents might exceed a certain ROS threshold, thus resulting in detrimental oxidative stress in the nanomaterial treated cells 58 .
Early apoptotic cells were comparable in abundance to untreated cells up to 12 h after exposure. However, early necrotic cells slightly increased from 12 to 17% at 3 h, although this increase was not significant 59 . On the other hand, viable cells diminished, whereas dead cells significantly accumulated at 12 h. Similarly, ZnOtreated BEAS-2B cells showed an increase in apoptotic cells but not in necrotic cells (Fig. 3C). As these results did not definitively establish apoptosis or necrosis as a driver of ZnO cytotoxicity, we quantified cleaved PARP, an apoptotic marker 60 .

Conclusion
The emergence of multi-drug resistance of vectors and microbes provides a major obstacle for the management of mosquito vectors, cancer, and microorganisms. Hence, there is an urgent need to develop a novel strategy to combat mosquito vectors, and management of cancer. The biosynthesized ZnONPs tested for the lower concentrations possessed larvicidal and pupicidal antimosquito-activities. Field experiments evidenced in addition that larval and pupal populations were reduced with time (24, 48, 72 h). They also boosted the predatory efficiency of the mosquito-fish Gambusia affinis and copepods at the breeding sites. So, it can be concluded that these nanoparticles are most effective in controlling the targeted mosquitoes. Moreover, administration of nanoparticles was shown as one of the vector control measures and further indirectly decreased disease transmission and this way assisted to manage diseases at the community and societal level of larger populations. This kind of bioinsecticide package will further decrease poverty and nuisance in mosquito endemic countries by killing mosquitoes and block disease transmission in a harmonious way and this promotes public health to the society. The same holds for conventional hazards imposed by chemicals in delivery matrices and using nanoparticles to reduce toxicity and side effects of drugs. Moreover, raw materials for the preparation of biosynthesized ZnONPs are easily available, cheap, when compared to other metal oxide nanoparticles like gold, palladium and silver. The final products provided high yields of approximately (85-95%) with high purity (97-99%). Hence, we conclude that the biogenesis of L. inermis-mediated ZnONPs could be used as a multipurpose agent against mosquitoe larvae, being antimicrobial and anticancer at the same time for societal benefit in the field of biomedical applications.