Biosynthesis of Co3O4 nanomedicine by using Mollugo oppositifolia L. aqueous leaf extract and its antimicrobial, mosquito larvicidal activities

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Mar 26, 2023

Biosynthesis of Co3O4 nanomedicine by using Mollugo oppositifolia L. aqueous leaf extract and its antimicrobial, mosquito larvicidal activities

Scientific Reports volume 13,

Scientific Reports volume 13, Article number: 9002 (2023) Cite this article

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Nanotechnology is a relatively revolutionary area that generates day-to-day advancement. It makes a significant impact on our daily life. For example, in parasitology, catalysis and cosmetics, nanoparticles possess distinctive possessions that make it possible for them in a broad range of areas. We utilized Mollugo oppositifolia L. aqueous leaf extract assisted chemical reduction method to synthesize Co3O4 nanoparticles. Biosynthesized Co3O4 Nps were confirmed via UV–Vis spectroscopy, scanning electron microscope, X-ray diffraction, EDX, Fourier-transform infrared, and HR-TEM analysis. The crystallite size from XRD studies revealed around 22.7 nm. The biosynthesized Co3O4 nanoparticle was further assessed for mosquito larvicidal activity against south-urban mosquito larvae Culex quinquefasciatus, and antimicrobial activities. The synthesized Co3O4 particle (2) displayed significant larvicidal activity towards mosquito larvae Culex quinquefasciatus with the LD50 value of 34.96 µg/mL than aqueous plant extract (1) and control Permethrin with the LD50 value of 82.41 and 72.44 µg/mL. When compared to the standard antibacterial treatment, Ciprofloxacin, the Co3O4 nanoparticle (2) produced demonstrates significantly enhanced antibacterial action against the pathogens E. coli and B. cereus. The MIC for Co3O4 nanoparticles 2 against C. albicans was under 1 μg/mL, which was much lower than the MIC for the control drug, clotrimale, which was 2 µg per milliliter. Co3O4 nanoparticles 2, with a MIC of 2 μg/mL, has much higher antifungal activity than clotrimale, whose MIC is 4 μg/mL, against M. audouinii.

Chemical insecticides are used for mosquito control, but they are harmful to non-target animals and trigger human health issues. Therefore, effective and economically friendly control systems must be targeted in order to manage this challenge effectively. In order to monitor mosquitoes successfully through several mechanisms, biopesticides can be created. Globally, mosquitoes transmit terrible diseases and parasites, such as measles, dengue, filariasis, etc. Mosquitoes are common and end in almost two million lives each year1. Many mosquito diseases, like damage of socioeconomic and manual work in subtropical and tropical countries, consume financial power, but vector-borne diseases are not protected in the climate of earth's ecosystems2. Anopheles stephensi is the primary vector of malaria in India. Malaria, while with a previous squeak of between 1.1 and 2.7 million, has been one of the main serious infectious diseases with a prevalence estimated at 300–500 million through health manifestations. Nearly 40 percent of people living in the biosphere also remain in tropical malaria sites3. For between 120 and 44 million citizens worldwide, the lymphatic filariasis agent of Culex quinquefasciatus, usually distributed through rainfall, is a recurring phenomenon4.

The specific mechanism underlying the larvicidal action of AgNPs is not entirely known, considering the existence of several research articles on the topic. The smaller size of AgNPs has led some authors to believe that they can easily penetrate the insect gut wall and bind to the sulfur and phosphorus group of deoxyribonucleic acid, causing cell death by interfering with normal functioning like replication. The mechanism of action of AgNPs towards larvae is poorly understood, with just a small number of publications available5,6,7,8,9. The effects of NPs on mosquito larvae were studied by Kumar et al. in terms of morphological, biochemical, physiological, and molecular alterations10.

Infectious illnesses, in general, constitute a severe danger to public health across the globe, particularly when antibiotic-resistant probiotic pathogens evolve. Gram-positive and Gram-negative strains of bacteria are both regarded to be a substantial public health concern. Antibiotics were used to manage diseases in both the community and hospital settings for many years11,12,13.

Mollugo oppositifolia L., often known as slim carpet weed, belongs to the Molluginaceae species (English). It's a thin, widespread, sleek, branching annual plant with 20 to 30 cm high branches that thrives in both dry and wet environments. Leaves are alternate or leathery, in tendrils of 4–5, uneven, oblanceolate or linear-lanceolate or occasionally rounded or sharp and apiculate at the apex, greatly tapering into the inconspicuous petiole. Flowers are white and borne in two or more axillary fascicles. Capsules are ellipsoid in shape and contain many dark brown seeds. Creaper and undesired roots14. In ethnomedicine, the herb is used for stomachic, earache, aperients, and skin problems. The leaves have a harsh flavor and are antiseptic. Mollugo subspecies have been shown to have antibacterial, anticancer, anti-inflammatory, and hepatoprotective properties15.

Due to their fascinating properties, nano-structure materials have drawn significant attention in recent years. Among these elements, much focus is drawn to research on fundamental characteristics and functional applications of transition-metal oxides16,17,18,19. Among the transition-metal oxides, cobalt oxides, Co3O4 and CoO are flexible materials that are stable in the natural environment20,21. In recent years, owing to their possible applications, much effort has been guided towards the synthesis and investigation of Co3O4 and CoO nanostructures22,23,24. Co3O4 is the thermodynamically stable type of cobalt oxide below 1164 K in ambient air, while Co3O4 is decomposed into CoO above this temperature25. Co3O4 is a natural spinel26 at room temperature and has several possible applications in gas sensors, magnetic materials, catalysts, and absorbers of solar energy27,28,29,30. Several processes, such as oxidation, microwave-assisted hydrothermal, ultrasonic, and hydrothermal have recently been developed for the preparation of Co3O431,32,33,34. CoO, on the other hand, crystallises in the structure of rock salt and has possible uses in many areas, such as lithium battery anodes, pigments, magnetoresistant reading heads, and gas sensors35,36,37. While there are a few studies on the synthesis of CoO in bulk form, through simple methods, this compound is hard to acquire in pure form, mostly polluted with Co3O4 and Co metal.

Cobalt nanoparticles (Co NPs) have gained a lot of interest recently owing to their unique electrical and magnetic characteristics and lower cost compared to noble metal nanoparticles (NPs)38,39. Biomedical researchers have investigated the potential of CoNPs as therapeutic agents for the therapy of disorders like microbial infection40,41. At low concentrations, CoNPs are safe for the body, have potent antimicrobial and antifungal activities, and fewer adverse effects than antibiotics42,43.

Yin and Wang demonstrated that in the existence of surfactant Na(AOT) at 130 °C in air, decomposition of Co2(CO)8 in toluene occurs in CoO nanocrystals combined with Co3O4 and Co44. Ye et al. developed CoO nanomaterials under solvothermal conditions by an esterification reaction45. Ghosh et al. synthesised pure CoO nanoparticles under solvothermal conditions by the decomposition of Co(II) cupferronate in decalin at 270 °C46. Very recently, via a spry roasting process, Guo et al. prepared CoO particles using the CoCl2 solution47. A basic synthesis strategy, different from those described above, is suggested in this article. Through green chemistry approach Mollugo oppositifolia L. aqueous leaf extract assisted strategy, we will report on the synthesis process of Co3O4 nanoparticles and evaluation of its mosquito larvicidal and antimicrobial activities.

The detailed schematic representation of biosynthesized Co3O4 nanoparticles is shown in Fig. 1a. FTIR spectra are often collected between 400 and 4000 cm−1. The FT-IR spectra of the biosynthesized Co3O4 NPs are shown in Fig. 1b. A wide peak at 3465.93 cm−1 indicates the presence of the N–H group, which may have appeared as an amine moiety. The presence of C–H functional group alkanes is indicated by a band between 2800 and 3000 cm−1. C=O was identified at 1644.01 cm−1 from the PVP moiety, as shown by spectral peaks. Both tetrahedral and octahedral Co–O vibrations are confirmed by the bands at 509.59 cm−1 and 584.80 cm−1, respectively. The functional groups of the capping agent and the synthesis of Co3O4 nanoparticles were authenticated by FT-IR analysis. In addition, The XRD pattern was employed to analyze the phase purity and crystalline nature of biosynthesized Co3O4 NPs, as shown in Fig. 1c.

(a) The schematic representation of biosynthesized Co3O4 nanoparticles. (b) FT-IR spectra. (c) XRD spectra and (d) UV–visible spectra of biosynthesized Co3O4 nanoparticles.

Pure face-centered cubic spinel phase structure of Co3O4 NPs was identified by diffraction peaks at 2 = 31.2°, 37.6°, 38.7°, 44.8°, 55.6°, 59.8°, and 66.3°, which were indexed to (220), (311), 222), 400, (422), 511, and 440) planes. Standard Co3O4 NPs were found to have diffraction peaks that were quite similar to those produced. The diffraction peaks all rather closely match the typical distribution for pure Co3O4 nanoparticles (JCPDS No. 00-042-1467). Certain peaks indicative of impurities have been detected. These pronounced peaks show that the resulting nanoparticles are very crystalline. The average crystallographic size may be determined from the observed primary diffracted peak by using the Scherer equation,

where, D(hkl) is the typical crystallographic dimension, k is shape constant (0.89), λ is the wavelength of the incident x-ray (Cukα source, λ = 0.15405 nm), β is the full width half maximum (FWHM), θ is the incident angle of x-ray. A 22.70 nm Co3O4 crystal was successfully produced.

Furthermore, UV–visible spectroscopy was used to investigate the optical absorption characteristics of the biosynthesized Co3O4 NPs at room temperature, and the results are shown in Fig. 1d. The formation of Co3O4 NPs is indicated by a UV–visible absorption peak at 409 nm. Our research focuses on two distinct absorption bands, between 200 and 340 nm and 336 and 409 nm. According to published research, these bands can be assigned to the O2– → Co2+ and O2– → Co3+ charge transfer processes, respectively. In addition, the plant extract shows an absorption peak at around 238 nm which confirms the successful formation of biosynthesized Co3O4 nanoparticles.

Scanning electron microscopy was used to regulate the resulting Co3O4 NPs' size and form (SEM). Scanning electron microscopy (SEM) scans confirmed the spherical shape of the biosynthesized Co3O4 NPs (Fig. 2a–c). The biosynthesized Co3O4 NPs were distributed in the wild as a population of uniformly sized particles. In addition, the EDX analysis confirmed the atomic composition of the biosynthesized Co3O4 NPs. The presence of cobalt and oxygen peaks in the EDX spectra confirmed that the material was really Co3O4 NPs (Fig. 2d). There was 3.58% cobalt and 64.20% oxygen by molecular weight. Extra peaks in the EDX spectra might be due to bioorganic or contaminant presence in the solution. The chemical composition of the biosynthesized Co3O4 nanoparticles is shown in Fig. 2e. Studies using scanning electron microscopy to map the nanoparticle proved its identity as Co3O4 (Fig. 2f). Cobalt is represented by the pink dots, whereas Oxygen is shown by the green ones. Detailed morphological features and chemical compositions of biosynthesized Co3O4 nanoparticles were analyzed by HR-TEM, obtained results are shown in Fig. 2g–j. TEM images demonstrate the existence of aggregated polycrystalline particles with restricted size distribution and a spherical shape. The particle size from TEM images is well-matched with the particle size predicted by the Debye–Scherrer equation. Figure 2j shows the elemental mapping of biosynthesized Co3O4 nanoparticles, which confirms the presence of Co and O elements with uniform distribution.

(a–c) FE-SEM morphology images (d–f) EDX spectra and elemental mapping (g–j) HR-TEM images and (j) elemental mapping of biosynthesized Co3O4 nanoparticles.

The biosynthesized Co3O4 particle (2) was much more active in contrast to Culex quinquefasciatus with an LD50 value of 34.96 μg/mL than the aqueous plant extract (1) and control Permethrin, which had LD50 values of 82.41 and 72.44 μg/mL, respectively. The aqueous plant extract (1) showed the least amount of activity against Culex quinquefasciatus, with LD50 values that were respectively 82.41 μg/mL. This was one of the samples that was tested. When compared to the positive control Permethrin, which had an LD50 value of 72.44 μg/mL, the manufactured Co3O4 nanoparticle (2) exhibited very high levels of activity, while the aqueous plant extract (1) exhibited only moderate levels of activity. The findings are shown in Table 1 below.

The antibacterial activity of ciprofloxacin was tested in vitro against four different bacteria: two Gram-negative (E. coli and Pseudomonas aeruginosa) and two Gram-positive (S. aureus and Bacillus cereus). The MIC values were determined using the standard agar method. Figure 3 and Table 2 displays the MIC values for both the synthesized Co3O4 nanoparticle (2) and the aqueous leaf extract of Mollugo oppositifolia L. (1). Compared to an aqueous leaf extract of Mollugo oppositifolia L., the antibacterial activity of the synthetic Co3O4 nanoparticle is much greater (1). Co3O4 nanoparticle (2) has significant antibacterial activity against E. coli, with a minimal inhibitory concentration (MIC) of 23.60 μg/mL compared to a MIC of 25.00 μg/mL for the control ciprofloxacin. Co3O4 nanoparticle (2) had a substantially lower MIC of 26.56 μg/mL than the 50.00 μg/mL of the control ciprofloxacin against B. cereus. The MIC for Co3O4 nanoparticle (2) against P. aeruginosa and S. aureus was 34 and 28 μg/mL, respectively, which is somewhat higher than the MIC for normal ciprofloxacin. Synthetic Co3O4 nanoparticle (2) substantially surpassed the reference activity in killing E. coli and B. cereus when compared to the gold standard antibacterial Ciprofloxacin.

Antibacterial image plates of biosynthesized Co3O4 nanoparticles (IZ—inhibition zone).

Fresh leaf extract 1 of Mollugo oppositifolia L. and synthetic nanoparticle 2 were both examined for their ability to inhibit the activity of four different types of fungi. When compared to compound 1, compound 2 is substantially more effective against fungi. Compound 2 effectively combats the fungal infections caused by Candida albicans and Malassezia audouinii. The minimal inhibitory concentration (MIC) of Compound 2 for C. albicans growth was 01 μg/mL, which was much lower than the control clotrimale (02 μg/mL). Compound 2 has an even lower MIC against M. audouinii than clotrimale, which has a MIC of 4 μg/mL. You can see the results in Table 3 and Fig. 4.

Antifungal image plates of biosynthesized Co3O4 nanoparticles.

The Co3O4 Nps, were studied for their docking behavior with 3OGN protein via Autodock Vina program. The Co3O4 Nps, shows excellent binding affinity (− 8.5 kcal/mol) than permethrin with the binding affinity of (− 4.4 kcal/mol) in 3OGN protein respectively. Hydrogen bonding is one of the significant factor in the stability of protein–ligand bonding, and the favorable bond distance amongst the H-donor and the H-acceptor atoms is less than 3.5 Å. The hydrogen bond distances of Co3O4 Nps, were less than 3.5 Å in respective 3OGN protein signifies strong hydrogen bonding. Co3O4 Nps, forms three hydrogen bond interaction with the receptor 3OGN. The amino acid residue Asp118 (bond length: 2.10), His121 (bond length: 1.63) and Phe123 (bond length: 1.98) were involved in hydrogen bonding contacts. The amino acid residues Tyr10, Pro11, and Ile87 were involved in hydrophobic interactions. The interactions of Co3O4 Nps with 3OGN protein were shown in Fig. 5. The control permethrin did not form any Hydrogen bond interaction with the receptor 3OGN. The amino acid residues Leu15, Leu19, Phe59, Leu76, Leu76, His77, Leu80, Ala88, Met89, Gly92, His111, Trp114, Phe123 and Leu124 were involved in hydrophobic interactions. The interactions of compound permethrin with 3OGN protein were shown in Fig. 6. The results shows that Co3O4 Nps having remarkable inhibition ability than control permethrin in larvicidal mosquito odorant binding protein 3OGN. The results were summarized in Table 4.

Docked complex (a), Helix (b), molecular surface (c), and 3D (d) interaction modes of compound Co3O4 Nps within the binding site of 3OGN protein.

Docked complex (a), molecular surface (b), 3D (c), and 2D (d) interaction modes of control permethrin within the binding site of 3OGN protein.

Progressive experience is an imperative of the hour for successful mosquito vector regulator. The current research highlights the recorded method of Mollugo oppositifolia L. aqueous leaf extract assisted synthesis of nanoparticles of Co3O4. Biosynthesized Co3O4 Nps were confirmed via UV–vis spectroscopy, Fourier-transform infrared spectroscopy, X-ray diffraction, scanning electron microscope, HR-TEM and mapping studies. In addition, Co3O4 nanoparticle was further evaluated for mosquito larvicidal, antibacterial and antifungal activities. When compared to an aqueous plant extract (1) and control Permethrin (LD50 = 82.41 and 72.44 μg/mL, respectively), the activity of the synthesized Co3O4 particle (2) against Culex quinquefasciatus was much higher. The synthesized Co3O4 nanoparticle (2) exhibits an antibacterial activity that is much greater than that of the control Ciprofloxacin in both the pathogens E. coli and B. cereus. When compared to the control Clotrimale, which had a MIC value of 2 μg/mL, the Co3O4 nanoparticles 2 had a MIC value of 1 μg/mL, which made them substantially more effective against C. albicans. In comparison, the antifungal activity of Co3O4 nanoparticles 2 against M. audouinii is much greater than that of Clotrimale, which has a minimal inhibitory concentration (MIC) value of 4 μg/mL. Consequently, Co3O4 nanoparticles might be a probable basis for emerging environmentally friendly bioactive compound, as well as ecological biopharmaceuticals and insecticides.

All chemical substances and solvents were purchased from Nice and Loba chemicals. High-purity solvents were utilized for synthesis processes without further purification. The bacterial strains E. coli, Pseudomonas aeruginosa, S. aureus and Bacillus cereus as well as different types of fungi were purchased from Iranian biological resource center, Pasture Institute of Iran.

The Mollugo oppositifolia L. used in this study was gathered from several locations in the greater Chennai region. Leaf waste from recent harvests was used in the production of Co3O4 Np. The collection of plant material and related studies complies with relevant institutional, national, and international guidelines and legislation.

The Mollugo oppositifolia L. plant species were used to generate the extract solution from the leaves of the plant. Greens from a plant that have been collected quite recently washed with deionized water and chopped very coarsely. Following the boiling of the plant material in 100 mL of distilled water at 100 °C, it was filtered and then stored at 4 °C for further examination.

Preparing cobalt oxide nanoparticles began with dissolving CoCl2⋅6H2O (0.1 g) in a sufficient amount of deionized water, followed by the addition of 10 mL of a solution containing an extract of the Mollugo oppositifolia L. plant. Then, for 3 h at room temperature, the mixture was agitated at a speed of 1000 rpm using a magnetic stirrer. The pH of the reaction mixture was adjusted by adding a 1 mL solution of 10% NaOH to the mixture. The precipitate was filtered and then evaporated for 12 h, the oven was set to 150 °C and let to do its thing. Following collection, the powder was calcined for 3 h at 500 °C before being ground into a fine powder.

Cobalt oxide nanoparticles were synthesized by using ultrasonic assisted chemical precipitation technique. UV–Visible spectra was recorded with V-730 UV–visible Spectrophotometer at a wavelength range between 200 and 800 nm. FT-IR spectra was recorded with Fourier transform infrared spectrometer (FT/IR-6600) (CHI 1000C) in the range 4000–400 cm−1, Powder XRD was assessed with X'Pert Pro by PANalytical, FE-SEM with EDX and Mapping were done with FESEM sigma essential by Zeiss Microscopy. HR-TEM images and mapping images of the biosynthesized Co3O4 nanoparticle are obtained from HR-TEM (Hitachi). Molecular docking studies were used to inspect the interaction, binding mode between compounds Co3O4 Nps, Permethrin and the mosquito odorant binding protein using Autodock vina 1.1.228. The crystal structure of mosquito odorant binding protein (PDB ID: 3OGN) was taken from Protein Data Bank (http://www.rcsb.org). The 3D assembly of the compounds Co3O4 Nps, and permethrin were achieved via ChemDraw Ultra 12.0 and Chem3D Pro 12.0 software. The input files for Autodock Vina were created by using Autodock Tools 1.5.6 program package. The search grid of 3OGN protein was fixed at center_x: 18.681, center_y: 49.66, and center_z: 11.409 with dimensions size_x: 22, size_y: 20, and size_z: 22 with spacing of 1.0 Å. The exhaustiveness value was set to 8. The other parameters were set to default for Vina docking and not mentioned. The compound having least binding affinity value is the best-scoring compound and the results were visually analyzed using Discovery studio 2019 program.

The biosynthesized Co3O4 nanoparticle was further assessed for larvicidal activity against south urban mosquito larvae Culex quinquefasciatus. Appraisals were made on 'a dead/alive premise. The evaluations are based on a rate size that ranges from 0 to 100, where 0 represents no activity at all and 100 represents outright murder. The bioassay was repeated a number of times, and the results of the bioactivity test served as the standard for each of these replications. The characteristics are compared with those of the positive control substance permethrin. The LD50 values of a few different dynamic title mixtures were determined by probit analysis, and the results were analyzed through the use of the SPSS v16 software.

The aqueous plant extract (1) and combined Co3O4 nanoparticle (2) were assessed for larvicidal activity against south urban mosquito larvae Culex quinquefasciatus. The assessment of larvicidal activity at the starter test convergence of 100 μg/mL in contrast to the 4th instar south-urban mosquito larvae Culex quinquefasciatus through water immersion strategy beneath relative stickiness 50–70%, photoperiod of 10:14 (light: dark), and temperature of (27 ± 2) °C. The tests were set up at the convergences of 100, 75, 50, 25 μg/mL by utilizing dissolvable Dimethylsulfoxide (DMSO). All the test measuring glasses comprising twenty Culex quinquefasciatus were assessed for 24 h later handling. The outcomes were documented by average percent mortality.

Kirby Bauer tested the antibacterial effectiveness of an aqueous plant extract (1) and a mixed Co3O4 nanoparticle suspension against Staphylococcus aureus, Escherichia coli, Klebsiella pneumophila, and Pseudomonas aeruginosa in vitro (2). Discs are the preferred method for dispersing molecules48. The antibacterial activity of ciprofloxacin was utilized as a standard. Bacteria were cultured on petri plates using nutrient agar. All of the synthesis was carried out in DMSO, and the chemicals were held on a filter paper disc that measured 5 mm in diameter and 1 mm in thickness. After 24 h incubation at 37 °C, the discs were tested for antibacterial activity by measuring the size of the inhibitory zone49,50 surrounding each one put on the plates that had previously been implanted. Minimum inhibitory concentrations (MIC) were used to compare the antibacterial activity of an aqueous plant extract (1) and Co3O4 nanoparticles (2).

The standardized disc–agar diffusion technique51,52 was used to assess the antifungal activity of aqueous plant extract (1) and combined Co3O4 nanoparticle (2). Microsporum audouinii (MTCC-8197), Candia albicans (MTCC-227), Cryptococcus neoformans (recultured) and Aspergillus niger (MTCC-872) were used to test antifungal activity. The materials were sterilised by filtering using 0.22 m Millipore filters after being dissolved in 10% dimethyl sulfoxide (DMSO) to a desired concentration of 30 mg/mL. Antifungal studies were then performed utilising disc diffusion technique with 100 L of solution containing 104 spore/mL of fungi dispersed over PDA medium. The discs (6 mm in diameter) were treated with 10 mL of the samples (300 g/disc) and put on the infected agar. The typical medicine was clotrimale. 10 percent DMSO was used to make negative controls. For fungus specimens, the inoculation plates were then incubated at 37 °C for 72 h. Fungi linked with plants were cultured at 27 °C. The zone of inhibition against the tested strains was used to assess antifungal activity. In this study, each test was carried out twice.

The datasets used and/or analysed during the current study available from the corresponding author on reasonable request.

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This research was supported by Hongik University's 'Project for the Establishment of Regionally Specialized Smart City Graduate School. This work was also supported by the International Science & Business Belt support program, through the Korea Innovation Foundation funded by the Ministry of Science and ICT.

PG Department of Chemistry, Shrimati Devkunvar Nanalal Bhatt Vaishnav College for Women, Chennai, India

P. Gowthami

School of Basic Sciences, Vels Institute of Science, Technology & Advanced Studies (VISTAS), Pallavaram, Chennai, India

P. Gowthami & A. Kosiha

Department of Chemistry, SRM Institute of Science and Technology (SRMIST), Ramapuram Campus, Chennai, 600 089, India

S. Meenakshi

Peri College of Arts and Science, Mannivakkam, Chennai, 600048, India

G. Boopathy

Department of Materials Science and Engineering, Hongik University, 2639, Sejong-ro, Jochiwon-eup, Sejong, 30016, Republic of Korea

A. G. Ramu & Dongjin Choi

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P.G.: conceptualization, investigation, writing—original draft. A.K.: investigation, visualization. S.M.: data curation, experimental instruments sources, sample analysis. G.B.: instruments sources, investigation, data curation, visualization. A.G.R.: data curation, experimental instruments sources, sample analysis. D.C.: conceptualization, writing—original draft, revision, supervision, project administration, funding acquisition.

Correspondence to A. Kosiha or Dongjin Choi.

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Gowthami, P., Kosiha, A., Meenakshi, S. et al. Biosynthesis of Co3O4 nanomedicine by using Mollugo oppositifolia L. aqueous leaf extract and its antimicrobial, mosquito larvicidal activities. Sci Rep 13, 9002 (2023). https://doi.org/10.1038/s41598-023-35877-z

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Received: 23 March 2023

Accepted: 25 May 2023

Published: 02 June 2023

DOI: https://doi.org/10.1038/s41598-023-35877-z

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