journal article·2025-01-23Open access

In vitro evaluation of silver-zinc oxide-eugenol nanocomposite for enhanced antimicrobial and wound healing applications in diabetic conditions

Hari Prasath Nagaiah, Malik Basha Samsudeen, Akshaya Rani Augustus, Karutha Pandian Shunmugiah

Discover Nano· Volume 20· Issue 1

Abstract

Diabetic wounds with chronic infections present a significant challenge, exacerbated by the growing issue of antimicrobial resistance, which often leads to delayed healing and increased morbidity. This study introduces a novel silver-zinc oxide-eugenol (Ag+ZnO+EU) nanocomposite, specifically designed to enhance antimicrobial activity and promote wound healing. The nanocomposite was thoroughly characterized using advanced analytical techniques, confirming its nanoscale structure, stability and chemical composition. The Ag+ZnO+EU nanocomposite demonstrated potent antimicrobial efficacy against a range of wound associated pathogens, including standard and clinical isolates of Staphylococcus aureus, Pseudomonas aeruginosa and Candida albicans. Minimum inhibitory concentrations of Ag+ZnO+EU for standard and clinical isolates were significantly lower than those of the individual components, highlighting the synergistic effect of the nanocomposite. Time-kill assays revealed rapid microbial eradication, achieving complete sterility within 240-min. Importantly, the nanocomposite effectively eliminated persister-like cells, which are typically resistant to conventional treatments, suggesting a potential solution for persistent infections. In vitro scratch assays using human keratinocyte cells demonstrated that the Ag+ZnO+EU nanocomposite significantly accelerated wound closure, with near-complete healing observed within 24-h, indicating enhanced cell migration and tissue regeneration. Additionally, the nanocomposite showed potential antidiabetic effects by increasing glucose uptake up to 97.21% in an in vitro assay using 2-[N-(7-nitrobenz-2-oxa-1,3-diazol-4-yl) amino]-2-deoxy-D-glucose, a fluorescent glucose analog, suggesting potential applications beyond wound healing. These findings highlight the Ag+ZnO+EU nanocomposite as a promising candidate for addressing both antimicrobial resistance and impaired wound healing in diabetic contexts.
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Research context

OpenAlex topics: Wound Healing and Treatments · Antimicrobial agents and applications · Nanoparticles: synthesis and applications

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (98)

Show source-provided references
1. International Diabetes Federation. IDF Diabetes Atlas, 10th edn. Brussels; 2021. Available at: https://www.diabetesatlas.org.
2. Umpierrez GE, Davis GM, ElSayed NA, Fadini GP, Galindo RJ, Hirsch IB, et al. Hyperglycaemic crises in adults with diabetes: a consensus report. Diabetologia. 2024;67:1455–79. https://doi.org/10.1007/s00125-024-06183-8.10.1007/s00125-024-06183-8 ↗
3. Chou YY, Hou CC, Wu CW, Huang DW, Tsai SL, Liu TH, et al. Risk factors that predict major amputations and amputation time intervals for hospitalised diabetic patients with foot complications. Int Wound J. 2022;19:1329–38. https://doi.org/10.1111/iwj.13727.10.1111/iwj.13727 ↗
4. Tuglo LS. Prevalence and determinants of lower extremity amputations among type I and type II diabetic patients: a multicenter-based study. Int Wound J. 2023;20:903–9. https://doi.org/10.1111/iwj.13935.10.1111/iwj.13935 ↗
5. Dhingra S, Rahman NAA, Peile E, Rahman M, Sartelli M, Hassali MA, et al. Microbial resistance movements: An overview of global public health threats posed by antimicrobial resistance and how best to counter. Front Public Health. 2020;8: 535668. https://doi.org/10.3389/fpubh.2020.535668.10.3389/fpubh.2020.535668 ↗
6. Mehraj I, Hamid A, Gani U, Iralu N, Manzoor T, Saleem BS. Combating antimicrobial resistance by employing antimicrobial peptides: immunomodulators and therapeutic agents against infectious diseases. ACS Appl Bio Mater. 2024;7:2023–35. https://doi.org/10.1021/acsabm.3c01104.10.1021/acsabm.3c01104 ↗
7. Naveed M, Waseem M, Mahkdoom I, Ali N, Asif F, Hassan J, et al. Transient comparison of techniques to counter multi-drug resistant bacteria: prime modules in curation of bacterial infections. Front Antibiot. 2024;2:1309107. https://doi.org/10.3389/frabi.2023.1309107.10.3389/frabi.2023.1309107 ↗
8. Clare G, Kempen JH, Pavésio C. Infectious eye disease in the 21st century—an overview. Eye. 2024;2024:1–14. https://doi.org/10.1038/s41433-024-02966-w.10.1038/s41433-024-02966-w ↗
9. Barman S, Kurnaz LB, Leighton R, Hossain MW, Decho AW, Tang C. Intrinsic antimicrobial resistance: molecular biomaterials to combat microbial biofilms and bacterial persisters. Biomaterials. 2024;311: 122690. https://doi.org/10.1016/j.biomaterials.2024.122690.10.1016/j.biomaterials.2024.122690 ↗
10. Jothi R, Hari Prasath N, Gowrishankar S, Pandian SK. Bacterial quorum-sensing molecules as promising natural inhibitors of candida albicans virulence dimorphism: an in silico and in vitro study. Front Cell Infect Microbiol. 2021;11: 781790. https://doi.org/10.3389/fcimb.2021.781790.10.3389/fcimb.2021.781790 ↗
11. Priya A, Nivetha S, Pandian SK. Synergistic interaction of piperine and thymol on attenuation of the biofilm formation, hyphal morphogenesis and phenotypic switching in Candida albicans. Front Cell Infect Microbiol. 2022;11: 780545. https://doi.org/10.3389/fcimb.2021.780545.10.3389/fcimb.2021.780545 ↗
12. Nagpal S, Mande SS. Environmental insults and compensative responses: when microbiome meets cancer. Discov Onc. 2023;14:1–18. https://doi.org/10.1007/s12672-023-00745-9.10.1007/s12672-023-00745-9 ↗
13. Dhanda G, Acharya Y, Haldar J. Antibiotic adjuvants: a versatile approach to combat antibiotic resistance. ACS Omega. 2023;8:10757–83. https://doi.org/10.1021/acsomega.3c00312.10.1021/acsomega.3c00312 ↗
14. Kamble E, Sanghvi P, Pardesi K. Synergistic effect of antibiotic combinations on Staphylococcus aureus biofilms and their persister cell populations. Biofilm. 2022;4: 100068. https://doi.org/10.1016/j.bioflm.2022.100068.10.1016/j.bioflm.2022.100068 ↗
15. Lebeaux D, Chauhan A, Létoffé S, Fischer F, De Reuse H, Beloin C, et al. pH-mediated potentiation of aminoglycosides kills bacterial persisters and eradicates in vivo biofilms. J Infect Dis. 2014;210:1357–66. https://doi.org/10.1093/infdis/jiu286.10.1093/infdis/jiu286 ↗
16. Wu M, Guo F, He X, Zheng D, Ye W, Li S, et al. Analysis of distribution and drug susceptibility test results of pathogenic bacteria in diabetic foot ulcers. Diabetes Therapy. 2024;15:1627–37. https://doi.org/10.1007/s13300-024-01601-x.10.1007/s13300-024-01601-x ↗
17. Rahman S, Sadaf S, Hoque ME, Mishra A, Mubarak NM, Malafaia G, et al. Unleashing the promise of emerging nanomaterials as a sustainable platform to mitigate antimicrobial resistance. RSC Adv. 2024;14:13862–99. https://doi.org/10.1039/d3ra05816f.10.1039/d3ra05816f ↗
18. Arshad F, Naikoo GA, Hassan IU, Chava SR, El-Tanani M, Aljabali AA, et al. Bioinspired and green synthesis of silver nanoparticles for medical applications: a green perspective. Appl Biochem Biotechnol. 2023;196:3636–69. https://doi.org/10.1007/s12010-023-04719-z.10.1007/s12010-023-04719-z ↗
19. Zhang J, Liu S, Han J, Wang Z, Zhang S. On the developmental toxicity of silver nanoparticles. Mater Des. 2021;203: 109611. https://doi.org/10.1016/j.matdes.2021.109611.10.1016/j.matdes.2021.109611 ↗
20. Makabenta JMV, Nabawy A, Li CH, Schmidt-Malan S, Patel R, Rotello VM. Nanomaterial-based therapeutics for antibiotic-resistant bacterial infections. Nat Rev Microbiol. 2020;19:23–36. https://doi.org/10.1038/s41579-020-0420-1.10.1038/s41579-020-0420-1 ↗
21. Singh TA, Sharma A, Tejwan N, Ghosh N, Das J, Sil PC. A state of the art review on the synthesis, antibacterial, antioxidant, antidiabetic and tissue regeneration activities of zinc oxide nanoparticles. Adv Colloid Interface Sci. 2021;295: 102495. https://doi.org/10.1016/j.cis.2021.102495.10.1016/j.cis.2021.102495 ↗
22. Halarnekar D, Ayyanar M, Gangapriya P, Kalaskar M, Redasani V, Gurav N, et al. Eco synthesized chitosan/zinc oxide nanocomposites as the next generation of nano-delivery for antibacterial, antioxidant, antidiabetic potential and chronic wound repair. Int J Biol Macromol. 2023;242: 124764. https://doi.org/10.1016/j.ijbiomac.2023.124764.10.1016/j.ijbiomac.2023.124764 ↗
23. Abdelghafar A, Yousef N, Askoura M. Zinc oxide nanoparticles reduce biofilm formation, synergize antibiotics action and attenuate Staphylococcus aureus virulence in host; an important message to clinicians. BMC Microbiol. 2022;22:1–17. https://doi.org/10.1186/s12866-022-02658-z.10.1186/s12866-022-02658-z ↗
24. Parlinska-Wojtan M, Depciuch J, Fryc B, Kus-Liskiewicz M. Green synthesis and antibacterial effects of aqueous colloidal solutions of silver nanoparticles using clove eugenol. Appl Organomet Chem. 2018;32: e4276. https://doi.org/10.1002/aoc.4276.10.1002/aoc.4276 ↗
25. Hajiagha MN, Kafil HS. Efflux pumps and microbial biofilm formation. Infect Genet Evol. 2023;112: 105459. https://doi.org/10.1016/j.meegid.2023.105459.1.10.1016/j.meegid.2023.105459.1 ↗
26. Konuk HB, Ergüden B. Phenolic –OH group is crucial for the antifungal activity of terpenoids via disruption of cell membrane integrity. Folia Microbiol (Praha). 2020;65:775–83. https://doi.org/10.1007/s12223-020-00787-4.10.1007/s12223-020-00787-4 ↗
27. Nagaiah HP, Periyakaruppan Murugesan PD, Ravindra Rupali CV, Shunmugiah KP. Pioneering topical ointment intervention for unprecedented antimicrobial and diabetic wound management with phenylpropanoids and nano-silver. AAPS J. 2024;26:1–19. https://doi.org/10.1208/s12248-024-00936-4.10.1208/s12248-024-00936-4 ↗
28. Ali R, Khamis T, Enan G, El-Didamony G, Sitohy B, Abdel-Fattah G. The healing capability of clove flower extract (CFE) in streptozotocin-induced (STZ-induced) diabetic rat wounds infected with multidrug resistant bacteria. Molecules. 2022;27:2270. https://doi.org/10.3390/molecules27072270.10.3390/molecules27072270 ↗
29. Gowrishankar S, Duncun Mosioma N, Karutha PS. Coral-associated bacteria as a promising antibiofilm agent against methicillin-resistant and -susceptible staphylococcus aureus biofilms. Evid Based Complement Altern Med. 2012;2012: 862374. https://doi.org/10.1155/2012/862374.10.1155/2012/862374 ↗
30. Kasthuri T, Barath S, Nandhakumar M, Karutha PS. Proteomic profiling spotlights the molecular targets and the impact of the natural antivirulent umbelliferone on stress response, virulence factors and the quorum sensing network of Pseudomonas aeruginosa. Front Cell Infect Microbiol. 2022;12: 998540. https://doi.org/10.3389/fcimb.2022.998540.10.3389/fcimb.2022.998540 ↗
31. Muthamil S, Prasath KG, Priya A, Precilla P, Pandian SK. Global proteomic analysis deciphers the mechanism of action of plant derived oleic acid against Candida albicans virulence and biofilm formation. Sci Rep. 2020;10:1–17. https://doi.org/10.1038/s41598-020-61918-y.10.1038/s41598-020-61918-y ↗
32. de Martín GN, Ramlaul K, Aylett CHS. Preparation of sample support films in transmission electron microscopy using a support floatation block. J Vis Exp. 2021. https://doi.org/10.3791/62321.10.3791/62321 ↗
33. Hong J, Mutalik S, Miola M, Gerlach D, Mehrabi KR, Ahmadi M, et al. Nickel boride (NixB) nanocrystals: from solid-state synthesis to highly colloidally stable inks. Chem Mater. 2023;35:1710–22. https://doi.org/10.1021/acs.chemmater.2c03478.10.1021/acs.chemmater.2c03478 ↗
34. Dey B, Narzary R, Chouhan L, Bhattacharjee S, Parida BN, Mondal A, et al. Crystal structure, optical and dielectric properties of Ag:ZnO composite-like compounds. J Mater Sci: Mater Electron. 2022;33:2855–68. https://doi.org/10.1007/s10854-021-07560-4.10.1007/s10854-021-07560-4 ↗
35. Kousar MU, Jabeen A, Fatima T, Hussain SZ, Zargar IA, Amin T, et al. Optimization of ultrasonic-assisted extraction of eugenol-rich fraction from basil leaves: characterization of extract for phenols, flavonoids and antioxidant activity. Food Chem Adv. 2023;3: 100374. https://doi.org/10.1016/j.focha.2023.100374.10.1016/j.focha.2023.100374 ↗
36. Yin Q, Zhou Q, Hu J, Weng J, Liu S, Yin L, Long L, Tong Y, Tang K, Bai S, Ou L. Fabrication of bimetallic Ag@ ZnO nanocomposite and its anti-cancer activity on cervical cancer via impeding PI3K/AKT/mTOR pathway. J Trace Elem Med Biol. 2024;84: 127437. https://doi.org/10.1016/j.jtemb.2024.127437.10.1016/j.jtemb.2024.127437 ↗
37. Zhang X, Bhuvana S, Loo LS. Characterization of layered silicate dispersion in polymer nanocomposites using Fourier transform infrared spectroscopy. J Appl Polym Sci. 2012;125:E175–80. https://doi.org/10.1002/app.36266.10.1002/app.36266 ↗
38. Kasthuri T, Swetha TK, Bhaskar JP, Pandian SK. Rapid-killing efficacy substantiates the antiseptic property of the synergistic combination of carvacrol and nerol against nosocomial pathogens. Arch Microbiol. 2022;204:1–21. https://doi.org/10.1007/s00203-022-03197-x.10.1007/s00203-022-03197-x ↗
39. Priya A, Selvaraj A, Divya D, Karthik Raja R, Pandian SK. In vitro and in vivo anti-infective potential of thymol against early childhood caries causing dual species Candida albicans and Streptococcus mutans. Front Pharmacol. 2021. https://doi.org/10.3389/fphar.2021.760768.10.3389/fphar.2021.760768 ↗
40. Zimmer BL. CLSI-M02; performance standards for antimicrobial disk susceptibility tests, 14th ed; 2024. p. 29.
41. Barros AC, Melo LF, Pereira A. Pseudomonas fluorescens cells’ recovery after exposure to BAC and DBNPA biocides. Antibiotics. 2022;11:1042. https://doi.org/10.3390/antibiotics11081042.10.3390/antibiotics11081042 ↗
42. Mohiuddin SG, Kavousi P, Orman MA. Flow-cytometry analysis reveals persister resuscitation characteristics. BMC Microbiol. 2020;20:1–13. https://doi.org/10.1186/s12866-020-01888-3.10.1186/s12866-020-01888-3 ↗
43. Dombach JL, Quintana JLJ, Detweiler CS. Staphylococcal bacterial persister cells, biofilms and intracellular infection are disrupted by JD1, a membrane-damaging small molecule. mBio. 2021. https://doi.org/10.1128/mbio.01801-21.10.1128/mbio.01801-21 ↗
44. Drew WL, Barry AL, O’Toole R, Sherris JC. Reliability of the Kirby-Bauer disc diffusion method for detecting methicillin-resistant strains of Staphylococcus aureus. Appl Microbiol. 1972;24:240–7. https://doi.org/10.1128/am.24.2.240-247.1972.10.1128/am.24.2.240-247.1972 ↗
45. Swetha TK, Vikraman A, Nithya C, Hari Prasath N, Pandian SK. Synergistic antimicrobial combination of carvacrol and thymol impairs single and mixed-species biofilms of Candida albicans and Staphylococcus epidermidis. Biofouling. 2020;36:1256–71. https://doi.org/10.1080/08927014.2020.1869949.10.1080/08927014.2020.1869949 ↗
46. Sherpa L, Nimmala A, Rao SVSN, Khan SA, Pathak AP, Tripathi A, et al. Refining shape and size of silver nanoparticles using ion irradiation for enhanced and homogeneous SERS activity. Discover Nano. 2024;19:1–19. https://doi.org/10.1186/s11671-024-03994-x.10.1186/s11671-024-03994-x ↗
47. Devi TB, Begum S, Ahmaruzzaman M. Photo-catalytic activity of Plasmonic Ag@AgCl nanoparticles (synthesized via a green route) for the effective degradation of Victoria Blue B from aqueous phase. J Photochem Photobiol B. 2016;160:260–70. https://doi.org/10.1016/j.jphotobiol.2016.03.033.10.1016/j.jphotobiol.2016.03.033 ↗
48. Seo YK, Kumar S, Kim GH. Analysis of assembling ZnO nanoparticles into nanogap electrodes for nanoscale electronic device applications. J Nanosci Nanotechnol. 2011;11:4852–62. https://doi.org/10.1166/jnn.2011.4140.10.1166/jnn.2011.4140 ↗
49. Mtavangu SG, Machunda RL, van der Bruggen B, Njau KN. In situ facile green synthesis of Ag–ZnO nanocomposites using Tetradenia riperia leaf extract and its antimicrobial efficacy on water disinfection. Sci Rep. 2022;12:1–14. https://doi.org/10.1038/s41598-022-19403-1.10.1038/s41598-022-19403-1 ↗
50. Stabryla LM, Moncure PJ, Millstone JE, Gilbertson LM. Particle-driven effects at the bacteria interface: a nanosilver investigation of particle shape and dose metric. ACS Appl Mater Interfaces. 2023;15:39027–38. https://doi.org/10.1021/acsami.3c00144.10.1021/acsami.3c00144 ↗
51. Rajendran R, Mani A. Photocatalytic, antibacterial and anticancer activity of silver-doped zinc oxide nanoparticles. J Saudi Chem Soc. 2020;24:1010–24. https://doi.org/10.1016/j.jscs.2020.10.008.10.1016/j.jscs.2020.10.008 ↗
52. Giroux MS, Zahra Z, Salawu OA, Burgess RM, Ho KT, Adeleye AS. Assessing the environmental effects related to quantum dot structure, function, synthesis and exposure. Environ Sci Nano. 2022;9:867–910. https://doi.org/10.1039/D1EN00712B.10.1039/D1EN00712B ↗
53. Saravanan H, Subramani T, Rajaramon S, David H, Sajeevan A, Sujith S, et al. Exploring nanocomposites for controlling infectious microorganisms: charting the path forward in antimicrobial strategies. Front Pharmacol. 2023;14:1282073. https://doi.org/10.3389/fphar.2023.1282073.10.3389/fphar.2023.1282073 ↗
54. Xue Q, Xiang Z, Wang S, Cong Z, Gao P, Liu X. Recent advances in nutritional composition, phytochemistry, bioactive and potential applications of Syzygium aromaticum L. (Myrtaceae). Front Nutr. 2022;9:1002147. https://doi.org/10.3389/fnut.2022.1002147.10.3389/fnut.2022.1002147 ↗
55. Vasiliev G, Kubo AL, Vija H, Kahru A, Bondar D, Karpichev Y, et al. Synergistic antibacterial effect of copper and silver nanoparticles and their mechanism of action. Sci Rep. 2023;13:1–15. https://doi.org/10.1038/s41598-023-36460-2.10.1038/s41598-023-36460-2 ↗
56. Babayevska N, Przysiecka Ł, Iatsunskyi I, Nowaczyk G, Jarek M, Janiszewska E, et al. ZnO size and shape effect on antibacterial activity and cytotoxicity profile. Sci Rep. 2022. https://doi.org/10.1038/s41598-022-12134-3.10.1038/s41598-022-12134-3 ↗
57. Ansar N, Shahid W, Irshad MA, Shahid S, Nawaz R, Irfan A, et al. Aloe-inspired eco-friendly synthesis of Ag/ZnO heterostructures: boosting photocatalytic potential. Sci Rep. 2024;14:1–11. https://doi.org/10.1038/s41598-024-61466-9.10.1038/s41598-024-61466-9 ↗
58. Alharthi FA, Alghamdi AA, Al-Zaqri N, Alanazi HS, Alsyahi AA, El MA, et al. Facile one-pot green synthesis of Ag–ZnO Nanocomposites using potato peeland their Ag concentration dependent photocatalytic properties. Sci Rep. 2020;10:1–14. https://doi.org/10.1038/s41598-020-77426-y002E.10.1038/s41598-020-77426-y002E ↗
59. El-Naggar NEA, Eltarahony M, Hafez EE, Bashir SI. Green fabrication of chitosan nanoparticles using Lavendula angustifolia, optimization, characterization and in-vitro antibiofilm activity. Sci Rep. 2023;13:1–24. https://doi.org/10.1038/s41598-023-37660-6.10.1038/s41598-023-37660-6 ↗
60. Meng A, Sun S, Li Z, Han J. Synthesis, characterization and dispersion behavior of ZnO/Ag nanocomposites. Adv Powder Technol. 2013;24:224–8. https://doi.org/10.1016/j.apt.2012.06.006.10.1016/j.apt.2012.06.006 ↗
61. Kuyukina MS, Makarova MV, Pistsova ON, Glebov GG, Osipenko MA, Ivshina IB. Exposure to metal nanoparticles changes zeta potentials of Rhodococcus cells. Heliyon. 2022;8: e11632. https://doi.org/10.1016/j.heliyon.2022.e11632.10.1016/j.heliyon.2022.e11632 ↗
62. Pramod K, Suneesh CV, Shanavas S, Ansari SH, Ali J. Unveiling the compatibility of eugenol with formulation excipients by systematic drug-excipient compatibility studies. J Anal Sci Technol. 2015;6:1–14. https://doi.org/10.1186/s40543-015-0073-2.10.1186/s40543-015-0073-2 ↗
63. Xiong G, Pal U, Serrano JG, Ucer KB, Williams RT. Photoluminesence and FTIR study of ZnO nanoparticles: the impurity and defect perspective. Phys Status Solidi (c). 2006;3:3577–81. https://doi.org/10.1002/pssc.200672164.10.1002/pssc.200672164 ↗
64. Jyoti K, Baunthiyal M, Singh A. Characterization of silver nanoparticles synthesized using Urtica dioica Linn. leaves and their synergistic effects with antibiotics. J Radiat Res Appl Sci. 2016;9:217–27. https://doi.org/10.1016/j.jrras.2015.10.002.10.1016/j.jrras.2015.10.002 ↗
65. Agreles MAA, Cavalcanti IDL, Cavalcanti IMF. Synergism between metallic nanoparticles and antibiotics. Appl Microbiol Biotechnol. 2022;106:3973–84. https://doi.org/10.1007/s00253-022-12001-1.10.1007/s00253-022-12001-1 ↗
66. Lou Z, Letsididi KS, Yu F, Pei Z, Wang H, Letsididi AR. Inhibitive effect of eugenol and its nanoemulsion on quorum sensing-mediated virulence factors and biofilm formation by Pseudomonas aeruginosa. J Food Prot. 2019;82:379–89. https://doi.org/10.4315/0362-028X.JFP-18-196.10.4315/0362-028X.JFP-18-196 ↗
67. Ghosh T, Das AB, Jena B, Pradhan C. Antimicrobial effect of silver zinc oxide (Ag-ZnO) nanocomposite particles. Front Life Sci. 2015;8:47–54. https://doi.org/10.1080/21553769.2014.952048.10.1080/21553769.2014.952048 ↗
68. Zeidan NK, Enany NM, Mohamed GG, Marzouk ES. The antibacterial effect of silver, zinc-oxide and combination of silver/zinc oxide nanoparticles coating of orthodontic brackets (an in vitro study). BMC Oral Health. 2022;22:1–14. https://doi.org/10.1186/s12903-022-02263-6.10.1186/s12903-022-02263-6 ↗
69. Rodríguez-Melcón C, Alonso-Calleja C, García-Fernández C, Carballo J, Capita R. Minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) for twelve antimicrobials (biocides and antibiotics) in eight strains of Listeria monocytogenes. J Biology. 2022;11:46. https://doi.org/10.3390/biology11010046.10.3390/biology11010046 ↗
70. Ju J, Xie Y, Yu H, Guo Y, Cheng Y, Qian H, et al. Analysis of the synergistic antifungal mechanism of eugenol and citral. LWT. 2020;123: 109128. https://doi.org/10.1016/j.lwt.2020.109128.10.1016/j.lwt.2020.109128 ↗
71. Huang T, Li X, Maier M, O’Brien-Simpson NM, Heath DE, O’Connor AJ. Using inorganic nanoparticles to fight fungal infections in the antimicrobial resistant era. Acta Biomater. 2023;158:56–79. https://doi.org/10.1016/j.actbio.2023.01.019.10.1016/j.actbio.2023.01.019 ↗
72. Peng H, Rossetto D, Mansy SS, Jordan MC, Roos KP, Chen IA. Treatment of wound infections in a mouse model using Zn2+-releasing phage bound to gold nanorods. ACS Nano. 2022;16:4756–74. https://doi.org/10.1021/acsnano.2c00048.10.1021/acsnano.2c00048 ↗
73. Walicka M, Raczyńska M, Marcinkowska K, Lisicka I, Czaicki A, Wierzba W, et al. Amputations of lower limb in subjects with diabetes mellitus: reasons and 30-day mortality. J Diabetes Res. 2021;2021:8866126. https://doi.org/10.1155/2021/8866126.10.1155/2021/8866126 ↗
74. Kido D, Mizutani K, Takeda K, Mikami R, Matsuura T, Iwasaki K, et al. Impact of diabetes on gingival wound healing via oxidative stress. PLoS One. 2017;12:e0189601. https://doi.org/10.1371/journal.pone.0189601.10.1371/journal.pone.0189601 ↗
75. Sutton JAF, Carnell OT, Lafage L, Gray J, Biboy J, Gibson JF, et al. Staphylococcus aureus cell wall structure and dynamics during host-pathogen interaction. PLoS Pathog. 2021;17: e1009468. https://doi.org/10.1371/journal.ppat.1009468.10.1371/journal.ppat.1009468 ↗
76. López CA, Zgurskaya H, Gnanakaran S. Molecular characterization of the outer membrane of Pseudomonas aeruginosa. BBA- Biomembranes. 2020;1862: 183151. https://doi.org/10.1016/j.bbamem.2019.183151.10.1016/j.bbamem.2019.183151 ↗
77. Ahmadipour S, Field RA, Miller GJ. Prospects for anti-Candida therapy through targeting the cell wall: a mini-review. The Cell Surface. 2021;7: 100063. https://doi.org/10.1016/j.tcsw.2021.100063.10.1016/j.tcsw.2021.100063 ↗
78. Liu C, Ponsero AJ, Armstrong DG, Lipsky BA, Hurwitz BL. The dynamic wound microbiome. BMC Med. 2020;18:1–12. https://doi.org/10.1186/s12916-020-01820-6.10.1186/s12916-020-01820-6 ↗
79. Ralhan K, Iyer KA, Diaz LL, Bird R, Maind A, Zhou QA. Navigating antibacterial frontiers: a panoramic exploration of antibacterial landscapes, resistance mechanisms and emerging therapeutic strategies. ACS Infect Dis. 2024;10:1483–519. https://doi.org/10.1021/acsinfecdis.4c00115.10.1021/acsinfecdis.4c00115 ↗
80. Roy S, Bahar AA, Gu H, Nangia S, Sauer K, Ren D. Persister control by leveraging dormancy associated reduction of antibiotic efflux. PLoS Pathog. 2021;17: e1010144. https://doi.org/10.1371/journal.ppat.1010144.10.1371/journal.ppat.1010144 ↗
81. Narayanaswamy VP, Keagy LL, Duris K, Wiesmann W, Loughran AJ, Townsend SM, et al. Novel glycopolymer eradicates antibiotic- and CCCP-induced persister cells in Pseudomonas aeruginosa. Front Microbiol. 2018;9: 367035. https://doi.org/10.3389/fmicb.2018.01724.10.3389/fmicb.2018.01724 ↗
82. Park J, Nabawy A, Doungchawee J, Mahida N, Foster K, Jantarat T, et al. Synergistic treatment of multidrug-resistant bacterial biofilms using silver nanoclusters incorporated into biodegradable nanoemulsions. ACS Appl Mater Interfaces. 2023;15:37205. https://doi.org/10.1021/acsami.3c06242.10.1021/acsami.3c06242 ↗
83. Lu M, Li Y, Wu MX. Bacteria-specific pro-photosensitizer kills multidrug-resistant Staphylococcus aureus and Pseudomonas aeruginosa. Commun Biol. 2021;4:1–12. https://doi.org/10.1038/s42003-021-01956-y.10.1038/s42003-021-01956-y ↗
84. Cheng G, Dai M, Ahmed S, Hao H, Wang X, Yuan Z. Antimicrobial drugs in fighting against antimicrobial resistance. Front Microbiol. 2016;7: 181062. https://doi.org/10.3389/fmicb.2016.00470.10.3389/fmicb.2016.00470 ↗
85. Zhou L, Zheng H, Tang Y, Yu W, Gong Q. Eugenol inhibits quorum sensing at sub-inhibitory concentrations. Biotechnol Lett. 2013;35:631–7. https://doi.org/10.1007/s10529-012-1126-x.10.1007/s10529-012-1126-x ↗
86. Chang CH, Tsai LH, Lee YC, Yao WC, Lin JJ. Synergistic effects of silicate-platelet supporting Ag and ZnO, offering high antibacterial activity and low cytotoxicity. Int J Mol Sci. 2023;24:7024. https://doi.org/10.3390/ijms24087024.10.3390/ijms24087024 ↗
87. Ellis T, Chiappi M, García-Trenco A, Al-Ejji M, Sarkar S, Georgiou TK, et al. Multimetallic microparticles increase the potency of rifampicin against intracellular Mycobacterium tuberculosis. ACS Nano. 2018;12:5228–40. https://doi.org/10.1021/acsnano.7b08264.10.1021/acsnano.7b08264 ↗
88. Shettigar K, Murali TS. Virulence factors and clonal diversity of Staphylococcus aureus in colonization and wound infection with emphasis on diabetic foot infection. Eur J Clin Microbiol Infect Dis. 2020;39:2235–46. https://doi.org/10.1007/s10096-020-03984-8.10.1007/s10096-020-03984-8 ↗
89. Wood SJ, Kuzel TM, Shafikhani SH. Pseudomonas aeruginosa: infections, animal modeling and therapeutics. Cells. 2023;12:199. https://doi.org/10.3390/cells12010199.10.3390/cells12010199 ↗
90. Naglik JR, Challacombe SJ, Hube B. Candida albicans secreted aspartyl proteinases in virulence and pathogenesis. Microbiol Mol Biol Rev. 2003;67:400. https://doi.org/10.1128/mmbr.67.3.400-428.2003.10.1128/mmbr.67.3.400-428.2003 ↗
91. Li L, Zhang J, Zhang Q, Zhang D, Xiang F, Jia J, et al. High glucose suppresses keratinocyte migration through the inhibition of p38 MAPK/autophagy pathway. Front Physiol. 2019;10: 434485. https://doi.org/10.3389/fphys.2019.00024.10.3389/fphys.2019.00024 ↗
92. Balkrishna A, Gohel V, Pathak N, Tomer M, Rawat M, Dev R, et al. Anti-hyperglycemic contours of Madhugrit are robustly translated in the Caenorhabditis elegans model of lipid accumulation by regulating oxidative stress and inflammatory response. Front Endocrinol (Lausanne). 2022;13:1064532. https://doi.org/10.3389/fendo.2022.1064532.10.3389/fendo.2022.1064532 ↗
93. Bommer C, Sagalova V, Heesemann E, Manne-Goehler J, Atun R, Bärnighausen T, et al. Global economic burden of diabetes in adults: projections from 2015 to 2030. Diabetes Care. 2018;41:963–70. https://doi.org/10.2337/dc17-1962.10.2337/dc17-1962 ↗
94. Sajjad A, Ali H, Zia M. Fabrication and evaluation of vitamin doped Zno/AgNPs nanocomposite based wheat gluten films: a promising findings for burn wound treatment. Sci Rep. 2023;13:1–19. https://doi.org/10.1038/s41598-023-43413-2.10.1038/s41598-023-43413-2 ↗
95. Paskeh MDA, Ghadyani F, Hashemi M, Abbaspour A, Zabolian A, Javanshir S, et al. Biological impact and therapeutic perspective of targeting PI3K/Akt signaling in hepatocellular carcinoma: promises and challenges. Pharmacol Res. 2023;187:106553. https://doi.org/10.1016/j.phrs.2022.106553.10.1016/j.phrs.2022.106553 ↗
96. Tao J, McCourt C, Sultana H, Nelson C, Driver J, Hackmanna TJ. Use of a fluorescent analog of glucose (2-NBDG) to identify uncultured rumen bacteria that take up glucose. Appl Environ Microbiol. 2019. https://doi.org/10.1128/AEM.03018-18.10.1128/AEM.03018-18 ↗
97. Qian H, Kuang Y, Su J, Chen M, Chen X, Lv C, et al. Reductive effect of acitretin on blood glucose levels in chinese patients with psoriasis. Front Med (Lausanne). 2021. https://doi.org/10.3389/fmed.2021.764216.10.3389/fmed.2021.764216 ↗
98. Lazzarini PA, Raspovic KM, Meloni M, van Netten JJ. A new declaration for feet’s sake: halving the global diabetic foot disease burden from 2% to 1% with next generation care. Diabetes Metab Res Rev. 2024;40:e3747. https://doi.org/10.1002/dmrr.3747.10.1002/dmrr.3747 ↗