Biofilms as a risk factor for infectious complications in surgery: a review of modern prevention and eradication methods

Cover Page


Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription or Fee Access

Abstract

This review focuses on the analysis of bacterial biofilms as one of the most significant risk factors for the development and chronicity of infectious complications in surgery. Biofilms are structured communities of microorganisms encased in a protective exopolysaccharide matrix, which exhibit high resistance to standard antibiotic therapy and host immune factors through a combination of mechanisms, including limited diffusion of antibacterial agents, the presence of metabolically inactive persister cells, and active horizontal gene transfer of resistance determinants.

This review systematizes data on the clinical significance of biofilms in implant-associated infections, chronic wounds, peritonitis, and mediastinitis. Modern diagnostic methods are examined in detail, highlighting the limitations of traditional microbiological culturing techniques and the significant potential of imaging approaches (specifically confocal microscopy), molecular genetic methods, and the value of detecting specific biofilm biomarkers.

The section on prevention emphasizes the methods for modifying implant surfaces and the application of antimicrobial coatings during surgical procedures. Eradication strategies are analyzed from the perspective of a combined approach, encompassing radical surgical debridement of the infectious focus, physical methods (negative pressure wound therapy with instillation, ultrasonic cavitation), and contemporary pharmacotherapy principles that involve local and systemic antibiotic delivery. Promising innovative directions are highlighted separately, including the use of quorum-sensing inhibitors, bacteriophages producing depolymerases, enzymatic matrix degradation, electrochemical methods, and nanotechnological systems for targeted delivery of antibacterial agents.

We emphasize the necessity of developing multimodal strategies that integrate surgical, physical, and pharmacological methods for the effective control of biofilm-associated infections, which is expected to subsequently reduce the incidence of postoperative complications.

Full Text

Restricted Access

About the authors

Diana F. Sangova

Izhevsk State Medical University

Author for correspondence.
Email: punk.scientist.fast@gmail.com
ORCID iD: 0009-0007-1165-6581
Russian Federation, Izhevsk

Elizaveta R. Krutikova

Izhevsk State Medical University

Email: yelizaveta.krutikova03@mail.ru
ORCID iD: 0009-0009-6758-7583
Russian Federation, Izhevsk

Adelina I. Alyavetdinova

Izhevsk State Medical University

Email: ildarovna28@bk.ru
ORCID iD: 0009-0002-0267-7536
Russian Federation, Izhevsk

Ilsur Sh. Shaydullin

Izhevsk State Medical University

Email: ilsur5555555555440@mail.ru
ORCID iD: 0009-0008-0233-4246
Russian Federation, Izhevsk

Ilmir A. Valiyakhmetov

Izhevsk State Medical University

Email: ilmirv7@gmail.com
ORCID iD: 0009-0003-5974-2295
Russian Federation, Izhevsk

Danil L. Garifyanov

Izhevsk State Medical University

Email: danil.garifyanow@yandex.ru
ORCID iD: 0009-0003-2334-9176
Russian Federation, Izhevsk

Elina M. Sadykova

Izhevsk State Medical University

Email: elinoshka50@gmail.com
ORCID iD: 0009-0001-6032-9671
Russian Federation, Izhevsk

Roman O. Volodin

Voronezh State Medical University

Email: gelog552@gmail.com
ORCID iD: 0009-0001-6216-898X
Russian Federation, Voronezh

Vladimir V. Salamatin

Voronezh State Medical University

Email: voci4ka@yandex.ru
ORCID iD: 0009-0008-6364-9292
Russian Federation, Voronezh

Leyla V. Guseynova

Irkutsk State Medical University

Email: brodskayaaal@gmail.com
ORCID iD: 0009-0002-7570-2093
Russian Federation, Irkutsk

Margarita L. Lbova

Izhevsk State Medical University

Email: margo.lbova@mail.ru
ORCID iD: 0009-0000-2519-863X
Russian Federation, Izhevsk

Angelina A. Korneeva

Irkutsk State Medical University

Email: korneevaangel03@mail.ru
ORCID iD: 0009-0007-6750-1589
Russian Federation, Irkutsk

References

  1. Uruén C, Chopo-Escuin G, Tommassen J, et al. Biofilms as promoters of bacterial antibiotic resistance and tolerance. Antibiotics (Basel). 2020;10(1):3. doi: 10.3390/antibiotics10010003 EDN: LURPRG
  2. Almatroudi A. Biofilm resilience: molecular mechanisms driving antibiotic resistance in clinical contexts. Biology (Basel). 2025;14(2):165. doi: 10.3390/biology14020165 EDN: RHHZXX
  3. Petukhova IN, Dmitrieva NV, Grigor’evskaya ZV, et al. Infections associated with biofilm formation. Zlokachestvennye opukholi. 2019;9(3S1):26–31. (In Russ.) doi: 10.18027/2224-5057-2019-9-3s1-26-31 EDN: OVRDJZ
  4. Harika K, Shenoy VP, Narasimhaswamy N, Chawla K. Detection of biofilm production and its impact on antibiotic resistance profile of bacterial isolates from chronic wound infections. J Glob Infect Dis. 2020;12(3):129–134. doi: 10.4103/jgid.jgid_150_19 EDN: YBHJIX
  5. Karygianni L, Ren Z, Koo H, Thurnheer T. Biofilm matrixome: extracellular components in structured microbial communities. Trends Microbiol. 2020;28(8):668–681. doi: 10.1016/j.tim.2020.03.016 EDN: ILFPKC
  6. Di Martino P. Extracellular polymeric substances, a key element in understanding biofilm phenotype. AIMS Microbiol. 2018;4(2):274–288. doi: 10.3934/microbiol.2018.2.274
  7. Erkihun M, Asmare Z, Endalamew K, et al. Medical scope of biofilm and quorum sensing during biofilm formation: systematic review. Bacteria. 2024;3(3):118–135. doi: 10.3390/bacteria3030008
  8. Sankaran J, Tan NJHJ, But KP, et al. Single microcolony diffusion analysis in Pseudomonas aeruginosa biofilms. NPJ Biofilms Microbiomes. 2019;5(1):35. doi: 10.1038/s41522-019-0107-4
  9. Campoccia D, Montanaro L, Arciola CR. Extracellular DNA (eDNA). A major ubiquitous element of the bacterial biofilm architecture. Int J Mol Sci. 2021;22(16):9100. doi: 10.3390/ijms22169100 EDN: UJZEWE
  10. Buzzo JR, Devaraj A, Gloag ES, et al. Z-form extracellular DNA is a structural component of the bacterial biofilm matrix. Cell. 2021;184(23):5740–5758.e17. doi: 10.1016/j.cell.2021.10.010 EDN: AWYLYL
  11. Ferguson DL, Gloag ES, Parsek MR, Wozniak DJ. Extracellular DNA enhances biofilm integrity and mechanical properties of mucoid Pseudomonas aeruginosa. J Bacteriol. 2023;205(10):e0023823. doi: 10.1128/jb.00238-23 EDN: KTLZSG
  12. Lin J, Cheng J. Quorum sensing in Pseudomonas aeruginosa and its relationship to biofilm development. In: Introduction to Biofilm Engineering. American Chemical Society. 2019. P. 1–16. doi: 10.1021/bk-2019-1323.ch001
  13. Wille J, Coenye T. Biofilm dispersion: The key to biofilm eradication or opening Pandora’s box? Biofilm. 2020;2:100027. doi: 10.1016/j.bioflm.2020.100027 EDN: DWAJTQ
  14. Stewart PS, White B, Boegli L, et al. Conceptual model of biofilm antibiotic tolerance that integrates phenomena of diffusion, metabolism, gene expression, and physiology. J Bacteriol. 2019;201(22):e00307–00319. doi: 10.1128/JB.00307-19
  15. Kunnath AP, Suodha Suoodh M, Chellappan DK, et al. Bacterial persister cells and development of antibiotic resistance in chronic infections: an update. Br J Biomed Sci. 2024;81:12958. doi: 10.3389/bjbs.2024.12958
  16. Soares A, Alexandre K, Etienne M. Tolerance and persistence of Pseudomonas aeruginosa in biofilms exposed to antibiotics: molecular mechanisms, antibiotic strategies and therapeutic perspectives. Front Microbiol. 2020;11:2057. doi: 10.3389/fmicb.2020.02057 EDN: IDFZFE
  17. Ayrapetyan M, Williams T, Oliver JD. Relationship between the viable but nonculturable state and antibiotic persister cells. J Bacteriol. 2018;200(20):e00249-18. doi: 10.1128/JB.00249-18 EDN: CQWMMH
  18. Michaelis C, Grohmann E. Horizontal gene transfer of antibiotic resistance genes in biofilms. Antibiotics (Basel). 2023;12(2):328. doi: 10.3390/antibiotics12020328 EDN: PZRNRU
  19. Abe K, Nomura N, Suzuki S. Biofilms: hot spots of horizontal gene transfer (HGT) in aquatic environments, with a focus on a new HGT mechanism. FEMS Microbiol Ecol. 2020;96(5):fiaa031. doi: 10.1093/femsec/fiaa031 EDN: WPMDIP
  20. Johnston EL, Zavan L, Bitto NJ, et al. Planktonic and biofilm-derived pseudomonas aeruginosa outer membrane vesicles facilitate horizontal gene transfer of plasmid DNA. Microbiol Spectr. doi: 10.1128/spectrum.05179-22 EDN: SOKDHM
  21. Liu HY, Prentice EL, Webber MA. Mechanisms of antimicrobial resistance in biofilms. NPJ Antimicrob Resist. 2024;2(1):27. doi: 10.1038/s44259-024-00046-3 EDN: HRCKJU
  22. Visperas A, Santana D, Klika AK, et al. Current treatments for biofilm-associated periprosthetic joint infection and new potential strategies. J Orthop Res. 2022;40(7):1477–1491. doi: 10.1002/jor.25345 EDN: XDKOAA
  23. Lyubimova LV, Bozhkova SA, Pchelova NN, et al. The role of culture-negative infection among infectious complications after total knee arthroplasty. Orthopaedic Genius. 2023;29(4):402–409. doi: 10.18019/1028-4427-2023-29-4-402-409 EDN: LUEAAK
  24. Tello-Díaz C, Palau M, Muñoz E, et al. Methicillin-susceptible staphylococcus aureus biofilm formation on vascular grafts: an in vitro study. Microbiol Spectr. doi: 10.1128/spectrum.03931-22 EDN: RGKNLY
  25. Ruke MG, Savai J. Diabetic foot infection, biofilm & new management strategy. Diabetes Research: Open Access. 2019;2019(1):7–22. doi: 10.36502/2019/droa.6152
  26. Dos Santos ACML, Hernandes RT, Montelli AC, et al. Clinical and microbiological factors predicting outcomes of nonfermenting gram-negative bacilli peritonitis in peritoneal dialysis. Sci Rep. 2021;11(1):12248. doi: 10.1038/s41598-021-91410-0 EDN: WOGAED
  27. Aref R, Ágnes B, Nasri A, Zsofia V. Effective combination of incisional negative pressure wound therapy and radical reconstructive surgery in the treatment of post-sternotomy mediastinitis caused by methicillin resistant Staphylococcus aureus. Biomed J Sci &Tech Res. 2018;2(5):BJSTR.MS.ID.000812. doi: 10.26717/BJSTR.2018.02.000812
  28. Grari O, Ezrari S, El Yandouzi I, et al. A comprehensive review on biofilm-associated infections: Mechanisms, diagnostic challenges, and innovative therapeutic strategies. The Microbe. 2025;8:100436. doi: 10.1016/j.microb.2025.100436
  29. Palan J, Nolan C, Sarantos K, et al. Culture-negative periprosthetic joint infections. EFORT Open Rev. 2019;4(10):585–594. doi: 10.1302/2058-5241.4.180067
  30. Godovalov AP, Karpunina TI. The determination of biofilm composition of Gram-positive bacteria. Clinical Laboratory Diagnostics. 2019;64(10):632–634. doi: 10.18821/0869-2084-2019-64-10-632-634 EDN: XIITJI
  31. Dassanayake RP, Falkenberg SM, Stasko JA, et al. Identification of a reliable fixative solution to preserve the complex architecture of bacterial biofilms for scanning electron microscopy evaluation. PLoS One. 2020;15(5):e0233973. doi: 10.1371/journal.pone.0233973 EDN: CDDIPG
  32. Reichhardt C, Parsek MR. Confocal laser scanning microscopy for analysis of pseudomonas aeruginosa biofilm architecture and matrix localization. Front Microbiol. 2019;10:677. doi: 10.3389/fmicb.2019.00677 EDN: ZHISPG
  33. Relucenti M, Familiari G, Donfrancesco O, et al. Microscopy methods for biofilm imaging: focus on SEM and VP-SEM pros and cons. Biology (Basel). 2021;10(1):51. doi: 10.3390/biology10010051 EDN: ETCZCY
  34. Baishya J, Everett JA, Chazin WJ, et al. The innate immune protein calprotectin interacts with and encases biofilm communities of Pseudomonas aeruginosa and Staphylococcus aureus. Front Cell Infect Microbiol. 2022;12:898796. doi: 10.3389/fcimb.2022.898796 EDN: DDKNXU
  35. Asghari E, Kiel A, Kaltschmidt BP, et al. Identification of microorganisms from several surfaces by MALDI-TOF MS: P. aeruginosa is leading in biofilm formation. Microorganisms. 2021;9(5):992. doi: 10.3390/microorganisms9050992 EDN: BIRRTU
  36. Madden DE, Olagoke O, Baird T, et al. Express yourself: quantitative real-time PCR assays for rapid chromosomal antimicrobial resistance detection in pseudomonas aeruginosa. Antimicrob Agents Chemother. 2022;66(5):e0020422. doi: 10.1128/aac.00204-22 EDN: YQDQOG
  37. Kamali E, Jamali A, Ardebili A, et al. Evaluation of antimicrobial resistance, biofilm forming potential, and the presence of biofilm-related genes among clinical isolates of Pseudomonas aeruginosa. BMC Res Notes. 2020;13(1):27. doi: 10.1186/s13104-020-4890-z EDN: SVTGKM
  38. Ingram JR, Cawley S, Coulman E, et al. Levels of wound calprotectin and other inflammatory biomarkers aid in deciding which patients with a diabetic foot ulcer need antibiotic therapy (INDUCE study). Diabet Med. 2018;35(2):255–261. doi: 10.1111/dme.13431
  39. Khatoon Z, McTiernan CD, Suuronen EJ, et al. Bacterial biofilm formation on implantable devices and approaches to its treatment and prevention. Heliyon. 2018;4(12):e01067. doi: 10.1016/j.heliyon.2018.e01067 EDN: GNXZDD
  40. Drugeon B, Rickard CM, Schults JA, et al. Chlorhexidine and povidone-iodine: Unmasking the unknown in catheter-related infection prevention, a narrative review. J Infect Public Health. 2025;18(9):102851. doi: 10.1016/j.jiph.2025.102851 EDN: FHKQCF
  41. Detusheva EV, Ershova ON, Fursova NK. The sensitivity of planktonic cultures and biofilms of gram-negative bacteria to commercial disinfectant and antiseptic preparations. Klin Lab Diagn. 2021;66(7):438–447. doi: 10.51620/0869-2084-2021-66-7-438-447 EDN: JVCOJG
  42. Morozov AM, Sergeev AN, Chervinets VM, et al. Methods of preventing surgical site infections. Ambulatornaya khirurgiya. 2024;21(1):168–176. doi: 10.21518/akh2024-013 EDN: CGFXTN
  43. Lai J, Li Q, He Y, et al. Glycemic control regimens in the prevention of surgical site infections: a meta-analysis of randomized clinical trials. Front Surg. 2022;9:855409. doi: 10.3389/fsurg.2022.855409 EDN: TMQRVP
  44. Morisaki S, Yoshii K, Tsuchida S, et al. The role of preoperative glycemic control in decreasing surgical site infections in lower extremity fractures. J Orthop Surg Res. 2023;18(1):700. doi: 10.1186/s13018-023-04204-7 EDN: FBLZFV
  45. Mu M, Liu S, DeFlorio W, et al. Influence of surface roughness, nanostructure, and wetting on bacterial adhesion. Langmuir. 2023;39(15):5426–5439. doi: 10.1021/acs.langmuir.3c00091 EDN: YRGJZP
  46. Spengler C, Nolle F, Mischo J, et al. Strength of bacterial adhesion on nanostructured surfaces quantified by substrate morphometry. Nanoscale. 2019;11(42):19713–19722. doi: 10.1039/c9nr04375f
  47. Plechev VV, Timerbulatov MV, Sufiyarov IF. Implantation antimicrobial prophylaxis in general and military field surgery. Creative Surgery and Oncology. 2024;14(4):336–344. doi: 10.24060/2076-3093-2024-14-4-336-344 EDN: STSOYJ
  48. Puges M, Bérard X, Vilain S, et al. Staphylococcus aureus adhesion and biofilm formation on vascular polyester grafts are inhibited in vitro by triclosan. Eur J Vasc Endovasc Surg. 2023;66(4):577–586. doi: 10.1016/j.ejvs.2023.07.018 EDN: HCLPED
  49. Mufty H, Van den Bergh M, Meuris B, et al. Clinical studies reporting on vascular graft coatings for the prevention of aortic graft infection: a systematic review and meta-analysis. Eur J Vasc Endovasc Surg. 2022;63(1):112–118. doi: 10.1016/j.ejvs.2021.09.020 EDN: DTDNSC
  50. Xu Y, Wang L, Xu W. Risk factors affect success rate of debridement, antibiotics and implant retention (DAIR) in periprosthetic joint infection. Arthroplasty. 2020;2(1):37. doi: 10.1186/s42836-020-00056-2 EDN: MCMEYH
  51. Zhang CF, He L, Fang XY, et al. Debridement, antibiotics, and implant retention for acute periprosthetic joint infection. Orthop Surg. 2020;12(2):463–470. doi: 10.1111/os.12641 EDN: OFOLWT
  52. Poilvache H, Ruiz-Sorribas A, Sakoulas G, et al. Synergistic effects of pulsed lavage and antimicrobial therapy against Staphylococcus aureus biofilms in an in-vitro model. Front Med (Lausanne). 2020;7:527. doi: 10.3389/fmed.2020.00527 EDN: QWQJPR
  53. Serena TE, Jalodi O, Serena L, et al. Evaluation of the combination of a biofilm-disrupting agent and negative pressure wound therapy: a case series. J Wound Care. 2021;30(1):9–14. doi: 10.12968/jowc.2021.30.1.9 EDN: MTNDAX
  54. Tahir S, Malone M, Hu H, et al. The effect of negative pressure wound therapy with and without instillation on mature biofilms in vitro. Materials (Basel). 2018;11(5):811. doi: 10.3390/ma11050811
  55. Diehm YF, Loew J, Will PA, et al. Negative pressure wound therapy with instillation and dwell time (NPWTi-d) with V. A. C. VeraFlo in traumatic, surgical, and chronic wounds-A helpful tool for decontamination and to prepare successful reconstruction. Int Wound J. 2020;17(6):1740–1749. doi: 10.1111/iwj.13462 EDN: BJERFO
  56. Russo A, Gatti A, Felici S, et al. Piezoelectric ultrasonic debridement as new tool for biofilm removal from orthopedic implants: A study in vitro. J Orthop Res. 2023;41(12):2749–2755. doi: 10.1002/jor.25599 EDN: TUNHLQ
  57. Berberich CE. Current concepts of local antibiotic delivery in bone and joint infections-a narrative review of techniques and clinical experiences. Microorganisms. 2025;13(10):2276. doi: 10.3390/microorganisms13102276 EDN: NFEOKB
  58. Ivantsov VA, Lashkovsky VV, Bogdanovich IP, Lazarevich SN. Treatment of deep periprosthetic infection of knee joint. Journal of the Grodno State Medical University. 2018;16(1):96–100. doi: 10.25298/2221-8785-2018-16-1-96-100 EDN: YREKJJ
  59. Cara A, Ferry T, Laurent F, Josse J. Prophylactic antibiofilm activity of antibiotic-loaded bone cements against Gram-negative bacteria. Antibiotics (Basel). 2022;11(2):137. doi: 10.3390/antibiotics11020137 EDN: GLVEIS
  60. Depypere M, Kuehl R, Metsemakers WJ, et al. Recommendations for systemic antimicrobial therapy in fracture-related infection: a consensus from an international expert group. J Orthop Trauma. 2020;34(1):30–41. doi: 10.1097/BOT.0000000000001626 EDN: CBAUZC
  61. Sharma S, Mohler J, Mahajan SD, et al. A review on formation, infection, antibiotic resistance, control measures, and innovative treatment. Microorganisms. 2023;11(6):1614. doi: 10.3390/microorganisms11061614 EDN: EULMCW
  62. Spitzmüller R, Gümbel D, Güthoff C, et al. Duration of antibiotic treatment and risk of recurrence after surgical management of orthopaedic device infections: a multicenter case-control study. BMC Musculoskelet Disord. 2019;20(1):184. doi: 10.1186/s12891-019-2574-4 EDN: OENIRU
  63. Bonnet E, Lourtet-Hascoët J. Combination antibiotic therapy for orthopedic infections. Antibiotics (Basel). 2025;14(8):761. doi: 10.3390/antibiotics14080761 EDN: EVFWHU
  64. Saqr AA, Aldawsari MF, Khafagy ES, et al. A novel use of allopurinol as a quorum-sensing inhibitor in Pseudomonas aeruginosa. Antibiotics (Basel). 2021;10(11):1385. doi: 10.3390/antibiotics10111385 EDN: YSNRXQ
  65. Murray EJ, Dubern JF, Chan WC, et al. A Pseudomonas aeruginosa PQS quorum-sensing system inhibitor with anti-staphylococcal activity sensitizes polymicrobial biofilms to tobramycin. Cell Chem Biol. 2022;29(7):1187–1199.e6. doi: 10.1016/j.chembiol.2022.02.007 EDN: DPCRGW
  66. Khayat MT, Abbas HA, Ibrahim TS, et al. Anti-quorum sensing activities of gliptins against Pseudomonas aeruginosa and Staphylococcus aureus. Biomedicines. 2022;10(5):1169. doi: 10.3390/biomedicines10051169 EDN: BBHHHZ
  67. Chegini Z, Khoshbayan A, Taati Moghadam M, et al. Bacteriophage therapy against Pseudomonas aeruginosa biofilms: a review. Ann Clin Microbiol Antimicrob. 2020;19(1):45. doi: 10.1186/s12941-020-00389-5 EDN: RZUPRD
  68. Topka-Bielecka G, Dydecka A, Necel A, et al. Bacteriophage-derived depolymerases against bacterial biofilm. Antibiotics (Basel). 2021;10(2):175. doi: 10.3390/antibiotics10020175 EDN: UUTSEA
  69. Rice CJ, Kelly SA, O’Brien SC, et al. Novel phage-derived depolymerase with activity against Proteus mirabilis biofilms. Microorganisms. 2021;9(10):2172. doi: 10.3390/microorganisms9102172 EDN: GJPJUH
  70. Mayorga-Ramos A, Carrera-Pacheco SE, Barba-Ostria C, Guamán LP. Bacteriophage-mediated approaches for biofilm control. Front Cell Infect Microbiol. 2024;14:1428637. doi: 10.3389/fcimb.2024.1428637 EDN: SPQDJW
  71. Kaplan JB, Sukhishvili SA, Sailer M, et al. Aggregatibacter actinomycetemcomitans Dispersin B: the quintessential antibiofilm enzyme. Pathogens. 2024;13(8):668. doi: 10.3390/pathogens13080668 EDN: XXAHFF
  72. Romanova YuM, Tutelyan AV, Sinitsyn AP, et al. Enzymes from carbohydrase group destroy biofilm matrix of gram-positive and gram-negative bacteria. Medical Alphabet. 2019;4(34):40–45. doi: 10.33667/2078-5631-2019-4-34(409)-40-45 EDN: AAQEOR
  73. Hari P, Kacharaju KR, Anumala N, et al. Application of bioelectric effect to reduce the antibiotic resistance of subgingival plaque biofilm: An in vitro study. J Indian Soc Periodontol. 2018;22(2):133–139. doi: 10.4103/jisp.jisp_320_17
  74. Chavez-Manini CA, Reza-López SA, Arzate-Quintana C, et al. Effect of electric current in viability, biofilm formation and antibiotic resistance of Pseudomonas aeruginosa: A systematic review. Indian J Med Microbiol. 2024;52:100735. doi: 10.1016/j.ijmmb.2024.100735 EDN: IICMDR
  75. Li H, Yang Z, Khan SA, et al. Characteristics of metallic nanoparticles (especially silver nanoparticles) as anti-biofilm agents. Antibiotics (Basel). 2024;13(9):819. doi: 10.3390/antibiotics13090819 EDN: TKGOTS
  76. Xu J, Li Y, Wang H, et al. Enhanced antibacterial and anti-biofilm activities of antimicrobial peptides modified silver nanoparticles. Int J Nanomedicine. 2021;16:4831–4846. doi: 10.2147/IJN.S315839 EDN: JSCOTI
  77. Ahsan A, Thomas N, Barnes TJ, et al. Lipid nanocarriers-enabled delivery of antibiotics and antimicrobial adjuvants to overcome bacterial biofilms. Pharmaceutics. 2024;16(3):396. doi: 10.3390/pharmaceutics16030396 EDN: UMMNJE

Supplementary files

Supplementary Files
Action
1. JATS XML
2. Fig. 1. Visual model of biofilm stability and therapeutic targets. ABT – antibiotic therapy; EPS – extracellular polymeric substance (matrix); QS – quorum sensing.

Download (165KB)

Copyright (c) 2026 Eco-Vector

License URL: https://eco-vector.com/for_authors.php#07

СМИ зарегистрировано Федеральной службой по надзору в сфере связи, информационных технологий и массовых коммуникаций (Роскомнадзор).
Регистрационный номер и дата принятия решения о регистрации СМИ: серия  ПИ № ФС 77 - 86296 от 11.12.2023 г
СМИ зарегистрировано Федеральной службой по надзору в сфере связи, информационных технологий и массовых коммуникаций (Роскомнадзор).
Регистрационный номер и дата принятия решения о регистрации СМИ: серия ЭЛ № ФС 77 - 80632 от 15.03.2021 г
.