Vancomycin-releasing cross-linked collagen sponges as wound dressings

. 2021 Feb 01 ; 21 (1) : 61-70. [epub] 20210201

Jazyk angličtina Země Bosna a Hercegovina Médium electronic

Typ dokumentu časopisecké články

Perzistentní odkaz   https://www.medvik.cz/link/pmid31782696

The study presents a novel vancomycin-releasing collagen wound dressing derived from Cyprinus carpio collagen type I cross-linked with carbodiimide which retarded the degradation rate and increased the stability of the sponge. Following lyophilization, the dressings were subjected to gamma sterilization. The structure was evaluated via scanning electron microscopy images, micro-computed tomography, and infrared spectrometry. The structural stability and vancomycin release properties were evaluated in phosphate buffered saline. Microbiological testing and a rat model of a wound infected with methicillin-resistant Staphylococcus aureus (MRSA) were then employed to test the efficacy of the treatment of the infected wound. Following an initial mass loss due to the release of vancomycin, the sponges remained stable. After 7 days of exposure in phosphate buffered saline (37°C), 60% of the material remained with a preserved collagen secondary structure together with a high degree of open porosity (over 80%). The analysis of the release of vancomycin revealed homogeneous distribution of the antibiotic both across and between the sponges. The release of vancomycin was retarded as proved by in vitro testing and further confirmed by the animal model from which measurable concentrations were observed in blood samples 24 hours after the subcutaneous implantation of the sponge, which was more than observed following intraperitoneal administration. The sponge was also highly effective in terms of reducing the number of colony-forming units in biopsies extracted from the infected wounds 4 days following the inoculation of the wounds with the MRSA solution. The presented sponges have ideal properties to serve as wound dressing for prevention of surgical site infection or treatment of already infected wounds.

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Schimmer C, Özkur M, Sinha B, Hain J, Gorski A, Hager B, et al. Gentamicin-collagen sponge reduces sternal wound complications after heart surgery:A controlled, prospectively randomized, double-blind study. J Thorac Cardiovasc Surg. 2012;143(1):194–200. https://doi.org/10.1016/j.jtcvs.2011.05.035. PubMed

Mishra PK, Ashoub A, Salhiyyah K, Aktuerk D, Ohri S, Raja SG, et al. Role of topical application of gentamicin containing collagen implants in cardiac surgery. J Cardiothorac Surg. 2014;9:122. https://doi.org/10.1186/1749-8090-9-122. PubMed PMC

Lukáč P, Hartinger JM, Mlček M, Popková M, Suchý T, Šupová M, et al. A novel gentamicin-releasing wound dressing prepared from freshwater fish Cyprinus carpio collagen cross-linked with carbodiimide. J Bioact Compat Polym. 2019;34(3):246–62. https://doi.org/10.1177/0883911519835143.

Suchý T, Šupová M, Klapková E, Horný L, Rýglová Š, Žaloudková M, et al. The sustainable release of vancomycin and its degradation products from nanostructured collagen/hydroxyapatite composite layers. J Pharm Sci. 2016;105(3):1288–94. https://doi.org/10.1016/s0022-3549(15)00175-6. PubMed

Suchý T, Šupová M, Klapková E, Adamková V, Závora J, Žaloudková M, et al. The release kinetics, antimicrobial activity and cytocompatibility of differently prepared collagen/hydroxyapatite/vancomycin layers: Microstructure vs nanostructure. Eur J Pharm Sci. 2017;100:219–29. https://doi.org/10.1016/j.ejps.2017.01.032. PubMed

Chiang HY, Herwaldt LA, Blevins AE, Cho E, Schweizer ML. Effectiveness of local vancomycin powder to decrease surgical site infections: A meta-analysis. Spine J. 2014;14(3):397–407. https://doi.org/10.1016/j.aorn.2015.01.018. PubMed

Hamman BL, Stout LY, Theologes TT, Sass DM, da Graca B, Filardo G. Relation between topical application of platelet-rich plasma and vancomycin and severe deep sternal wound infections after a first median sternotomy. Am J Cardiol. 2014;113(8):1415–9. https://doi.org/10.1016/j.amjcard.2013.12.046. PubMed

Vander Salm TJ, Okike ON, Pasque MK, Pezzella AT, Lew R, Traina V, et al. Reduction of sternal infection by application of topical vancomycin. J Thorac Cardiovasc Surg. 1989;98(4):618–22. https://doi.org/10.1016/S0022-5223(19)34366-1. PubMed

Stein GE, Wells EM. The importance of tissue penetration in achieving successful antimicrobial treatment of nosocomial pneumonia and complicated skin and soft-tissue infections caused by methicillin-resistant Staphylococcus aureus:Vancomycin and linezolid. Curr Med Res Opin. 2010;26(3):571–88. https://doi.org/10.1185/03007990903512057. PubMed

Buttaro MA, Gimenez MI, Greco G, Barcan L, Piccaluga F. High active local levels of vancomycin without nephrotoxicity released from impacted bone allografts in 20 revision hip arthroplasties. Acta Orthop. 2005;76(3):336–40. https://doi.org/10.1080/00016470510030797. PubMed

Armaghani SJ, Menge TJ, Lovejoy SA, Mencio GA, Martus JE. Safety of topical vancomycin for pediatric spinal deformity:Nontoxic serum levels with supratherapeutic drain levels. Spine (Phila Pa 1976) 2014;39(20):1683–7. https://doi.org/10.1097/brs.0000000000000465. PubMed

Charriere G, Bejot M, Schnitzler L, Ville G, Hartmann DJ. Reactions to a bovine collagen implant. Clinical and immunologic study in 705 patients. J Am Acad Dermatol. 1989;21(6):1203–8. https://doi.org/10.1016/s0190-9622(89)70330-3. PubMed

John P, Lazarus F, George JP, Selvam A, Prabhuji ML. Adjunctive effects of a piscean collagen-based controlled-release chlorhexidine chip in the treatment of chronic periodontitis:A clinical and microbiological study. J Clin Diagn Res. 2015;9(5):C70–4. https://doi.org/10.7860/jcdr/2015/11534.5965. PubMed PMC

Yamada S, Yamamoto K, Ikeda T, Yanagiguchi K, Hayashi Y. Potency of fish collagen as a scaffold for regenerative medicine. Biomed Res Int. 2014;2014:302932. https://doi.org/10.1155/2014/302932. PubMed PMC

Chou CH, Chen YG, Lin CC, Lin SM, Yang KC, Chang SH. Bioabsorbable fish scale for the internal fixation of fracture: A preliminary study. Tissue Eng Part A. 2014;20(17-18):2493–502. https://doi.org/10.1089/ten.tea.2013.0174. PubMed

Lambert L, Novakova M, Lukac P, Cechova D, Sukenikova L, Hrdy J, et al. Evaluation of the immunogenicity of a vascular graft covered with collagen derived from the European carp (Cyprinus carpio) and bovine collagen. Biomed Res Int. 2019;2019:5301405. https://doi.org/10.1155/2019/5301405. PubMed PMC

Bae I, Osatomi K, Yoshida A, Osako K, Yamaguchi A, Hara K. Biochemical properties of acid-soluble collagens extracted from the skins of underutilised fishes. Food Chem. 2008;108(1):49–54. https://doi.org/10.1016/j.foodchem.2007.10.039.

Harrell CR, Djonov V, Fellabaum C, Volarevic V. Risks of using sterilization by gamma radiation: The other side of the coin. Int J Med Sci. 2018;15(3):274–9. https://doi.org/10.7150/ijms.22644. PubMed PMC

Grus T, Lambert L, Mlcek M, Chlup H, Honsova E, Spacek M, et al. In vivo evaluation of short-term performance of new three-layer collagen-based vascular graft designed for low-flow peripheral vascular reconstructions. Biomed Res Int. 2018;2018:3519596. https://doi.org/10.1155/2018/3519596. PubMed PMC

Bell E, Ivarsson B, Merrill C. Production of a tissue-like structure by contraction of collagen lattices by human fibroblasts of different proliferative potential in vitro. Proc Natl Acad Sci U S A. 1979;76(3):1274–8. https://doi.org/10.1073/pnas.76.3.1274. PubMed PMC

Suchý T, Šupová M, Sauerová P, Verdánová M, Sucharda Z, Rýglová Š, et al. The effects of different cross-linking conditions on collagen-based nanocomposite scaffolds-an in vitro evaluation using mesenchymal stem cells. Biomed Mater. 2015;10:065008. https://doi.org/10.1088/1748-6041/10/6/065008. PubMed

Jiřík M, Bartoš M, Tomášek P, Malečková A, Kural T, Horáková J, et al. Generating standardized image data for testing and calibrating quantification of volumes, surfaces, lengths, and object counts in fibrous and porous materials using X-ray microtomography. Microsc Res Tech. 2018;81(6):551–68. https://doi.org/10.1002/jemt.23011. PubMed

Hildebrand T, Rüegsegger P. A new method for the model-independent assessment of thickness in three-dimensional images. J Microsc. 1997;185(1):67–75. https://doi.org/10.1046/j.1365-2818.1997.1340694.x.

Remy E, Thiel E. Medial axis for chamfer distances:Computing look-up tables and neighbourhoods in 2D or 3D. Pattern Recognit Lett. 2002;23(6):649–61. https://doi.org/10.1016/s0167-⇏(01)00141-6.

Jackson M, Choo LP, Watson PH, Halliday WC, Mantsch HH. Beware of connective tissue proteins:Assignment and implications of collagen absorptions in infrared spectra of human tissues. Biochim Biophys Acta. 1995;1270(1):1–6. https://doi.org/10.1016/0925-4439(94)00056-v. PubMed

Pielesz A. Temperature-dependent FTIR spectra of collagen and protective effect of partially hydrolysed fucoidan. Spectrochim Acta A Mol Biomol Spectrosc. 2014;118:287–93. https://doi.org/10.1016/j.saa.2013.08.056. PubMed

Moise-Broder PA, Forrest A, Birmingham MC, Schentag JJ. Pharmacodynamics of vancomycin and other antimicrobials in patients with Staphylococcus aureus lower respiratory tract infections. Clin Pharmacokinet. 2004;43(13):925–42. https://doi.org/10.2165/00003088-200443130-00005. PubMed

Šíma M, Hartinger J, Cikánková T, Slanař O. Importance of vancomycin loading doses in intermittent infusion regimens. J Infect Chemother. 2018;24(4):247–50. https://doi.org/10.1016/j.jiac.2017.11.002. PubMed

Šíma M, Hronová K, Hartinger J, Slanař O. A simulation of loading doses for vancomycin continuous infusion regimens in intensive care. Infect Dis (Lond) 2017;49(9):674–9. https://doi.org/10.1080/23744235.2017.132∥. PubMed

Ruszczak Z, Friess W. Collagen as a carrier for on-site delivery of antibacterial drugs. Adv Drug Deliv Rev. 2003;55(12):1679–98. https://doi.org/10.1016/j.addr.2003.08.007. PubMed

Morávek J, Málek P. Comparison of serum and coagulum antibiotic levels with respect to protected blood coagulum. Czech Med. 1986;9(4):187–90. PubMed

Suchý T, Šupová M, Bartoš M, Sedláček R, Piola M, Soncini M, et al. Dry versus hydrated collagen scaffolds:Are dry states representative of hydrated states? J Mater Sci Mater Med. 2018;29(3):20. https://doi.org/10.1007/s10856-017-6024-2. PubMed

Šíma M, Hartinger J, ŠtenglováNetíkováI, SlanařO. Creatinine clearance estimations for vancomycin maintenance dose adjustments. Am J Ther. 2018;25(5):e602–4. https://doi.org/10.1097/mjt.0000000000000616. PubMed

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