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Comparison of the Impact of NaIO 4 -Accelerated, Cu 2+ /H 2 O 2 -Accelerated, and Novel Ion-Accelerated Methods of Poly(l-DOPA) Coating on Collagen-Sealed Vascular Prostheses: Strengths and Weaknesses.

التفاصيل البيبلوغرافية
العنوان: Comparison of the Impact of NaIO 4 -Accelerated, Cu 2+ /H 2 O 2 -Accelerated, and Novel Ion-Accelerated Methods of Poly(l-DOPA) Coating on Collagen-Sealed Vascular Prostheses: Strengths and Weaknesses.
المؤلفون: Fornal M; Chair and Department of Biochemistry and Biotechnology, Medical University of Lublin, Chodźki 1, 20-093 Lublin, Poland., Krawczyńska A; Faculty of Materials Science and Engineering, Warsaw University of Technology, 141 Wołoska, 02-507 Warsaw, Poland., Belcarz A; Chair and Department of Biochemistry and Biotechnology, Medical University of Lublin, Chodźki 1, 20-093 Lublin, Poland.
المصدر: ACS applied materials & interfaces [ACS Appl Mater Interfaces] 2024 Aug 07; Vol. 16 (31), pp. 40515-40530. Date of Electronic Publication: 2024 Jul 23.
نوع المنشور: Journal Article; Comparative Study
اللغة: English
بيانات الدورية: Publisher: American Chemical Society Country of Publication: United States NLM ID: 101504991 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1944-8252 (Electronic) Linking ISSN: 19448244 NLM ISO Abbreviation: ACS Appl Mater Interfaces Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Washington, D.C. : American Chemical Society
مواضيع طبية MeSH: Copper*/chemistry , Copper*/pharmacology , Coated Materials, Biocompatible*/chemistry , Coated Materials, Biocompatible*/pharmacology , Hydrogen Peroxide*/chemistry , Anti-Bacterial Agents*/chemistry , Anti-Bacterial Agents*/pharmacology , Blood Vessel Prosthesis* , Collagen*/chemistry, Humans
مستخلص: Sensitive biomaterials subjected to surface modification require delicate methods to preserve their structures and key properties. These include collagen-sealed polyester vascular prostheses. For their functionalization, coating with polycatecholamines (PCAs) can be used. PCAs change some important biological properties of biomaterials, e.g., hydrophilicity, bioactivity, antibacterial activity, and drug binding. The coating process can be stimulated by oxidants, organic solvents, or process conditions. However, these factors may change the properties of the PCA layer and the matrix itself. In this work, collagen-sealed vascular grafts were functionalized with a poly(l-DOPA) (PLD) layer using novel seawater-inspired ion combination as an accelerator, compared to the sodium periodate, Cu 2+ /H 2 O 2 mixture, and accelerator-free reference methods. Then, poly(l-DOPA) was used as the interface for antibiotic binding. The coated prostheses were characterized (SEM, FIB-SEM, FTIR, UV/vis), and their important functional parameters (mechanical, antioxidant, hemolytic, and prothrombotic properties, bioactivity, stability in human blood and simulated body fluid (SBF), antibiotic binding, release, and antibacterial activity) were compared. It was found that although sodium periodate increased the strength and drug-binding capacity of the prosthesis, it also increased the blood hemolysis risk. Cu 2+ /H 2 O 2 destabilized the mechanical properties of the coating and the graft. The seawater-inspired ion-accelerated method was efficient, stable, and matrix- and human blood-friendly, and it stimulated hydroxyapatite formation on the prosthesis surface. The results lead to the conclusion that selection of the PCA formation accelerator should be based on a careful analysis of the biological properties of medical devices. They also suggest that the ion-accelerated method of PLD coating on medical devices may be highly effective and safer than the oxidant-accelerated coating method.
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فهرسة مساهمة: Keywords: biological activity; catecholamine polymerization acceleration; hydrogen peroxide; mono-/divalent ions; periodate; vascular grafts
المشرفين على المادة: 789U1901C5 (Copper)
0 (Coated Materials, Biocompatible)
BBX060AN9V (Hydrogen Peroxide)
0 (Anti-Bacterial Agents)
9007-34-5 (Collagen)
تواريخ الأحداث: Date Created: 20240724 Date Completed: 20240808 Latest Revision: 20240820
رمز التحديث: 20240820
مُعرف محوري في PubMed: PMC11310904
DOI: 10.1021/acsami.4c05979
PMID: 39044622
قاعدة البيانات: MEDLINE
الوصف
تدمد:1944-8252
DOI:10.1021/acsami.4c05979