Antibacterial and antioxidant activity of gold and silver nanoparticles in dextran–polyacrylamide copolymers

IF 4.1 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Anton Tkachenko, Sadin Özdemir, Gülşah Tollu, Nadir Dizge, Kasim Ocakoglu, Volodymyr Prokopiuk, Anatolii Onishchenko, Vasyl Сhumachenko, Pavlo Virych, Vadym Pavlenko, Nataliya Kutsevol
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引用次数: 0

Abstract

Search for new antimicrobial agents is of great significance due to the issue of antimicrobial resistance, which nowadays has become more important than many diseases. The aim of this study was to evaluate the toxicity and biological effects of a dextran-graft-polyacrylamide (D-PAA) polymer-nanocarrier with/without silver or gold nanoparticles (AgNPs/D-PAA and AuNPs/D-PAA, respectively) to analyze their potential to replace or supplement conventional antibiotic therapy. The toxicity of nanocomplexes against eukaryotic cells was assessed on primary dermal fibroblasts using scratch, micronucleus and proliferation assays. DPPH (2,2-diphenyl-1-picrylhydrazylradical) assay was used to evaluate the antioxidant capacity of D-PAA, AgNPs/D-PAA and AuNPs/D-PAA. DNA cleavage, antimicrobial and biofilm inhibition effects of nanocomplexes were investigated. Nanocomplexes were found to be of moderate toxicity against fibroblasts with no genotoxicity observed. AgNPs/D-PAA reduced motility and proliferation at lower concentrations compared with the other studied nanomaterials. AgNPs/D-PAA and AuNPs/D-PAA showed radical scavenging capacities in a dose-dependent manner. The antimicrobial activity of AgNPs/D-PAA against various bacteria was found to be much higher compared to D-PAA and AuNPs/D-PAA, especially against E. hirae, E. faecalis and S. aureus, respectively. D-PAA, AgNPs/D-PAA and AuNPs/D-PAA showed DNA-cleaving and biofilm inhibitory activity, while AgNPs/D-PAA displayed the highest anti-biofilm activity. AgNPs/D-PAA and AuNPs/D-PAA were characterized by good antimicrobial activity. According to the findings of the study, AgNPs/D-PAA and AuNPs/D-PAA can be evaluated as alternatives for the preparation of new antimicrobial agents, the fight against biofilms, sterilization and disinfection processes. Our findings confirm the versatility of nanosystems based on dextran–polyacrylamide polymers and indicate that AgNPs/D-PAA and AuNPs/D-PAA can be evaluated as alternatives for the preparation of novel antimicrobial agents.

Abstract Image

葡聚糖-聚丙烯酰胺共聚物中金和银纳米粒子的抗菌和抗氧化活性。
由于抗菌剂耐药性问题,寻找新的抗菌剂具有重要意义。本研究旨在评估含有/不含银或金纳米粒子(分别为 AgNPs/D-PAA 和 AuNPs/D-PAA)的葡聚糖接枝聚丙烯酰胺(D-PAA)聚合物纳米载体的毒性和生物效应,分析其替代或补充传统抗生素疗法的潜力。使用划痕、微核和增殖试验评估了纳米复合物对真核细胞的毒性。DPPH(2,2-二苯基-1-苦基肼自由基)试验用于评估 D-PAA、AgNPs/D-PAA 和 AuNPs/D-PAA 的抗氧化能力。研究了纳米复合物的 DNA 裂解、抗菌和生物膜抑制效果。结果发现,纳米复合物对成纤维细胞的毒性适中,未观察到遗传毒性。与所研究的其他纳米材料相比,AgNPs/D-PAA 在较低浓度下就能减少运动和增殖。AgNPs/D-PAA 和 AuNPs/D-PAA 的自由基清除能力与剂量有关。与 D-PAA 和 AuNPs/D-PAA 相比,AgNPs/D-PAA 对各种细菌的抗菌活性要高得多,尤其是对平肠杆菌、粪大肠杆菌和金黄色葡萄球菌。D-PAA、AgNPs/D-PAA 和 AuNPs/D-PAA 显示出 DNA 切断和生物膜抑制活性,而 AgNPs/D-PAA 显示出最高的抗生物膜活性。AgNPs/D-PAA 和 AuNPs/D-PAA 具有良好的抗菌活性。根据研究结果,AgNPs/D-PAA 和 AuNPs/D-PAA 可作为制备新型抗菌剂、抗生物膜、杀菌和消毒过程的替代品进行评估。我们的研究结果证实了基于葡聚糖-聚丙烯酰胺聚合物的纳米系统的多功能性,并表明 AgNPs/D-PAA 和 AuNPs/D-PAA 可作为制备新型抗菌剂的替代品进行评估。
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来源期刊
Biometals
Biometals 生物-生化与分子生物学
CiteScore
5.90
自引率
8.60%
发文量
111
审稿时长
3 months
期刊介绍: BioMetals is the only established journal to feature the important role of metal ions in chemistry, biology, biochemistry, environmental science, and medicine. BioMetals is an international, multidisciplinary journal singularly devoted to the rapid publication of the fundamental advances of both basic and applied research in this field. BioMetals offers a forum for innovative research and clinical results on the structure and function of: - metal ions - metal chelates, - siderophores, - metal-containing proteins - biominerals in all biosystems. - BioMetals rapidly publishes original articles and reviews. BioMetals is a journal for metals researchers who practice in medicine, biochemistry, pharmacology, toxicology, microbiology, cell biology, chemistry, and plant physiology who are based academic, industrial and government laboratories.
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