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银纳米粒子在具有生物活性的共聚物 Pluronic F68 共同稳定下的抗菌效果。

Antimicrobial effectiveness of silver nanoparticles co-stabilized by the bioactive copolymer pluronic F68.

机构信息

Department of Chemical Engineering of the Polytechnic School, University of São Paulo (USP), São Paulo, Brazil.

出版信息

J Nanobiotechnology. 2012 Nov 29;10:43. doi: 10.1186/1477-3155-10-43.


DOI:10.1186/1477-3155-10-43
PMID:23193983
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3570368/
Abstract

BACKGROUND: Silver nanoparticles (AgNps) have attracted much interest in biomedical engineering, since they have excellent antimicrobial properties. Therefore, AgNps have often been considered for incorporation into medical products for skin pathologies to reduce the risk of contamination. This study aims at evaluating the antimicrobial effectiveness of AgNps stabilized by pluronic™ F68 associated with other polymers such as polyvinyl alcohol (PVA) and polyvinylpyrrolidone (PVP). METHODS: AgNps antimicrobial activity was evaluated using the minimum inhibitory concentration (MIC) method. The action spectrum was evaluated for different polymers associated with pluronic™ F68 against the gram negative bacteria P. aeuroginosa and E. coli and the gram positive bacteria S. Aureus. RESULTS: AgNps stabilized with PVP or PVA and co-stabilized with pluronic™ F68 are effective against E. coli and P. aeruginosa microorganisms, with MIC values as low as 0.78% of the concentration of the original AgNps dispersion. The antimicrobial action against S. aureus is poor, with MIC values not lower than 25%. CONCLUSIONS: AgNps stabilized by different polymeric systems have shown improved antimicrobial activity against gram-negative microorganisms in comparison to unstabilized AgNps. Co-stabilization with the bioactive copolymer pluronic™ F68 has further enhanced the antimicrobial effectiveness against both microorganisms. A poor effectiveness has been found against the gram-positive S. aureus microorganism. Future assays are being delineated targeting possible therapeutic applications.

摘要

背景:由于具有优异的抗菌性能,银纳米粒子(AgNps)在生物医学工程中引起了广泛关注。因此,AgNps 常被考虑纳入用于治疗皮肤疾病的医疗产品中,以降低污染风险。本研究旨在评估由聚醚多元醇 F68 稳定的 AgNps 与其他聚合物(如聚乙烯醇(PVA)和聚乙烯吡咯烷酮(PVP))结合的抗菌效果。

方法:采用最低抑菌浓度(MIC)法评估 AgNps 的抗菌活性。评估了不同聚合物与聚醚多元醇 F68 联合作用对革兰氏阴性菌铜绿假单胞菌和大肠杆菌和革兰氏阳性菌金黄色葡萄球菌的作用光谱。

结果:用 PVP 或 PVA 稳定的 AgNps 与聚醚多元醇 F68 共同稳定,对大肠杆菌和铜绿假单胞菌微生物有效,MIC 值低至原始 AgNps 分散体浓度的 0.78%。对金黄色葡萄球菌的抗菌作用较差,MIC 值不低于 25%。

结论:与未稳定的 AgNps 相比,用不同聚合物体系稳定的 AgNps 对革兰氏阴性微生物表现出更好的抗菌活性。与生物活性共聚物聚醚多元醇 F68 共同稳定进一步增强了对两种微生物的抗菌效果。对革兰氏阳性金黄色葡萄球菌微生物的效果较差。正在设计未来的试验,以针对可能的治疗应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ff/3570368/721871114248/1477-3155-10-43-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ff/3570368/721871114248/1477-3155-10-43-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77ff/3570368/721871114248/1477-3155-10-43-1.jpg

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[6]
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本文引用的文献

[1]
Development and characterization of silver-based antimicrobial ethylene-vinyl alcohol copolymer (EVOH) films for food-packaging applications.

J Agric Food Chem. 2012-5-18

[2]
The antithrombotic and antimicrobial properties of PEG-protected silver nanoparticle coated surfaces.

Biomaterials. 2012-1-28

[3]
Antimicrobial activity of spherical silver nanoparticles prepared using a biocompatible macromolecular capping agent: evidence for induction of a greatly prolonged bacterial lag phase.

J Nanobiotechnology. 2010-12-21

[4]
The bactericidal effect of silver nanoparticles.

Nanotechnology. 2005-10

[5]
Influence of Pluronic® F68 on ceftazidime biological activity in parenteral solutions.

J Pharm Sci. 2010-8-26

[6]
Pluronic block copolymer-mediated interactions of organic compounds with noble metal nanoparticles for SERS analysis.

Langmuir. 2010-4-6

[7]
Review of health safety aspects of nanotechnologies in food production.

Regul Toxicol Pharmacol. 2009-2

[8]
Pluronic block copolymers: evolution of drug delivery concept from inert nanocarriers to biological response modifiers.

J Control Release. 2008-9-10

[9]
Delivery systems to increase the selectivity of antibiotics in phagocytic cells.

J Control Release. 2008-2-11

[10]
Pluronic F127-g-poly(acrylic acid) copolymers as in situ gelling vehicle for ophthalmic drug delivery system.

Int J Pharm. 2008-2-28

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