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用于药物递送的载抗生素纳米网中的纳米颗粒。

Nanoparticles in an antibiotic-loaded nanomesh for drug delivery.

作者信息

Fuller Melanie A, Carey Ashley, Whiley Harriet, Kurimoto Rio, Ebara Mitsuhiro, Köper Ingo

机构信息

Institute for NanoScale Science and Technology, Flinders University Bedford Park South Australia 5042 Australia

College of Science and Engineering, Flinders University Bedford Park South Australia 5042 Australia.

出版信息

RSC Adv. 2019 Sep 24;9(52):30064-30070. doi: 10.1039/c9ra06398f. eCollection 2019 Sep 23.

Abstract

Antibiotic loaded nanomeshes were fabricated by electrospinning polycaprolactone, a biocompatible polymer, with 12.5% w/w Colistin, 1.4% w/w Vancomycin and either cationic or anionic gold nanoparticles in varying combinations. The resulting nanomeshes had different antibiotic release profiles, with citrate capped gold nanoparticles combined with Colistin having the highest sustained release over 14 days for a 4 mg, 1.5 cm nanomesh. The electrospinning parameters were optimised to ensure the spinning of a homogenous mesh and the addition of antibiotics was confirmed through H NMR and ATR-FTIR. This research, as a proof of concept, suggests an opportunity for fabricating nanomeshes which contain gold nanoparticles as a drug release mechanism for antibiotics.

摘要

通过静电纺丝聚己内酯(一种生物相容性聚合物)与12.5% w/w的黏菌素、1.4% w/w的万古霉素以及不同组合的阳离子或阴离子金纳米颗粒来制备负载抗生素的纳米网。所得的纳米网具有不同的抗生素释放曲线,对于一个4毫克、1.5厘米的纳米网,柠檬酸盐包覆的金纳米颗粒与黏菌素结合在14天内具有最高的持续释放量。对静电纺丝参数进行了优化,以确保纺出均匀的网,并通过核磁共振氢谱(H NMR)和衰减全反射傅里叶变换红外光谱(ATR-FTIR)证实了抗生素的添加。作为概念验证,这项研究表明了制造包含金纳米颗粒作为抗生素药物释放机制的纳米网的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e667/9072143/4219c686ac15/c9ra06398f-f2.jpg

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