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壳聚糖-聚乙二醇载阿莫西林纳米粒作为新型药物递送系统的制备、表征及其抗菌和细胞毒性活性评价

Preparation, characterization, and evaluation of antibacterial and cytotoxic activity of chitosan-polyethylene glycol nanoparticles loaded with amoxicillin as a novel drug delivery system.

作者信息

Güncüm Enes, Işıklan Nuran, Anlaş Ceren, Bulut Elif, Bakırel Tülay

机构信息

Faculty of Veterinary Medicine, Department of Pharmacology and Toxicology, Kırıkkale University, Yahşihan, Kırıkkale, Turkey.

Faculty of Science and Arts, Department of Chemistry, Kırıkkale University, Yahşihan, Kırıkkale, Turkey.

出版信息

J Biomater Sci Polym Ed. 2023 Aug;34(12):1660-1682. doi: 10.1080/09205063.2023.2179269. Epub 2023 Feb 16.

DOI:10.1080/09205063.2023.2179269
PMID:36756763
Abstract

In this study, nanoparticles of amoxicillin (AMX) were prepared using chitosan (CHI) and polyethylene glycol (PEG). The physicochemical properties of the particles were investigated by FT-IR, DSC, SEM, and zeta potential analyses. The nanoparticles showed a spherical shape, and the average size of formulations was within the range of 696.20 ± 24.86 - 359.53 ± 7.41 nm. Zeta potential data demonstrated that the formulations had positive surface charges with a zeta potential range of 21.38 ± 2.28 - 7.73 ± 1.66 mV. FTIR analysis showed that the drug was successfully entrapped in the nanoparticles. DSC results suggested that the drug was present in amorphous form in the polymer matrix. release studies demonstrated that the release pattern consisted of two phases, with an initial burst release followed by a controlled and sustained release. The MTT assay results on mouse fibroblast cell line indicated that the prepared formulations did not affect the viability of the cells. In the antibacterial activity test, it was found that the drug-loaded nanoparticles have AMX-equivalent antibacterial activity against , and . These findings revealed that the obtained nanoparticles might be a promising and safe nanocarrier system for efficient delivery of AMX.

摘要

在本研究中,使用壳聚糖(CHI)和聚乙二醇(PEG)制备了阿莫西林(AMX)纳米颗粒。通过傅里叶变换红外光谱(FT-IR)、差示扫描量热法(DSC)、扫描电子显微镜(SEM)和zeta电位分析对颗粒的物理化学性质进行了研究。纳米颗粒呈球形,制剂的平均粒径在696.20±24.86 - 359.53±7.41 nm范围内。zeta电位数据表明,制剂表面带正电荷,zeta电位范围为21.38±2.28 - 7.73±1.66 mV。傅里叶变换红外光谱分析表明药物成功包封在纳米颗粒中。差示扫描量热法结果表明药物以无定形形式存在于聚合物基质中。释放研究表明,释放模式包括两个阶段,先是初始突释,然后是控释和缓释。对小鼠成纤维细胞系的MTT试验结果表明,所制备的制剂不影响细胞活力。在抗菌活性测试中,发现载药纳米颗粒对……具有与阿莫西林等效的抗菌活性。这些发现表明,所获得的纳米颗粒可能是一种有前景且安全的纳米载体系统,用于高效递送阿莫西林。

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