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功能化磷酸化纤维素微球:设计、表征及载氟沙星的负载和释放性能。

Functionalized phosphorylated cellulose microspheres: Design, characterization and ciprofloxacin loading and releasing properties.

机构信息

Key Laboratory for Green Chemical Process of Ministry of Education, Hubei Key Laboratory for Novel Reactor and Green Chemistry Technology, School of Chemical Engineering and Pharmacy, Wuhan Institute of Technology, LiuFang Campus, No. 206, Guanggu 1st Road, Donghu New & High Technology Development Zone, Wuhan 430205, Hubei Province, PR China.

School of Materials Science and Engineering, Zhengzhou University, No.100 Science Avenue, Zhengzhou City, 450001, Henan Province, PR China; College of Food Science and Technology Huazhong Agricultural University, Wuhan 430205, Hubei Province, PR China.

出版信息

Carbohydr Polym. 2021 Feb 15;254:117421. doi: 10.1016/j.carbpol.2020.117421. Epub 2020 Nov 24.

Abstract

In this work, functionalized phosphorylated cellulose microspheres (CMP) were designed as a carrier for the ciprofloxacin (CIP) drug delivery system. The CMP has been developed from cellulose microspheres (CM) and phosphoric acid via an esterification reaction. CIP, an antibiotic drug as a model, was loaded onto CIP via hydrogen bonds and electrostatic interactions. A series of test results showed that the CIP was successfully incorporated and released from the prepared CMP without the loss of structural integrity or changing its functionality. The release kinetics and mechanism suggest that CIP release follows first-order kinetics and non-Fickian diffusion mechanism. The cytotoxicity behavior of CMP enables the material as a suitable vehicle for the safe release of CIP. The CIP loaded microspheres exhibited a significant antibacterial effect due to the CIP release and diffusion from the microspheres. This study provides insight into the design of suitable cellulose microspheres for CIP delivery.

摘要

在这项工作中,功能化磷酸化纤维素微球(CMP)被设计为环丙沙星(CIP)药物输送系统的载体。CMP 是通过酯化反应从纤维素微球(CM)和磷酸制备的。CIP,作为一种抗生素药物,通过氢键和静电相互作用加载到 CIP 上。一系列测试结果表明,CIP 已成功掺入并从制备的 CMP 中释放出来,而不会损失结构完整性或改变其功能。释放动力学和机制表明,CIP 释放遵循一级动力学和非菲克扩散机制。CMP 的细胞毒性行为使该材料成为 CIP 安全释放的合适载体。负载 CIP 的微球由于 CIP 从微球中的释放和扩散而表现出显著的抗菌作用。这项研究为设计适合 CIP 传递的纤维素微球提供了思路。

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