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使用羧甲基纤维素 - 氯 - 聚(乳酸 - 共 - 衣康酸)水凝胶控制释放抗生素阿莫西林药物。

Controlled release of antibiotic amoxicillin drug using carboxymethyl cellulose-cl-poly(lactic acid-co-itaconic acid) hydrogel.

作者信息

Sood S, Gupta Vinod Kumar, Agarwal Shilpi, Dev Kamal, Pathania Deepak

机构信息

School of Chemistry, Shoolini University, Solan 173212, Himachal Pradesh, India.

Department of Applied Department, University of Johannesburg, Johannesburg, South Africa.

出版信息

Int J Biol Macromol. 2017 Aug;101:612-620. doi: 10.1016/j.ijbiomac.2017.03.103. Epub 2017 Mar 23.

Abstract

In this paper, microwave assisted preparation of carboxymethyl cellulose-cl-poly(lactic acid-co-itaconic acid) (CMC-cl-P(LA-co-IA)) hydrogel was reported via facile graft copolymerization using N,N-methylene-bis-acrylamide (MBA) and potassium persulphate as cross linker and initiator. Different reaction parameters were optimized to achieve good yield. The formation of hydrogel was confirmed by characterization techniques such as Fourier transform infrared spectroscopy, field emission scanning electron microscopy, X-ray diffraction, thermo gravimetric analysis, transmission electron microscopy etc. The antimicrobial activities of the hydrogel were studied against Staphylococcus aureus and Escherichia coli. About 95% killing of bacteria was recorded after 24h. The controlled release of amoxicillin drug from hydrogel was evaluated as a function of pH and time. Maximum drug release of 98% was recorded at 2.2 pH after 7h. The kinetic studies showed non-Fickian diffusion of the drug.

摘要

本文报道了通过使用N,N-亚甲基双丙烯酰胺(MBA)和过硫酸钾作为交联剂和引发剂,通过简便的接枝共聚反应微波辅助制备羧甲基纤维素-cl-聚(乳酸-共-衣康酸)(CMC-cl-P(LA-co-IA))水凝胶。优化了不同的反应参数以获得良好的产率。通过傅里叶变换红外光谱、场发射扫描电子显微镜、X射线衍射、热重分析、透射电子显微镜等表征技术证实了水凝胶的形成。研究了水凝胶对金黄色葡萄球菌和大肠杆菌的抗菌活性。24小时后记录到约95%的细菌杀灭率。评估了阿莫西林药物从水凝胶中的控释情况与pH值和时间的关系。在7小时后,在pH 2.2时记录到最大药物释放率为98%。动力学研究表明药物的扩散为非菲克扩散。

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