生物响应性杂化纳米纤维通过生理温度下的玻璃化转变开关实现药物控制释放。

Bioresponsive Hybrid Nanofibers Enable Controlled Drug Delivery through Glass Transition Switching at Physiological Temperature.

机构信息

Empa, Swiss Federal Laboratories for Materials Science and Technology, Laboratory for Biointerfaces, Lerchenfeldstrasse 5, 9014 St. Gallen, Switzerland.

Empa, Swiss Federal Laboratories for Materials Science and Technology, Laboratory for Biomimetic Membranes and Textiles, Lerchenfeldstrasse 5, 9014 St. Gallen, Switzerland.

出版信息

ACS Appl Bio Mater. 2021 May 17;4(5):4271-4279. doi: 10.1021/acsabm.1c00099. Epub 2021 Apr 14.

Abstract

To avoid excessive usage of antibiotics and antimicrobial agents, smart wound dressings permitting controlled drug release for treatment of bacterial infections are highly desired. In search of a sensitive stimulus to activate drug release under physiological conditions, we found that the glass transition temperature () of a polymer or polymer blend can be an ideal parameter because a thermal stimulus can regulate drug release at the physiological temperature of 37 °C. A well-tuned for a controlled drug release from fibers at 37 °C was achieved by varying the blending ratio of Eudragit® RS 100 and poly(methyl methacrylate). Octenidine, an antimicrobial agent often used in wound treatment, was encapsulated into the polymer blend during the electrospinning process and evaluated for its controlled release based on modulation of temperature. The thermal switch of the nanofibrous membranes can be turned "on" at physiological temperature (37 °C) and "off" at room temperature (25 °C), conferring a controlled release of octenidine. It was found that octenidine can be released in an amount at least 8.5 times higher (25 mg·L) during the "on" stage compared to the "off" stage after 24 h, which was regulated by the wet (34.8-36.5 °C). The "on"/"off" switch for controlled drug release can moreover be repeated at least 5 times. Furthermore, the fabricated nanofibrous membranes displayed a distinctive antibacterial activity, causing a log3 reduction of the viable cells for both Gram negative and positive pathogens at 37 °C, when the thermal switch was "on". This study forms the groundwork for a treatment concept where no external stimulus is needed for the release of antimicrobials at physiological conditions, and will help reduce the overuse of antibiotics by allowing controlled drug release.

摘要

为避免过度使用抗生素和抗菌剂,人们非常希望开发能够控制药物释放以治疗细菌感染的智能伤口敷料。在寻找一种能在生理条件下激活药物释放的敏感刺激物时,我们发现聚合物或聚合物共混物的玻璃化转变温度 (Tg) 可以作为一个理想的参数,因为热刺激可以在 37°C 的生理温度下调节药物释放。通过改变 Eudragit® RS 100 和聚甲基丙烯酸甲酯的共混比,实现了在 37°C 从纤维中控制药物释放的良好调节 Tg。在静电纺丝过程中,将抗菌剂奥替尼啶包埋在聚合物共混物中,并根据温度的调节来评估其控制释放。纳米纤维膜的热开关可以在生理温度(37°C)下“开启”,在室温(25°C)下“关闭”,从而控制奥替尼啶的释放。研究发现,与“关闭”阶段相比,在 24 小时后“开启”阶段奥替尼啶的释放量至少高 8.5 倍(25mg·L),这是由湿 Tg(34.8-36.5°C)调节的。此外,这种“开启”/“关闭”控制药物释放的开关可以至少重复 5 次。此外,所制备的纳米纤维膜在“开启”状态下显示出独特的抗菌活性,在 37°C 时,对革兰氏阴性和阳性病原体的活菌数分别减少了 3 个对数,这为在生理条件下无需外部刺激即可释放抗菌剂的治疗概念奠定了基础,并将有助于减少抗生素的过度使用,实现药物的控制释放。

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