Stimuli-triggered multilayer films in response to temperature and ionic strength changes for controlled favipiravir drug release

被引:42
|
作者
Xu, Li [1 ]
He, Lang [1 ]
Li, Yinzhao [1 ]
Cai, Tingwei [1 ]
Zhang, Jianhua [2 ]
Chu, Zihan [1 ]
Shen, Xiaochen [3 ]
Cai, Raymond [1 ]
Shi, Haifeng [1 ]
Zhu, Chunyin [1 ]
机构
[1] Jiangsu Univ, Inst Life Sci, Zhenjiang 212013, Jiangsu, Peoples R China
[2] NOD topia GuangZhou Biotechnol Co Ltd, Guangzhou 510599, Guangdong, Peoples R China
[3] China Tobacco Jiangsu Ind Co Ltd, Nanjing 210019, Jiangsu, Peoples R China
关键词
nanoparticles; block copolymer micelles; favipiravir; self-assembly; drug delivery; nisin; POLYELECTROLYTE MULTILAYERS; COPOLYMER MICELLES; PEPTIDES; HYDROGEL; WATER; NANOCOMPOSITE; NANOPARTICLES; ARCHITECTURES; GROWTH; GENE;
D O I
10.1088/1748-605X/ad2a3b
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The block copolymer micelles and natural biopolymers were utilized to form layer-by-layer (LbL) films via electrostatic interaction, which were able to effectively load and controllably release favipiravir, a potential drug for the treatment of coronavirus epidemic. The LbL films demonstrated reversible swelling/shrinking behavior along with the manipulation of temperature, which could also maintain the integrity in the structure and the morphology. Due to dehydration of environmentally responsive building blocks, the drug release rate from the films was decelerated by elevating environmental temperature and ionic strength. In addition, the pulsed release of favipiravir was observed from the multilayer films under the trigger of temperature, which ensured the precise control in the content of the therapeutic reagents at a desired time point. The nanoparticle-based LbL films could be used for on-demand in vitro release of chemotherapeutic reagents.
引用
收藏
页数:13
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