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Preparation of thermo-responsive drug-loaded nanofibrous films created by electrospinning.
Li, Jianbo; Peng, Chengwei; Wang, Zhimei; Ren, Jie.
Afiliación
  • Li J; Institute of Nano and Biopolymeric Materials, School of Materials Science and Engineering, Key Laboratory of Advanced Civil Engineering Materials, Ministry of Education, Tongji University 4800 Caoan Road Shanghai 201804 China lijianbo@tongji.edu.cn +86-21-33515906 +86-21-33515906.
  • Peng C; Institute of Nano and Biopolymeric Materials, School of Materials Science and Engineering, Key Laboratory of Advanced Civil Engineering Materials, Ministry of Education, Tongji University 4800 Caoan Road Shanghai 201804 China lijianbo@tongji.edu.cn +86-21-33515906 +86-21-33515906.
  • Wang Z; Institute of Nano and Biopolymeric Materials, School of Materials Science and Engineering, Key Laboratory of Advanced Civil Engineering Materials, Ministry of Education, Tongji University 4800 Caoan Road Shanghai 201804 China lijianbo@tongji.edu.cn +86-21-33515906 +86-21-33515906.
  • Ren J; Institute of Nano and Biopolymeric Materials, School of Materials Science and Engineering, Key Laboratory of Advanced Civil Engineering Materials, Ministry of Education, Tongji University 4800 Caoan Road Shanghai 201804 China lijianbo@tongji.edu.cn +86-21-33515906 +86-21-33515906.
RSC Adv ; 8(31): 17551-17557, 2018 May 09.
Article en En | MEDLINE | ID: mdl-35539269
We prepared thermosensitive and biocompatible drug-loaded nanofibrous films by an electrospinning technique using a block copolymer, poly(N-isopropylacrylamide)-b-poly(l-lactide) (PNLA), and poly(l-lactide) (PLLA). The copolymer PNLA was synthesized by the radical polymerization of N-isopropylacrylamide (NIPAAm), followed by the ring-opening polymerization of l-lactide. The properties of PNIPAAm and PNLA were selectively discussed based on the results of NMR, FT-IR, GPC, and CA analyses. Because of the low molecular weight of PNIPAAm and PNLA and the hydrolysis of PNLA resulting from its hydrophilicity, these copolymers were inappropriate for electrospinning separately. Hence, a mixture of PNLA and PLLA was used to prepare electrospun nanofibrous films. SEM images of the PNLA/PLLA electrospun films showed that homogeneous fibres with smooth surfaces were obtained. In vitro release studies indicated that the drug-release rate of the PNLA/PLLA electrospun nanofibrous films can be adjusted by the content and molecular weight of PNLA and by the environmental temperature. The results demonstrate that electrospinning is a promising way to create stimuli-responsive fibrous films with potential applications in the design of controllable drug delivery systems.

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: RSC Adv Año: 2018 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: RSC Adv Año: 2018 Tipo del documento: Article