Study on thermo-sensitive intelligent targeting type drug carriers (II) microcapsules with grafted thermo-sensitive gates.
- Author:
Xiaojie JU
1
;
Liangyin CHU
;
Yan LI
Author Information
1. School of Chemical Engineering, Sichuan University, Chengdu 610065, China.
- Publication Type:Journal Article
- MeSH:
Acrylic Resins;
chemistry;
Biocompatible Materials;
Capsules;
Delayed-Action Preparations;
Drug Carriers;
Drug Delivery Systems;
Humans;
Polymers;
Porosity;
Temperature
- From:
Journal of Biomedical Engineering
2004;21(6):999-1002
- CountryChina
- Language:Chinese
-
Abstract:
Environmental stimuli-responsive microcapsules are getting more and more interests because of their potential applications in site-specific and time- and rate-programmed controlled-release. In this study, thermo-responsive microcapsules with linear grafted poly(N-isopropylacrylamide) (PNIPAM) gates on the inner pore surface were prepared, and the thermo-responsive controlled-release experiments were carried out. Interfacial polymerization was introduced to prepare polyamide porous microcapsules, and plasma-graft pore-filling polymerization was used to graft PNIPAM into the pore of the microcapsule membranes. The experimental results showed that PNIPAM-grafted microcapsules were featured with thermo-responsiveness due to the thermoresponsive swollen-shrunken property of PNIPAM chains grafted on the inner pore surface of the microcapsule membrane. At temperatures below the lower critical solution temperature (LCST), the linear grafted PNIPAM chains on the inner pore surface were in the swollen state, and the pores in the membrane were closed and the solute molecules were restrained to pass, as a result the release rate was low. In contrast, the grafted PNIPAM chains were in the shrunken state at temperatures above the LCST, and therefore the pores in the membrane were open, and a high release rate was the result.