Abstract
A drug delivery system is synthesized by using poly(N-isopropylacrylamide)-b-poly( l-alanine) (PNIPAAm-b-PAla) block copolymers with different molecular weights, in which the molecular weight can be controlled by adjusting concentration ratio of the PNIPAAm-NH 2 and l-Ala-NCA. The lower critical solution temperature (LCST) of the copolymer is a little lower than that of the pure PNIPAAm. Furthermore, with the increase of chain length of the poly( l-alanine) block, the LCST shifts to much lower value. The FT-IR, DSC and TEM characterizations of the products indicated that the amphiphilic PNIPAAm-b-PAla block copolymer can self-assemble into a spherical core–shell micelle structure. This micelle carrier exhibits a reversible phase transition within a very narrow temperature range (about 4 °C). This drug delivery system not only shows good dissolution and hydrophilicity, but also is biodegradable. As a drug carrier of adriamycin (ADR), the PNIPAAm-b-PAla and ADR can form the core–shell micelle easily without precipitation, which prolongs the release time (it is more than 20 h here) of the ADR. Accordingly, this PNIPAAm-b-PAla copolymer is an excellent carrier for controlling drug delivery and release.
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