期刊
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS
卷 62, 期 1, 页码 110-116出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.ejpb.2005.07.006
关键词
protein adsorption; temperature-sensitive liposome; poly(N-isopropylacrylamide); surface modification
In the field of the temperature sensitive drug delivery systems, we studied on the surface modification of liposomes, by using poly(N-isopropylacrylamide-co-acrylamide) (PNIPAM-AAM) and polyethyleneglycol (PEG) to increase the release of doxorubicin (DOX) from liposomes and prolong the stability of liposomes in the presence of serum. The release of DOX from the PNIPAM-AAM/PEG modified liposomes is enhanced around the transition temperature of the polymer. In addition, the stability of the PNIPAM-AAM/PEG modified liposomes in serum shows a high level comparing with polymer unmodified liposomes. These results suggest that the modification on the surface of liposomes, with both PNIPAM-AAM and PEG enhances the drug release from liposomes and reduces the protein adsorption in serum. (c) 2005 Elsevier B.V. All rights reserved.
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