4.7 Article

Synthesis of temperature and pH-responsive crosslinked micelles from polypeptide-based graft copolymer

期刊

JOURNAL OF COLLOID AND INTERFACE SCIENCE
卷 359, 期 2, 页码 436-442

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2011.04.037

关键词

Poly(N-isopropylacrylamide); Poly(L-glutamic acid); Self-assembly; Cross linked micelles

资金

  1. National Natural Science Foundation of China [50773081, 50973108, 50733003, 50425309]
  2. Ministry of Science and Technology of China [2007DFR5020]
  3. Jilin Science and Technology Bureau [20095003, 20096018]

向作者/读者索取更多资源

A polypeptide-based double hydrophilic graft copolymer was synthesized by the sequential grafting of poly(N-isopropylacrylamide) (PNIPAM) and 2-hydroxyethyl methacrylate (HEMA) onto poly(L-glutamic acid) (PGA) backbone. The copolymers were sensitive to both temperature and pH. The phase transition and aggregation behaviors of the graft copolymers in aqueous solutions were investigated by the turbidity measurements and dynamic laser scattering (DLS). The light transmittance decrease of the copolymers at temperature above lower critical solution temperature (LCST) was remarkably weakened at pH around 6.5 due to the coil to alpha helix change of PGA chain induced by pH. The copolymers can self-assembly into micelles with PNIPAM cores in the aqueous solution at pH 8.0 and 60 degrees C. Subsequently, polymerization of HEMA led to the facile preparation of crosslinked micelles, which were observed directly by transmission electron microscopy (TEM). The temperature controlled shrinkage behaviors of crosslinked micelles highly depended on the pH values of the solution. The crosslinked micelles aggregated at pH 5.0 due to the increased hydrophobic interactions among them induced by the protonation of PGA component. These crosslinked micelles have promising applications as intelligent drug delivery vehicles. (C) 2011 Elsevier Inc. All rights reserved.

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