The current study synthesized amphiphilic thermal/pH-sensitive block copolymers PNiPAAm-b-PHpr by condensation polymerization of trans-4-hydroxy-L-proline (Hpr) initiated from hydroxy-terminated poly (N-isopropylacrylamide) (PNiPAAm) as the macroinitiator in the presence of the catalyst, SnOct(2). H-1 NMR, FTIR, and gel permeation chromatography (GPC) characterized these copolymers. Their solutions showed reversible changes in optical properties: transparent below a lower critical solution temperature (LCST) and opaque above the LCST. The LCST values depended on the polymer composition and the media. With critical micelle concentrations (CMCs) in the range of 1.23-3.73 mg L-1, the block copolymers formed micelles in the aqueous phase owing to their amphiphilic characteristics. Increased hydrophobic segment length or decreased hydrophilic segment length in an amphiphilic diblock copolymer produced lower CMC values. The current work proved the core-shell structure of micelles by H-1 NMR analyses of the micelles in D2O. Transmission electron microscopy analyzed micelle morphology, showing a spherical core-shell structure. The micelles had an average size in the range of 170210 nm (blank), and 195280 nm (with drug). Observations showed high drug entrapment efficiency and drug-loading content for the drug micelles. Crown Copyright (C) 2010 Published by Elsevier Ltd. All rights reserved.