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Frontiers of Chemistry in China

ISSN 1673-3495

ISSN 1673-3614(Online)

CN 11-5726/O6

Front Chem Chin    2009, Vol. 4 Issue (1) : 104-109    https://doi.org/10.1007/s11458-009-0006-y
RESEARCH ARTICLE
Micellization and controlled release properties of methoxy poly(ethylene glycol)-b-poly(D,L-lactide-co-trimethylene carbonate)
Jieming GAO, Yingzhi GUO, Zhongwei GU(), Xingdong ZHANG
National Engineering Research Center for Biomaterials, Sichuan University, Chengdu 610064, China
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Abstract

Amphiphilic block copolymers composed of D,L-lactide, trimethylene carbonate and methoxy poly(ethylene glycol) (PETLA) were synthesized with ring-opening copolymerization. Studies on the micellization and drug-controlled release behavior of PETLA were performed. Both of the copolymers and the micelles were characterized with the methods of 1H nuclear magnetic resonance (1H-NMR), fluorescence spectroscopy, gel permeation chromatographic (GPC), dynamic light scattering (DLS), transmission electron microscopy (TEM) and ultraviolet-visible spectroscopy (UV). As a result, the critical micelle concentration of the copolymer was decreased with the increase of the hydrophobic chain length. DLS resulys indicated the diameters of the micelle were increased with increasing of hydrophobic length. TEM photographs illustrated that micelles MT1 were regularly spherical with the diameter from 30 nm to 40 nm. Taking 9-nitro-20(S)-camptothecin (9-NC) for the model drug, the release profiles in vitro show that the release behavior from micelles was controllable and nearly in zero order after the initial burst release.

Keywords biodegradable      methoxy poly(ethylene glycol)-b-poly(D      L-lactide-co-trimethylene carbonate)      micelle      controlled release     
Corresponding Author(s): GU Zhongwei,Email:zwgu@scu.edu.cn   
Issue Date: 05 March 2009
 Cite this article:   
Jieming GAO,Yingzhi GUO,Zhongwei GU, et al. Micellization and controlled release properties of methoxy poly(ethylene glycol)-b-poly(D,L-lactide-co-trimethylene carbonate)[J]. Front Chem Chin, 2009, 4(1): 104-109.
 URL:  
https://academic.hep.com.cn/fcc/EN/10.1007/s11458-009-0006-y
https://academic.hep.com.cn/fcc/EN/Y2009/V4/I1/104
CopolymerFeed aMn ˉbProduct a,cMn ˉcMn ˉdMw ˉ/Mn ˉdYield/%
mPEG∶LA∶TMCmPEG∶LA∶TMC
PETLA111.5∶30∶70300018.5∶35.1∶64.9260029001.0575.5
PETLA25.4∶30∶7040006.7∶33.2∶66.8390041001.2589.7
PETLA33.8∶30∶7050003.7∶28.8∶71.2530053001.4394.1
PETLA42.9∶30∶7060002.5∶29.1∶70.9680067001.5389.7
Tab.1  H-NMR and GPC characterization of PETLA copolymers
Fig.1  Synthesis of copolymer PETLA
Fig.2  H-NMR spectra of block copolymer PETLA2
Fig.3  Plots of the intensity ratio / from pyrene emission spectra versus concentrations (g/L) of copolymers from PETLA1 to PETLA4 in tri-distilled water
Fig.4  GPC chromatograms of micelle MT1, from which peak molecular weight of MT1 and PETLA1 were 241 919 and 2363 respectively
MicellesMw of micelle aMw of copolymer aDiameter /nm b
MT1277 500270032.7 ± 5.3
MT2462 200400048.3 ± 6.4
MT3644 800510061.3 ± 10.2
Tab.2  Micelles molecular weight and size analysis through GPC and DLS
Fig.5  Transmission electron micrographs of micelle MT1 composed of copolymer PETLA1
Fig.6  9-NC release profile from MT1 to MT4
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