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Preparation and characterization of tri-block poly(lactide)-poly(ethylene glycol)-poly(lactide) nanogels for controlled release of naltrexone
被引:46
作者:
Asadi, H.
[1
,2
]
Rostamizadeh, K.
[1
]
Salari, D.
[2
]
Hamidi, M.
[3
]
机构:
[1] Zanjan Univ Med Sci, Sch Pharm, Dept Med Chem, Zanjan 4513956184, Iran
[2] Univ Tabriz, Fac Chem, Dept Appl Chem, Tabriz, Iran
[3] Zanjan Univ Med Sci, Sch Pharm, Dept Pharmaceut, Zanjan 4513956184, Iran
关键词:
PLA-PEG-PLA;
Nanogels;
Crosslinking;
Naltrexone;
Sustained release;
POLY(ETHYLENE GLYCOL);
TRIBLOCK COPOLYMER;
BIODEGRADABLE NANOPARTICLES;
DRUG-DELIVERY;
PLA;
PEG;
POLY(L-LACTIDE);
MORPHOLOGY;
HYDROGELS;
MICELLES;
D O I:
10.1016/j.ijpharm.2011.06.035
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Tr-block poly( lactide)-poly(ethylene glycol)-poly(lactide) (PLA-PEG-PLA) copolymers and related acrylated derivative were synthesized and used to prepare micelles and nanogels for controlled release of naltrexone. The resulting copolymers, micelles and nanogels were characterized by various techniques such as proton nuclear magnetic resonance spectroscopy, Fourier transform infrared spectroscopy, gel permeation chromatography, fluorescence spectrometry, differential scanning calorimetry, photon correlation spectroscopy and scanning electron microscopy. The nanogels exhibited high encapsulation efficiency around 60% and excellent stability for long periods of time. The drug release profiles of micelles and nanogels were compared and it was found that the naltrexone loaded nanogels offered a steady and long-term release pattern for different periods of time up to 35 days, depending on the crosslinker concentration, compared to the micelles. The size of nanogels could be manipulated easily in the range of 128-200 nm by variations in polymer concentration used in the nanogels preparation step. From the results obtained it can be concluded that PIA-PEG-PLA nanogels can be considered as a promising carrier for drug delivery purpose. (C) 2011 Elsevier B.V. All rights reserved.
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页码:356 / 364
页数:9
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