Preparation and Characterization of Venlafaxine Hydrochloride-Loaded Chitosan Nanoparticles and In Vitro Release of Drug

被引:67
作者
Shah, Sunil [1 ]
Pal, Angshuman [1 ]
Kaushik, V. K. [2 ]
Devi, Surekha [1 ]
机构
[1] Maharaja Sayajirao Univ Baroda, Fac Sci, Dept Chem, Baroda 390002, Gujarat, India
[2] Reliance Ind Ltd, Ctr Res & Dev, Vadodara Mfg Div, Vadodara 391934, India
关键词
chitosan; nanoparticles; venlafaxine hydrochloride; ionic gelation; DELIVERY-SYSTEM; INSULIN; ABSORPTION; MICROSPHERES; IMPROVEMENT; BEHAVIOR; CHITIN; ENHANCEMENT; ADSORPTION;
D O I
10.1002/app.29807
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The venlafaxine hydrochloride (VHL)-loaded chitosan nanoparticles were prepared by ionic gelation of chitosan (CS) using tripolyphosphate (TPP). The nanoparticles were characterized using FTIR, differential scanning calorimetry, X-ray diffraction, dynamic light scattering, transmission electron microscopy, and X-ray photoelectron spectroscopy. The effect of concentration of CS, polyethylene glycol (PEG), VHL and CS/TPP mass ratio on the particle size and zeta potential of nanoparticles was examined. The particle size of CS/TPP nanoparticles and VHL-loaded CS/TPP nanoparticles was within the range of 200-400 nm with positive surface charge. In the case of VHL-loaded nanoparticles and PEG-coated CS/TPP nano-particles, the particle size increases and surface charge decreases with increasing concentration of VHL and PEG. Both placebo and VHL-loaded CS/TPP nanoparticles were observed to be spherical in nature. PEG coafing on the surface of CS/TPP nanoparticles was confirmed by XPS analysis. Maximum drug entrapment efficiency (70%) was observed at 0.6 mg/mL drug concentration. In vitro drug release study at 37 degrees C +/- 0.5 degrees C and pH 7.4 exhibited initial burst release followed by a steady release. (C) 2009 Wiley Periodicals, Inc. J Appl Polym Sci 112: 2876-2887, 2009
引用
收藏
页码:2876 / 2887
页数:12
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