In vitro aceclofenac release from IPN matrix tablets composed of chitosan-tamarind seed polysaccharide

被引:13
|
作者
Jana, Sougata [1 ]
Sen, Kalyan Kumar [1 ]
Basu, Sanat Kumar [2 ]
机构
[1] Gupta Coll Technol Sci, Dept Pharmaceut, Asansol 713301, WB, India
[2] Jadavpur Univ, Dept Pharmaceut Technol, Div Pharmaceut, Kolkata 700032, WB, India
关键词
Chitosan; Tamarind seed polysaccharide; Matrix tablet; RESPONSE-SURFACE METHODOLOGY; CONTROLLED DRUG-DELIVERY; METFORMIN HCL; MUCOADHESIVE BEADS; VIVO EVALUATION; NATURAL GUMS; XANTHAN GUM; POLYMER; FORMULATION; MICROSPHERES;
D O I
10.1016/j.ijbiomac.2014.01.037
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This communication describes the formulation and in vitro evaluation of IPN matrix tablets of aceclofenac. IPN microparticles using chitosan and tamarind seed polysaccharide blend was prepared using glutaraldehyde as cross-linker. The drug entrapment efficiency and average particle size of these microparticles was found to be 91.97 +/- 130% and 498.12 +/- 38.67 mu m, respectively. These IPN microparticles were characterized by scanning electron microscopy (SEM) and powder X-ray diffraction (P-XRD) study. These microparticles were compressed with tablet excipients through direct compression technique. These matrix tablets showed sustained aceclofenac release over 8 h. These matrix tablets might be helpful to minimize dosing frequency and reduction of various side effects during prolong period of treatment. (c) 2014 Published by Elsevier B.V.
引用
收藏
页码:241 / 245
页数:5
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