Aceclofenac-loaded unsaturated esterified alginate/gellan gum microspheres: In vitro and in vivo assessment

被引:69
作者
Jana, Sougata [1 ]
Das, Arindam [1 ]
Nayak, Amit Kumar [2 ]
Sen, Kalyan Kumar [1 ]
Basu, Sanat Kumar [1 ]
机构
[1] Gupta Coll Technol Sci, Dept Pharmaceut, Asansol 713301, WB, India
[2] Seemanta Inst Pharmaceut Sci, Dept Pharmaceut, Mayurbhanj 757086, Odisha, India
关键词
Alginate; Drug delivery; Drug release; Microspheres; Oral drug delivery; FTIR; ORAL DELIVERY; BEADS; FORMULATION; GLICLAZIDE; OPTIMIZATION; PARAMETERS; GELATION; RELEASE; ACID; SIZE;
D O I
10.1016/j.ijbiomac.2013.03.015
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
Aceclofenac-loaded alginate/gellan gum microspheres for prolonged aceclofenac release were prepared through maleic anhydride-induced unsaturated esterification. The drug entrapment efficiency of these microspheres was found 39.30 +/- 1.28% to 98.46 +/- 0.40% and their average particle sizes were 270-490 mu m. These microspheres were characterized by FTIR, DSC, P-XRD and SEM analysis. The in vitro dissolution indicated prolonged sustained release of aceclofenac over 6 h, which also followed the Korsmeyer-Peppas model (R-2 = 0.9571-0.9952). The microspheres prepared through 3% (w/v) maleic anhydride-induced esterification exhibited comparatively slower drug-release. Most of the microspheres were followed Fickian diffusion mechanism except the microspheres containing higher gellan gum content, which followed anomalous (non-Fickian) diffusion. The in vivo results showed sustained systemic absorption of aceclofenac in rabbits and excellent anti-inflammatory activity in carrageenan-induced rats after oral administration over prolonged period. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:129 / 137
页数:9
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