کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
600244 1454299 2013 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Aceclofenac-loaded chitosan-tamarind seed polysaccharide interpenetrating polymeric network microparticles
موضوعات مرتبط
مهندسی و علوم پایه مهندسی شیمی شیمی کلوئیدی و سطحی
پیش نمایش صفحه اول مقاله
Aceclofenac-loaded chitosan-tamarind seed polysaccharide interpenetrating polymeric network microparticles
چکیده انگلیسی

The present work deals with the preparation, characterization and evaluation of glutaraldehyde cross-linked chitosan-tamarind seed polysaccharide (TSP) interpenetrating polymeric network (IPN) microparticles for prolonged aceclofenac release. The drug entrapment efficiency of these microparticles was found 85.84 ± 1.75 to 91.97 ± 1.30% and their average particle sizes were ranged from 490.55 ± 23.24 to 621.60 ± 53.57 μm. These chitosan-TSP IPN microparticles were characterized by FTIR, DSC, and SEM analyses. The in vitro drug release from these aceclofenac-loaded chitosan-TSP IPN microparticles showed sustained release of aceclofenac over 8 h and followed the Korsmeyer-Peppas model (R2 = 0.9809–0.9828) with anomalous (non-Fickian) diffusion drug release mechanism. The in vivo studies exhibited sustained anti-inflammatory activity in carrageenan-induced rats over prolonged period after oral administration of these newly developed aceclofenac-loaded IPN microparticles.

Figure optionsDownload as PowerPoint slideHighlights
► Aceclofenac-loaded chitosan-TSP IPN microparticles were prepared.
► Drug entrapment efficiency of these microparticles were 85.84 ± 1.75 to 91.97 ± 1.30%.
► The in vitro drug release showed sustained drug release over 8 h.
► The drug release followed Korsmeyer-Peppas model with anomalous diffusion mechanism.
► Sustained anti-inflammatory activity was seen in rats after oral administration.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Colloids and Surfaces B: Biointerfaces - Volume 105, 1 May 2013, Pages 303–309
نویسندگان
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