Manna Sreejan, Sarkar Saurav, Sahu Ranabir, Dua Tarun Kumar, Paul Paramita, Jana Sougata, Nandi Gouranga
Department of Pharmaceutical Technology, University of North Bengal, Dist. - Darjeeling 734013, West Bengal, India; Department of Pharmaceutical Technology, Brainware University, Barasat, Kolkata, West Bengal 700125, India.
Department of Pharmaceutical Technology, University of North Bengal, Dist. - Darjeeling 734013, West Bengal, India.
Int J Biol Macromol. 2024 Nov;280(Pt 2):135901. doi: 10.1016/j.ijbiomac.2024.135901. Epub 2024 Sep 21.
This investigation focuses on the extraction, characterization, and evaluation of taro (Colocasia esculenta) stolon polysaccharide (TSP) as a tablet binding agent, which is obtained from edible taro stolon. TSP was subjected to phytochemical screening and characterized by FTIR, DSC, TGA, DTA, XRD, particle size, polydispersity index, zeta potential, rheological behavior, and SEM. The tablets prepared with varying concentrations of TSP (2.5 %, 5 %, 7.5 %, and 10 % w/w) and diclofenac sodium (DS) were evaluated and compared with the same concentrations of gum acacia and PVP K-30. The presence of carbohydrates was confirmed by Molisch's test. The FTIR spectra established the compatibility of the drug with excipients. The SEM images revealed asymmetric and elongated particles of TSP powder. The hydration kinetics study showed matrix hydration and water penetration velocity within the range of 0.602-0.753 g/g and 0.112-0.189 cm/g.h, respectively. The tablets showed drug release of >75 % at 45 min. The release-exponent value above 0.89 indicated a super case II drug transport combining matrix erosion and diffusion. Optimum tablet hardness and very low friability, even at 2.5 % binder concentration, suggested the potential application of the novel TSP as a tablet binder in the formulation of the tablets.
本研究聚焦于从可食用的芋头匍匐茎中提取、表征和评估芋头(芋属植物)匍匐茎多糖(TSP)作为片剂粘合剂。对TSP进行了植物化学筛选,并通过傅里叶变换红外光谱(FTIR)、差示扫描量热法(DSC)、热重分析法(TGA)、差热分析法(DTA)、X射线衍射法(XRD)、粒度分析、多分散指数、zeta电位、流变学行为和扫描电子显微镜(SEM)进行表征。用不同浓度的TSP(2.5%、5%、7.5%和10% w/w)和双氯芬酸钠(DS)制备片剂,并与相同浓度的阿拉伯胶和聚乙烯吡咯烷酮K-30进行评估和比较。通过莫利施试验证实了碳水化合物的存在。FTIR光谱确定了药物与辅料的相容性。SEM图像显示TSP粉末颗粒不对称且呈细长状。水合动力学研究表明,基质水合和水渗透速度分别在0.602 - 0.753 g/g和0.112 - 0.189 cm/g·h范围内。片剂在45分钟时药物释放率>75%。释放指数值高于0.89表明存在结合基质侵蚀和扩散的超Ⅱ型药物转运。即使在粘合剂浓度为2.5%时,片剂仍具有最佳硬度和极低的脆碎度,这表明新型TSP作为片剂粘合剂在片剂配方中具有潜在应用价值。