Characterization of Taro ( Colocasia esculenta) ) stolon polysaccharide and evaluation of its potential as a tablet binder in the formulation of matrix tablet

被引:0
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作者
Manna, Sreejan [1 ,2 ]
Sarkar, Saurav [1 ]
Sahu, Ranabir [1 ]
Dua, Tarun Kumar [1 ]
Paul, Paramita [1 ]
Jana, Sougata [3 ]
Nandi, Gouranga [1 ]
机构
[1] Univ North Bengal, Dept Pharmaceut Technol, Darjeeling 734013, West Bengal, India
[2] Brainware Univ, Dept Pharmaceut Technol, Kolkata 700125, West Bengal, India
[3] Directorate Hlth Serv, Dept Hlth & Family Welf, Kolkata, India
关键词
Taro ( Colocasia esculenta ) stolon polysaccharide; Diclofenac sodium; Tablet binder; RELEASE; DICLOFENAC; GUM; EXTRACTION; DELIVERY; MUCILAGE; PECTIN; AGENT; BEADS;
D O I
10.1016/j.ijbiomac.2024.135901
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 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.
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页数:14
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