HPMC-based gastroretentive dual working matrices coated with Ca+2 ion crosslinked alginate-fenugreek gum gel membrane

被引:23
作者
Bera, Hriday [1 ,2 ]
Gaini, Chakravarthy [2 ]
Kumar, Sanoj [2 ]
Sarkar, Srimanta [3 ]
Boddupalli, Shashank [2 ]
Ippagunta, Sohitha Reddy [2 ]
机构
[1] AIMST Univ, Fac Pharm, Semeling 08100, Kedah, Malaysia
[2] Gokaraju Rangaraju Coll Pharm, Hyderabad 500090, Andhra Pradesh, India
[3] Dr Reddys Lab Ltd, Formulat & Dev, Hyderabad 500090, Andhra Pradesh, India
来源
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2016年 / 67卷
关键词
Gastroretentive drug delivery system; Floating; Swelling; Alginate; Fenugreek gum; Hydroxypropylmethylcellulose; Quetiapine fumarate; IN-VITRO EVALUATION; DRUG-RELEASE; GASTRIC RETENTION; DELIVERY SYSTEMS; TABLETS; BEADS; DESIGN; RISPERIDONE; SIZE; HCL;
D O I
10.1016/j.msec.2016.05.016
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
082905 [生物质能源与材料]; 100103 [病原生物学];
摘要
Novel alginate-fenugreek gum (FG) gel membrane coated hydroxypropylmethylcellulose (HPMC) based matrix tablets were developed for intragastric quetiapine fumarate (QF) delivery by combining floating and swelling mechanisms. The effects of polymer blend ratios [HPMC K4M:HPMC E15] and citric acid contents on time taken for 50% drug release (t(50%), min) and drug release at 8 h (Q(8) h. %) were studied to optimize the core tablets by 3(2) factorial design. The optimized tablets (F-O) exhibited t(50%) of 247.67 +/- 3.51 min and Q(8) h of 71.11 +/- 032% with minimum errors in prediction. The optimized tablets were coated with Ca+2 ions crosslinked alginate-FG gel membrane by diffusion-controlled interfacial complexation technique. The biopolymeric-coated optimized matrices exhibited superior buoyancy, preferred swelling characteristics and slower drug release rate. The drug release profiles of the QF-loaded uncoated and coated optimized matrices were best fitted in Korsmeyer-Peppas model with anomalous diffusion driven mechanism. The uncoated and coated tablets containing QF were also characterized for drug-excipients compatibility, thermal behaviour and surface morphology by FTIR, DSC and SEM analyses, respectively. Thus, the newly developed alginate-FG gel membrane coated HPMC matrices are appropriate for intragastric delivery of QF over a prolonged period of time with greater therapeutic benefits. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:170 / 181
页数:12
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