Alginate-sterculia gum gel-coated oil-entrapped alginate beads for gastroretentive risperidone delivery

被引:62
|
作者
Bera, Hriday [1 ]
Kandukuri, Saisharan Goud [1 ]
Nayak, Amit Kumar [2 ]
Boddupalli, Shashank [1 ]
机构
[1] Gokaraju Rangaraju Coll Pharm, Dept Ind Pharm, Hyderabad 500090, Andhra Pradesh, India
[2] Seemanta Inst Pharmaceut Sci, Dept Pharmaceut, Jharpokharia 757086, Odisha, India
关键词
Alginate; Sterculia gum; Olive oil; Floatation; Mucoadhesion; Risperidone; IN-VITRO EVALUATION; DRUG-DELIVERY; CALCIUM SILICATE; FORMULATION; SYSTEM; MUCOADHESIVE; MICROSPHERES; RELEASE;
D O I
10.1016/j.carbpol.2014.12.009
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Novel floating-mucoadhesive oil-entrapped alginate beads coated with crossslinked alginate-sterculia gum gel membrane was developed for gastroretentive risperidone delivery. Oil-entrapped alginate beads containing risperidone as core were prepared by ionotropic gelation technique. Effects of polymer to drug ratio and oil to water ratio on drug entrapment efficiency (%) and cumulative drug release after 8 h (%) were studied to optimize the core beads by a 32 factorial design. The optimized beads (F-O) demonstrated drug entrapment efficiency of 83.73 +/- 0.81% and cumulative drug release of 70.84 +/- 0.27% after 8 h. The biopolymeric-coated optimized beads exhibited excellent buoyancy, better ex vivo mucoadhesion and slower drug release rate. The drug release profiles of risperidone-loaded uncoated and coated beads were best fitted in Korsmeyer-Peppas model with Fickian diffusion mechanism. The beads were also examined for the drug-excipients compatibility, drug crystallinity and surface morphology by FTIR, P-XRD and SEM analyses, respectively. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:74 / 84
页数:11
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