Controlled Release of an Antihypertensive Drug through Interpenetrating Polymer Network Hydrogel Tablets of Tamarind Seed Polysaccharide and Sodium Alginate

被引:20
作者
Kulkarni, Raghavendra V. [1 ]
Baraskar, Vaibhav V. [1 ]
Alange, Vijaykumar V. [1 ]
Naikawadi, Akram A. [2 ]
Sa, Biswanath [3 ]
机构
[1] BLDEA, Dept Pharmaceut Technol, Coll Pharm, Bijapur 586103, Karnataka, India
[2] Bijapur Liberal Dist Educ Univ, Shri BM Patil Med Coll, Dept Pharmacol, Bijapur 586103, Karnataka, India
[3] Jadavpur Univ, Dept Pharmaceut Technol, Div Pharmaceut, Kolkata, India
来源
JOURNAL OF MACROMOLECULAR SCIENCE PART B-PHYSICS | 2013年 / 52卷 / 11期
关键词
drug release; interpenetrating polymer network; ion exchange resins; sodium alginate; tamarind seed polysaccharide; CARBOXYMETHYL CELLULOSE; IN-VITRO; BEADS; CARRAGEENAN; DELIVERY; GELATIN;
D O I
10.1080/00222348.2013.789327
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The application of interpenetrating polymer network (IPN) hydrogel tablets of tamarind seed polysaccharide and sodium alginate for controlled release of a water-soluble antihypertensive drug, propranolol HCl (PPL), was investigated. The IPN tablets loaded with PPL or PPL-resin complex (resinate) were prepared by a wet granulation/covalent cross-linking method. Fourier Transform Infrared Spectroscopic confirmed the cross-linking reaction and IPN formation, while X-ray Diffraction and Scanning Electron Microscopy studies confirmed the amorphous dispersion of the drug within the IPN tablets. The plain drug PPL showed complete release within 1 h, while drug release from the resinate was prolonged for 2.5 h and the IPN matrices showed drug release up to 24 h. The drug release rate from the IPN matrices was affected by polymer concentration and cross-linking time; the higher the cross-linking time, the slower was the drug release. The drug release mechanism was found to be of a non-Fickian type.
引用
收藏
页码:1636 / 1650
页数:15
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