Dynamic release of riboflavin from a starch-based semi IPN via partial enzymatic degradation: part II

被引:13
作者
Bajpai, SK [1 ]
Saxena, S [1 ]
机构
[1] Govt Model Sci Coll Autuonomous, Dept Chem, Polymer Res Lab, Jabalpur 482001, MP, India
关键词
swelling; drug release; degradation; enzyme; zero-order;
D O I
10.1016/j.reactfunctpolym.2004.04.004
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The dynamic release of riboflavin from the starch - cross-linked polyacrylic acid semi IPN has been studied at the physiological temperature 37 degreesC. The gel demonstrated nearly 39% drug in the amylase-free phosphate buffer of pH 7.4 while in the presence of 1.30 IU per ml enzyme activity in the release media, the gel underwent enzymatic degradation to release nearly 75% drug. The gel exhibited complex H-bonded structure in the lower pH thus demonstrating almost minimum release (i.e. 20%) in the release medium of pH 2.0. The amount of drug released was found to increase with the starch content in the gels. Similarly, with the increase in the initial water content, the quantity of drug released was also observed to increase. The degree of cross-linking was found to affect the release behavior. However, the gels demonstrated nearly 'zero-order release' for maximum as well as minimum concentration of cross-linker in the gels. A linear dependency between square of diameter of the gel and t(1/2) i.e. time required for 50% release was also observed. Finally, the gastrointestinal transit time and agitation speed also affected the release behavior. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:115 / 129
页数:15
相关论文
共 36 条
[1]   TARGETING DRUGS TO THE COLON - DELIVERY SYSTEMS FOR ORAL-ADMINISTRATION [J].
ASHFORD, M ;
FELL, JT .
JOURNAL OF DRUG TARGETING, 1994, 2 (03) :241-257
[2]   Enzymatically degradable and pH-sensitive hydrogels for colon-targeted oral drug delivery. I. Synthesis and characterization [J].
Bajpai, SK ;
Saxena, S .
JOURNAL OF APPLIED POLYMER SCIENCE, 2004, 92 (06) :3630-3643
[3]   Dynamic release of riboflavin from a colon-targeted delivery device: an in vitro study [J].
Bajpai, SK ;
Sonkusley, J .
REACTIVE & FUNCTIONAL POLYMERS, 2003, 55 (02) :197-210
[4]  
Bajpai SK, 2002, IRAN POLYM J, V11, P187
[5]   Hydrogels for oral drug delivery of peptides: synthesis and characterization [J].
Bajpai, SK .
JOURNAL OF APPLIED POLYMER SCIENCE, 2002, 83 (08) :1717-1729
[6]   Colon-specific oral delivery of vitamin B2 from poly(acrylamide-co-maleic acid) hydrogels:: An in vitro study [J].
Bajpai, SK ;
Bajpai, M ;
Kalla, KG .
JOURNAL OF APPLIED POLYMER SCIENCE, 2002, 84 (06) :1133-1145
[7]   Hydrogels for colon-specific oral drug delivery: Synthesis and characterization [J].
Bajpai, SK ;
Sonkusley, SJ .
JOURNAL OF MACROMOLECULAR SCIENCE-PURE AND APPLIED CHEMISTRY, 2001, 38 (04) :365-381
[8]   Mechanisms of solute and drug transport in relaxing, swellable, hydrophilic glassy polymers [J].
Brazel, CS ;
Peppas, NA .
POLYMER, 1999, 40 (12) :3383-3398
[9]   SWELLING OF POLYMER SYSTEMS IN SOLVENTS .2. MATHEMATICS OF DIFFUSION [J].
BUCKLEY, DJ ;
BERGER, M .
JOURNAL OF POLYMER SCIENCE, 1962, 56 (163) :175-&
[10]   Effects of acrylic acid on preparation and swelling properties of pH-sensitive dextran hydrogels [J].
Chiu, HC ;
Lin, YF ;
Hsu, YH .
BIOMATERIALS, 2002, 23 (04) :1103-1112