Structure-properties relationship in cross-linked high-amylose starch for use in controlled drug release

被引:0
作者
Ispas-Szabo, P
Ravenelle, F
Hassan, I
Preda, M
Mateescu, MA
机构
[1] Univ Quebec, Dept Chem Biochem, Montreal, PQ H3C 3P8, Canada
[2] Univ Quebec, Dept Earth Sci, Montreal, PQ H3C 3P8, Canada
关键词
amylose; cross-linking; crystallinity; X-ray diffraction; FTIR; drug release;
D O I
暂无
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
Cross-linked high-amylose starch (CLHAS), obtained by high-amylose starch cross-linking, was recently introduced as an excipient (Contramid(TM)) for monolithic dosage forms that are able to control drug release over 18-24 h. These control properties are related to tablet swelling and are strongly dependent on the degree of the cross-linking of CLHAS. The permeability of solutes through CLHAS hydrogels depends on the chemical structure of the polymer. The aim of this study was to obtain a better understanding of how modifications in CLHAS molecular structures at the level of long-range and short-range order during the cross-linking and processing conditions relate to the release properties of the CLHAS matrices. Structural parameters such as crystallinity contribute significantly to the physical and mechanical aspects of starch products. X-ray diffractometry, FTIR spectroscopy, dissolution tests in vitro, and mechanical hardness (of dry tablets) were found to be sensitive to the cross-linking degree (cld) variation. Best release properties and highest mechanical hardness were obtained from CLHAS matrices with low-to-moderate crystallinity, where the V- and the B-type structures coexist with amorphous regions. X-ray and FTIR profiles of dry CLHAS powders were found to be predictive for release properties of CLHAS tablets. (C) 2000 Elsevier Science S.A. All rights reserved.
引用
收藏
页码:163 / 175
页数:13
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