Cross-linked high amylose starch derivatives as matrices for controlled release of high drug loadings

被引:72
作者
Mulhbacher, J
Ispas-Szabo, P
Lenaerts, V
Mateescu, MA
机构
[1] Univ Quebec, Dept Chem & Biochem, Montreal, PQ H3C 3P8, Canada
[2] Labopharm Inc, Laval, PQ, Canada
关键词
high amylose starch; excipients; drug controlled release; high drug loading; starch derivatives;
D O I
10.1016/S0168-3659(01)00425-4
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Selection of hydrogels as excipients in controlled drug release systems depends on the characteristics of the gel and of the drug. Three types of derivatives were synthesized from cross-linked high amylose starch (HASCL-6) by substitution of hydroxylic groups with cationic (carboxymethyl: CM), anionic (aminoethyl: AE) and acetate (Ac) groups. These new polymeric excipients are able to control the release over 20 h from monolithic tablets loaded with 20 to 60% drug. Three drugs were used as model tracer: acetaminophen (uncharged), acetylsalicylic acid (having an acidic group) and metformin (having a basic group). It was found that the release of ionic drugs from CM-HASCL-6 and AE-HASCL-6 matrices can be partially controlled by ionic interaction between pendant groups of polymer and drugs. The substitution degree of HASCL-6 derivatives can also be varied to modulate the drug's release time. These derivatives represent a novel generation of pharmaceutical excipients, recommended for high loading dosage formulations. (C) 2001 Elsevier Science B.V. All rights. reserved.
引用
收藏
页码:51 / 58
页数:8
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