Controlled release from solid dispersion composed of poly(ethylene oxide)-Carbopol® interpolymer complex with various cross-linking degrees of Carbopol®

被引:69
作者
Ozeki, T [1 ]
Yuasa, H [1 ]
Kanaya, Y [1 ]
机构
[1] Tokyo Univ Pharm & Life Sci, Sch Pharm, Lab Med & Pharmaceut Technol, Hachioji, Tokyo 1920392, Japan
关键词
controlled release; solid dispersion; cross-linking degree; Carbopol (R); poly(ethylene oxide);
D O I
10.1016/S0168-3659(99)00202-3
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Solid dispersion composed of the poly(ethylene oxide) (PEO)-Carbopol(R) (CP) interpolymer complex containing phenacetin (PHE) was prepared by using six grades of CP having various cross-linking degrees. We attempted to control the medicine release from the PEO-CP solid dispersion by varying the CP grade. The powder X-ray diffraction pattern and differential scanning calorimetry curves suggested that PHE existed in the amorphous state, and PEO in the crystalline state disappeared in the solid dispersions. The release profile of PHE varied depending on the CP grade. A small release rate was observed at CP910 and CP971P that are cross-linked at low and middle degrees, respectively. The Fourier transform-infrared (FT-IR) spectra showed that the amount of the PEO-CP complex formed by hydrogen bonding changed depending on the CP grade. With the cross-linked CP, a good correlation was observed between the hydrogen bonding percent and the percent released of the PHE after 60 min (D-60 (min)), indicating that PHE release was controlled by the amount of PEO-CP complex formation in the solid dispersion. These results show that it is feasible to control the medicine release from PEO-CP solid dispersion by varying the CP grade. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:287 / 295
页数:9
相关论文
共 39 条
[1]   POLY(ETHYLENE OXIDE) (PEO) AND DIFFERENT MOLECULAR-WEIGHT PEO BLENDS MONOLITHIC DEVICES FOR DRUG RELEASE [J].
APICELLA, A ;
CAPPELLO, B ;
DELNOBILE, MA ;
LAROTONDA, MI ;
MENSITIERI, G ;
NICOLAI, L .
BIOMATERIALS, 1993, 14 (02) :83-90
[2]  
BAILY FE, 1964, J POLYM SCI A, V2, P397
[3]  
BEKTUROV EA, 1981, ADV POLYM SCI, V41, P99
[4]   ORAL ABSORPTION OF GRISEOFULVIN IN DOGS - INCREASED ABSORPTION VIA SOLID DISPERSION IN POLYETHYLENE GLYCOL-6000 [J].
CHIOU, WL ;
RIEGELMAN, S .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1970, 59 (07) :937-+
[5]   Development of a novel controlled-release system for gastric retention [J].
Deshpande, AA ;
Shah, NH ;
Rhodes, CT ;
Malick, W .
PHARMACEUTICAL RESEARCH, 1997, 14 (06) :815-819
[6]  
FUJII M, 1988, CHEM PHARM BULL, V36, P2186
[7]   Solid-state stability assessment of controlled release tablets containing Carbopol® 971P [J].
Goskonda, VR ;
Reddy, IK ;
Durrani, MJ ;
Wilber, W ;
Khan, MA .
JOURNAL OF CONTROLLED RELEASE, 1998, 54 (01) :87-93
[8]  
GRAHAM NB, 1984, BIOMATERIALS, V5, P27, DOI 10.1016/0142-9612(84)90063-2
[9]  
Hirasawa N, 1999, CHEM PHARM BULL, V47, P417, DOI 10.1248/cpb.47.417
[10]   INTERPOLYMER COMPLEX BETWEEN POLY(ETHYLENE OXIDE) AND POLY(CARBOXYLIC ACID) [J].
IKAWA, T ;
ABE, K ;
HONDA, K ;
TSUCHIDA, E .
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, 1975, 13 (07) :1505-1514