The use of hypromellose in oral drug delivery

被引:261
作者
Li, CL
Martini, LG
Ford, JL
Roberts, M
机构
[1] Liverpool John Moores Univ, Sch Pharm & Chem, Liverpool L3 3AF, Merseyside, England
[2] GlaxoSmithKline, Harlow CM19 5AW, Essex, England
关键词
D O I
10.1211/0022357055957
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Hypromellose, formerly known as hydroxypropylmethylcellulose (HPMC), is by far the most commonly employed cellulose ether used in the fabrication of hydrophilic matrices. Hypromellose provides the release of a drug in a controlled manner, effectively increasing the duration of release of a drug to prolong its therapeutic effect. This review provides a current insight into hypromellose and its applicability to hydrophilic matrices in order to highlight the basic parameters that affect its performance. Topics covered include the chemical, thermal and mechanical properties of hypromellose, hydration of the polymer matrices, the mechanism of drug release and the influence of tablet geometry on drug-release rate. The inclusion of drug-release modifiers within hypromellose matrices, the effects of dissolution media and the influence of both the external environment and microenvironment pH within the gel matrix on the properties of the polymer are also discussed.
引用
收藏
页码:533 / 546
页数:14
相关论文
共 111 条
[1]   A method for quantifying differential expansion within hydrating hydrophilic matrixes by tracking embedded fluorescent microspheres [J].
Adler, J ;
Jayan, A ;
Melia, CD .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1999, 88 (03) :371-377
[2]   Optimisation of floating matrix tablets and evaluation of their gastric residence time [J].
Baumgartner, S ;
Kristl, J ;
Vrecer, F ;
Vodopivec, P ;
Zorko, B .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2000, 195 (1-2) :125-135
[3]   SWELLING AND DRUG-RELEASE IN HYDROGEL MATRICES - POLYMER VISCOSITY AND MATRIX POROSITY EFFECTS [J].
BETTINI, R ;
COLOMBO, P ;
MASSIMO, G ;
CATELLANI, PL ;
VITALI, T .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 1994, 2 (03) :213-219
[4]   Translocation of drug particles in HPMC matrix gel layer: effect of drug solubility and influence on release rate [J].
Bettini, R ;
Catellani, PL ;
Santi, P ;
Massimo, G ;
Peppas, NA ;
Colombo, P .
JOURNAL OF CONTROLLED RELEASE, 2001, 70 (03) :383-391
[5]  
Bonferoni MC, 1996, STP PHARMA SCI, V6, P277
[6]   Influence of the viscosity grade and the particle size of HPMC on metronidazole release from matrix tablets [J].
CamposAldrete, ME ;
VillafuerteRobles, L .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 1997, 43 (02) :173-178
[7]   Anti-tack action of polyvinylpyrrolidone on hydroxypropylmethyleellulose solution [J].
Chan, LW ;
Wong, TW ;
Chua, PC ;
York, P ;
Heng, PWS .
CHEMICAL & PHARMACEUTICAL BULLETIN, 2003, 51 (02) :107-112
[8]  
Chary RBR, 1999, DRUG DEV IND PHARM, V25, P685
[9]   INFLUENCE OF SHAPE FACTORS ON KINETICS OF DRUG RELEASE FROM MATRIX TABLETS .1. THEORETICAL [J].
COBBY, J ;
MAYERSOHN, M ;
WALKER, GC .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1974, 63 (05) :725-732
[10]   Analysis of the swelling and release mechanisms from drug delivery systems with emphasis on drug solubility and water transport [J].
Colombo, P ;
Bettini, R ;
Santi, P ;
DeAscentiis, A ;
Peppas, NA .
JOURNAL OF CONTROLLED RELEASE, 1996, 39 (2-3) :231-237