Microemulsion formulation for enhanced absorption of poorly soluble drugs - II. In vivo study

被引:164
作者
Kawakami, K
Yoshikawa, T
Hayashi, T
Nishihara, Y
Masuda, K
机构
[1] Shionogi & Co Ltd, Dev Res Labs, Fukushima Ku, Osaka 5530002, Japan
[2] Shionogi & Co Ltd, R&D Labs, Mfg Technol R&D Labs, Amagasaki, Hyogo 6600813, Japan
关键词
microemulsion; oral administration; bioavailability; fed state; toxicity;
D O I
10.1016/S0168-3659(02)00050-0
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Oral administration study of microemulsion formulations, which are known to improve the bioavailability of poorly soluble drugs, was performed using rats. Nitrendipine was used as a poorly soluble model drug, and its absorption was enhanced significantly by employing the microemulsion formulations compared to a suspension or an oil solution. The effect of the fed state on the oral absorption of nitrendipine became insignificant with the microemulsion formulations. although it affected the absorption from the suspension formulation significantly. The absorption behavior also varied with the type of surfactant. The absorption from Tween 80-based formulation was very rapid, while HCO-60-based formulation showed prolonged plasma concentration profile. However. the absorption from BL-9EX (polyoxyethylene alkyl ether)-based formulation was hardly observed. Damage to the gastrointestinal mucosa, which seems to be a serious problem of surfactant-based formulations, also differed with the type of surfactant employed. HCO-60 and Tween 80-based formulations were mild to the organs. while BL-9EX-based formulation caused serious damage. The behavior and absorption mechanism of the microemulsion formulations are discussed. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:75 / 82
页数:8
相关论文
共 21 条
[1]   Combinatorial chemistry [J].
Borman, S .
CHEMICAL & ENGINEERING NEWS, 1998, 76 (14) :47-+
[2]   SELF-EMULSIFYING DRUG DELIVERY SYSTEMS - FORMULATION AND BIOPHARMACEUTIC EVALUATION OF AN INVESTIGATIONAL LIPOPHILIC COMPOUND [J].
CHARMAN, SA ;
CHARMAN, WN ;
ROGGE, MC ;
WILSON, TD ;
DUTKO, FJ ;
POUTON, CW .
PHARMACEUTICAL RESEARCH, 1992, 9 (01) :87-93
[3]   DISSOLUTION BEHAVIOR AND CHARACTERIZATION OF DIAZEPAM-PULLULAN COGROUND MIXTURES [J].
CHOUDHARI, KB ;
SANGHAVI, NM .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1993, 89 (03) :207-211
[4]   Comparison of cyclosporin A pharmacokinetics of a new microemulsion formulation and standard oral preparation in patients with psoriasis [J].
Erkko, P ;
Granlund, H ;
Nuutinen, M ;
Reitamo, S .
BRITISH JOURNAL OF DERMATOLOGY, 1997, 136 (01) :82-88
[5]   Interaction of a self-emulsifying lipid drug delivery system with the everted rat intestinal mucosa as a function of droplet size and surface charge [J].
Gershanik, T ;
Benzeno, S ;
Benita, S .
PHARMACEUTICAL RESEARCH, 1998, 15 (06) :863-869
[6]  
HANANO M, 1987, PHARMACOKINETICS
[7]  
KAWAKAMI K, J CONTROL RELEASE
[8]   REDUCED INTERINDIVIDUAL AND INTRAINDIVIDUAL VARIABILITY IN CYCLOSPORINE PHARMACOKINETICS FROM A MICROEMULSION FORMULATION [J].
KOVARIK, JM ;
MUELLER, EA ;
VANBREE, JB ;
TETZLOFF, W ;
KUTZ, K .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1994, 83 (03) :444-446
[9]  
KRAUSE HP, 1988, ARZNEIMITTEL-FORSCH, V38-2, P1593
[10]  
LANGENBUCHER F, 1982, PHARM IND, V44, P1166