Controlled drug release from pellets containing water-insoluble drugs dissolved in a self-emulsifying system

被引:50
作者
Serratoni, Mauro
Newton, Michael
Booth, Steven
Clarke, Ashley
机构
[1] Univ London, Sch Pharm, London WC1N 1AX, England
[2] Merck Sharp & Dohme Ltd, Dev Labs, Hoddesdon, England
关键词
controlled drug release; film coating; pellets; self-emulsifying systems; water-insoluble drugs;
D O I
10.1016/j.ejpb.2006.07.011
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The aim of the study was to provide a controlled release system, which could be used for the oral administration of highly water-insoluble drugs. Pellets have been prepared by extrusion/spheronization containing two model drugs (methyl and propyl parabens) of low water solubility. One type of pellets contained the drugs mixed with lactose and microcrystalline cellulose (MCC) and the other types of pellets contained the model drugs dissolved in a self-emulsifying system (4.8%) consisting of equal parts of mono-diglycerides and polysorbate 80 and MCC. Pellets of all types in the same size fraction (1.4-2.0 mm) were coated to different levels of weight gain, with ethylcellulose, talc and glycerol. A sample of pellets containing methyl parabens in the self-emulsifying system was pre-coated with a film of hydroxypropylmethyl cellulose from an aqueous solution and then coated as above. Dissolution experiments established that the presence of the self-emulsifying system enhanced the drug release of both model drugs and that the film coating considerably reduced the drug release from pellets made with just water, lactose and MCC. The coating reduced the drug release from the pellets containing the self-emulsifying system to a lesser extent but in relation to the quantity of coat applied to the pellets. The application of a sub-coating of hydroxypropylmethyl cellulose was able to reduce the release rate of methyl parabens self-emulsifying system ethyl cellulose coated pellets. Thus, the formulation approach offers the possibility of formulating and controlling the in vitro release of water-insoluble drugs from solid oral dosage forms. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:94 / 98
页数:5
相关论文
共 9 条
[1]   The influence of pellet shape and film coating on the filling of pellets into hard shell capsules [J].
Chopra, R ;
Podczeck, F ;
Newton, JM ;
Alderborn, G .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2002, 53 (03) :327-333
[2]   INTRA SUBJECT AND INTERSUBJECT VARIATION OF ERYTHROMYCIN ABSORPTION FROM SINGLE-UNIT AND MULTIPLE-UNIT ENTERIC-COATED PRODUCTS [J].
GRAFFNER, C ;
JOSEFSSON, K ;
STOCKMAN, O .
BIOPHARMACEUTICS & DRUG DISPOSITION, 1986, 7 (02) :163-171
[3]  
JOSEFSSON K, 1986, CURR THER RES CLIN E, V39, P131
[4]   The influence of formulation variables on the properties of pellets containing a self-emulsifying mixture [J].
Newton, M ;
Petersson, J ;
Podczeck, F ;
Clarke, A ;
Booth, S .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2001, 90 (08) :987-995
[5]   A SHAPE FACTOR TO CHARACTERIZE THE QUALITY OF SPHEROIDS [J].
PODCZECK, F ;
NEWTON, JM .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1994, 46 (02) :82-85
[6]  
Rowe RaymondC., 2003, Handbook of Pharmaceutical Excipients
[7]  
SCHEIDEL B, 1993, ARZNEIMITTEL-FORSCH, V43-2, P1211
[8]   The influence of core materials and film coating on the drug release from coated pellets [J].
Sousa, JJ ;
Sousa, A ;
Moura, MJ ;
Podczeck, F ;
Newton, JM .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2002, 233 (1-2) :111-122
[9]   Comparative bioavailability study in dogs of a self-emulsifying formulation of progesterone presented in a pellet and liquid form compared with an aqueous suspension of progesterone [J].
Tuleu, C ;
Newton, M ;
Rose, J ;
Euler, D ;
Saklatvala, R ;
Clarke, A ;
Booth, S .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2004, 93 (06) :1495-1502