The Developability Classification System: Application of Biopharmaceutics Concepts to Formulation Development

被引:292
作者
Butler, James M. [1 ]
Dressman, Jennifer B. [2 ]
机构
[1] GlaxoSmithKline R&D, Pharmaceut Dev, Harlow, Essex, England
[2] Goethe Univ Frankfurt, Inst Pharmaceut Technol, Frankfurt, Germany
关键词
biopharmaceutics classification system (BCS); bioequivalence; oral absorption; developability; biorelevant media; solubility; permeability; dissolution rate; ORAL-DRUG ABSORPTION; IN-VIVO; MEFENAMIC-ACID; INTESTINAL PERMEABILITY; P-GLYCOPROTEIN; GASTROINTESTINAL ABSORPTION; JEJUNAL PERMEABILITY; REGIONAL ABSORPTION; DISSOLUTION RATE; GASTRIC-ACIDITY;
D O I
10.1002/jps.22217
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A revised classification system for oral drugs was developed using the biopharmaceutics classification system (BCS) as a starting point. The revised system is designed to have a greater focus on drug developability. Intestinal solubility, the compensatory nature of solubility and permeability in the small intestine and an estimate of the particle size needed to overcome dissolution rate limited absorption were all considered in the revised system. The system was then validated by comparison with literature on the in vivo performance of a number of test compounds. Observations on the test compounds were consistent with the revised classification, termed the developability classification system (DCS), showing it to be of greater value in predicting what factors are critical to in vivo performance than the widely used BCS. (C) 2010 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 99:4940-4954, 2010
引用
收藏
页码:4940 / 4954
页数:15
相关论文
共 106 条
[1]   Application of hydrogen bonding calculations in property based drug design [J].
Abraham, MH ;
Ibrahim, A ;
Zissimos, AM ;
Zhao, YH ;
Comer, J ;
Reynolds, DP .
DRUG DISCOVERY TODAY, 2002, 7 (20) :1056-1063
[2]   THE EFFECT OF MANNITOL ON THE ORAL BIOAVAILABILITY OF CIMETIDINE [J].
ADKIN, DA ;
DAVIS, SS ;
SPARROW, RA ;
HUCKLE, PD ;
WILDING, IR .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1995, 84 (12) :1405-1409
[3]   In vitro and in vivo evaluation of a fast-disintegrating lyophilized dry emulsion tablet containing griseofulvin [J].
Ahmed, Iman Saad ;
Hassan, Mona Aboul-Einien .
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES, 2007, 32 (01) :58-68
[4]   Evaluation of oral mucoadhesive microspheres in man on the basis of the pharmacokinetics of furosemide and riboflavin, compounds with limited gastrointestinal absorption sites [J].
Akiyama, Y ;
Nagahara, N ;
Nara, E ;
Kitano, M ;
Iwasa, S ;
Yamamoto, I ;
Azuma, J ;
Ogawa, Y .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1998, 50 (02) :159-166
[5]   Development of a partially automated solubility screening (PASS) assay for early drug development [J].
Alsenz, Jochem ;
Meister, Eva ;
Haenel, Elisabeth .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2007, 96 (07) :1748-1762
[6]   A THEORETICAL BASIS FOR A BIOPHARMACEUTIC DRUG CLASSIFICATION - THE CORRELATION OF IN-VITRO DRUG PRODUCT DISSOLUTION AND IN-VIVO BIOAVAILABILITY [J].
AMIDON, GL ;
LENNERNAS, H ;
SHAH, VP ;
CRISON, JR .
PHARMACEUTICAL RESEARCH, 1995, 12 (03) :413-420
[7]   Influence of polyethylene glycol 400 on the gastrointestinal absorption of ranitidine [J].
Basit, AW ;
Podczeck, F ;
Newton, JM ;
Waddington, WA ;
Ell, PJ ;
Lacey, LF .
PHARMACEUTICAL RESEARCH, 2002, 19 (09) :1368-1374
[8]   BIOAVAILABILITY OF MICRONIZED GRISEOFULVIN FROM CORN OIL-IN-WATER EMULSION, AQUEOUS SUSPENSION, AND COMMERCIAL TABLET DOSAGE FORMS IN HUMANS [J].
BATES, TR ;
SEQUEIRA, JA .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1975, 64 (05) :793-797
[9]   REDUCED BIOAVAILABILITY AND EFFECT OF FUROSEMIDE GIVEN WITH FOOD [J].
BEERMANN, B ;
MIDSKOV, C .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1986, 29 (06) :725-727
[10]   PAMPA-excipient classification gradient map [J].
Bendels, Stefanie ;
Tsinman, Oksana ;
Wagner, Bjorn ;
Lipp, Dana ;
Parrilla, Isabelle ;
Kansy, Manfred ;
Avdeef, Alex .
PHARMACEUTICAL RESEARCH, 2006, 23 (11) :2525-2535