COMPARATIVE STUDIES ON 8 DISSOLUTION METHODS USING 21 COMMERCIAL CHLORAMPHENICOL TABLETS AND A NON-DISINTEGRATING BENZOIC-ACID TABLET

被引:32
作者
OGATA, H
SHIBAZAKI, T
INOUE, T
EJIMA, A
机构
[1] Division of Drug, National Institute of Hygienic Sciences, Tokyo, 1‐18‐1, Kamiyoga Setagaya‐ku
关键词
Benzoic acid—dissolution rate; tablet; eight testing systems compared; Chloramphenicol—dissolution rates; tablets and powder; Dissolution rates—chloramphenicol tablets and powder; benzoic acid tablet; Dissolution testing systems—eight systems compared; chloramphenicol tablets and powder;
D O I
10.1002/jps.2600680614
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Eight dissolution methods (beaker, rotating basket, oscillating basket, solubility simulator, rotating flask, and column) were evaluated using 21 commercial film‐coated chloramphenicol (I) tablets and a nondisintegrating benzoic acid (II) tablet. The relative agitating intensities obtained from different dissolution methods were compared through the relative zero‐order nondisintegrating tablet dissolution rate constants. Correlation coefficients between I dissolution rate parameters (lag time, T20, T50. and T80) were determined. Significant correlation was observed for the lag time among seven methods, and all pairwise regression lines passed through zero except one. The regression line slopes reflected the relative destructive force intensities produced by each dissolution method on the coated I tablet films. The seven dissolution methods could be classified into two main groups according to correlations of four dissolution rate parameters. This classification criterion agreed well with that based on the agitation method. However, dissolution methods may not be interchangeable even though they belong to the same dissolution method group. Copyright © 1979 Wiley‐Liss, Inc., A Wiley Company
引用
收藏
页码:708 / 712
页数:5
相关论文
共 16 条
[1]   USE OF PHYSICAL AND ANIMAL MODELS TO ASSESS BIOAVAILABILITY [J].
BARR, WH .
PHARMACOLOGY, 1972, 8 (1-3) :55-101
[2]  
BATHE RV, 1975, PHARM ACTA HELV, V50, P3
[3]   APPARATUS FOR DETERMINING RATE OF DRUG RELEASE FROM SOLID DOSAGE FORMS [J].
BAUN, DC ;
WALKER, GC .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1969, 58 (05) :611-&
[4]   QUANTITATIVE CORRELATION OF ABSORPTION AND IN-VITRO DISSOLUTION KINETICS OF ASPIRIN FROM SEVERAL DOSAGE FORMS [J].
GIBALDI, M ;
WEINTRAUB, H .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1970, 59 (05) :725-+
[5]   THE PHYSICS OF TABLET COMPRESSION .2. THE INFLUENCE OF DEGREE OF COMPRESSION ON PROPERTIES OF TABLETS [J].
HIGUCHI, T ;
RAO, AN ;
BUSSE, LW ;
SWINTOSKY, JV .
JOURNAL OF THE AMERICAN PHARMACEUTICAL ASSOCIATION-SCIENTIFIC EDITION, 1953, 42 (04) :194-200
[6]  
IKEDA M, 1971, 91ST ANN M PHARM SOC, P323
[7]   EFFECTS OF HARDNESS ON DISINTEGRATION TIME AND DISSOLUTION RATE OF UNCOATED CAFFEINE TABLETS [J].
KITAZAWA, S ;
JOHNO, I ;
ITO, Y ;
TERAMURA, S ;
OKADA, J .
JOURNAL OF PHARMACY AND PHARMACOLOGY, 1975, 27 (10) :765-770
[8]   PHYSICOCHEMICAL BASIS OF THE BUFFERED ACETYLSALICYLIC ACID CONTROVERSY [J].
LEVY, G ;
HAYES, BA .
NEW ENGLAND JOURNAL OF MEDICINE, 1960, 262 (21) :1053-1058
[9]  
Nernst W, 1904, Z PHYS CHEM, V47, P52, DOI [10.1515/zpch-1904-4704, DOI 10.1515/ZPCH-1904-4704]
[10]  
Noyes A.A., 1897, J AM CHEM SOC, V19, P930