Highly compressible paracetamol - II. Compression properties

被引:34
作者
Garekani, HA [1 ]
Ford, JL [1 ]
Rubinstein, MH [1 ]
Rajabi-Siahboomi, AR [1 ]
机构
[1] Liverpool John Moores Univ, Sch Pharm & Chem, Liverpool L3 3AF, Merseyside, England
关键词
paracetamol; polyvinylpyrrolidone; agglomerated particles; compression force; compression speed; crushing strength; elastic recovery; elastic energy/plastic energy ratio;
D O I
10.1016/S0378-5173(00)00551-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Paracetamol particles crystallized in the presence of polyvinylpyrrolidone (PVP) exhibited an obvious improvement in their compression properties compared to untreated paracetamol. Paracetamol particles crystallized in the presence of 0.5% w/v PVP 10 000 or PVP 50 000 produced tablets with improved crushing strength with no tendency to cap even at high compression speeds. The very low values of strain rate sensitivity (SRS) and the lack of reduction in crushing strength with increasing compression speed for these particles, were indicative of a high degree of fragmentation during compression. The results of elastic recoveries and elastic energies of tablets were indicative of much less elastic behaviour of these particles than untreated paracetamol. The low elastic energy/plastic energy (EE/PE) ratio for paracetamol crystallized in the presence of PVP indicated that, contrary to untreated paracetamol, a minor portion of compression energy was utilized as elastic energy. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:101 / 110
页数:10
相关论文
共 19 条
[1]  
ABDELILLAH E, 1995, P 14 PHARM TECH C SP, V2, P368
[2]   PLASTIC-FLOW DURING COMPRESSION OF DIRECTLY COMPRESSIBLE FILLERS AND ITS EFFECT ON TABLET STRENGTH [J].
DAVID, ST ;
AUGSBURGER, LL .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1977, 66 (02) :155-159
[3]   A new pure paracetamol for direct compression: The orthorhombic form [J].
DiMartino, P ;
GuyotHermann, AM ;
Conflant, P ;
Drache, M ;
Guyot, JC .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1996, 128 (1-2) :1-8
[4]  
DUBERG M, 1982, ACTA PHARM SUEC, V19, P421
[5]   COMPRESSION ABILITY IMPROVEMENT BY SOLVATION DESOLVATION PROCESS - APPLICATION TO PARACETAMOL FOR DIRECT COMPRESSION [J].
FACHAUX, JM ;
HERMANN, AMG ;
GUYOT, JC ;
CONFLANT, P ;
DRACHE, M ;
HUVENNE, JP ;
BOUCHE, R .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1993, 99 (2-3) :99-107
[6]   Formation and compression characteristics of prismatic polyhedral and thin plate-like crystals of paracetamol [J].
Garekani, HA ;
Ford, JL ;
Rubinstein, MH ;
Rajabi-Siahboomi, AR .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1999, 187 (01) :77-89
[7]   Highly compressible paracetamol: I: crystallization and characterization [J].
Garekani, HA ;
Ford, JL ;
Rubinstein, MH ;
Rajabi-Siahboomi, AR .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2000, 208 (1-2) :87-99
[8]  
GAREKANI HA, 1996, THESIS LIVERPOOL J M
[9]   DIRECT COMPRESSION CHARACTERISTICS OF XYLITOL [J].
GARR, JSM ;
RUBINSTEIN, MH .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1990, 64 (2-3) :223-226
[10]   AN INVESTIGATION INTO THE CAPPING OF PARACETAMOL AT INCREASING SPEEDS OF COMPRESSION [J].
GARR, JSM ;
RUBINSTEIN, MH .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1991, 72 (02) :117-122