Crystallization of paracetamol from ethanol-water solutions in the presence of polymers

被引:13
作者
Kachrimanis, K [1 ]
Malamataris, S [1 ]
机构
[1] Univ Thessaloniki, Sch Pharm, Dept Pharmaceut Technol, GR-54006 Salonika, Greece
关键词
D O I
10.1211/0022357991776949
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We have examined the effect of polymer nature and concentration on yield and micromeritic, melting and compression properties of paracetamol crystals obtained from ethanol-water solutions using the solvent-change technique. Agar, gelatin, polyethyleneglycol (PEG) and polyvinylpyrrolidone (PVP) were the polymers used. These four polymers have different solubility in ethanol and water. It was found that the yield of crystallization may increase by up to 8% with agar, gelatin and PEG, polymers that are insoluble in ethanol, while the soluble PVP reduces yield by 14%. The size of crystals increased due to the addition of polymers and changed almost in parallel with the crystal yield for agar and gelatin. Gelatin resulted in the biggest crystals, agar in the most equidimensional (aspect ratio 1 . 45 and roundness 1 . 47) and PVP in the most elongated (aspect ratio 1 . 89;and roundness 2 . 13). PEG resulted in the most agglomerated crystals. Yield pressure, P-y, decreased in the following order: agar > PEG > gelatin > PVP, which is the same order for the enthalpy of fusion. Gelatin and PEG significantly decreased the elastic recovery of tablets (0 . 05 level), probably due to plastic deformation of crystals and fragmentation of agglomerates, respectively. Crystallization of paracetamol in the presence of polymers by the solvent-change (ethanol-water) technique may permit increase of crystal yield, alteration of crystal shape and improvement of compression behaviour during tableting.
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页码:1219 / 1227
页数:9
相关论文
共 20 条
[1]   MODIFICATION OF ACETAMINOPHEN CRYSTALS - INFLUENCE OF GROWTH IN AQUEOUS-SOLUTIONS CONTAINING PARA-ACETOXYACETANILIDE ON CRYSTAL PROPERTIES [J].
CHOW, AHL ;
CHOW, PKK ;
WANG, ZS ;
GRANT, DJW .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1985, 24 (2-3) :239-258
[2]   THE ROLE OF THE SOLVENT IN CRYSTAL-GROWTH FROM SOLUTION [J].
DAVEY, RJ .
JOURNAL OF CRYSTAL GROWTH, 1986, 76 (03) :637-644
[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]   TRUE DENSITY AND THERMAL EXPANSIVITY OF PHARMACEUTICAL SOLIDS - COMPARISON OF METHODS AND ASSESSMENT OF CRYSTALLINITY [J].
DUNCANHEWITT, WC ;
GRANT, DJW .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1986, 28 (01) :75-84
[5]  
ELSAID Y, 1995, STP PHARMA SCI, V5, P232
[6]   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
[7]   STUDIES ON PARACETAMOL CRYSTALS PRODUCED BY GROWTH IN AQUEOUS-SOLUTIONS [J].
FEMIOYEWO, MN ;
SPRING, MS .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1994, 112 (01) :17-28
[8]  
GAREKANI HA, 1996, PHARMACOL RES S, V13, P9
[9]  
HECKEL RW, 1961, T METALL SOC AIME, V221, P671
[10]   Crystallisation conditions and physicomechanical properties of ibuprofen-Eudragit® S100 spherical crystal agglomerates prepared by the solvent-change technique [J].
Kachrimanis, K ;
Ktistis, G ;
Malamataris, S .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 1998, 173 (1-2) :61-74