INFERRING THERMODYNAMIC STABILITY RELATIONSHIP OF POLYMORPHS FROM MELTING DATA

被引:213
作者
YU, L
机构
[1] Lilly Research Laboratories, Eli Lilly & Company, Lilly Corporate Center, Indianapolis, Indiana
关键词
D O I
10.1002/jps.2600840812
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
This study investigates the possibility of inferring the thermodynamic stability relationship of polymorphs from their melting data, Thermodynamic formulas are derived for calculating the Gibbs free energy difference (Delta G) between two polymorphs and its temperature slope from mainly the temperatures and heats of melting. This information is then used to estimate Delta G, thus relative stability, at other temperatures by extrapolation. Both linear and nonlinear extrapolations are considered. Extrapolating Delta G to zero gives an estimation of the transition (or virtual transition) temperature, from which the presence of monotropy or enantiotropy is inferred. This procedure is analogous to the use of solubility data measured near the ambient temperature to estimate a transition point at higher temperature. For several systems examined, the two methods are in good agreement. The qualitative rule introduced this way for inferring the presence of monotropy or enantiotropy is approximately the same as The Heat of Fusion Rule introduced previously on a statistical mechanical basis. This method is applied to 96 pairs of polymorphs from the literature. In most cases, the result agrees with the previous determination. The deviation of the calculated transition temperatures from their previous values (n = 18) is 2% on average and 7% at maximum.
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页码:966 / 974
页数:9
相关论文
共 26 条
[2]   POLYMORPHIC DIFFERENCES IN ALPHA-FORM AND BETA-FORM CRYSTALS OF 2R, 4S, 6-FLUORO-2-METHYL-SPIRO[CHROMAN-4,4'-IMIDAZOLINE]-2',5-DIONE (M79175) AS DETERMINED BY X-RAY-DIFFRACTION, INFRARED-SPECTROSCOPY, AND DIFFERENTIAL SCANNING CALORIMETRY [J].
ASHIZAWA, K ;
UCHIKAWA, K ;
HATTORI, T ;
SATO, T ;
MIYAKE, Y .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1988, 77 (07) :635-637
[3]   CONFORMATIONAL STUDY OF 2 POLYMORPHS OF SPIPERONE - POSSIBLE CONSEQUENCES ON THE INTERPRETATION OF PHARMACOLOGICAL ACTIVITY [J].
AZIBI, M ;
DRAGUETBRUGHMANS, M ;
BOUCHE, R ;
TINANT, B ;
GERMAIN, G ;
DECLERCQ, JP ;
VANMEERSSCHE, M .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1983, 72 (03) :232-235
[4]   POLYMORPHISM OF BUTYROPHENONES RELATED TO HALOPERIDOL [J].
AZIBI, M ;
DRAGUETBRUGHMANS, M ;
BOUCHE, R .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1984, 73 (04) :512-515
[5]   CHARACTERIZATION OF POLYMORPHISM OF GEPIRONE HYDROCHLORIDE [J].
BEHME, RJ ;
BROOKE, D ;
FARNEY, RF ;
KENSLER, TT .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1985, 74 (10) :1041-1046
[6]  
BERNSTEIN J, 1978, J AM CHEM SOC, V100, P673, DOI 10.1021/ja00471a001
[7]  
BUERGER MJ, 1951, PHASE TRANSFORMATION, pCH6
[8]  
BURGER A, 1979, MIKROCHIM ACTA, V2, P273
[9]   POLYMORPHISM OF PHARMACEUTICALS AND OTHER MOLECULAR-CRYSTALS .1. THEORY OF THERMODYNAMIC RULES [J].
BURGER, A ;
RAMBERGER, R .
MIKROCHIMICA ACTA, 1979, 2 (3-4) :259-271
[10]  
Byrn S.R, 1982, SOLID STATE CHEM DRU