How does residual water affect the solid-state degradation of drugs in the amorphous state?

It is widely recognized in the pharmaceutical field that exposure of solid drugs (small molecules or proteins) to high relative humidity and the resulting association of water vapor with the solid generally accelerate the rate of chemical degradation.1 Although there are true solid-state reactions that take place only in the crystalline state or to a much lesser extent in the liquid or solution state than in the crystal,2,3 most instabilities observed for drugs occur in solution much more readily than in the solid state; when they do occur over practical time scales in the solid state, it is very likely that the reaction is taking place in the more disordered amorphous regions of the solid.4 Indeed, it has been shown in a number of cases that under otherwise identical conditions reactivity of a particular substance in the amorphous state is greater than that in the crystalline state.5-8 Generally, for reactions occurring in the amorphous solid state, the rate of reactivity increases with increasing water content, and this can be attributed to the ability of the amorphous solid to absorb water vapor into its bulk structure, forming an amorphous solution.9,10 In a few cases it has been reported that a certain amount of water must be present to ensure chemical stability, e.g., lipid peroxidation rates decrease with the addition of small amounts of water;11,12 however, a destabilizing effect of absorbed water is more generally the case for the major types of drug degradations, e.g., hydrolysis, oxidation, or deamidation. An examination of the literature indicates that discussions concerning solid-state reactivity in the amorphous state have followed along two lines. In some work correlations appear to exist between the rate of reactivity and the glass transition temperature, Tg, strongly supporting the role of water as a plasticizer in facilitating chemical reactivity by increasing molecular mobility.13,14 In other studies, a lack of correlation with Tg and reactivity well below Tg has been shown to occur, and there also appears to be a better correlation of reactivity with water activity, aw, defined as: aw ) p/po (1)

[1]  Howard Maskill,et al.  The physical basis of organic chemistry , 1985 .

[2]  B. Brooks,et al.  Book reviewComprehensive chemical kinetics, vol. 25, diffusion-limited reactions : By S. A. Rice; published by Elsevier, Amsterdam, 1985; 404 pp.; price, Dfl. 365 , 1986 .

[3]  L. Bell,et al.  Differentiating between the Effects of Water Activity and Glass Transition Dependent Mobility on a Solid State Chemical Reaction: Aspartame Degradation , 1994 .

[4]  J. Carstensen,et al.  Chemical stability of indomethacin in the solid amorphous and molten states. , 1993, Journal of pharmaceutical sciences.

[5]  A kinetic and x-ray diffraction study of the solid state rearrangement of methyl p-dimethylaminobenzenesulfonate. Reaction rate enhancement due to proper orientation in a crystal , 1977 .

[6]  C. Angell,et al.  The protein-glass analogy: New insight from homopeptide comparisons , 1994 .

[7]  Samuel Glasstone,et al.  Textbook of physical chemistry , 1941 .

[8]  Enhancement of a chemical reaction rate by proper orientation of reacting molecules in the solid state , 1975 .

[9]  W. Garner Chemistry of the solid state , 1955 .

[10]  Raymond F. Schultz Studies in Ester Hydrolysis Equilibria--Formic Acid Esters , 1939 .

[11]  C. Angell,et al.  Glass-forming liquids, anomalous liquids, and polyamorphism in liquids and biopolymers , 1994 .

[12]  J. Hodge Dehydrated Foods, Chemistry of Browning Reactions in Model Systems , 1953 .

[13]  F. Franks Water activity: a credible measure of food safety and quality? , 1991 .

[14]  Edward L Cussler,et al.  Diffusion: Mass Transfer in Fluid Systems , 1984 .

[15]  G. Brenner,et al.  Cefoxitin sodium: solution and solid-state chemical stability studies. , 1979, Journal of pharmaceutical sciences.

[16]  H. Sillescu,et al.  Translational and rotational diffusion in supercooled orthoterphenyl close to the glass transition , 1992 .

[17]  T. Labuza Oxidative Changes in Foods at Low and Intermediate Moisture Levels , 1975 .

[18]  C. Ingold,et al.  Structure and Mechanism in Organic Chemistry , 1953 .

[19]  M. Pikal,et al.  Thermal Decomposition of Amorphous β-Lactam Antibacterials , 1977 .

[20]  George Zografi,et al.  The molecular basis of moisture effects on the physical and chemical stability of drugs in the solid state , 1990 .

[21]  C. Bamford,et al.  Comprehensive Chemical Kinetics , 1976 .

[22]  A. Fainberg,et al.  Correlation of Solvolysis Rates. IV.1 Solvent Effects on Enthalpy and Entropy of Activation for Solvolysis of t-Butyl Chloride2 , 1957 .

[23]  C. Reichardt,et al.  Solvent Effects in Organic Chemistry , 1979 .

[24]  P. Lillford,et al.  The glassy state in foods , 1993 .

[25]  B. Giese C. Reichardt: Solvent Effects in Organic Chemistry, Monographs in Modern Chemistry, Vol. 3. Verlag Chemie, Weinheim, New York 1979. 355 Seiten, Preis: DM 108,- , 1980 .

[26]  C. Eckhardt,et al.  General Theoretical Concepts for Solid State Reactions: Quantitative Formulation of the Reaction Cavity, Steric Compression, and Reaction-Induced Stress Using an Elastic Multipole Representation of Chemical Pressure , 1995 .

[27]  Henry Eyring,et al.  Basic chemical kinetics , 1980 .