Cefoxitin Sodium: Solution and Solid-State Chemical Stability Studies

Studies were undertaken to provide the basic physicochemical information necessary for preparing a suitable parenteral formulation of cefoxitin sodium. Emphasis was placed on the physicochemical properties of the compound in solution and in the solid state. Cefoxitin sodium is very soluble in water...

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Veröffentlicht in:Journal of pharmaceutical sciences 1979-07, Vol.68 (7), p.863-866
Hauptverfasser: Oberholtzer, Earl R., Brenner, Gerald S.
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Brenner, Gerald S.
description Studies were undertaken to provide the basic physicochemical information necessary for preparing a suitable parenteral formulation of cefoxitin sodium. Emphasis was placed on the physicochemical properties of the compound in solution and in the solid state. Cefoxitin sodium is very soluble in water and exhibits apparent first-order decomposition in this medium at pH 3-9. Maximum stability in water is at pH 5-7. Under these pH conditions, cefoxitin sodium loses about 10% of its activity in 2 days at 25°. Thermal decomposition rates for amorphous and crystalline cefoxitin sodium samples were determined. Amorphous cefoxitin sodium was considerably less stable than its corresponding crystalline form. Solid-state decomposition plots are biphasic, displaying initial rapid losses followed by a slower decay period. The extent of loss in the crystalline solid at the end of the more rapid initial phase can be correlated with the water content of the solid.
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Pharm. Sci</addtitle><description>Studies were undertaken to provide the basic physicochemical information necessary for preparing a suitable parenteral formulation of cefoxitin sodium. Emphasis was placed on the physicochemical properties of the compound in solution and in the solid state. Cefoxitin sodium is very soluble in water and exhibits apparent first-order decomposition in this medium at pH 3-9. Maximum stability in water is at pH 5-7. Under these pH conditions, cefoxitin sodium loses about 10% of its activity in 2 days at 25°. Thermal decomposition rates for amorphous and crystalline cefoxitin sodium samples were determined. Amorphous cefoxitin sodium was considerably less stable than its corresponding crystalline form. Solid-state decomposition plots are biphasic, displaying initial rapid losses followed by a slower decay period. 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Solid-state decomposition plots are biphasic, displaying initial rapid losses followed by a slower decay period. The extent of loss in the crystalline solid at the end of the more rapid initial phase can be correlated with the water content of the solid.</abstract><cop>Washington</cop><pub>Elsevier Inc</pub><pmid>458604</pmid><doi>10.1002/jps.2600680720</doi><tpages>4</tpages></addata></record>
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source MEDLINE; Wiley Online Library All Journals; Alma/SFX Local Collection
subjects amorphous and crystalline solids
Antibiotics-cefoxitin sodium
Antibiotics—cefoxitin sodium, chemical stability, amorphous and crystalline solids, water content
Biological Assay
Cefoxitin - analysis
Cefoxitin sodium-chemical stability
Cefoxitin sodium—chemical stability, amorphous and crystalline solids, water content
Cephalosporins - analysis
Chemical Phenomena
chemical stability
Chemistry, Physical
Chromatography, High Pressure Liquid
Chromatography, Thin Layer
Crystallization
Drug Stability
Kinetics
Solutions
Spectrophotometry, Ultraviolet
Stability-cefoxitin sodium
Stability—cefoxitin sodium, amorphous and crystalline solids, water content
Time Factors
water content
title Cefoxitin Sodium: Solution and Solid-State Chemical Stability Studies
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