A New Parenteral Emulsion for the Administration of Taxol |
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Authors: | B. D. Tarr T. G. Sambandan S. H. Yalkowsky |
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Affiliation: | (1) Department of Pharmaceutical Sciences, University of Arizona, Tucson, Arizona, 85721;(2) Present address: College of Pharmacy, Washington State University, Pullman, Washington, 99164;(3) Present address: Stauffer Chemical Co, San Francisco, California |
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Abstract: | Taxol (NSC-125973) is a poorly soluble plant product that exhibits excellent antimitotic properties. This study involves the development of a new formulation for taxol. The stability of taxol in a 50% triacetin emulsion as well as possible methods of intravenous administration of this dosage form was examined. A stable emulsion was found at taxol concentrations of 10 and 15 mg/ml of emulsion. The 50% triacetin emulsion showed an intravenous LD50 of 1.2 ml/kg in Swiss-Webster mice. The 10 mg/ml taxol formulation was demonstrated to be stable upon addition to 5% dextrose iv fluids provided that small packing systems were used. The taxol–triacetin emulsion can also be intravenously injected at various rates, and it may prove to be a useful formulation for taxol. |
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Keywords: | taxol formulation water-soluble emulsion toxicity of triacetin |
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