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Director, Clinical Pharmaceutics Research, The University of Texas, MD Anderson Cancer Center, Houston, TX
Research Investigator, Clinical Pharmaceutics Research, The University of Texas, MD Anderson Cancer Center
Reprints: Mr. Trissel, Division of Pharmacy Unit 90, UTMD Anderson Cancer Center, 1515 Holcombe Blvd., Houston, TX 77030-4095, fax 713/796-1910,
BACKGROUND: Palonosetron HCl is a selective 5-HT3 receptor antagonist used for the prevention of chemotherapy-induced nausea and vomiting. Palonosetron HCl may be administered with other drugs by Y-site administration, including doxorubicin HCI and epirubicin HCI. Consequently, stability and compatability information are needed to verify the acceptability of such Y-site administration.
OBJECTIVE: To evaluate the physical and chemical stability of undiluted palonosetron HCl 50 µg/mL with doxorubicin HCl 1 mg/mL and epirubicin HCl 0.5 mg/mL during simulated Y-site administration.
METHODS: Triplicate samples of palonosetron HCl with each of the anthracycline chemotherapy drugs were tested. Samples were stored and evaluated for up to 4 hours at room temperature near 23 °C. Physical stability was assessed using turbidimetric and particulate measurement, as well as visual inspection. Chemical stability was assessed by HPLC.
RESULTS: All of the admixtures were clear and red-orange when viewed in normal fluorescent room light and with a Tyndall beam. Measured turbidity and particulate content were low initially and remained low throughout the study. The drug concentration was unchanged in any of the samples throughout the study.
CONCLUSIONS: Palonosetron HCl is physically and chemically stable with doxorubicin HCl and epirubicin HCl during simulated Y-site administration of these drugs over 4 hours at ambient room temperature.
Key Words: compatibility, doxorubicin, epirubicin, palonosetron, stability
Published Online, December 21, 2004. www.theannals.com, DOI 10.1345/aph.1E408
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