Journal of Pharmacy and Pharmacology · 1980 · 103 citations · 10 references
MedicineOncologyPharmacologyCancer PharmacologyChemotherapyPharmacokinetics Of Anticancer AgentsCytotoxic ChemotherapyMelanoma PharmacotherapyOncology PharmacologyPharmacokinetics Of Anticancer DrugsIntraperitoneal AdministrationMitomycin C TherapyMitomycin C TreatmentParent Drug ReleasePharmacokinetics Of Cytotoxic ChemotherapySustained Release Kinetics
A high molecular weight derivative of mitomycin C (MMC), mitomycin C-dextran conjugate (MMC-D) has been synthesized and its biological and pharmacological properties investigated. MMC is released from MMC-D in vitro with a half-life of 24 h. After intraperitoneal injection of MMC-D, free MMC could be detected in plasma and urine of mouse for 5--8 h, while MMC administered as a free form was eliminated rapidly. After MMC-D, given to mice bearing Ehrlich ascites carcinoma or B16 melanoma there was a reduction in toxicitst that the high molecular weight MMC-dextran derivative is a kind of pro-drug which persists in the body giving a sustained release of free MMC thus significantly increasing the antitumour activity of the parent drug.
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Gregory Gregoriadis · Nature · 1977 · 389 citations
Isolation of new fractions of antitumor mitomycins.
Shigetoshi WAKAKI, Hirofuto Marumo, K Tomioka et al. · PubMed · 1958 · 213 citations