The effect of verapamil on the pharmacokinetics of adriamycin
โ Scribed by D. J. Kerr; J. Graham; J. Cummings; J. G. Morrison; G. G. Thompson; M. J. Brodie; S. B. Kaye
- Publisher
- Springer
- Year
- 1986
- Tongue
- English
- Weight
- 363 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0344-5704
No coin nor oath required. For personal study only.
โฆ Synopsis
The concurrent administration of adriamycin (intravenous) and verapamil (oral) is of considerable interest because of experimental data suggesting that resistance to adriamycin may be overcome by this means. The potential for a pharmacokinetic interaction between the two drugs has therefore been investigated in five patients with small cell lung cancer treated with combination chemotherapy comprising adriamycin, VP16, vincristine and cyclophosphamide. The data indicate that a significant interaction takes place. Adriamycin peak levels, terminal half-life and the volume of distribution at steady state are higher, whereas plasma drug clearance and the volume of the central compartment are lower with co-administration of verapamil. There was no evidence of enhanced drug toxicity in this study; however, the data should be considered in the interpretation of clinical trials in which adriamycin and verapamil are used together, both in terms of toxicity and tumour response.
๐ SIMILAR VOLUMES
The effects of gender on the pharmacokinetics of verapamil and its active metabolite, norverapamil, following single oral dose (80 mg, Isoptin) to 12 healthy male (mean age: 25.75+/-2.42 years, mean body weight: 70.59+/-9.94 kg) and 12 healthy female subjects (mean age: 24.08+/-2.84 years, mean body
The systemic bioavailability of the calcium channel blocker verapamil HCl after sublingual (SL) administration has been clinically demonstrated. [1][2][3][4][5] Therefore, this compound was chosen as a model compound for evaluation during establishment of a preclinical rabbit model for intra-oral dr