Effect of various cyclodextrins on solution stability and dissolution rate of doxorubicin hydrochloride
- 1 February 1992
- journal article
- Published by Elsevier in International Journal of Pharmaceutics
- Vol. 79 (1-3) , 289-299
- https://doi.org/10.1016/0378-5173(92)90121-h
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- An intravenous toxicity study of 2-hydroxypropyl-β-cyclodextrin, a useful drug solubilizer, in rats and monkeys☆International Journal of Pharmaceutics, 1990
- Effect of cyclodextrins on anthracycline stability in acidic aqueous mediaInternational Journal of Clinical Pharmacy, 1988
- Characterization, Dissolution and Diffusion Properties of Tolbutamide-β-Cyclodextrin Complex SystemDrug Development and Industrial Pharmacy, 1988
- Aspects of the degradation kinetics of doxorubicin in aqueous solutionInternational Journal of Pharmaceutics, 1986
- Characterization, dissolution and bioavailability in rats of ibuprofen-β-cyclodextrin complex systemInternational Journal of Pharmaceutics, 1986
- Dissolution behavior of prednisolone from solid dispersion systems with cyclodextrins and polyvinylpyrrolidone.CHEMICAL & PHARMACEUTICAL BULLETIN, 1986
- Aspects of the chemical stability of doxorubicin and seven other anthracydines in acidic solutionInternational Journal of Clinical Pharmacy, 1985
- Doxorubicin decomposition on storage. Effect of pH, type of buffer and liposome encapsulationInternational Journal of Pharmaceutics, 1985
- Treatment of tissue extravasation by antitumor agentsCancer, 1982
- Therapy of local toxicities caused by extravasation of cancer chemotherapeutic drugsCancer Treatment Reviews, 1980