Formulation of Long-Acting Quinacrine Hydrochloride Pellets in Different Matrices I
- 1 January 1985
- journal article
- research article
- Published by Taylor & Francis in Drug Development and Industrial Pharmacy
- Vol. 11 (12) , 2143-2154
- https://doi.org/10.3109/03639048509087777
Abstract
In this study, quinacrine hydrochloride, which is a very soluble drug in water was selected as the active ingredient to formulate a long-acting dosage form. The prolonged release form is obtained by incorporating the drug in an inert solid matrix. Since it is believed that if the correct matrix and hardness is chosen the drug release can be controlled. The effect of different fatty acids, fatty alcohols, polymers and waxes individually or in combinations were investigated.This publication has 15 references indexed in Scilit:
- Sustained Release from Inert Wax Matrixes II: Effect of Surfactants on Tripelennamine Hydrochloride ReleaseJournal of Pharmaceutical Sciences, 1978
- Sustained Release from Inert Wax Matrixes I: Drug-Wax CombinationsJournal of Pharmaceutical Sciences, 1978
- The Clinical Efficacy of the Repeated Transcervical Instillation of Quinacrine for Female SterilizationInternational Journal of Gynecology & Obstetrics, 1976
- Clinical evaluation of quinacrine hydrochloride for sterilization of the human femaleContraception, 1976
- Chemically induced tubal occlusion in the human female using intrauterine instillation of ouinacrineContraception, 1975
- Transvaginal chemical sterilization: Clinical use of quinacrine plus potentiating adjuvantsContraception, 1975
- Chemically induced tubal occlusion in the human female following a single instillation of quinacrineContraception, 1973
- Human Fertility Control by Transvaginal Application of Quinacrine on the Fallopian TubeFertility and Sterility, 1970
- Alterations in fertility induced by unilateral intrauterine instillation of cytotoxic compounds in ratsAmerican Journal of Obstetrics and Gynecology, 1968
- Oral Prolonged Action Medicaments: Their Pharmaceutical Control and Therapeutic AspectsJournal of Pharmacy and Pharmacology, 1959