Timed-release depot for anticancer agents
β Scribed by Seymour Yolles; Thomas D. Leafe; Francis J. Meyer
- Book ID
- 102404703
- Publisher
- John Wiley and Sons
- Year
- 1975
- Tongue
- English
- Weight
- 183 KB
- Volume
- 64
- Category
- Article
- ISSN
- 0022-3549
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β¦ Synopsis
The timed-release of anticancer agents from composites with poly(1actic acid) was studied in rats. In the case of cyclophosphamide-poly(1actic acid) composites, 67% of the administered dose was released within 34 days. With cis-dichlorodiammineplatinum (II), the amount of drug released was only 9.3% within the same period. This difference might be attributed to the different solubilities of these two drugs in the polymer. Electron spectroscopy chemical analysis, a new tool, was used to investigate the extent of diffusion of drugs in polymer films.
Keyphrases 0 Cyclophosphamide-timed-release formulation with poly(1actic acid), release characteristics, electron spectra cis-Dichlorodiammineplatinum (11)-timed-release formulation with poly(1actic acid), release characteristics, electron spectra Anticancer agents-poly(1actic acid) timed-release formulations of cyclophosphamide and cis -dichlorodiammineplatinum (11) 0 Timed-release formulations-cyclophosphamide and cisdichlorodiammineplatinum (11) with poly(1actic acid)
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## Abstract A new type of photolabile carbonylβprotecting group was utilized in releasing anticancer agents upon irradiation at 350 nm in an aqueous environment. (Β© WileyβVCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)