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Anti-Tumor Effect of Mitoxantrone-Loaded Bovine Casein Microspheres on Ehrlich Ascites Carcinoma in Mice

Drug Delivery , Volume 3 (2) – Jan 1, 1996

Details

Publisher
Informa UK Ltd
Copyright
© 1996 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted
Subject
Research Article
ISSN
1071-7544
eISSN
1521-0464
D.O.I.
10.3109/10717549609031176
Publisher site
See Article on Publisher Site

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Anti-Tumor Effect of Mitoxantrone-Loaded Bovine Casein Microspheres on Ehrlich Ascites Carcinoma in Mice

Abstract

This work was supported with a grant SP/SO/D-21/89 from the Department of Science and Technology, Government of India. A. J. thanks the Director, TBG&RI for collaboration and Prof. E. P. Goldberg of the University of Florida, USA for a generous gift of mitoxantrone. Glutaraldehyde cross-linked bovine casein microspheres loaded with the antineoplastic agent mitoxantrone were prepared and in vitro release of the drug into phosphate buffer was examined at 37°C. In the absence of any proteolytic enzymes, the release reached a steady state within a week, releasing only 17–40% of the incorporated drug, depending on the initial payload. In the presence of an enzyme such as protease, however, 100% release was seen in vitro in 2–3 days. The antitumor effect of mitoxantroneloaded microspheres was evaluated in Swiss albino mice bearing Ehrlich ascites carcinoma (EAC) by intraperitoneal injections. The mean survival time of mice receiving 1 mg of mitoxantrone as free drug was 4.6 ± 0.67 days as opposed 37.7 ± 2.9 days for mice receiving equivalent amount of drug encapsulated in microspheres ( p <. 001). The percent T/C ratio of the animals receiving treatment via microsphere modality was 219.2, as opposed to 26.7 for the group receiving therapy using free drug. There was no significant increase in the body weight of animals receiving the drug-loaded microspheres. It is demonstrated that sustained delivery of mitoxantrone intraperitoneally using casein microspheres would be a promising approach in the treatment of EAC
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