Abstract |
The present study aimed to assess the antitumor effect of glycosphingolipid-incorporated liposomes (glycosphingosomes) in combination with liposomal doxorubicin (Lip-Dox) in a mouse model of fibrosarcoma. Glycosphingosomes were prepared by incorporating glycosphingolipids isolated from Sphingomonas paucimobilis into the liposomes of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine, cholesterol, and cardiolipin. Tumors were induced by administering dimethyl-α- benzanthracene, and tumor-bearing mice were treated with various formulations of Dox, including free Dox, Lip-Dox, or glycosphingosomes + Lip-Dox. Mice were observed for 90 days to monitor their survival and tumor size. Free Dox, but not Lip-Dox or a combination of glycosphingosomes and Lip-Dox, caused the substantial depletion of leukocytes and significantly increased the levels of lactate dehydrogenase and creatinine kinase in mice. Tumor-bearing mice treated with a combination of glycosphingosomes and Lip-Dox showed restricted tumor growth and increased survival when compared to those treated with free Dox or Lip-Dox. The results of the present study suggest that a combination of glycosphingosomes and Lip-Dox may prove to be very effective in the treatment of tumors.
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Authors | Masood A Khan, Ahmed N Aljarbou, Yousef H Aldebasi, Mohammed S Alorainy, Arif Khan |
Journal | International journal of nanomedicine
(Int J Nanomedicine)
Vol. 10
Pg. 6331-8
( 2015)
ISSN: 1178-2013 [Electronic] New Zealand |
PMID | 26504383
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- liposomal doxorubicin
- 1,2-Dipalmitoylphosphatidylcholine
- colfosceril palmitate
- Polyethylene Glycols
- 9,10-Dimethyl-1,2-benzanthracene
- Doxorubicin
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Topics |
- 1,2-Dipalmitoylphosphatidylcholine
(analogs & derivatives, chemistry)
- 9,10-Dimethyl-1,2-benzanthracene
(toxicity)
- Animals
- Cell Proliferation
(drug effects)
- Chemistry, Pharmaceutical
- Doxorubicin
(analogs & derivatives, chemistry, pharmacology, therapeutic use)
- Female
- Fibrosarcoma
(chemically induced, drug therapy, pathology)
- Mice
- Polyethylene Glycols
(chemistry, pharmacology, therapeutic use)
- Survival Analysis
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