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Therapy of a xenografted human colonic carcinoma using cisplatin or doxorubicin encapsulated in long-circulating pegylated stealth liposomes

โœ Scribed by Jan Vaage; Dorothy Donovan; Eirin Wipff; Robert Abra; Gail Colbern; Paul Uster; Peter Working


Publisher
John Wiley and Sons
Year
1999
Tongue
French
Weight
62 KB
Volume
80
Category
Article
ISSN
0020-7136

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โœฆ Synopsis


We compared the therapeutic effects of low doses of cisplatin and doxorubicin hydrochloride encapsulated in longcirculating liposomes composed of cholesterol/hydrogenated soy phosphatidylcholine-polyethylene glycol-distearoyl-phosphatidyl-ethanolamine. The encapsulation of cisplatin and doxorubicin in these liposomes made ineffectively low doses of the free drugs able to inhibit the growth of and affect cures of a human colonic carcinoma growing in nude mice. Liposome-encapsulated cisplatin had minor systemic toxic side effects indicated by an average 9% weight loss which was recovered 3-4 weeks after the last treatment. Toxicity was not observed in mice treated with liposome-encapsulated doxorubicin.


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Background. This study compared the therapeutic effects of doxorubicin hydrochloride in saline and in sterically stabilized, long-circulating liposomes composed of hydrogenated soy phosphatidylcholine/cholesteroljpolyethylene glycol-distearoyl-phosphatidyl-ethanolamine (Doxil]. Methods. The drug fo