Vaage J, Donovan D, Wipff E, Abra R, Colbern G, Uster P, Working P
Department of Immunology, Roswell Park Cancer Institute, Buffalo, NY 14263, USA.
Int J Cancer. 1999 Jan 5;80(1):134-7. doi: 10.1002/(sici)1097-0215(19990105)80:1<134::aid-ijc24>3.0.co;2-q.
We compared the therapeutic effects of low doses of cisplatin and doxorubicin hydrochloride encapsulated in long-circulating 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.
我们比较了低剂量顺铂和盐酸阿霉素包裹于由胆固醇/氢化大豆磷脂酰胆碱 - 聚乙二醇 - 二硬脂酰磷脂酰乙醇胺组成的长循环脂质体中的治疗效果。顺铂和阿霉素包裹于这些脂质体后,使低剂量的游离药物能有效抑制裸鼠体内人结肠癌的生长并影响其治愈情况。脂质体包裹的顺铂有轻微的全身毒性副作用,表现为平均体重减轻9%,在最后一次治疗后3 - 4周恢复。用脂质体包裹的阿霉素治疗的小鼠未观察到毒性。