Peeters P A, Huiskamp C W, Eling W M, Crommelin D J
Department of Pharmaceutics, Faculty of Pharmacy, University of Utrecht, The Netherlands.
Parasitology. 1989 Jun;98 Pt 3:381-6. doi: 10.1017/s003118200006145x.
In this study, the advantage of the use of chloroquine (CQ) containing liposomes (lipCQ) over free CQ in the chemotherapy of murine malaria (Plasmodium berghei) was demonstrated. The maximum permissible dose per intraperitoneal injection was 0.8 and 10 mg for CQ and lipCQ, respectively. An increase in therapeutic and prophylactic efficacy of lipCQ in comparison with free CQ at a 0.8 mg CQ dose level was found. It was possible to obtain 100% efficacy (injection at day 5 after infection; parasitaemia 4-8%) with one single intraperitoneal injection of 6 mg lipCQ. Moreover, the ability to increase the doses of CQ per injection after liposome encapsulation allowed successful treatment of infections with CQ-resistant Plasmodium berghei which could not be cured by a 7-day course with the maximum tolerable dose of free CQ of 0.8 mg/mouse/day.
在本研究中,已证明在鼠疟(伯氏疟原虫)化疗中,含氯喹(CQ)的脂质体(lipCQ)比游离CQ具有优势。腹腔注射时,CQ和lipCQ的最大允许剂量分别为0.8毫克和10毫克。发现在0.8毫克CQ剂量水平下,lipCQ的治疗和预防效果比游离CQ有所提高。单次腹腔注射6毫克lipCQ可获得100%的疗效(感染后第5天注射;寄生虫血症4 - 8%)。此外,脂质体包封后能够增加每次注射CQ的剂量,从而成功治疗对CQ耐药的伯氏疟原虫感染,而用游离CQ最大耐受剂量0.8毫克/小鼠/天进行7天疗程无法治愈这种感染。