Uno T, Yamaguchi T, Li X K, Suzuki Y, Hashimoto H, Harada Y, Kimura T, Kazui T
First Department of Surgery, Hamamatsu University School of Medicine, Shizuoka, Japan.
Lipids. 1997 May;32(5):543-8. doi: 10.1007/s11745-997-0069-1.
We developed a water-in-oil-in-water-type (W/O/W)-type multiple emulsion of a new tacrolimus formulation. A potential approach to avoid the complications of systemic immunosuppression and simultaneously enhance immunosuppressive efficacy is to deliver immunosuppressive agents locally to the site of the target organs. The W/O/W emulsion is dispersed oil drops containing smaller water droplets that allow the delivery of drugs preferentially to the reticuloendothelial systems (RES). Since the liver and the spleen are primary components of the RES, and the brain and the kidney have a poor RES, we hypothesized that a W/O/W emulsion of tacrolimus would possess the pharmacokinetic benefits of local immunosuppression. We evaluated this hypothesis in a rat model. The tacrolimus levels of whole blood, the liver, spleen, brain, and kidney in rats given intravenous emulsions of tacrolimus (W/O/W group) were compared with a group administered tacrolimus alone (T group). There were no significant differences between the pharmacokinetic parameters of W/O/W group and T group based on whole blood data. However, the W/O/W group had significantly decreased tacrolimus levels in the brain and kidney, and significantly increased levels in the liver and spleen compared with the T group. These data suggest that the W/O/W emulsion is applicable as an intravenous drug carrier for local immunosuppression.
我们研发了一种新型他克莫司制剂的水包油包水型(W/O/W型)多重乳液。避免全身免疫抑制并发症并同时提高免疫抑制疗效的一种潜在方法是将免疫抑制剂局部递送至靶器官部位。W/O/W乳液是分散有较小水滴的油滴,可使药物优先递送至网状内皮系统(RES)。由于肝脏和脾脏是RES的主要组成部分,而脑和肾的RES较少,我们推测他克莫司的W/O/W乳液将具有局部免疫抑制的药代动力学优势。我们在大鼠模型中评估了这一假设。将给予他克莫司静脉乳液的大鼠(W/O/W组)的全血、肝脏、脾脏、脑和肾中的他克莫司水平与单独给予他克莫司的组(T组)进行比较。基于全血数据,W/O/W组和T组的药代动力学参数之间没有显著差异。然而,与T组相比,W/O/W组脑和肾中的他克莫司水平显著降低,肝脏和脾脏中的水平显著升高。这些数据表明,W/O/W乳液可作为局部免疫抑制的静脉药物载体。