Yoshida Takayuki, Nakanishi Kiyo, Yoshioka Tatsunobu, Tsutsui Yuuki, Maeda Atsushi, Kondo Hiromu, Sako Kazuhiro
Drug Delivery, Pharmaceutical Research and Technology Labs., Astellas Pharma Inc., 180 Ozumi, Yaizu, Shizuoka 425-0072, Japan.
Drug Delivery, Pharmaceutical Research and Technology Labs., Astellas Pharma Inc., 180 Ozumi, Yaizu, Shizuoka 425-0072, Japan.
Eur J Pharm Biopharm. 2016 Mar;100:58-65. doi: 10.1016/j.ejpb.2015.12.006. Epub 2015 Dec 31.
Oral oil formulations have been reported to deliver drugs into the lymph. Lymphatic delivery of immunomodulatory drugs can more efficiently expose the drugs to T-cells in lymph, consequently induce higher efficacy and lower side effects. In this study, effects of tacrolimus oral oil formulations on drug blood exposure, and on inhibition of T-cell's interleukin-2 (IL-2) production were investigated in rats. Oil formulations (sunflower oil, cacao butter, medium chain triglyceride, and palm oil) dissolving tacrolimus showed lower drug blood concentration than a solid dispersion formulation (SDF). The sunflower oil, and cacao butter formulations suppressed drug blood exposure to 50% of the SDF, and inhibited T-cell's IL-2 production similar to the SDF. In vitro digestion tests indicated that slower digestion of the oils might reduce amount and rate of tacrolimus blood absorption. The cacao butter formulations showed 3.0 times more rapid tacrolimus absorption to lymphatic fluid than the SDF. Ratio of the rate constants of absorption into lymph to that into blood was higher in oil formulations (15 times in cacao butter, 15 times sunflower oil, and 3.5 times palm oil) than in the SDF. These results indicated that the oral oil formulations might be suitable for reduced tacrolimus blood concentration for low systemic side effects, and keep high lymph concentration for high efficacy in organ transplantation patients.
据报道,口服油制剂可将药物输送至淋巴。免疫调节药物的淋巴输送能更有效地使药物作用于淋巴中的T细胞,从而提高疗效并降低副作用。在本研究中,研究了他克莫司口服油制剂对大鼠药物血药暴露以及对T细胞白细胞介素-2(IL-2)产生的抑制作用。溶解他克莫司的油制剂(向日葵油、可可脂、中链甘油三酯和棕榈油)的血药浓度低于固体分散体制剂(SDF)。向日葵油和可可脂制剂将药物血药暴露抑制至SDF的50%,并与SDF类似地抑制T细胞的IL-2产生。体外消化试验表明,油类消化较慢可能会降低他克莫司的血药吸收量和吸收速率。可可脂制剂的他克莫司向淋巴液的吸收速度比SDF快3.0倍。油制剂中他克莫司向淋巴的吸收速率常数与向血液的吸收速率常数之比高于SDF(可可脂为15倍,向日葵油为15倍,棕榈油为3.5倍)。这些结果表明,口服油制剂可能适合降低他克莫司血药浓度以减少全身副作用,并保持高淋巴浓度以提高器官移植患者的疗效。