Jang Ji-Hun, Jeong Seung-Hyun, Lee Yong-Bok
College of Pharmacy, Chonnam National University, 77 Yongbong-ro, Buk-Gu, Gwangju 61186, Korea.
Pharmaceutics. 2020 Oct 16;12(10):978. doi: 10.3390/pharmaceutics12100978.
Methotrexate, which is widely used in the treatment of cancer and immune-related diseases, has limitations in use because of its low bioavailability, short half-life, and tissue toxicity. Thus, in this study, a nano-sized water-in-oil-in-water (W/O/W) double emulsion containing methotrexate was prepared to enhance its lymphatic delivery and bioavailability. Based on the results from solubility testing and a pseudo-ternary diagram study, olive oil as the oil, Labrasol as a surfactant, and ethanol as a co-surfactant, were selected as the optimal components for the nanoemulsion. The prepared nanoemulsion was evaluated for size, zeta potential, encapsulation efficiency, pH, morphology, and in vitro release profiles. Furthermore, pharmacokinetics and lymphatic targeting efficiency were assessed after oral and intravenous administration of methotrexate-loaded nanoemulsion to rats. Mean droplet size, zeta potential, encapsulation efficiency, and pH of formulated nanoemulsion were 173.77 ± 5.76 nm, -35.63 ± 0.78 mV, 90.37 ± 0.96%, and 4.07 ± 0.03, respectively. In vitro release profile of the formulation indicated a higher dissolution and faster rate of methotrexate than that of free drug. The prepared nanoemulsion showed significant increases in maximum plasma concentration, area under the plasma concentration-time curve, half-life, oral bioavailability, and lymphatic targeting efficiency in both oral and intravenous administration. Therefore, our research proposes a methotrexate-loaded nanoemulsion as a good candidate for enhancing targeted lymphatic delivery of methotrexate.
甲氨蝶呤广泛应用于癌症和免疫相关疾病的治疗,但由于其生物利用度低、半衰期短和组织毒性,在使用上存在局限性。因此,在本研究中,制备了一种含有甲氨蝶呤的纳米级水包油包水(W/O/W)双重乳液,以提高其淋巴输送和生物利用度。基于溶解度测试和伪三元相图研究的结果,选择橄榄油作为油相、Labrasol作为表面活性剂、乙醇作为助表面活性剂作为纳米乳液的最佳成分。对制备的纳米乳液进行了粒径、zeta电位、包封率、pH值、形态和体外释放曲线的评估。此外,在给大鼠口服和静脉注射载有甲氨蝶呤的纳米乳液后,评估了其药代动力学和淋巴靶向效率。所制备纳米乳液的平均液滴尺寸、zeta电位、包封率和pH值分别为173.77±5.76nm、-35.63±0.78mV、90.37±0.96%和4.07±0.03。该制剂的体外释放曲线表明,甲氨蝶呤的溶出度更高,速率比游离药物更快。所制备的纳米乳液在口服和静脉给药后,其最大血浆浓度、血浆浓度-时间曲线下面积、半衰期、口服生物利用度和淋巴靶向效率均显著提高。因此,我们的研究提出载有甲氨蝶呤的纳米乳液是增强甲氨蝶呤靶向淋巴输送的良好候选物。