Drug Delivery, Disposition and Dynamics, Monash Institute of Pharmaceutical Sciences, Monash University (Parkville Campus), 381 Royal Pde, Parkville, Victoria 3052, Australia.
Phosphagenics Limited, 11 Duerdin Street, Clayton, Victoria 3168, Australia.
J Control Release. 2017 Dec 28;268:400-406. doi: 10.1016/j.jconrel.2017.10.039. Epub 2017 Oct 31.
Phosphorylated tocopherols are a new class of lipid excipients that have demonstrated potential in pharmaceutical applications. Their ability to solubilise poorly water soluble drugs indicates their potential utility in improving bioavailability of drugs where solubility limits their bioavailability. In this study a commercial mixture of phosphorylated tocopherols, TPM was combined with medium chain triglyceride (MCT) as a formulation for CoQ, and in vitro and in vivo performance compared to the effect of addition of alternative tocopherol-based excipients. In in vitro digestion experiments, CoQ was poorly solubilised in the digesting MCT as anticipated. Addition of TPM facilitated the enhanced solubilisation of CoQ as did vitamin E TPGS (TPGS). Other tocopherol derivatives (tocopherol acetate, tocopherol) were less effective at solubilising the active during the digestion process. The trends in in vitro solubilisation were conserved in the in vivo bioavailability of CoQ after oral administration to rats, with TPM and TPGS formulations providing approximately double the exposure of MCT alone, while the addition of the other tocopherol derivatives reduced the overall exposure. Collectively, the results indicate potential of TPM as a new solubilising excipient for use in oral drug delivery for poorly water soluble drugs.
磷酸生育酚是一类新的脂质赋形剂,已在药物应用中显示出潜力。它们能够增溶水溶性差的药物,表明它们在提高药物生物利用度方面具有潜在的应用价值,因为溶解度限制了药物的生物利用度。在这项研究中,一种商业的磷酸生育酚混合物 TPM 与中链甘油三酯 (MCT) 结合作为 CoQ 的配方,与添加替代生育酚赋形剂的效果进行了体外和体内性能比较。在体外消化实验中,CoQ 在消化 MCT 中溶解度差,如预期的那样。TPM 的添加促进了 CoQ 的增溶,维生素 E TPGS (TPGS) 也是如此。其他生育酚衍生物(醋酸生育酚、生育酚)在消化过程中对活性物质的增溶作用效果较差。在大鼠口服给予 CoQ 后的体内生物利用度研究中,体外增溶的趋势得以保持,TPM 和 TPGS 制剂提供的暴露量约为单独 MCT 的两倍,而添加其他生育酚衍生物则降低了总体暴露量。总的来说,这些结果表明 TPM 作为一种新的增溶剂赋形剂,可用于水溶性差的口服药物递送。