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含 SHetA2 的阴道栓剂治疗宫颈发育不良:每日剂量的药代动力学和初步安全性特征。

Vaginal Suppositories Containing SHetA2 to Treat Cervical Dysplasia: Pharmacokinetics of Daily Doses and Preliminary Safety Profile.

机构信息

Department of Pharmaceutical Sciences, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma 73104.

Department of Pharmaceutical Sciences, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma 73104; Genetics and Bioengineering Department, Yeditepe University, Istanbul, Turkey.

出版信息

J Pharm Sci. 2020 Jun;109(6):2000-2008. doi: 10.1016/j.xphs.2020.02.016. Epub 2020 Feb 27.

Abstract

SHetA2 is a new drug with potential to treat cervical dysplasia, but only 0.02% of the dose is absorbed into the cervix after oral administration. By contrast, 23.9% of the dose is absorbed into the cervix after vaginal administration. This study determines the pharmacokinetic and pharmacodynamic parameters after daily vaginal doses of SHetA2 in suppositories and assesses its safety. Daily dosed mice maintained therapeutic concentrations of SHetA2 in the cervix for 65 h. The steady-state area under the curve concentration versus time (AUC) after the last dose was similar to that after a single dose indicating that there was no drug accumulation in the cervix. By contrast, the maximum drug concentration (C) was smaller in the daily dosed group (52.19 μg/g) than after a single dose (121.84 μg/g), whereas the half-life (t) was also shorter in the daily dosed group (9.94 h) than after a single dose (23.32 h). Notably, daily vaginal doses of SHetA2 reduced the levels of cyclin D1 (the pharmacodynamic endpoint) to a larger extent (∼45%) than after the administration of a single dose (∼26%). No adverse effects were observed in the mice for the duration of the study; thus, daily vaginal doses of SHetA2 appear to be safe.

摘要

SHetA2 是一种有潜力治疗宫颈发育不良的新药,但口服后只有 0.02%的剂量被吸收到宫颈。相比之下,阴道给药后 23.9%的剂量被吸收到宫颈。本研究旨在确定阴道给予栓剂后每日剂量的 SHetA2 的药代动力学和药效学参数,并评估其安全性。每日剂量的小鼠在宫颈中维持治疗浓度的 SHetA2 长达 65 小时。最后一次给药后的稳态 AUC 与单次给药相似,表明宫颈内无药物蓄积。相比之下,每日剂量组的 C 最大值(52.19μg/g)小于单次剂量组(121.84μg/g),而半衰期(t)也小于单次剂量组(9.94 h)。值得注意的是,与单次给药相比(约 26%),每日阴道给予 SHetA2 能更大程度地降低细胞周期蛋白 D1 水平(药效学终点)(约 45%)。在研究期间,小鼠未观察到任何不良反应;因此,每日阴道给予 SHetA2 似乎是安全的。

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