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优化阴道栓剂配方,以递送 SHetA2 作为治疗宫颈发育不良的新方法。

Optimization of a Vaginal Suppository Formulation to Deliver SHetA2 as a Novel Treatment for Cervical Dysplasia.

机构信息

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

Department of Obstetrics and Gynecology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma 73104.

出版信息

J Pharm Sci. 2018 Feb;107(2):638-646. doi: 10.1016/j.xphs.2017.09.018. Epub 2017 Oct 6.

Abstract

Cervical dysplasia induced by the human papilloma virus unpredictably progresses to cervical cancer. Therapeutic options are invasive and affect the patient's quality of life. SHetA2 has demonstrated therapeutic efficacy against human and murine human papilloma virus-induced tumors, but its oral bioavailability is <1%. An optimized vaginal suppository formulation can deliver SHetA2 in sufficient doses to prevent cervical dysplasia. The quality by design approach was employed to optimize the suppository formulation consisting of cocoa butter as base with 5% Kolliphor and 40% SHetA2. The suppository had a content uniformity of 105.44 ± 0.42%, melted in <8 min, and had a complete release of SHetA2 in water. Administration of the suppository to mice-achieved cervix concentrations that were significantly higher than the SHetA2 therapeutic concentration, with the maximum concentration (C = 336.78 μg/g) being more than 100-fold the therapeutic SHetA2 concentration. Furthermore, the levels of cyclin D1 protein decreased 9-fold indicating a correlation of drug concentrations with the pharmacodynamic endpoint. These proof-of-concept studies suggest that the SHetA2 optimized vaginal suppository formulation may have a potential use in the prevention of cervical dysplasia, but detailed efficacy studies are required to confirm this assumption.

摘要

人乳头瘤病毒引起的宫颈发育不良不可预测地进展为宫颈癌。治疗选择具有侵入性,并影响患者的生活质量。SHetA2 已被证明对人乳头瘤病毒诱导的人类和鼠类肿瘤具有治疗效果,但口服生物利用度<1%。优化的阴道栓剂配方可以提供足够剂量的 SHetA2 来预防宫颈发育不良。采用质量源于设计方法优化栓剂配方,以可可脂为基质,含 5%Kolliphor 和 40%SHetA2。栓剂的含量均匀度为 105.44±0.42%,<8 分钟内融化,在水中完全释放 SHetA2。将栓剂给予小鼠,可使宫颈浓度明显高于 SHetA2 的治疗浓度,最大浓度(C=336.78μg/g)超过治疗 SHetA2 浓度的 100 倍。此外,细胞周期蛋白 D1 蛋白的水平降低了 9 倍,表明药物浓度与药效终点相关。这些概念验证研究表明,优化的 SHetA2 阴道栓剂配方可能具有预防宫颈发育不良的潜力,但需要详细的疗效研究来证实这一假设。

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