泊洛沙姆
泊洛沙姆407
阴道内给药
生物利用度
化学
体内
子宫
剂型
药理学
色谱法
西地那非
医学
阴道
外科
内科学
生物
共聚物
有机化学
生物技术
聚合物
作者
Jinmei Ren,Shuxia Wang,Zhaoli Wu,Chenghao Zhang,Qing Zhang,Xinran Cui,Jiaxin Liu,Jingling Tang
标识
DOI:10.1080/1061186x.2025.2546491
摘要
Sildenafil citrate (SC) could promote uterine lining development, leading to successful embryo implantation. Due to the low oral bioavailability of the first-pass elimination of SC, it is necessary to develop a gel for vaginal administration to improve the efficacy. A vaginal gel was prepared using the cold method in order to increase the retention of SC in the uterus, which allows for prolonged contact between SC and the vaginal mucosa. A poloxamer-based thermosensitive in situ gel containing SC (SC-Tsgel) and a HPMC-based standard gel containing SC (SC-Cogel) were prepared. The rheological properties, in vitro drug release, and in vivo retention in the uterus of SC-Tsgel and SC-Cogel were compared. The average dosage of SC from SC-Tsgel and SC-Cogel were 5.72 and 5.94 mg/mL, respectively. The poloxamer gel and the HPMC gel containing SC had pH values of 4.53 and 5.02, respectively. The gel formulations significantly prolonged the time it took for drugs to be released following a release study. SC-Tsgel and SC-Cogel administered vaginally increased the duration of drug administration compared to SC solutions injected through the tail vein. Nevertheless, compared with tail vein injection of SC solutions or vaginal administration of the SC-Cogel, the retention of SC in the uterus was increased significantly after vaginal administration of the SC-Tsgel. Novel formulations of SC prepared with poloxamer 407 show promise as vaginal medication preparations for the management of a thin endometrium.
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