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In Vitro / In Vivo Correlation of Travoprost Release from a Biodegradable Hydrogel Punctum Plug for the Treatment of Glaucoma

机译:从可生物降解的水凝胶点状塞中释放的Travoprost的体外/体内相关性用于治疗青光眼

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?Purpose?To demonstrate an in vitro / in vivo correlation (IVIVC) of sustained release travoprost from biodegradable hydrogel punctum plugs in an animal model compared to dissolution testing.?Methods?The Travoprost Punctum Plug (OTX-TP3) is comprised of travoprost encapsulated in polylactide microparticles that are entrapped within a dried biodegradable PEG hydrogel matrix and sized for insertion into the vertical canaliculus. Upon insertion the hydrogel swells to conform to the vertical canaliculus to ensure plug retention and release travoprost for a period of 3 months. Drug release rate from OTX-TP3 was assessed in vitro in PBS at pH 7.4, incubated at 37 C through complete dissolution and in vivo after subcutaneous implantation of two plugs in the scapular region of Sprague Dawley rats (n=40). Excision of 10 plugs from 5 rats per time point was performed and drug content per plug was determined via extraction and RP-HPLC.?Results?The daily in vitro and in vivo release of travoprost from OTX-TP3 was plotted over the duration of the studies (Figure One). Results demonstrate a sustained drug release relationship between the two studies and establish a 3-month drug release profile in an animal model correlating to conventional in vitro dissolution testing (Figure Two). For dose comparison purposes the daily amount of travoprost administered in a Travatan Z eye drop (from Travatan Z NDA #21-994) is presented in Figure One.?Conclusions?The in vivo release results show good agreement with standard in vitro dissolution testing and demonstrate a suitable model for the development of an IVIVC. Sustained release of travoprost from biodegradable plugs can deliver travoprost for a period of 3 months in an in vivo animal model that meets or exceeds the daily dose from eye drops. ?View OriginalDownload SlideView OriginalDownload Slide?View OriginalDownload SlideView OriginalDownload Slide? Keywords: 503 drug toxicity/drug effects ? 607 nanotechnology ? 633 outflow: trabecular meshwork ?.
机译:目的:为了证明与动物模型中的溶出度测试相比,动物模型中可生物降解的水凝胶穿刺塞的缓释曲伏前列素的体外/体内相关性(IVIVC)。方法:特拉沃前列素点缀塞(OTX-TP3)是由特拉沃前列素包封的聚丙交酯微粒中的多糖被截留在干燥的可生物降解的PEG水凝胶基质中,其大小可插入垂直小管中。插入后,水凝胶溶胀以适应垂直小管,以确保塞子保留并释放特拉沃前列素3个月。在pH 7.4的PBS中体外评估OTX-TP3的药物释放速率,在完全溶解的条件下于37°C孵育,并在Sprague Dawley大鼠的肩region骨区域(n = 40)皮下植入两个栓塞后在体内进行体内评估。在每个时间点从5只大鼠中切除10个栓塞,并通过提取和RP-HPLC测定每个栓塞的药物含量。结果:绘制了OTX-TP3在体外和体内的travoprost的每日体内和体外释放情况。研究(图一)。结果证明了这两项研究之间的持续药物释放关系,并在与常规体外溶出度测试相关的动物模型中建立了3个月的药物释放曲线(图二)。为了进行剂量比较,图一显示了Travatan Z滴眼液中Travoprost的每日给药量(来自Travatan Z NDA#21-994)。结论:体内释放结果与标准的体外溶出度测试和演示用于开发IVIVC的合适模型。从生物可降解栓塞中持续释放travoprost可以在达到或超过滴眼剂日剂量的体内动物模型中将travoprost递送3个月。查看原始下载幻灯片查看原始下载幻灯片查看原始下载幻灯片查看原始下载幻灯片关键字:503药物毒性/药物作用? 607纳米技术633流出:小梁网。

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