Department of Pharmaceutics and Drug Delivery, School of Pharmacy, The University of Mississippi, University, MS 38677, USA.
College of Pharmacy, The University of Texas at Austin, Austin, TX 78712, USA.
Int J Pharm. 2019 Jul 20;566:520-531. doi: 10.1016/j.ijpharm.2019.06.021. Epub 2019 Jun 8.
Cefuroxime Axetil (CA) is a poorly soluble, broad spectrum antibiotic which undergoes enzymatic degradation in gastrointestinal tract. The objective of the present study was to develop lipid-based gastro-retentive floating drug delivery systems containing CA using hot-melt extrusion (HME) to improve absorption. Selected formulations of CA and lipids were extruded using a twin screw hot-melt extruder. Milled extrudates were characterized for dissolution, floating strength, and micromeritic properties. Solid-state characterization was performed using differential scanning calorimetry (DSC), scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy, and hot-stage microscopy. In vitro characterization demonstrated that the formulations exhibited a sustained drug release profile for 12 h. All formulations showed desired floating and flow properties. Solid-state characterization revealed no phase separation and no chemical interactions between the drug and excipients. Based on in vitro study results, an optimized formulation (F8) was further evaluated for in vivo performance. Oral bioavailability (C and AUC) of F8 was significantly higher than that of pure CA. This study describes the use of lipid-based gastro-retentive floating drug delivery systems to achieve desired sustained release profile for more complete dissolution which could potentially reduce enzymatic degradation. This study also highlights the effectiveness of HME technology to improve dissolution and bioavailability.
头孢呋辛醋乙酯(CA)是一种难溶性的广谱抗生素,在胃肠道中会发生酶降解。本研究的目的是开发含有 CA 的基于脂质的胃滞留型漂浮药物传递系统,以改善吸收。使用双螺杆热熔挤出机对 CA 和脂质的选定配方进行挤出。对挤出的细粒进行溶解、漂浮强度和微粉特性的表征。使用差示扫描量热法(DSC)、扫描电子显微镜(SEM)、傅里叶变换红外(FTIR)光谱和热台显微镜对固态特性进行了表征。体外特性研究表明,这些配方可在 12 小时内实现药物的持续释放。所有配方均表现出所需的漂浮和流动性能。固态特性研究表明,药物与赋形剂之间没有相分离,也没有发生化学相互作用。基于体外研究结果,对优化配方(F8)进行了体内性能评估。F8 的口服生物利用度(C 和 AUC)明显高于纯 CA。本研究描述了使用基于脂质的胃滞留型漂浮药物传递系统来实现所需的持续释放曲线,以促进更完全的溶解,从而有可能减少酶降解。本研究还强调了热熔挤出技术在改善溶解和生物利用度方面的有效性。