Bhagurkar Ajinkya M, Repka Michael A, Murthy S Narasimha
Department of Pharmaceutics and Drug Delivery, School of Pharmacy, University of Mississippi, University, Mississippi 38677.
Department of Pharmaceutics and Drug Delivery, School of Pharmacy, University of Mississippi, University, Mississippi 38677; Pii Center for Pharmaceutical Technology, School of Pharmacy, University of Mississippi, University, Mississippi 38677.
J Pharm Sci. 2017 Apr;106(4):1085-1091. doi: 10.1016/j.xphs.2016.12.015. Epub 2016 Dec 28.
The main aim of this study was to investigate the feasibility of preparing nanostructured lipid carrier (NLC) utilizing hot-melt extrusion (HME) coupled with probe sonication. The process parameters for HME and sonication were optimized and a modified screw configuration was used for extrusion. Lidocaine-loaded NLCs were successfully prepared by the proposed method with particle size <50 nm and polydispersity index <0.3. Transmission electron microscopy revealed the spherical nature of the particles. The second objective was to develop NLCs for topical controlled delivery of drug for pain management in cutaneous wounds. The entrapment efficiency of drug-loaded NLCs was found to be 73.9%. The formulation was subjected to permeation studies across porcine epidermis using a Franz diffusion setup. The drug permeation from the NLC-loaded carbopol gel was found to be sustained as compared to permeation from the gel without lipids. Furthermore, mechanistic studies were performed using tape stripped and intact skin models to ascertain the fact that the predominant rate controlling process was release of drug from the NLCs. In summary, the conventional HME process can be modified for continuous manufacturing of NLCs, which are otherwise prepared by batch processing involving multiple and complicated processing steps.
本研究的主要目的是探讨利用热熔挤出(HME)结合探头超声处理制备纳米结构脂质载体(NLC)的可行性。对HME和超声处理的工艺参数进行了优化,并采用改良的螺杆配置进行挤出。通过该方法成功制备了载利多卡因的NLC,其粒径<50 nm,多分散指数<0.3。透射电子显微镜显示颗粒呈球形。第二个目标是开发用于皮肤伤口疼痛管理的局部控释药物的NLC。载药NLC的包封率为73.9%。使用Franz扩散装置对该制剂进行了跨猪表皮的渗透研究。与不含脂质的凝胶相比,载NLC的卡波姆凝胶的药物渗透具有持续性。此外,使用胶带剥离和完整皮肤模型进行了机理研究,以确定主要的速率控制过程是药物从NLC中的释放。总之,传统的HME工艺可以进行改进,以连续生产NLC,否则NLC是通过涉及多个复杂加工步骤的分批工艺制备的。