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一步挤出法制备高浓度利多卡因脂质纳米载体(LNC)分散体。

One-step extrusion of concentrated lidocaine lipid nanocarrier (LNC) dispersions.

机构信息

Case Western Reserve University Department of Macromolecular Science and Engineering, 2100 Adelbert Rd., Cleveland, OH 44106, United States.

University of Minnesota College of Science and Engineering Characterization Facility, 312 Church St SE, Minneapolis, MN 55455, United States.

出版信息

Int J Pharm. 2020 Nov 15;589:119817. doi: 10.1016/j.ijpharm.2020.119817. Epub 2020 Aug 29.

Abstract

Lipid nanocarriers (LNCs) have been successfully produced by many methods including high pressure homogenization, sonication and microemulsification, but it remains very difficult to produce dispersions with greater than 30% LNCs, volume average particle diameter less than 150 nm, and concentration of drugs useful for topical products. This research is the first to propose and demonstrate extrusion to manufacture highly concentrated drug containing LNC dispersions continuously and economically in a single step. By treating crude emulsions in a twin-screw extruder which has sections for homogenizing, mixing and fast-cooling inside the extruder, lidocaine-loaded LNC dispersions were successfully generated with lipid concentration up to 60% and particle diameters less than 50 nm. Electrical conductivity and birefringence measurements indicate that in the lidocaine system, lamellar microemulsions are intermediate structures and compositions with low lipid concentrations that do not present evidence of lamellar structures fail to give nanoparticles when processed. This paper also presents a new method for measuring kinetics of drug release from nanoparticles based on pH stat titration. Sufficiently precise data from pH stat titration allows determination of rate laws for release occurring on a time scale of minutes versus hours or days. The release rate of lidocaine from extruded 35% lipid nanoparticles was constant (zero order release kinetics) through the first hour (40% of drug release), a valuable property for drug delivery.

摘要

脂质纳米载体(LNCs)已经通过多种方法成功制备,包括高压匀质法、超声法和微乳液法,但仍然很难制备出脂质纳米载体浓度大于 30%、体积平均粒径小于 150nm 且载药量适用于局部产品的分散体。本研究首次提出并证明了挤出法可在一步连续、经济地制备高浓度载药 LNC 分散体。通过在双螺杆挤出机中处理粗乳液,该挤出机内部具有均质、混合和快速冷却的部分,成功制备了载有盐酸利多卡因的 LNC 分散体,脂质浓度高达 60%,粒径小于 50nm。电导率和双折射测量表明,在利多卡因体系中,层状微乳液是中间结构和组成,脂质浓度较低,没有层状结构的证据,而在处理过程中没有形成纳米颗粒。本文还提出了一种基于 pH -stat 滴定法测量纳米颗粒药物释放动力学的新方法。pH-stat 滴定法提供了足够精确的数据,可以确定在分钟到小时或几天的时间尺度上发生的释放速率定律。挤出的 35%脂质纳米颗粒中盐酸利多卡因的释放速率在最初的 1 小时内保持恒定(零级释放动力学)(药物释放的 40%),这是药物传递的一个有价值的特性。

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