Sugiura Shinji, Kuroiwa Takashi, Kagota Tetsuro, Nakajima Mitsutoshi, Sato Seigo, Mukataka Sukekuni, Walde Peter, Ichikawa Sosaku
Food Engineering Division, National Food Research Institute, Tsukuba 305-8642, Japan.
Langmuir. 2008 May 6;24(9):4581-8. doi: 10.1021/la703509r. Epub 2008 Apr 1.
A novel technique called the "lipid-coated ice droplet hydration method" is presented for the preparation of giant vesicles with a controlled size between 4 and 20 microm and entrapment yields for water-soluble molecules of up to about 30%. The method consists of three main steps. In the first step, a monodisperse water-in-oil emulsion with a predetermined average droplet diameter between 4 and 20 microm is prepared by microchannel emulsification, using sorbitan monooleate (Span 80) and stearylamine as emulsifiers and hexane as oil. In the second step, the water droplets of the emulsion are frozen and separated from the supernatant hexane solution by precipitation, followed by a removal of the supernatant and followed by the replacement of Span 80 by using a hexane solution containing egg yolk phosphatidylcholine, cholesterol, and stearylamine (5:5:1, molar ratio). This procedure is performed at -10 degrees C to keep the water droplets of the emulsion in a frozen state and thereby to avoid extensive water droplet coalescence. In the third step, hexane is evaporated at -4 to -7 degrees C and an external water phase is added to the remaining mixture of lipids and water droplets to form giant vesicles that have an average size in the range of that of the initial emulsion droplets (4-20 microm). The entrapment yield and the lamellarity of the vesicles obtained depend on the lipid/water droplet ratio and on the composition of the external water phase. At high lipid/water droplet ratio, the giant vesicles have a thicker membrane (indicating multilamellarity) and a higher entrapment yield than in the case of a low lipid/water droplet ratio. The highest entrapment yield ( approximately 35%) is obtained if the added external water phase contains preformed unilamellar egg phosphatidylcholine vesicles with an average diameter of 50 nm. The addition of these small vesicles minimizes the water droplet coalescence during the third step of the vesicle preparation, thereby decreasing the extent of release of water-soluble molecules originally present in the water droplets. The GVs prepared can be extruded through polycarbonate membranes to yield large unilamellar vesicles with about 100 nm diameter. This size reduction, however, leads to a decrease in the entrapment yield to about 12% due to solute leakage from the vesicles during the extrusion process.
本文介绍了一种名为“脂质包裹冰滴水合方法”的新技术,用于制备尺寸可控在4至20微米之间的巨型囊泡,水溶性分子的包封率高达约30%。该方法包括三个主要步骤。第一步,使用脱水山梨醇单油酸酯(司盘80)和硬脂胺作为乳化剂,己烷作为油相,通过微通道乳化制备平均液滴直径在4至20微米之间的单分散油包水乳液。第二步,将乳液中的水滴冷冻,通过沉淀与上层清液己烷溶液分离,然后去除上层清液,接着用含有蛋黄磷脂酰胆碱、胆固醇和硬脂胺(摩尔比为5:5:1)的己烷溶液替换司盘80。此操作在-10℃下进行,以使乳液中的水滴保持冷冻状态,从而避免水滴大量聚并。第三步,在-4至-7℃下蒸发己烷,并向剩余的脂质和水滴混合物中加入外部水相,以形成平均尺寸在初始乳液液滴范围内(4 - 20微米)的巨型囊泡。所得囊泡的包封率和层数取决于脂质/水滴比例以及外部水相的组成。在高脂质/水滴比例下,巨型囊泡具有更厚的膜(表明为多层结构),且包封率比低脂质/水滴比例时更高。如果添加的外部水相含有平均直径为50 nm的预制单层卵磷脂囊泡,则可获得最高包封率(约35%)。添加这些小囊泡可使囊泡制备第三步中的水滴聚并最小化,从而减少最初存在于水滴中的水溶性分子的释放程度。制备的巨型囊泡可通过聚碳酸酯膜挤出,以产生直径约为100 nm的大单层囊泡。然而,这种尺寸减小会导致包封率因挤出过程中溶质从囊泡泄漏而降至约12%。