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[一种从单分散乳液制备囊泡的新方法,旨在控制尺寸并提高包封率]

[Novel method for preparing vesicles from a monodisperse emulsion aimed at controlling the size and improving the entrapment yield].

作者信息

Ichikawa Sosaku, Kuroiwa Takashi

机构信息

Graduate School of Life and Environmental Sciences, University of Tsukuba, Tsukuba City, Japan.

出版信息

Yakugaku Zasshi. 2008 May;128(5):681-6. doi: 10.1248/yakushi.128.681.

Abstract

A vesicle is a compartment composed of lipid bilayer of amphiphilic molecules. The vesicle is applied to carriers of drugs, cosmetics and functional food ingredients in industries. Vesicles are also applied as a model for artificial cell membrane and expected as micro- and nano-reactors. They are generally prepared by the hydration of dry lipid film, but there is no method to prepare vesicles of a controlled size and high entrapment yield of hydrophilic materials inside them. In this article, a microchannel (MC) emulsification method was applied to prepare vesicles aimed at controlling the size and improving the entrapment yield. Firstly, monodisperse water-in-oil (W/O) emulsions were prepared by the MC emulsification method. In this process, hydrophilic materials to be entrapped were contained inside the water droplets of the emulsions. Keeping the water droplets frozen, the emulsifier was replaced by a bilayer-forming lipid mixture, and then the oil phase was evaporated. After hydration of lipid layers surrounding the water droplets, vesicles were formed. We call this preparation "lipid-coated ice droplet hydration method". The final sizes of the prepared vesicles were comparable to the original emulsion droplet sizes. This means that the size of vesicles can be controlled by controlling the size of original water droplets of the W/O emulsions. Furthermore, calcein as a hydrophilic fluorescent marker and biopolymers, such as enzyme and polysaccharide, were entrapped into the internal water phases of vesicles. The method proposed in this study enables the formation of vesicles with a controlled size and high entrapment yields, potentially useful for expanding the application fields of vesicles as biocompatible carriers and micro- and nano-reactors for biochemical reactions.

摘要

囊泡是由两亲性分子的脂质双层组成的隔室。在工业中,囊泡被用作药物、化妆品和功能性食品成分的载体。囊泡还被用作人工细胞膜的模型,并有望成为微型和纳米反应器。它们通常通过干燥脂质膜的水合作用制备,但目前尚无制备尺寸可控且内部亲水性材料包封率高的囊泡的方法。在本文中,采用微通道(MC)乳化法制备囊泡,旨在控制其尺寸并提高包封率。首先,通过MC乳化法制备单分散的油包水(W/O)乳液。在此过程中,待包封的亲水性材料包含在乳液的水滴内部。保持水滴冷冻,将乳化剂替换为形成双层的脂质混合物,然后蒸发油相。在水滴周围的脂质层水合后,形成囊泡。我们将这种制备方法称为“脂质包被冰滴水化法”。制备的囊泡的最终尺寸与原始乳液滴的尺寸相当。这意味着可以通过控制W/O乳液原始水滴的尺寸来控制囊泡的尺寸。此外,将作为亲水性荧光标记物的钙黄绿素以及酶和多糖等生物聚合物包封到囊泡的内部水相中。本研究提出的方法能够形成尺寸可控且包封率高的囊泡,这对于扩大囊泡作为生物相容性载体以及生化反应的微型和纳米反应器的应用领域可能具有重要意义。

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