A novel filtration approach to create small unilamellar liposomes for drug delivery

Steven A. Roberts, N. Neelaveni, Nitin Agrawal
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引用次数: 2

Abstract

Nanoscale drug carriers have quickly risen to the forefront of translational research and promise to play a prominent role in point of care applications. The protocol for synthesizing these particles typically relies on extensive secondary post processing techniques (e.g. extrusion, dialysis, or ultracentrifugation) that are time consuming and can lead to a net loss in either the number of particles or amount of encapsulated molecules. Here we utilize filter centrifugation to efficiently purify and concentrate liposomal particle solutions. Using this technique, we are able to remove 99.99% of nonencapsulated molecules from solution in less than half of the time required for ultracentrifugation without net loss of particles from the solution.
一种新的过滤方法,以创建用于药物递送的小单层脂质体
纳米级药物载体已经迅速上升到转化研究的前沿,并有望在护理点应用中发挥突出作用。合成这些颗粒的方案通常依赖于广泛的二次后处理技术(例如挤出、透析或超离心),这些技术耗时且可能导致颗粒数量或包封分子数量的净损失。在这里,我们利用过滤离心有效地纯化和浓缩脂质体颗粒溶液。使用这种技术,我们能够在不到超离心所需时间的一半的时间内从溶液中去除99.99%的非封装分子,而不会从溶液中净损失颗粒。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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