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Shrinkage of pegylated and non-pegylated liposomes in serum

机译:血清中聚乙二醇化和非聚乙二醇化脂质体的收缩

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摘要

An essential requisite for the design of nanodelivery systems is the ability to characterize the size, homogeneity and zeta potential of nanoparticles. Such properties can be tailored in order to create the most efficient drug delivery platforms. An important question is whether these characteristics change upon systemic injection. Here, we have studied the behavior of phosphatidylcholine/cholesterol liposomes exposed to serum proteins. The results reveal a serum-induced reduction in the size and homogeneity of both pegylated and non-pegylated liposomes, implicating the possible role of osmotic forces. In addition, changes to zeta-potential were observed upon exposing liposomes to serum. The liposomes with polyethylene glycol expressed different characteristics than their non-polymeric counterparts, suggesting the potential formation of a denser protein corona around the non-pegylated liposomes.
机译:纳米传递系统设计的基本要求是能够表征纳米粒子的大小,均质性和ζ电势。可以定制此类属性,以创建最有效的药物输送平台。一个重要的问题是这些特征在全身注射后是否会改变。在这里,我们研究了暴露于血清蛋白的磷脂酰胆碱/胆固醇脂质体的行为。结果揭示了血清诱导的聚乙二醇化和非聚乙二醇化脂质体的大小和均一性的降低,暗示了渗透力的可能作用。另外,将脂质体暴露于血清后观察到ζ电位的变化。具有聚乙二醇的脂质体表现出与非聚合脂质体不同的特性,表明在非聚乙二醇化脂质体周围可能形成更致密的蛋白质电晕。

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