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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Asymmetric-flow field-flow fractionation for measuring particle size, drug loading and (in)stability of nanopharmaceuticals. The joint view of European Union Nanomedicine Characterization Laboratory and National Cancer Institute - Nanotechnology Characterization Laboratory
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Asymmetric-flow field-flow fractionation for measuring particle size, drug loading and (in)stability of nanopharmaceuticals. The joint view of European Union Nanomedicine Characterization Laboratory and National Cancer Institute - Nanotechnology Characterization Laboratory

机译:用于测量粒度,药物载荷和(IN)纳米药物稳定性的不对称流场流动分馏。 欧盟纳米医生表征实验室和国家癌症研究所的联合观 - 纳米技术特征实验室

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Asymmetric-flow field-flow fractionation (AF4) has been recognized as an invaluable tool for the characterisation of particle size, polydispersity, drug loading and stability of nanopharmaceuticals. However, the application of robust and high quality standard operating procedures (SOPs) is critical for accurate measurements, especially as these complex drug nanoformulations are most often inherently polydisperse. In this review we describe a unique international collaboration that lead to the development of a robust SOP for the measurement of physical-chemical properties of nanopharmaceuticals by multi detector AF4 (MD-AF4) involving two state of the art infrastructures in the field of nanomedicine, the European Union Nanomedicine Characterization Laboratory (EUNCL) and the National Cancer Institute-Nanotechnology Characterisation Laboratory (NCI-NCL). We present examples of how MD-AF4 has been used for the analysis of key quality attributes, such as particle size, shape, drug loading and stability of complex nanomedicine formulations. The results highlight that MD-AF4 is a very versatile analytical technique to obtain critical information on a material particle size distribution, polydispersity and qualitative information on drug loading. The ability to conduct analysis in complex physiological matrices is an additional very important advantage of MD-AF4 over many other analytical techniques used in the field for stability studies. Overall, the joint NCI-NCL/EUNCL experience demonstrates the ability to implement a powerful and highly complex analytical technique such as MD-AF4 to the demanding quality standards set by the regulatory authorities for the pre-clinical safety characterization of nanomedicines. (C) 2020 Published by Elsevier B.V.
机译:非对称流场流动分馏(AF4)已被公认为表征纳米药物粒径、多分散性、载药量和稳定性的宝贵工具。然而,稳健和高质量标准操作规程(SOP)的应用对于精确测量至关重要,尤其是因为这些复杂的药物纳米制剂通常具有内在的多分散性。在这篇综述中,我们描述了一项独特的国际合作,该合作导致开发了一个强大的SOP,用于通过多探测器AF4(MD-AF4)测量纳米药物的物理化学性质,涉及纳米医学领域的两个最先进的基础设施,欧盟纳米医学表征实验室(EUNCL)和国家癌症研究所纳米技术表征实验室(NCI-NCL)。我们展示了MD-AF4如何用于分析关键质量属性的示例,如粒径、形状、载药量和复杂纳米药物制剂的稳定性。结果表明,MD-AF4是一种非常通用的分析技术,可以获得材料粒度分布、多分散性和载药量定性信息的关键信息。在复杂的生理基质中进行分析的能力是MD-AF4相对于稳定性研究领域中使用的许多其他分析技术的另一个非常重要的优势。总的来说,NCI-NCL/EUNCL的联合经验表明,有能力实施强大且高度复杂的分析技术,如MD-AF4,以达到监管机构为纳米药物临床前安全性特征设定的严格质量标准。(C) 2020年爱思唯尔公司出版。

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