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Comparison of the physical characteristics of monodisperse non-ionic surfactant vesicles (NISV) prepared using different manufacturing methods

机译:使用不同制造方法制备的单分散非离子表面活性剂囊泡(NISV)的物理特性比较

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摘要

Non-ionic surfactant vesicles (NISV) are synthetic membrane vesicles formed by self-assembly of a non-ionic surfactant, often in a mixture with cholesterol and a charged chemical species. Different methods can be used to manufacture NISV, with the majority of these requiring bulk mixing of two phases. This mixing process is time-consuming and leads to the preparation of large and highly dispersed vesicles, which affects the consistency of the final product and could hinder subsequent regulatory approval. In this study, we have compared the physical characteristics of NISV prepared using two conventional methods (thin-film hydration method and heating method) with a recently introduced microfluidic method. The resulting particles from these methods were assessed for their physical characteristics and in vitro cytotoxicity. Through microfluidics, nano-sized NISV were prepared in seconds, through rapid and controlled mixing of two miscible phases (lipids dissolved in alcohol and an aqueous medium) in a microchannel, without the need of a size reduction step, as required for the conventional methods. Stability studies over two months showed the particles were stable regardless of the method of preparation and there were no differences in terms of EC50 on A375 and A2780 cell lines. However, this work demonstrates the flexibility and ease of applying lab-on-chip microfluidics for the preparation of NISV that could be used to significantly improve formulation research and development, by enabling the rapid manufacture of a consistent end-product, under controlled conditions.
机译:非离子表面活性剂囊泡(NISV)是通过非离子表面活性剂自组装形成的合成膜囊泡,通常与胆固醇和带电化学物质混合。可以使用不同的方法来制造NISV,其中大多数方法需要两相的本体混合。该混合过程很费时,并且导致制备大且高度分散的囊泡,这影响了最终产品的稠度并可能阻碍随后的监管批准。在这项研究中,我们将使用两种常规方法(薄膜水化方法和加热方法)制备的NISV的物理特性与最近引入的微流体方法进行了比较。从这些方法得到的颗粒的物理特性和体外细胞毒性进行了评估。通过微流控技术,通过在微通道中快速可控地混合两个可混溶相(脂类溶解在乙醇和水性介质中),无需常规方法所需的减小尺寸步骤,即可在几秒钟内制备出纳米级NISV 。超过两个月的稳定性研究表明,无论采用何种制备方法,颗粒均稳定,并且A375和A2780细胞系的EC50均无差异。但是,这项工作证明了使用芯片实验室微流体制备NISV的灵活性和易用性,可通过在受控条件下快速制造稳定的最终产品来显着改善制剂的研发。

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