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使用3D打印的离心式反应器快速制备纳米级脂质体:配方、表征及超分辨率成像

Rapid Production of Nanoscale Liposomes Using a 3D-Printed Reactor-In-A-Centrifuge: Formulation, Characterisation, and Super-Resolution Imaging.

作者信息

He Yongqing, Grandi Davide De, Chandradoss Stanley, LuTheryn Gareth, Cidonio Gianluca, Nunes Bastos Ricardo, Pereno Valerio, Carugo Dario

机构信息

Department of Pharmaceutics, School of Pharmacy, University College London, London WC1N 1AX, UK.

Institute of Biomedical Engineering (IBME), Department of Engineering Science, University of Oxford, Parks Road, Oxford OX1 3PJ, UK.

出版信息

Micromachines (Basel). 2023 Sep 12;14(9):1763. doi: 10.3390/mi14091763.

Abstract

Nanoscale liposomes have been extensively researched and employed clinically for the delivery of biologically active compounds, including chemotherapy drugs and vaccines, offering improved pharmacokinetic behaviour and therapeutic outcomes. Traditional laboratory-scale production methods often suffer from limited control over liposome properties (e.g., size and lamellarity) and rely on laborious multistep procedures, which may limit pre-clinical research developments and innovation in this area. The widespread adoption of alternative, more controllable microfluidic-based methods is often hindered by complexities and costs associated with device manufacturing and operation, as well as the short device lifetime and the relatively low liposome production rates in some cases. In this study, we demonstrated the production of liposomes comprising therapeutically relevant lipid formulations, using a cost-effective 3D-printed reactor-in-a-centrifuge (RIAC) device. By adjusting formulation- and production-related parameters, including the concentration of polyethylene glycol (PEG), temperature, centrifugation time and speed, and lipid concentration, the mean size of the produced liposomes could be tuned in the range of 140 to 200 nm. By combining selected experimental parameters, the method was capable of producing liposomes with a therapeutically relevant mean size of ~174 nm with narrow size distribution (polydispersity index, PDI ~0.1) at a production rate of >8 mg/min. The flow-through method proposed in this study has potential to become an effective and versatile laboratory-scale approach to simplify the synthesis of therapeutic liposomal formulations.

摘要

纳米级脂质体已被广泛研究并在临床上用于递送生物活性化合物,包括化疗药物和疫苗,具有改善的药代动力学行为和治疗效果。传统的实验室规模生产方法往往对脂质体性质(如大小和层数)的控制有限,且依赖繁琐的多步程序,这可能会限制该领域的临床前研究进展和创新。替代的、更可控的基于微流体的方法的广泛采用常常受到与设备制造和操作相关的复杂性和成本的阻碍,以及设备寿命短和在某些情况下脂质体生产率相对较低的问题。在本研究中,我们展示了使用具有成本效益的3D打印的离心式反应器(RIAC)设备生产包含治疗相关脂质制剂的脂质体。通过调整与制剂和生产相关的参数,包括聚乙二醇(PEG)浓度、温度、离心时间和速度以及脂质浓度,所生产脂质体的平均大小可在140至200纳米范围内调节。通过组合选定的实验参数,该方法能够以>8毫克/分钟的生产率生产平均大小约为174纳米且具有窄尺寸分布(多分散指数,PDI约为0.1)的治疗相关脂质体。本研究中提出的流通方法有可能成为一种有效且通用的实验室规模方法,以简化治疗性脂质体制剂的合成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/42f5/10535575/3554a472933f/micromachines-14-01763-g001.jpg

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