Abstract

Microfluidics has recently emerged as a new method of manufacturing liposomes, which allows for reproducible mixing in miliseconds on the nanoliter scale. Here we investigate microfluidics-based manufacturing of liposomes. The aim of these studies was to assess the parameters in a microfluidic process by varying the total flow rate (TFR) and the flow rate ratio (FRR) of the solvent and aqueous phases. Design of experiment and multivariate data analysis were used for increased process understanding and development of predictive and correlative models. High FRR lead to the bottom-up synthesis of liposomes, with a strong correlation with vesicle size, demonstrating the ability to in-process control liposomes size; the resulting liposome size correlated with the FRR in the microfluidics process, with liposomes of 50nm being reproducibly manufactured. Furthermore, we demonstrate the potential of a high throughput manufacturing of liposomes using microfluidics with a four-fold increase in the volumetric flow rate, maintaining liposome characteristics. The efficacy of these liposomes was demonstrated in transfection studies and was modelled using predictive modeling. Mathematical modelling identified FRR as the key variable in the microfluidic process, with the highest impact on liposome size, polydispersity and transfection efficiency. This study demonstrates microfluidics as a robust and high-throughput method for the scalable and highly reproducible manufacture of size-controlled liposomes. Furthermore, the application of statistically based process control increases understanding and allows for the generation of a design-space for controlled particle characteristics.

Highlights

  • Liposomes are well established as delivery systems and immunological adjuvants and there are a wide range of methods employed in their production

  • The results indicate that the flow rate ratio (FRR) in the microfluidic process has a strong relevance to the formation of size-controlled vesicles with multivariate data analysis (MVDA) studies confirm the significance of FRR in the microfluidics process for the formation of liposomes

  • Homogenous liposomes suspensions can be prepared in a high throughput method setup

Read more

Summary

Introduction

Liposomes are well established as delivery systems and immunological adjuvants and there are a wide range of methods employed in their production. Homogenization techniques, shear or pressure induced size reduction, circumvent protein or lipid degradation and are frequently used to reduce the size and lamellarity of MLV (Wagner and Vorauer-Uhl, 2011). As an alternative to these methods, microfluidics is a relatively new area of liposome synthesis, where the small dimensions in a micromixer allow for fast mixing, dominated by diffusion or convection (Whitesides, 2006). Microfluidics refers to fluid handling methods in a controlled volume, typically below millimeter scales, which allows for implementation of the mixing process into planar chips (Squires and Quake, 2005).

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call