Can We Simplify Liposome Manufacturing Using a Complex DoE Approach?

Microfluidic liposome production presents a streamlined pathway for expediting the translation of liposomal formulations from the laboratory setting to clinical applications. Using this production method, resultant liposome characteristics can be tuned through the control of both the formulation parameters (including the lipids and solvents used) and production parameters (including the production speed and mixing ratio). Therefore, the aim of this study was to investigate the relationship between not only total flow rate (TFR), the fraction of the aqueous flow rate over the organic flow rate (flow rate ratio (FRR)), and the lipid concentration, but also the solvent selection, aqueous buffer, and production temperature. To achieve this, we used temperature, applying a design of experiment (DoE) combined with machine learning. This study demonstrated that liposome size and polydispersity were influenced by manipulation of not only the total flow rate and flow rate ratio but also through the lipids, lipid concentration, and solvent selection, such that liposome attributes can be in-process controlled, and all factors should be considered within a manufacturing process as impacting on liposome critical quality attributes.

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Publication Details

Journal
Pharmaceutics
Published
2024-09-01
DOI
https://doi.org/10.3390/pharmaceutics16091159
Citations
9
Primary Topic
Microfluidic and Bio-sensing Technologies
Type
article
Field-Weighted Citation Impact
1.66
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article

Can We Simplify Liposome Manufacturing Using a Complex DoE Approach?

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9 citations
Pharmaceutics
Microfluidic and Bio-sensing Technologies
1.66
article

Can We Simplify Liposome Manufacturing Using a Complex DoE Approach?

Hans Coppenolle, Martin Kovářík, Yvonne Perrie, Sanket Shah, René Holm, Tatsiana Khamiakova, Sarah Lindsay, Olympia Tumolva
article en
9 citations

Abstract

Microfluidic liposome production presents a streamlined pathway for expediting the translation of liposomal formulations from the laboratory setting to clinical applications. Using this production method, resultant liposome characteristics can be tuned through the control of both the formulation parameters (including the lipids and solvents used) and production parameters (including the production speed and mixing ratio). Therefore, the aim of this study was to investigate the relationship between not only total flow rate (TFR), the fraction of the aqueous flow rate over the organic flow rate (flow rate ratio (FRR)), and the lipid concentration, but also the solvent selection, aqueous buffer, and production temperature. To achieve this, we used temperature, applying a design of experiment (DoE) combined with machine learning. This study demonstrated that liposome size and polydispersity were influenced by manipulation of not only the total flow rate and flow rate ratio but also through the lipids, lipid concentration, and solvent selection, such that liposome attributes can be in-process controlled, and all factors should be considered within a manufacturing process as impacting on liposome critical quality attributes.

PharmaceuticsVol. 16(9)
Johnson & Johnson (United States) (US), Janssen (Belgium) (BE), University of Southern Denmark (DK), University of Strathclyde (GB)
Openalex Percentile: Top 17%
Microfluidic and Bio-sensing Technologies
1.66
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