The Use of a Staggered Herringbone Micromixer for the Preparation of Rigid Liposomal Formulations Allows Efficient Encapsulation of Antigen and Adjuvant.

Fernando Lozano Vigario, Noémi Anna Nagy, Meike H The, Rinske Sparrius, Joke A Bouwstra, Alexander Kros, Wim Jiskoot, Esther C de Jong, Bram Slütter

Journal: Journal of pharmaceutical sciences 2022;111(4):1050-1057

PMID: 35114210

Abstract

Anionic liposomal formulations have previously shown to have intrinsic tolerogenic capacity and these properties have been related to the rigidity of the particles. The combination of highly rigid anionic liposomes to deliver tolerogenic adjuvants and antigen peptides has potential applications for the treatment of autoimmune and inflammatory diseases. However, the preparation of these highly rigid anionic liposomes using traditional methods such as lipid film hydration presents problems in terms of scalability and loading efficiency of some costly tolerogenic adjuvants like 1-α,25-dihydroxyvitaminD3. Here we propose the use of an off-the-shelf staggered herringbone micromixer for the preparation of these formulations and performed a systematic study on the effect of temperature and flow conditions on the size and polydispersity index of the formulations. Furthermore, we show that the system allows for the encapsulation of a wide variety of peptides and significantly higher loading efficiency of 1-α,25-dihydroxyvitaminD3 compared to the traditional lipid film hydration method, without compromising their non-inflammatory interaction with dendritic cells. Therefore, the microfluidics method presented here is a valuable tool for the preparation of highly rigid tolerogenic liposomes in a fast, size-tuneable and scalable manner.

Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.

Address: Division of BioTherapeutics, Leiden Academic Centre for Drug Research, Leiden University, the Netherlands.; Department of Experimental Immunology, Amsterdam University Medical Centre, Amsterdam Institute for Infection & Immunity, University of Amsterdam, Amsterdam, the Netherlands.; Department of Supramolecular & Biomaterials Chemistry, Leiden Institute of Chemistry, Leiden University, the Netherlands.; Division of BioTherapeutics, Leiden Academic Centre for Drug Research, Leiden University, the Netherlands. Electronic address: [email protected].

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