The Effect of Cryoprotectants and Storage Conditions on the Transfection Efficiency, Stability, and Safety of Lipid‐Based Nanoparticles for mRNA and DNA Delivery

Author:

Kafetzis Konstantinos N.1,Papalamprou Natalia1,McNulty Elisha1,Thong Kai X.2,Sato Yusuke3,Mironov Aleksandr4,Purohit Atul5,Welsby Philip J.6,Harashima Hideyoshi3,Yu‐Wai‐Man Cynthia2,Tagalakis Aristides D.1ORCID

Affiliation:

1. Department of Biology Edge Hill University Ormskirk L39 4QP UK

2. Faculty of Life Sciences & Medicine King's College London London SE1 7EH UK

3. Faculty of Pharmaceutical Sciences Hokkaido University Kita‐12, Nishi‐6, Kita‐ku Sapporo 060–0812 Japan

4. Electron Microscopy Core Facility (RRID: SCR_021147) Faculty of Biology Medicine and Health University of Manchester Manchester M13 9PT UK

5. Oncology Drug Discovery & Women's Health Group Department of Metabolism Digestion & Reproduction Imperial College London London W12 0HS UK

6. Medical School Edge Hill University Ormskirk L39 4QP UK

Abstract

AbstractLipid‐based nanoparticles have recently shown great promise, establishing themselves as the gold standard in delivering novel RNA therapeutics. However, research on the effects of storage on their efficacy, safety, and stability is still lacking. Herein, the impact of storage temperature on two types of lipid‐based nanocarriers, lipid nanoparticles (LNPs) and receptor‐targeted nanoparticles (RTNs), loaded with either DNA or messenger RNA (mRNA), is explored and the effects of different cryoprotectants on the stability and efficacy of the formulations are investigated. The medium‐term stability of the nanoparticles was evaluated by monitoring their physicochemical characteristics, entrapment and transfection efficiency, every two weeks over one month. It is demonstrated, that the use of cryoprotectants protects nanoparticles against loss of function and degradation in all storage conditions. Moreover, it is shown that the addition of sucrose enables all nanoparticles to remain stable and maintain their efficacy for up to a month when stored at −80 °C, regardless of cargo or type of nanoparticle. DNA‐loaded nanoparticles also remain stable in a wider variety of storage conditions than mRNA‐loaded ones. Importantly, these novel LNPs show increased GFP expression that can signify their future use in gene therapies, beyond the established role of LNPs in RNA therapeutics.

Funder

Medical Research Council

Publisher

Wiley

Subject

Pharmaceutical Science,Biomedical Engineering,Biomaterials

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