mRNA exhibits therapeutic potential across considerable applications, encompassing viral vaccines, protein replacement therapies, immunotherapy, cell therapy, and genome editing. In order to elicit therapeutic effects, mRNA molecule needs to reach and enter specific target cells and generate a sufficient quantity of the desired proteins. Abnova offers mRNA mixing services for several nanoparticle carriers, including lipid nanoparticles (LNPs) and liposomes, employing either microfluidic mixing devices (Precision NanoSystems) or manual mixing methods. Microfluidic technology (Precision NanoSystems) enables the fabrication of mRNA nanoparticle carrier complex under reproducible, scalable, and controlled mixing conditions. In contrast, manual mixing presents a simpler and cost-effective alternative method.

Lipid Nanoparticles (LNPs)
Lipid nanoparticles (LNPs) consist of ionizable lipids, structural lipids, cholesterol, and PEG-grafted lipids, each playing a distinct role in the particle structure. The ionizable lipid is a key component, capable of acquiring a positive charge at a reduced pH. This allows it to bind to the negatively charged phosphate backbone of nucleic acid cargo, forming an actively enriched core protected by a lipid exterior. LNPs can be customized for various therapeutic targets, and the efficacy of the LNP hinges on these essential components.

Liposomes
Liposomes, characterized by spherical lipid bilayers surrounding an aqueous cavity, represent another rapidly advancing lipid-based nanomedicine. The selection of specific lipids and liposome properties can influence factors such as the rate of drug release, circulation time, and target organ. Hydrophobic actives can be encapsulated within the lipid bilayer's fatty chains, attached to elements on the surface, or contained within the aqueous core, offering versatility in drug delivery design.

Mixing Flowchart

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Nanoparticle Carrier Components

Nanoparticle_Carrier_Components.jpg (383 KB)

 

 

Examples

Bioluminescent Imaging Following Intramuscular Injection of Reporter Lipid K LNP Prepared Using Microfluidic Device Mixing (Precision NanoSystems) in BALB/c Mice

 

mRNA_nanoparticle_carrier_mixing_exp1.jpg (343 KB)

 

The mouse experiments were conducted in quadruple repeat. Female BALB/c mice were individually injected with 40 μg of Luc-encoding reporter mRNA LNP, which was prepared using the microfluidic device (Precision NanoSystems), through the intramuscular route. IVIS Spectrum images were captured at 4 and 24 hours post-injection.

 

 

Bioluminescent Imaging Following Intramuscular Injection of Reporter Lipid K LNP Prepared Using Manual Mixing in BALB/c Mice

 

mRNA_nanoparticle_carrier_mixing_exp2.jpg (338 KB)

 

The mouse experiments were conducted in quadruple repeat. Female BALB/c mice were individually injected with 40 μg of Luc-encoding reporter mRNA LNP, which was manually mixed, through the intramuscular route. IVIS Spectrum images were captured at 4 and 24 hours post-injection.

 

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