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Updated: Jul 16, 2026

Generation of Cationic Nanoliposomes for the Efficient Delivery of In Vitro Transcribed Messenger RNA
Published on: February 1, 2019
DOTAP/UDCA vesicles: novel approach in oligonucleotide delivery
Barbara Ruozi1, Renata Battini, Monica Montanari
1Department of Pharmaceutical Sciences, University of Modena and Reggio Emilia, Modena, Italy.
Ursodeoxycholic acid (UDCA) additive enhances DOTAP liposome delivery of oligonucleotides. These modified liposomes show improved cellular uptake and stability without toxicity, offering a promising gene delivery approach.
Area of Science:
- Biochemistry
- Nanotechnology
- Molecular Biology
Background:
- Cationic liposomes like DOTAP are used for oligonucleotide delivery.
- Improving liposome stability and cellular uptake is crucial for effective gene therapy.
- Ursodeoxycholic acid (UDCA) is a hydrophilic bile acid with potential formulation applications.
Purpose of the Study:
- To investigate the effect of UDCA as an additive to DOTAP cationic liposomes.
- To evaluate the impact on cellular uptake and localization of oligonucleotides.
- To assess the stability and toxicity of the novel DOTAP-UDCA formulations.
Main Methods:
- Nuclear magnetic resonance (NMR) for UDCA incorporation.
- Gel electrophoresis to analyze oligonucleotide-liposome complexes.
- Cytofluorimetric and confocal microscopy for cellular uptake and localization studies in HaCaT cells.
Main Results:
- DOTAP-UDCA vesicles (MixVes) were successfully formed at various molar ratios.
- UDCA incorporation enhanced liposome stability, flexibility, and activity.
- MixVes at 1:0.25 and 1:0.5 molar ratios significantly increased oligonucleotide cellular uptake compared to DOTAP alone.
- Confocal microscopy confirmed altered cellular localization of the oligonucleotides.
Conclusions:
- Formulating DOTAP liposomes with UDCA creates more stable and effective gene delivery vehicles.
- Specific UDCA ratios (1:0.25, 1:0.5) optimize oligonucleotide cellular uptake.
- These UDCA-modified liposomes demonstrate a promising, non-toxic approach for oligonucleotide delivery.
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