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Updated: May 5, 2026

Delivery of Therapeutic siRNA to the CNS Using Cationic and Anionic Liposomes
Published on: July 23, 2016
Preparation and in-vitro Evaluation of an Antisense-containing Cationic Liposome against Non-small Cell Lung Cancer:
Mostafa Saffari1, Farshad H Shirazi, Mohammad Ali Oghabian
1Department of Pharmaceutics, School of Pharmacy, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Abstract:
The current methods for treatment of cancers are inadequate and more specific methods such as gene therapy are in progress. Among different vehicles, cationic liposomes are frequently used for delivery of genetic material. This investigation aims to prepare and optimize DOTAP cationic liposomes containing an antisense oligonuclotide (AsODN) against protein kinase C alpha in non-small cells lung cancer (NSCLC). To perform this investigation, two different methods of ethanol injection and thin film hydration were used to prepare AsODN-loaded DOTAP liposomes. The formulated liposomes were then evaluated for their morphology, particle size, zeta potential and encapsulation efficiency, and the best formulation was chosen. In-vitro growth inhibitory effect of encapsulated ODN on A549 cells were evaluated by MTT and colonogenic assay. The physical and serum stability of liposomal ODN were also evaluated. Thin film hydration method resulted in large liposomes that required downsizing by extrusion with an encapsulation efficiency of 13%. Ethanol injection, in a single step gave liposomes with a small size of 115 nm and an encapsulation efficiency of around 90% which were physically stable for 6 months. The optimized liposome could protect oligonucleotides from degradation by nuclease. Cell studies showed a 20% sequence-specific inhibition of cell growth in MTT assay and revealed an LC50 of 103 nM in colonogenic studies. In conclusion, ethanol injection was able to provide suitable liposomes from the permanently charged DOTAP. Also the resulted liposomes were able to inhibit the growth of lung cancer cells.
Insights
DOTAP cationic liposomes effectively delivered antisense oligonucleotides to inhibit non-small cell lung cancer (NSCLC) growth. This gene therapy approach shows promise for improved cancer treatment strategies.
Area of Science:
- Nanomedicine
- Gene Therapy
- Oncology
Background:
- Current cancer treatments are insufficient, necessitating advanced therapies like gene therapy.
- Cationic liposomes are promising vehicles for delivering genetic material.
- Targeting protein kinase C alpha is a strategy for non-small cell lung cancer (NSCLC).
Purpose of the Study:
- To prepare and optimize DOTAP cationic liposomes for delivering an antisense oligonucleotide (AsODN) against protein kinase C alpha in NSCLC.
- Evaluate the efficacy and stability of AsODN-loaded liposomes for lung cancer treatment.
Main Methods:
- Two methods, ethanol injection and thin film hydration, were used to formulate AsODN-loaded DOTAP liposomes.
- Liposomes were characterized for morphology, particle size, zeta potential, and encapsulation efficiency.
- In-vitro studies using MTT and colonogenic assays assessed growth inhibition in A549 lung cancer cells.
Main Results:
- Ethanol injection yielded optimized liposomes (115 nm) with high encapsulation efficiency (~90%) and stability.
- Liposomal AsODN protected against nuclease degradation.
- A 20% sequence-specific inhibition of A549 cell growth was observed, with an LC50 of 103 nM.
Conclusions:
- Ethanol injection is a suitable method for preparing stable DOTAP liposomes.
- The developed liposomal AsODN formulation effectively inhibits non-small cell lung cancer cell growth.
- This study supports the potential of liposomal gene therapy for NSCLC treatment.
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