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Co-delivery of doxorubicin and erlotinib through liposomal nanoparticles for glioblastoma tumor regression using an in vitro brain tumor model
Using tiny fat-based particles to deliver two cancer drugs together for shrinking brain tumor cells in a lab model
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Abstract
Dual functionalized liposomes achieved approximately 52% tumor cell death in an in vitro brain tumor model.
- The developed liposomal delivery system is designed to enhance the transport of chemotherapeutics across the blood-brain barrier.
- Surface modification with transferrin allows for targeted delivery to glioma cells.
- The inclusion of a cell-penetrating peptide increases the internalization of doxorubicin and Erlotinib into tumor cells.
- In vitro studies indicated significantly higher apoptosis in glioblastoma cells treated with dual functionalized liposomes.
- Cellular uptake studies showed efficient internalization of drugs in glioblastoma and brain endothelial cells.
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