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MSN-LFA is an experimental hybrid nanocarrier system designed for targeted cancer therapy. It consists of mesoporous silica nanoparticles (MSNs) that provide a high surface area and pore volume for drug loading, a lipid coating that enhances physicochemical stability and controls drug release, and folic acid (FA) ligands for active targeting. The system specifically targets the Folate receptor alpha (FRα), which is overexpressed in various malignancies, including aggressive breast cancer (e.g., MCF-7 cells), while remaining low in normal tissues. By utilizing receptor-mediated endocytosis, MSN-LFA improves the intracellular accumulation of chemotherapeutic agents like doxorubicin, thereby increasing cytotoxic efficacy and potentially reducing systemic side effects such as cardiotoxicity.
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