Gastrointestinal cancers are the third leading cause of cancer-related mortality worldwide. Most current chemotherapeutics are administered intravenously, causing discomfort and stress to patients, and high costs due to multiple hospitalizations required. Furthermore, hospitalization is dangerous for immunocompromised cancer patients, due to drug-resistant pathogens widespread in hospitals. Multidrug resistance (MDR) is a major hindrance to curative cancer therapy. One of the major mechanisms of MDR is enhanced energy-dependent efflux of numerous hydrophobic cytotoxic drugs, which diffuse into cells through the plasma membrane. This ATP-dependent efflux is mediated by transmembrane transporters of the ATP-binding cassette (ABC) superfamily. We developed a novel β-CN-based target-activated nanoparticle system for oral delivery of synergistic combinations of hydrophobic chemotherapeutic drugs and MDR chemosensitizers.
Research
Biomed
Target-activated nanoparticles for treatment of MDR gastric cancer
Relevant publications:
β-Casein micelles for oral delivery of SN-38 and elacridar to overcome BCRP-mediated multidrug resistance in gastric cancer
European Journal of Pharmaceutics and Biopharmaceutics, Volume 133 (2018) 240-249
Re-assembled Casein Micelles for Oral Delivery of Chemotherapeutic Combinations to Overcome Multidrug Resistance in Gastric Cancer
J Mol Clin Med. (2018), Vol 1, 52-61.
Beta-Casein Based Nano-Vehicles for Oral Delivery of Chemotherapeutic Drugs: Drug-Protein Interactions and Mitoxantrone Loading Capacity
Nanomedicine: Nanotechnology, Biology and Medicine 6 , 547-555,(2010).
Beta-casein Nanoparticles as an Oral Delivery System for Chemotherapeutic Drugs: Impact of Drug Structure and Properties on Co-assembly
Pharmaceutical Research 27, 2175–2186 , (2010) .
β-Casein Nanoparticle-Based Oral Drug Delivery System for Potential Treatment of Gastric Carcinoma: Stability, Target-Activated Release and Cytotoxicity
European Journal of Pharmaceutics and Biopharmaceutics 80 (2) (2012), 298–305.
β-Casein Nano-vehicles for Oral Delivery of Chemotherapeutic Combinations Overcoming P-glycoprotein-Mediated Multidrug Resistance in Human Gastric Cancer
Oncotarget, 7 (2016), No. 17, 23322- 23334