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Jyh-Ping Chen

Jyh-Ping Chen

Chang Gung University, Taiwan

Title: Thermosensitive Magnetoliposome Nanodrugs for Cancer Therapy

Biography

Biography: Jyh-Ping Chen

Abstract

Thermosensitive Magnetic Liposomes Were Developed For Controlled Release Of A Thrombolytic Drug And Anticancer Chemical/Gene Drugs For Thrombolysis And Glioma Treatment. As The FDA Has Approved The Application Of Liposome-Encapsulated Anticancer Drugs In Clinical Practice, Magnetic Liposome Formed By Entrapping Iron Oxide Magnetic Nanoparticles (MNP) In Phospholipids Could Be A Safe Platform For Drug Delivery. By Incorporating (Phospholipiddipalmitoylphosphatidylcholine, DPPC) With A Melting Temperature (Tm) Slightly Above The Physiological Temperature In The Liposome, The Thermosensitive Magnetic Liposome Was Designed For Controlled Release Of Entrapped Drugs Subject To Temperature Increase From 37 Oc To 43 Oc Or Through A Hyperthermia Effect Induced By An Alternating Magnetic Field (AMF). In Addition, The Co-Entrapped MNP Could Be Used For Magnetic Targeted Delivery Of The Cargo In The Liposome Under The Guidance Of A Magnet. The Temperature-Sensitive Liposomes Were Synthesized From DPPC, Distearolyphosphatidylethanolamine-N-Poly(Ethylene Glycol)2000 (DSPE-PEG2000), Cholesterol (CH) And Bis-Dodecyl Dimethyl Bromide (DDAB). Citric Acid Modified Iron Oxide MNP Were Encapsulated Into The Liposome Along With Anticancer Chemical Drug (Irinotecan, CPT11)/Gene Drug (SLP2 Shrna) To Prepare Thermosensitive Cationic Magnetic Liposome-CPT11-Shrna (TCML-CPT11-Shrna). The Composition Of Phospholipids Was First Optimized Followed By Physicochemical Analysis By DLS, Cryo-TEM, FTIR, TGA, DSC, SQUID, Zeta Potential And XRD. Enhanced Drug Release Was Confirmed By Temperature Change From 37 Oc To 43 Oc Or In The Presence Of An AMF. Furthermore, In Vitro Cell Culture Experiments Confirmed That The Drug Carriers Exhibited No Cytotoxicity Against Fibroblasts And Cancer Cells. The Drug-Loaded Carriers Also Showed Better Therapeutic Effect Toward Killing Cancer Cells Compared With Free Drugs. The Blood Hemolysis Assay Showed Non-Hemolytic Activity, Indicating Good Blood Compatibility. Finally, In Vivo Experiments Using Xenograft Tumor Mouse Model With U87 Human Glioblastoma Cells With Magnetic Guidance And AMF Treatment Demonstrated The Efficacy And Safety Of Treatment Using TCML-CPT11-Shrna.