Publication Type : Journal Article
Thematic Areas : Nanosciences and Molecular Medicine
Publisher : ACS Biomaterials Science and Engineering, American Chemical Society.
Source : ACS Biomaterials Science and Engineering, American Chemical Society, Volume 2, Number 5, p.768-779 (2016)
Url : https://www.scopus.com/inward/record.uri?eid=2-s2.0-85001514211&doi=10.1021%2facsbiomaterials.5b00511&partnerID=40&md5=206a99b5df9a5864ed368d04cd5223e1
Keywords : alginic acid, animal experiment, animal model, animal tissue, article, asialoglycoprotein receptor, atomic force microscopy, biodegradability, controlled drug release, controlled study, cytotoxicity, doxorubicin, drug release, galactose, human, human cell, liver tumor, male, nanoparticle, nonhuman, priority journal, radiofrequency ablation, radiofrequency ablation device, rat, scintigraphy, technetium 99m, Tin, zeta potential
Campus : Kochi
School : Center for Nanosciences
Center : Amrita Center for Nanosciences and Molecular Medicine Move, Nanosciences
Department : Nanosciences and Molecular Medicine
Year : 2016
Abstract : Radiofrequency ablation (RFA) and doxorubicin (Dox) chemotherapy are separately approved for liver cancer therapy; however, both have limited success in the clinic due to suboptimal/nonuniform heating and systemic side effects, respectively. Here, we report a biodegradable nanoparticle (NP) system showing excellent RF hyperthermic response together with the ability to locally deliver Dox in the liver under RF trigger and control. The nanosystem was prepared by doping a clinically permissible dose (∼4.3 wt %, 0.03 ppm) of stannous ions in alginate nanoparticles (∼100 nm) coloaded with Dox at ∼13.4 wt % concentration and surface conjugated with galactose for targeting asialo-glycoprotein receptors in liver tumors. Targeted NP-uptake and increased cytotoxicity when combined with RF exposure was demonstrated in HEPG2 liver cancer cells. Following in vitro (chicken liver phantom) demonstration of locally augmented RF thermal response, in vivo scintigraphic imaging of 99Tc-labeled NPs was performed to optimize liver localization in Sprague-Dawley (SD) rats. RF ablation was performed in vivo using a cooled-tip probe, and uniformly enhanced (∼44%) thermal ablation was demonstrated with magnetic resonance imaging along with RF-controlled Dox release. In orthotopic rat liver tumor models, real-time infrared imaging revealed significantly higher (∼20 °C) RF thermal response at the tumor site, resulting in uniform augmented ablation (∼80%) even at a low RF power exposure of 15 W for just 1 min duration. Being a clinically acceptable, biodegradable material, alginate nanoparticles hold strong translational potential for augmented RF hyperthermia combined with triggered drug release.
Cite this Research Publication : V. H. Somasundaram, Pillai, R., Malarvizhi, G., Anusha Ashokan, Gowd, S., Peethambaran, R., Palaniswamy, S., Unni, A. K. K., Shantikumar V Nair, and Dr. Manzoor K., “Biodegradable Radiofrequency Responsive Nanoparticles for Augmented Thermal Ablation Combined with Triggered Drug Release in Liver Tumors”, ACS Biomaterials Science and Engineering, vol. 2, pp. 768-779, 2016.