| Literature DB >> 33434989 |
Siheng Su1, Jilong Wang1, Evan Vargas1, Junhua Wei1, Raul Martínez-Zaguilán2, Souad R Sennoune2, Michelle L Pantoya1, Shiren Wang3, Jharna Chaudhuri1, Jingjing Qiu1.
Abstract
Brain cancer is a fatal disease that is difficult to treat because of poor targeting and low permeability of chemotherapeutic drugs through the blood brain barrier. In a comparison to current treatments, such as surgery followed by chemotherapy and/or radiotherapy, photothermal therapy is a remarkable noninvasive therapy developed in recent years. In this work, porphyrin immobilized nanographene oxide (PNG) was synthesized and bioconjugated with a peptide to achieve enhanced and targeted photothermal therapy for brain cancer. PNG was dispersed into the agar based artificial tissue model and demonstrated a photo-to-thermal conversion efficiency of 19.93% at a PNG concentration of only 0.5 wt %, with a heating rate of 0.6 °C/s at the beginning of irradiation. In comparison, 0.5 wt % graphene oxide (GO) indicated a photo-to-thermal conversion efficiency of 12.20% and a heating rate of 0.3 °C/s. To actively target brain tumor cells without harming healthy cells and tissues surrounding the laser path, a tripeptide l-arginyl-glycyl-l-aspartic (RGD) was further grafted to PNG. The photothermal therapy effects of PNG-RGD completely eliminated the tumor in vivo, indicating its excellent therapeutic effect for the treatment of brain cancer.Entities:
Keywords: graphene oxide; photothermal; porphyrin; targeting
Year: 2016 PMID: 33434989 DOI: 10.1021/acsbiomaterials.6b00290
Source DB: PubMed Journal: ACS Biomater Sci Eng ISSN: 2373-9878