Spiky Gold Nanoparticles for the Photothermal Eradication of Colon Cancer Cells
Authors:
- Paolo Emidio CostantiniPCPaolo Emidio Costantini
- Matteo Di GiosiaMGMatteo Di Giosia
- Luca UlfoLULuca Ulfo
- Annapaola PetrosinoAPAnnapaola Petrosino
- Roberto SaporettiRSRoberto Saporetti
- Carmela FimognariCarmela Fimognari
- Pier Paolo PompaPier Paolo Pompa
- Alberto DanielliADAlberto Danielli
- Eleonora TurriniEleonora Turrini
- Luca BoselliLuca Boselli
- Matteo CalvaresiMatteo Calvaresi
Open Access
- 18 June 2021
- journal article
- research article
- Published by MDPI AG in Nanomaterials
- Vol. 11 (6) , 1608
Abstract
Colorectal cancer (CRC) is a widespread and lethal disease. Relapses of the disease and metastasis are very common in instances of CRC, so adjuvant therapies have a crucial role in its treatment. Systemic toxic effects and the development of resistance during therapy limit the long-term efficacy of existing adjuvant therapeutic approaches. Consequently, the search for alternative strategies is necessary. Photothermal therapy (PTT) represents an innovative treatment for cancer with great potential. Here, we synthesize branched gold nanoparticles (BGNPs) as attractive agents for the photothermal eradication of colon cancer cells. By controlling the NP growth process, large absorption in the first NIR biological window was obtained. The FBS dispersed BGNPs are stable in physiological-like environments and show an extremely efficient light-to-heat conversion capability when irradiated with an 808-nm laser. Sequential cycles of heating and cooling do not affect the BGNP stability. The uptake of BGNPs in colon cancer cells was confirmed using flow cytometry and confocal microscopy, exploiting their intrinsic optical properties. In dark conditions, BGNPs are fully biocompatible and do not compromise cell viability, while an almost complete eradication of colon cancer cells was observed upon incubation with BGNPs and irradiation with an 808-nm laser source. The PTT treatment is characterized by an extremely rapid onset of action that leads to cell membrane rupture by induced hyperthermia, which is the trigger that promotes cancer cell death.Keywords
Funding Information
- Associazione Italiana per la Ricerca sul Cancro (22318, 22894)
This publication has 72 references indexed in Scilit:
- Gold Nanoparticles Induce Autophagosome Accumulation through Size-Dependent Nanoparticle Uptake and Lysosome ImpairmentACS Nano, 2011
- Specific Cell Targeting with Nanobody Conjugated Branched Gold Nanoparticles for Photothermal TherapyACS Nano, 2011
- Monodispersed and size-controlled multibranched gold nanoparticles with nanoscale tuning of surface morphologyNanoscale, 2011
- Controllable Synthesis of Stable Urchin-like Gold Nanoparticles Using Hydroquinone to Tune the Reactivity of Gold ChlorideThe Journal of Physical Chemistry C, 2011
- Physical−Chemical Aspects of Protein Corona: Relevance toin Vitroandin VivoBiological Impacts of NanoparticlesJournal of the American Chemical Society, 2011
- Effects of Cell Culture Media on the Dynamic Formation of Protein−Nanoparticle Complexes and Influence on the Cellular ResponseACS Nano, 2010
- Nanoshell-Enabled Photothermal Cancer Therapy: Impending Clinical ImpactAccounts of Chemical Research, 2008
- Plasmonic photothermal therapy (PPTT) using gold nanoparticlesLasers in Medical Science, 2007
- Microscale Heat Transfer Transduced by Surface Plasmon Resonant Gold NanoparticlesThe Journal of Physical Chemistry C, 2007
- Cancer Cell Imaging and Photothermal Therapy in the Near-Infrared Region by Using Gold NanorodsJournal of the American Chemical Society, 2006