Gold nanoparticle mediated combined cancer therapy
Autor: | Devika B. Chithrani, Kyle Bromma, Caterina Di Ciano-Oliveira, Monique van Prooijen, Gaetano Zafarana, Celina Yang |
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Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
Drug
medicine.medical_treatment media_common.quotation_subject Biomedical Engineering Pharmaceutical Science 02 engineering and technology 010402 general chemistry Bleomycin 01 natural sciences lcsh:RC254-282 chemistry.chemical_compound Radiation dose enhancer medicine Gold nanoparticles Physical and Theoretical Chemistry Clonogenic assay media_common Chemotherapy Cancer 021001 nanoscience & nanotechnology medicine.disease lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens 3. Good health 0104 chemical sciences Radiation therapy Oncology chemistry Colloidal gold Cancer cell Drug delivery Cancer research DNA damage 0210 nano-technology Combined therapy |
Zdroj: | Cancer Nanotechnology, Vol 9, Iss 1, Pp 1-14 (2018) |
ISSN: | 1868-6966 1868-6958 |
DOI: | 10.1186/s12645-018-0039-3 |
Popis: | Background The combined use of radiation therapy and chemotherapy is commonly being used in cancer treatment. The side effects of the treatment can be further minimized through targeted delivery of anticancer drugs and local enhancement of the radiation dose. Gold nanoparticles (GNPs) can play a significant role in this regard since GNPs can be used as radiation dose enhancers and anticancer drug carriers. Anticancer drug, bleomycin, was chosen as the model drug, since it could be easily conjugated onto GNPs through the gold–thiol bond. Methods Gold nanoparticles of size 10 nm were synthesized using the citrate reduction method. The surface of The GNPs was modified with a peptide sequence (CKKKKKKGGRGDMFG) containing the RGD domain and anticancer drug, bleomycin. Human breast cancer cells (MDA-MB-231) were incubated with 0.3 nM concentration of GNP–drug complex for 16 h prior to irradiation with a 2 Gy single fraction of 6 MV X-rays. After the treatment, cells were trypsinized and seeded in 60 mm dishes for clonogenic assay. Damage to DNA was probed using immunofluorescence assay. Results Cancer cells internalized with the GNP–drug complex had a 32 ± 9% decrease in cell survival and statistically significant enhancement in DNA (deoxyribonucleic acid) damage as compared to control cells (irradiated with no GNPs) after receiving a radiation dose of 2 Gy with 6 MV photons. Conclusions The experimental results demonstrate that GNP-mediated chemoradiation has the potential to improve cancer care in the near future through enhancement of the local radiation dose and controlled delivery of anticancer drugs. |
Databáze: | OpenAIRE |
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