期刊
JOURNAL OF LABELLED COMPOUNDS & RADIOPHARMACEUTICALS
卷 56, 期 13, 页码 663-671出版社
WILEY
DOI: 10.1002/jlcr.3087
关键词
gold nanoparticles; radiolabeled nanoparticles; Lys(3)-bombesin; radiolabeled peptides; nanoparticle-peptide; Tat peptide; lutetium-177; technetium-99m
资金
- Mexican National Council of Science and Technology [CONACYT-SEP-CB-2010-01-150942]
Radiolabeled gold nanoparticles may function simultaneously as radiotherapy and thermal ablation systems. The gastrin-releasing peptide receptor (GRP-r) is overexpressed in prostate cancer, and Lys(3)-bombesin is a peptide that binds with high affinity to the GRP-r. HIV Tat(49-57) is a cell-penetrating peptide that reaches the DNA. In cancer cells, Lu-177 shows efficient crossfire effect, whereas Tc-99m that is internalized in the cancer cell nuclei acts as an effective system of targeted radiotherapy because of the biological Auger effect. The aim of this research was to evaluate the in vitro potential of Tc-99m-labeled and Lu-177-labeled gold nanoparticles conjugated to Tat(49-57)-Lys(3)-bombesin peptides (Tc-99m/Lu-177-AuNP-Tat-BN) as a plasmonic photothermal therapy and targeted radiotherapy system in PC3 prostate cancer cells. Peptides were conjugated to AuNPs (5nm) by spontaneous reaction with the thiol group of cysteine (Cys). The effect on PC3 cell viability after laser heating of the AuNP-Tat-BN incubated with the cancer cells was conducted using an Nd:YAG laser pulsed for 5ns at 532nm (0.65W/cm(2)). For the Tc-99m/Lu-177-AuNP-Tat-BN to be obtained, the Lu-177-DOTA-Gly-Gly-Cys and Tc-99m-HYNIC-octreotide radiopeptides were first prepared and added simultaneously to a solution of AuNP-Tat-BN. Tc-99m/Lu-177-AuNP-Tat-BN (20Bq/cell) was incubated with PC3 cells, and the effect on the cell proliferation was evaluated after 3days. Fluorescence images of Tc-99m/Lu-177-AuNP-Tat-BN internalized in nuclei of PC3 were also obtained. After laser irradiation, the presence of AuNP-Tat-BN caused a significant increase in the temperature of the medium (46.4 vs 39.5 degrees C of that without AuNP) resulting in a significant decrease in PC3 cell viability down to 1.3%. After treatment with Tc-99m/Lu-177-AuNP-Tat-BN, the PC3 cell proliferation was inhibited. The nanosystem exhibited properties suitable for plasmonic photothermal therapy and targeted radiotherapy in the treatment of prostate cancer.
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