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Blood Plasma Stabilized Gold Nanoclusters for Personalized Tumor Theranostics

SIMPLE SUMMARY: Cancer is a disease that has a high fatality rate over the world. Nanotechnology is one of the most promising current approaches for developing novel diagnostic and treatment methods in accomplishing more personalized medicine. Personalized gold nanoclusters have potential to be used...

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Autores principales: Jarockyte, Greta, Poderys, Vilius, Barzda, Virginijus, Karabanovas, Vitalijus, Rotomskis, Ricardas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9030650/
https://www.ncbi.nlm.nih.gov/pubmed/35454798
http://dx.doi.org/10.3390/cancers14081887
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author Jarockyte, Greta
Poderys, Vilius
Barzda, Virginijus
Karabanovas, Vitalijus
Rotomskis, Ricardas
author_facet Jarockyte, Greta
Poderys, Vilius
Barzda, Virginijus
Karabanovas, Vitalijus
Rotomskis, Ricardas
author_sort Jarockyte, Greta
collection PubMed
description SIMPLE SUMMARY: Cancer is a disease that has a high fatality rate over the world. Nanotechnology is one of the most promising current approaches for developing novel diagnostic and treatment methods in accomplishing more personalized medicine. Personalized gold nanoclusters have potential to be used in cancer theranostics. We demonstrate that biocompatible gold nanoclusters could be synthesized directly in human blood plasma. Such gold nanoclusters have a wide photoluminescence band in the optical tissue window and generate reactive oxygen species under irradiation with visible light, thus are suitable for cancer theranostics. ABSTRACT: Personalized cancer theranostics has a potential to increase efficiency of early cancer diagnostics and treatment, and to reduce negative side-effects. Protein-stabilized gold nanoclusters may serve as theranostic agents. To make gold nanoclusters personalized and highly biocompatible, the clusters were stabilized with human plasma proteins. Optical properties of synthesized nanoclusters were investigated spectroscopically, and possible biomedical application was evaluated using standard cell biology methods. The spectroscopic investigations of human plasma proteins stabilized gold nanoclusters revealed that a wide photoluminescence band in the optical tissue window is suitable for cancer diagnostics. High-capacity generation of singlet oxygen and other reactive oxygen species was also observed. Furthermore, the cluster accumulation in cancer cells and the photodynamic effect were evaluated. The results demonstrate that plasma proteins stabilized gold nanoclusters that accumulate in breast cancer cells and are non-toxic in the dark, while appear phototoxic under irradiation with visible light. The results positively confirm the utility of plasma protein stabilized gold nanoclusters for the use in cancer diagnostics and treatment.
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spelling pubmed-90306502022-04-23 Blood Plasma Stabilized Gold Nanoclusters for Personalized Tumor Theranostics Jarockyte, Greta Poderys, Vilius Barzda, Virginijus Karabanovas, Vitalijus Rotomskis, Ricardas Cancers (Basel) Article SIMPLE SUMMARY: Cancer is a disease that has a high fatality rate over the world. Nanotechnology is one of the most promising current approaches for developing novel diagnostic and treatment methods in accomplishing more personalized medicine. Personalized gold nanoclusters have potential to be used in cancer theranostics. We demonstrate that biocompatible gold nanoclusters could be synthesized directly in human blood plasma. Such gold nanoclusters have a wide photoluminescence band in the optical tissue window and generate reactive oxygen species under irradiation with visible light, thus are suitable for cancer theranostics. ABSTRACT: Personalized cancer theranostics has a potential to increase efficiency of early cancer diagnostics and treatment, and to reduce negative side-effects. Protein-stabilized gold nanoclusters may serve as theranostic agents. To make gold nanoclusters personalized and highly biocompatible, the clusters were stabilized with human plasma proteins. Optical properties of synthesized nanoclusters were investigated spectroscopically, and possible biomedical application was evaluated using standard cell biology methods. The spectroscopic investigations of human plasma proteins stabilized gold nanoclusters revealed that a wide photoluminescence band in the optical tissue window is suitable for cancer diagnostics. High-capacity generation of singlet oxygen and other reactive oxygen species was also observed. Furthermore, the cluster accumulation in cancer cells and the photodynamic effect were evaluated. The results demonstrate that plasma proteins stabilized gold nanoclusters that accumulate in breast cancer cells and are non-toxic in the dark, while appear phototoxic under irradiation with visible light. The results positively confirm the utility of plasma protein stabilized gold nanoclusters for the use in cancer diagnostics and treatment. MDPI 2022-04-08 /pmc/articles/PMC9030650/ /pubmed/35454798 http://dx.doi.org/10.3390/cancers14081887 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Jarockyte, Greta
Poderys, Vilius
Barzda, Virginijus
Karabanovas, Vitalijus
Rotomskis, Ricardas
Blood Plasma Stabilized Gold Nanoclusters for Personalized Tumor Theranostics
title Blood Plasma Stabilized Gold Nanoclusters for Personalized Tumor Theranostics
title_full Blood Plasma Stabilized Gold Nanoclusters for Personalized Tumor Theranostics
title_fullStr Blood Plasma Stabilized Gold Nanoclusters for Personalized Tumor Theranostics
title_full_unstemmed Blood Plasma Stabilized Gold Nanoclusters for Personalized Tumor Theranostics
title_short Blood Plasma Stabilized Gold Nanoclusters for Personalized Tumor Theranostics
title_sort blood plasma stabilized gold nanoclusters for personalized tumor theranostics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9030650/
https://www.ncbi.nlm.nih.gov/pubmed/35454798
http://dx.doi.org/10.3390/cancers14081887
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