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Magnetic-luminescent YbPO(4):Er,Dy microspheres designed for tumor theranostics with synergistic effect of photodynamic therapy and chemotherapy

In this paper, magnetic and fluorescent bifunctional YbPO(4):Er,Dy microspheres were synthesized via a simple solvothermal method. The prepared microspheres exposed to 980 nm near-infrared (NIR) laser light emitted bright upconversion fluorescence (450–570 nm) after calcination at high temperatures...

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Detalles Bibliográficos
Autores principales: Wang, Wei, Xu, Dong, Wei, Xiaojun, Chen, Kezheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4211918/
https://www.ncbi.nlm.nih.gov/pubmed/25364246
http://dx.doi.org/10.2147/IJN.S62678
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author Wang, Wei
Xu, Dong
Wei, Xiaojun
Chen, Kezheng
author_facet Wang, Wei
Xu, Dong
Wei, Xiaojun
Chen, Kezheng
author_sort Wang, Wei
collection PubMed
description In this paper, magnetic and fluorescent bifunctional YbPO(4):Er,Dy microspheres were synthesized via a simple solvothermal method. The prepared microspheres exposed to 980 nm near-infrared (NIR) laser light emitted bright upconversion fluorescence (450–570 nm) after calcination at high temperatures (>800°C). Results of magnetic resonance studies demonstrated that the YbPO(4):Er,Dy microspheres are more suitable to be used as a transverse relaxation time (negative) contrast magnetic resonance imaging agent. The microspheres successfully entered the human hepatocellular carcinoma cells and presented low toxicity. A well-selected photodynamic therapy (PDT) drug, merocyanine 540 (MC540) with an ultraviolet–visible spectroscopy absorption maximum of 540 nm, was loaded onto the microspheres to obtain YbPO(4):Er,Dy-MC540. Since the upconversion fluorescence emitting from the microspheres could be absorbed by MC540 with a small absorption/emission disparity, YbPO(4):Er,Dy-MC540 could kill the hepatocellular carcinoma cells via PDT mechanism effectively. In other words, being upconverting particles, the prepared microspheres acted as light transducers in the NIR light-triggered PDT process. A chemotherapy drug, doxorubicin, was further loaded onto YbPO(4):Er,Dy-MC540 to achieve enhanced antitumor effect based on synergistic therapeutic efficacy of PDT and chemotherapy. It is expected that the prepared YbPO(4):Er,Dy microspheres have applications in tumor theranostics including magnetic-fluorescent bimodal imaging and NIR light-triggered PDT.
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spelling pubmed-42119182014-10-31 Magnetic-luminescent YbPO(4):Er,Dy microspheres designed for tumor theranostics with synergistic effect of photodynamic therapy and chemotherapy Wang, Wei Xu, Dong Wei, Xiaojun Chen, Kezheng Int J Nanomedicine Original Research In this paper, magnetic and fluorescent bifunctional YbPO(4):Er,Dy microspheres were synthesized via a simple solvothermal method. The prepared microspheres exposed to 980 nm near-infrared (NIR) laser light emitted bright upconversion fluorescence (450–570 nm) after calcination at high temperatures (>800°C). Results of magnetic resonance studies demonstrated that the YbPO(4):Er,Dy microspheres are more suitable to be used as a transverse relaxation time (negative) contrast magnetic resonance imaging agent. The microspheres successfully entered the human hepatocellular carcinoma cells and presented low toxicity. A well-selected photodynamic therapy (PDT) drug, merocyanine 540 (MC540) with an ultraviolet–visible spectroscopy absorption maximum of 540 nm, was loaded onto the microspheres to obtain YbPO(4):Er,Dy-MC540. Since the upconversion fluorescence emitting from the microspheres could be absorbed by MC540 with a small absorption/emission disparity, YbPO(4):Er,Dy-MC540 could kill the hepatocellular carcinoma cells via PDT mechanism effectively. In other words, being upconverting particles, the prepared microspheres acted as light transducers in the NIR light-triggered PDT process. A chemotherapy drug, doxorubicin, was further loaded onto YbPO(4):Er,Dy-MC540 to achieve enhanced antitumor effect based on synergistic therapeutic efficacy of PDT and chemotherapy. It is expected that the prepared YbPO(4):Er,Dy microspheres have applications in tumor theranostics including magnetic-fluorescent bimodal imaging and NIR light-triggered PDT. Dove Medical Press 2014-10-20 /pmc/articles/PMC4211918/ /pubmed/25364246 http://dx.doi.org/10.2147/IJN.S62678 Text en © 2014 Wang et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Wang, Wei
Xu, Dong
Wei, Xiaojun
Chen, Kezheng
Magnetic-luminescent YbPO(4):Er,Dy microspheres designed for tumor theranostics with synergistic effect of photodynamic therapy and chemotherapy
title Magnetic-luminescent YbPO(4):Er,Dy microspheres designed for tumor theranostics with synergistic effect of photodynamic therapy and chemotherapy
title_full Magnetic-luminescent YbPO(4):Er,Dy microspheres designed for tumor theranostics with synergistic effect of photodynamic therapy and chemotherapy
title_fullStr Magnetic-luminescent YbPO(4):Er,Dy microspheres designed for tumor theranostics with synergistic effect of photodynamic therapy and chemotherapy
title_full_unstemmed Magnetic-luminescent YbPO(4):Er,Dy microspheres designed for tumor theranostics with synergistic effect of photodynamic therapy and chemotherapy
title_short Magnetic-luminescent YbPO(4):Er,Dy microspheres designed for tumor theranostics with synergistic effect of photodynamic therapy and chemotherapy
title_sort magnetic-luminescent ybpo(4):er,dy microspheres designed for tumor theranostics with synergistic effect of photodynamic therapy and chemotherapy
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4211918/
https://www.ncbi.nlm.nih.gov/pubmed/25364246
http://dx.doi.org/10.2147/IJN.S62678
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