Sonodynamic therapy in combination with photodynamic therapy shows enhanced long-term cure of brain tumor

Abstract This article presents the construction of a multimodality platform that can be used for efficient destruction of brain tumor by a combination of photodynamic and sonodynamic therapy. For in vivo studies, U87 patient-derived xenograft tumors were implanted subcutaneously in SCID mice. For th...

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Autores principales: Ballav M. Borah, Joseph Cacaccio, Farukh A. Durrani, Wiam Bshara, Steven G. Turowski, Joseph A. Spernyak, Ravindra K. Pandey
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Publicado: Nature Portfolio 2020
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Acceso en línea:https://doaj.org/article/a02153428d9443d0abc09e951259cca0
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spelling oai:doaj.org-article:a02153428d9443d0abc09e951259cca02021-12-02T16:18:05ZSonodynamic therapy in combination with photodynamic therapy shows enhanced long-term cure of brain tumor10.1038/s41598-020-78153-02045-2322https://doaj.org/article/a02153428d9443d0abc09e951259cca02020-12-01T00:00:00Zhttps://doi.org/10.1038/s41598-020-78153-0https://doaj.org/toc/2045-2322Abstract This article presents the construction of a multimodality platform that can be used for efficient destruction of brain tumor by a combination of photodynamic and sonodynamic therapy. For in vivo studies, U87 patient-derived xenograft tumors were implanted subcutaneously in SCID mice. For the first time, it has been shown that the cell-death mechanism by both treatment modalities follows two different pathways. For example, exposing the U87 cells after 24 h incubation with HPPH [3-(1′-hexyloxy)ethyl-3-devinyl-pyropheophorbide-a) by ultrasound participate in an electron-transfer process with the surrounding biological substrates to form radicals and radical ions (Type I reaction); whereas in photodynamic therapy, the tumor destruction is mainly caused by highly reactive singlet oxygen (Type II reaction). The combination of photodynamic therapy and sonodynamic therapy both in vitro and in vivo have shown an improved cell kill/tumor response, that could be attributed to an additive and/or synergetic effect(s). Our results also indicate that the delivery of the HPPH to tumors can further be enhanced by using cationic polyacrylamide nanoparticles as a delivery vehicle. Exposing the nano-formulation with ultrasound also triggered the release of photosensitizer. The combination of photodynamic therapy and sonodynamic therapy strongly affects tumor vasculature as determined by dynamic contrast enhanced imaging using HSA-Gd(III)DTPA.Ballav M. BorahJoseph CacaccioFarukh A. DurraniWiam BsharaSteven G. TurowskiJoseph A. SpernyakRavindra K. PandeyNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 10, Iss 1, Pp 1-13 (2020)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Ballav M. Borah
Joseph Cacaccio
Farukh A. Durrani
Wiam Bshara
Steven G. Turowski
Joseph A. Spernyak
Ravindra K. Pandey
Sonodynamic therapy in combination with photodynamic therapy shows enhanced long-term cure of brain tumor
description Abstract This article presents the construction of a multimodality platform that can be used for efficient destruction of brain tumor by a combination of photodynamic and sonodynamic therapy. For in vivo studies, U87 patient-derived xenograft tumors were implanted subcutaneously in SCID mice. For the first time, it has been shown that the cell-death mechanism by both treatment modalities follows two different pathways. For example, exposing the U87 cells after 24 h incubation with HPPH [3-(1′-hexyloxy)ethyl-3-devinyl-pyropheophorbide-a) by ultrasound participate in an electron-transfer process with the surrounding biological substrates to form radicals and radical ions (Type I reaction); whereas in photodynamic therapy, the tumor destruction is mainly caused by highly reactive singlet oxygen (Type II reaction). The combination of photodynamic therapy and sonodynamic therapy both in vitro and in vivo have shown an improved cell kill/tumor response, that could be attributed to an additive and/or synergetic effect(s). Our results also indicate that the delivery of the HPPH to tumors can further be enhanced by using cationic polyacrylamide nanoparticles as a delivery vehicle. Exposing the nano-formulation with ultrasound also triggered the release of photosensitizer. The combination of photodynamic therapy and sonodynamic therapy strongly affects tumor vasculature as determined by dynamic contrast enhanced imaging using HSA-Gd(III)DTPA.
format article
author Ballav M. Borah
Joseph Cacaccio
Farukh A. Durrani
Wiam Bshara
Steven G. Turowski
Joseph A. Spernyak
Ravindra K. Pandey
author_facet Ballav M. Borah
Joseph Cacaccio
Farukh A. Durrani
Wiam Bshara
Steven G. Turowski
Joseph A. Spernyak
Ravindra K. Pandey
author_sort Ballav M. Borah
title Sonodynamic therapy in combination with photodynamic therapy shows enhanced long-term cure of brain tumor
title_short Sonodynamic therapy in combination with photodynamic therapy shows enhanced long-term cure of brain tumor
title_full Sonodynamic therapy in combination with photodynamic therapy shows enhanced long-term cure of brain tumor
title_fullStr Sonodynamic therapy in combination with photodynamic therapy shows enhanced long-term cure of brain tumor
title_full_unstemmed Sonodynamic therapy in combination with photodynamic therapy shows enhanced long-term cure of brain tumor
title_sort sonodynamic therapy in combination with photodynamic therapy shows enhanced long-term cure of brain tumor
publisher Nature Portfolio
publishDate 2020
url https://doaj.org/article/a02153428d9443d0abc09e951259cca0
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