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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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) |
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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 |
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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 |
work_keys_str_mv |
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