Development of a rat capnoperitoneum phantom to study drug aerosol deposition in the context of anticancer research on peritoneal carcinomatosis
Abstract Pressurized Intraperitoneal Aerosol Chemotherapy (PIPAC) is a promising approach with a high optimization potential for the treatment of peritoneal carcinomatosis. To study the efficacy of PIPAC and drugs, first rodent cancer models were developed. But inefficient drug aerosol supply and kn...
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oai:doaj.org-article:b1a0f240eea44bb2911eaa2667ca43562021-11-14T12:19:26ZDevelopment of a rat capnoperitoneum phantom to study drug aerosol deposition in the context of anticancer research on peritoneal carcinomatosis10.1038/s41598-021-01332-02045-2322https://doaj.org/article/b1a0f240eea44bb2911eaa2667ca43562021-11-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-01332-0https://doaj.org/toc/2045-2322Abstract Pressurized Intraperitoneal Aerosol Chemotherapy (PIPAC) is a promising approach with a high optimization potential for the treatment of peritoneal carcinomatosis. To study the efficacy of PIPAC and drugs, first rodent cancer models were developed. But inefficient drug aerosol supply and knowledge gaps concerning spatial drug distribution can limit the results based on such models. To study drug aerosol supply/deposition, computed tomography scans of a rat capnoperitoneum were used to deduce a virtual and a physical phantom of the rat capnoperitoneum (RCP). RCP qualification was performed for a specific PIPAC method, where the capnoperitoneum is continuously purged by the drug aerosol. In this context, also in-silico analyses by computational fluid dynamic modelling were conducted on the virtual RCP. The physical RCP was used for ex-vivo granulometric analyses concerning drug deposition. Results of RCP qualification show that aerosol deposition in a continuous purged rat capnoperitoneum depends strongly on the position of the inlet and outlet port. Moreover, it could be shown that the droplet size and charge condition of the drug aerosol define the deposition efficiency. In summary, the developed virtual and physical RCP enables detailed in-silico and ex-vivo analyses on drug supply/deposition in rodents.Daniel GöhlerAntje GeldnerRalf GritzkiFranz LohseStephan GroßeJulien SobiloClemens FelsmannJonathan R. BuggischAlain Le PapeAndreas RudolphMichael StintzUrs Giger-PabstNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-12 (2021) |
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Medicine R Science Q Daniel Göhler Antje Geldner Ralf Gritzki Franz Lohse Stephan Große Julien Sobilo Clemens Felsmann Jonathan R. Buggisch Alain Le Pape Andreas Rudolph Michael Stintz Urs Giger-Pabst Development of a rat capnoperitoneum phantom to study drug aerosol deposition in the context of anticancer research on peritoneal carcinomatosis |
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Abstract Pressurized Intraperitoneal Aerosol Chemotherapy (PIPAC) is a promising approach with a high optimization potential for the treatment of peritoneal carcinomatosis. To study the efficacy of PIPAC and drugs, first rodent cancer models were developed. But inefficient drug aerosol supply and knowledge gaps concerning spatial drug distribution can limit the results based on such models. To study drug aerosol supply/deposition, computed tomography scans of a rat capnoperitoneum were used to deduce a virtual and a physical phantom of the rat capnoperitoneum (RCP). RCP qualification was performed for a specific PIPAC method, where the capnoperitoneum is continuously purged by the drug aerosol. In this context, also in-silico analyses by computational fluid dynamic modelling were conducted on the virtual RCP. The physical RCP was used for ex-vivo granulometric analyses concerning drug deposition. Results of RCP qualification show that aerosol deposition in a continuous purged rat capnoperitoneum depends strongly on the position of the inlet and outlet port. Moreover, it could be shown that the droplet size and charge condition of the drug aerosol define the deposition efficiency. In summary, the developed virtual and physical RCP enables detailed in-silico and ex-vivo analyses on drug supply/deposition in rodents. |
format |
article |
author |
Daniel Göhler Antje Geldner Ralf Gritzki Franz Lohse Stephan Große Julien Sobilo Clemens Felsmann Jonathan R. Buggisch Alain Le Pape Andreas Rudolph Michael Stintz Urs Giger-Pabst |
author_facet |
Daniel Göhler Antje Geldner Ralf Gritzki Franz Lohse Stephan Große Julien Sobilo Clemens Felsmann Jonathan R. Buggisch Alain Le Pape Andreas Rudolph Michael Stintz Urs Giger-Pabst |
author_sort |
Daniel Göhler |
title |
Development of a rat capnoperitoneum phantom to study drug aerosol deposition in the context of anticancer research on peritoneal carcinomatosis |
title_short |
Development of a rat capnoperitoneum phantom to study drug aerosol deposition in the context of anticancer research on peritoneal carcinomatosis |
title_full |
Development of a rat capnoperitoneum phantom to study drug aerosol deposition in the context of anticancer research on peritoneal carcinomatosis |
title_fullStr |
Development of a rat capnoperitoneum phantom to study drug aerosol deposition in the context of anticancer research on peritoneal carcinomatosis |
title_full_unstemmed |
Development of a rat capnoperitoneum phantom to study drug aerosol deposition in the context of anticancer research on peritoneal carcinomatosis |
title_sort |
development of a rat capnoperitoneum phantom to study drug aerosol deposition in the context of anticancer research on peritoneal carcinomatosis |
publisher |
Nature Portfolio |
publishDate |
2021 |
url |
https://doaj.org/article/b1a0f240eea44bb2911eaa2667ca4356 |
work_keys_str_mv |
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