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...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: 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
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2021
Materias:
R
Q
Acceso en línea:https://doaj.org/article/b1a0f240eea44bb2911eaa2667ca4356
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:b1a0f240eea44bb2911eaa2667ca4356
record_format dspace
spelling 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)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle 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
description 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 AT danielgohler developmentofaratcapnoperitoneumphantomtostudydrugaerosoldepositioninthecontextofanticancerresearchonperitonealcarcinomatosis
AT antjegeldner developmentofaratcapnoperitoneumphantomtostudydrugaerosoldepositioninthecontextofanticancerresearchonperitonealcarcinomatosis
AT ralfgritzki developmentofaratcapnoperitoneumphantomtostudydrugaerosoldepositioninthecontextofanticancerresearchonperitonealcarcinomatosis
AT franzlohse developmentofaratcapnoperitoneumphantomtostudydrugaerosoldepositioninthecontextofanticancerresearchonperitonealcarcinomatosis
AT stephangroße developmentofaratcapnoperitoneumphantomtostudydrugaerosoldepositioninthecontextofanticancerresearchonperitonealcarcinomatosis
AT juliensobilo developmentofaratcapnoperitoneumphantomtostudydrugaerosoldepositioninthecontextofanticancerresearchonperitonealcarcinomatosis
AT clemensfelsmann developmentofaratcapnoperitoneumphantomtostudydrugaerosoldepositioninthecontextofanticancerresearchonperitonealcarcinomatosis
AT jonathanrbuggisch developmentofaratcapnoperitoneumphantomtostudydrugaerosoldepositioninthecontextofanticancerresearchonperitonealcarcinomatosis
AT alainlepape developmentofaratcapnoperitoneumphantomtostudydrugaerosoldepositioninthecontextofanticancerresearchonperitonealcarcinomatosis
AT andreasrudolph developmentofaratcapnoperitoneumphantomtostudydrugaerosoldepositioninthecontextofanticancerresearchonperitonealcarcinomatosis
AT michaelstintz developmentofaratcapnoperitoneumphantomtostudydrugaerosoldepositioninthecontextofanticancerresearchonperitonealcarcinomatosis
AT ursgigerpabst developmentofaratcapnoperitoneumphantomtostudydrugaerosoldepositioninthecontextofanticancerresearchonperitonealcarcinomatosis
_version_ 1718429307703918592