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Mass spectrometry detection of inhaled drug in distal fibrotic lung

BACKGROUND: Currently the only available therapies for fibrotic Interstitial Lung Disease are administered systemically, often causing significant side effects. Inhaled therapy could avoid these but to date there is no evidence that drug can be effectively delivered to distal, fibrosed lung. We set...

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Autores principales: Mikolasch, Theresia A., Oballa, Eunice, Vahdati-Bolouri, Mitra, Jarvis, Emily, Cui, Yi, Cahn, Anthony, Terry, Rebecca L., Sahota, Jagdeep, Thakrar, Ricky, Marshall, Peter, Porter, Joanna C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092847/
https://www.ncbi.nlm.nih.gov/pubmed/35546672
http://dx.doi.org/10.1186/s12931-022-02026-5
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author Mikolasch, Theresia A.
Oballa, Eunice
Vahdati-Bolouri, Mitra
Jarvis, Emily
Cui, Yi
Cahn, Anthony
Terry, Rebecca L.
Sahota, Jagdeep
Thakrar, Ricky
Marshall, Peter
Porter, Joanna C.
author_facet Mikolasch, Theresia A.
Oballa, Eunice
Vahdati-Bolouri, Mitra
Jarvis, Emily
Cui, Yi
Cahn, Anthony
Terry, Rebecca L.
Sahota, Jagdeep
Thakrar, Ricky
Marshall, Peter
Porter, Joanna C.
author_sort Mikolasch, Theresia A.
collection PubMed
description BACKGROUND: Currently the only available therapies for fibrotic Interstitial Lung Disease are administered systemically, often causing significant side effects. Inhaled therapy could avoid these but to date there is no evidence that drug can be effectively delivered to distal, fibrosed lung. We set out to combine mass spectrometry and histopathology with rapid sample acquisition using transbronchial cryobiopsy to determine whether an inhaled drug can be delivered to fibrotic, distal lung parenchyma in participants with Interstitial Lung Disease. METHODS: Patients with radiologically and multidisciplinary team confirmed fibrotic Interstitial Lung Disease were eligible for this study. Transbronchial cryobiopsies and endobronchial biopsies were taken from five participants, with Interstitial Lung Disease, within 70 min of administration of a single dose of nebulised ipratropium bromide. Thin tissue cryosections were analysed by Matrix Assisted Laser Desorption/Ionization-Mass Spectrometry imaging and correlated with histopathology. The remainder of the cryobiopsies were homogenised and analysed by Liquid Chromatography—tandem Mass Spectrometry. RESULTS: Drug was detected in proximal and distal lung samples from all participants. Fibrotic regions were identified in research samples of four of the five participants. Matrix Assisted Laser Desorption/Ionization-Mass Spectrometry imaging showed co-location of ipratropium with fibrotic regions in samples from three participants. CONCLUSIONS: In this proof of concept study, using mass spectrometry, we demonstrate for the first-time that an inhaled drug can deposit in distal fibrotic lung parenchyma in patients with Interstitial Lung Disease. This suggests that drugs to treat pulmonary fibrosis could potentially be administered by the inhaled route. Trial registration A prospective clinical study approved by London Camden and Kings Cross Research Ethics Committee and registered on clinicaltrials.gov (NCT03136120) SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12931-022-02026-5.
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spelling pubmed-90928472022-05-12 Mass spectrometry detection of inhaled drug in distal fibrotic lung Mikolasch, Theresia A. Oballa, Eunice Vahdati-Bolouri, Mitra Jarvis, Emily Cui, Yi Cahn, Anthony Terry, Rebecca L. Sahota, Jagdeep Thakrar, Ricky Marshall, Peter Porter, Joanna C. Respir Res Research BACKGROUND: Currently the only available therapies for fibrotic Interstitial Lung Disease are administered systemically, often causing significant side effects. Inhaled therapy could avoid these but to date there is no evidence that drug can be effectively delivered to distal, fibrosed lung. We set out to combine mass spectrometry and histopathology with rapid sample acquisition using transbronchial cryobiopsy to determine whether an inhaled drug can be delivered to fibrotic, distal lung parenchyma in participants with Interstitial Lung Disease. METHODS: Patients with radiologically and multidisciplinary team confirmed fibrotic Interstitial Lung Disease were eligible for this study. Transbronchial cryobiopsies and endobronchial biopsies were taken from five participants, with Interstitial Lung Disease, within 70 min of administration of a single dose of nebulised ipratropium bromide. Thin tissue cryosections were analysed by Matrix Assisted Laser Desorption/Ionization-Mass Spectrometry imaging and correlated with histopathology. The remainder of the cryobiopsies were homogenised and analysed by Liquid Chromatography—tandem Mass Spectrometry. RESULTS: Drug was detected in proximal and distal lung samples from all participants. Fibrotic regions were identified in research samples of four of the five participants. Matrix Assisted Laser Desorption/Ionization-Mass Spectrometry imaging showed co-location of ipratropium with fibrotic regions in samples from three participants. CONCLUSIONS: In this proof of concept study, using mass spectrometry, we demonstrate for the first-time that an inhaled drug can deposit in distal fibrotic lung parenchyma in patients with Interstitial Lung Disease. This suggests that drugs to treat pulmonary fibrosis could potentially be administered by the inhaled route. Trial registration A prospective clinical study approved by London Camden and Kings Cross Research Ethics Committee and registered on clinicaltrials.gov (NCT03136120) SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12931-022-02026-5. BioMed Central 2022-05-11 2022 /pmc/articles/PMC9092847/ /pubmed/35546672 http://dx.doi.org/10.1186/s12931-022-02026-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visithttp://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Mikolasch, Theresia A.
Oballa, Eunice
Vahdati-Bolouri, Mitra
Jarvis, Emily
Cui, Yi
Cahn, Anthony
Terry, Rebecca L.
Sahota, Jagdeep
Thakrar, Ricky
Marshall, Peter
Porter, Joanna C.
Mass spectrometry detection of inhaled drug in distal fibrotic lung
title Mass spectrometry detection of inhaled drug in distal fibrotic lung
title_full Mass spectrometry detection of inhaled drug in distal fibrotic lung
title_fullStr Mass spectrometry detection of inhaled drug in distal fibrotic lung
title_full_unstemmed Mass spectrometry detection of inhaled drug in distal fibrotic lung
title_short Mass spectrometry detection of inhaled drug in distal fibrotic lung
title_sort mass spectrometry detection of inhaled drug in distal fibrotic lung
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092847/
https://www.ncbi.nlm.nih.gov/pubmed/35546672
http://dx.doi.org/10.1186/s12931-022-02026-5
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