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Uncovering the regional localization of inhaled salmeterol retention in the lung
Treatment of respiratory disease with a drug delivered via inhalation is generally held as being beneficial as it provides direct access to the lung target site with a minimum systemic exposure. There is however only limited information of the regional localization of drug retention following inhala...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6058612/ https://www.ncbi.nlm.nih.gov/pubmed/29587546 http://dx.doi.org/10.1080/10717544.2018.1455762 |
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author | Bäckström, Erica Hamm, Gregory Nilsson, Anna Fihn, Britt-Marie Strittmatter, Nicole Andrén, Per Goodwin, Richard J. A. Fridén, Markus |
author_facet | Bäckström, Erica Hamm, Gregory Nilsson, Anna Fihn, Britt-Marie Strittmatter, Nicole Andrén, Per Goodwin, Richard J. A. Fridén, Markus |
author_sort | Bäckström, Erica |
collection | PubMed |
description | Treatment of respiratory disease with a drug delivered via inhalation is generally held as being beneficial as it provides direct access to the lung target site with a minimum systemic exposure. There is however only limited information of the regional localization of drug retention following inhalation. The aim of this study was to investigate the regional and histological localization of salmeterol retention in the lungs after inhalation and to compare it to systemic administration. Lung distribution of salmeterol delivered to rats via nebulization or intravenous (IV) injection was analyzed with high-resolution mass spectrometry imaging (MSI). Salmeterol was widely distributed in the entire section at 5 min after inhalation, by 15 min it was preferentially retained in bronchial tissue. Via a novel dual-isotope study, where salmeterol was delivered via inhalation and d(3)-salmeterol via IV to the same rat, could the effective gain in drug concentration associated with inhaled delivery relative to IV, expressed as a site-specific lung targeting factor, was 5-, 31-, and 45-fold for the alveolar region, bronchial sub-epithelium and epithelium, respectively. We anticipate that this MSI-based framework for quantifying regional and histological lung targeting by inhalation will accelerate discovery and development of local and more precise treatments of respiratory disease. |
format | Online Article Text |
id | pubmed-6058612 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-60586122018-08-17 Uncovering the regional localization of inhaled salmeterol retention in the lung Bäckström, Erica Hamm, Gregory Nilsson, Anna Fihn, Britt-Marie Strittmatter, Nicole Andrén, Per Goodwin, Richard J. A. Fridén, Markus Drug Deliv Original Article Treatment of respiratory disease with a drug delivered via inhalation is generally held as being beneficial as it provides direct access to the lung target site with a minimum systemic exposure. There is however only limited information of the regional localization of drug retention following inhalation. The aim of this study was to investigate the regional and histological localization of salmeterol retention in the lungs after inhalation and to compare it to systemic administration. Lung distribution of salmeterol delivered to rats via nebulization or intravenous (IV) injection was analyzed with high-resolution mass spectrometry imaging (MSI). Salmeterol was widely distributed in the entire section at 5 min after inhalation, by 15 min it was preferentially retained in bronchial tissue. Via a novel dual-isotope study, where salmeterol was delivered via inhalation and d(3)-salmeterol via IV to the same rat, could the effective gain in drug concentration associated with inhaled delivery relative to IV, expressed as a site-specific lung targeting factor, was 5-, 31-, and 45-fold for the alveolar region, bronchial sub-epithelium and epithelium, respectively. We anticipate that this MSI-based framework for quantifying regional and histological lung targeting by inhalation will accelerate discovery and development of local and more precise treatments of respiratory disease. Taylor & Francis 2018-03-28 /pmc/articles/PMC6058612/ /pubmed/29587546 http://dx.doi.org/10.1080/10717544.2018.1455762 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Bäckström, Erica Hamm, Gregory Nilsson, Anna Fihn, Britt-Marie Strittmatter, Nicole Andrén, Per Goodwin, Richard J. A. Fridén, Markus Uncovering the regional localization of inhaled salmeterol retention in the lung |
title | Uncovering the regional localization of inhaled salmeterol retention in the lung |
title_full | Uncovering the regional localization of inhaled salmeterol retention in the lung |
title_fullStr | Uncovering the regional localization of inhaled salmeterol retention in the lung |
title_full_unstemmed | Uncovering the regional localization of inhaled salmeterol retention in the lung |
title_short | Uncovering the regional localization of inhaled salmeterol retention in the lung |
title_sort | uncovering the regional localization of inhaled salmeterol retention in the lung |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6058612/ https://www.ncbi.nlm.nih.gov/pubmed/29587546 http://dx.doi.org/10.1080/10717544.2018.1455762 |
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