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Efficient Nebulization and Pulmonary Biodistribution of Polymeric Nanocarriers in an Acute Lung Injury Preclinical Model
Acute respiratory distress syndrome (ARDS) is a clinical syndrome characterized by acute hypoxemic respiratory failure. Pneumonia and sepsis are the most common causes, turning ARDS into a critical public health problem. Despite recent advances in pharmacological strategies, clinical trials have not...
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Published in: | Small science 2024-09, Vol.4 (9), p.n/a |
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creator | Solé‐Porta, Anna Areny‐Balagueró, Aina Camprubí‐Rimblas, Marta Fernández Fernández, Elena O’Sullivan, Andrew Giannoccari, Rossella MacLoughlin, Ronan Closa, Daniel Artigas, Antonio Roig, Anna |
description | Acute respiratory distress syndrome (ARDS) is a clinical syndrome characterized by acute hypoxemic respiratory failure. Pneumonia and sepsis are the most common causes, turning ARDS into a critical public health problem. Despite recent advances in pharmacological strategies, clinical trials have not demonstrated a reduction in ARDS‐associated mortality. This is in part connected to the singularity of the pulmonary physiological barrier, which hampers drug delivery, specifically at distal areas. To this aim, the use of polymeric nanocarriers as a platform for the efficient delivery of therapeutics to the lungs by nebulization is introduced. Herein, poly(lactic‐co‐glycolic acid) (PLGA) nanocapsules (NCs) loaded with human serum albumin, as an inhalable nanotherapeutic are prepared. The production of stable NCs aerosols in the inhalable range is achieved using a commercial device, while the nanocarrier's physicochemical parameters are only minimally altered after nebulization. Importantly, in vivo studies with healthy and acute lung injury animals show that after inhalation, the NCs are homogeneously distributed throughout the lungs, arriving at the distal areas. The NCs are internalized by alveolar type II cells, avoiding macrophage‐mediated lung clearance. These features make the PLGA NCs excellent vehicles for noninvasive pulmonary delivery, facilitating a ready‐to‐be‐used nanomedicine.
Poly(lactic‐co‐glycolic acid) nanocapsules (NCs) are investigated as inhalable nanotherapeutics. Stable aerosols can be produced using a commercial nebulizer without any significant alteration of the NCs. In vivo studies with healthy and acute lung injury animals show NCs homogeneously distributed throughout the lungs, arriving at even distal areas. NCs are internalized by alveolar type II cells, avoiding macrophage‐mediated lung clearance. |
doi_str_mv | 10.1002/smsc.202400066 |
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Poly(lactic‐co‐glycolic acid) nanocapsules (NCs) are investigated as inhalable nanotherapeutics. Stable aerosols can be produced using a commercial nebulizer without any significant alteration of the NCs. In vivo studies with healthy and acute lung injury animals show NCs homogeneously distributed throughout the lungs, arriving at even distal areas. NCs are internalized by alveolar type II cells, avoiding macrophage‐mediated lung clearance.</description><identifier>ISSN: 2688-4046</identifier><identifier>EISSN: 2688-4046</identifier><identifier>DOI: 10.1002/smsc.202400066</identifier><language>eng</language><publisher>Weinheim: John Wiley & Sons, Inc</publisher><subject>Aerosols ; Biodistribution ; Drug delivery systems ; Drug dosages ; Drug therapy ; Efficiency ; Growth factors ; Health care ; inhalation ; Inhalers ; lung ; Lungs ; Microscopy ; Mortality ; nanocarriers ; Nanomaterials ; poly(lactic‐co‐glycolic acid) ; Proteins ; vibrating mesh nebulizer</subject><ispartof>Small science, 2024-09, Vol.4 (9), p.n/a</ispartof><rights>2024 The Author(s). Small Science published by Wiley‐VCH GmbH</rights><rights>2024. This work is published under https://creativecommons.org/licenses/by/4.0/ (the "License"). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><orcidid>0000-0001-6464-7573 ; 0000-0002-4085-5324 ; 0000-0002-3164-1607 ; 0000-0002-8029-1017 ; 0000-0003-3797-3095 ; 0000-0002-5823-2731 ; 0000-0002-6129-4087 ; 0000-0001-9611-1781 ; 0000-0002-5434-1260</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3115310717/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3115310717?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,11562,25753,27924,27925,37012,44590,46052,46476,75126</link.rule.ids></links><search><creatorcontrib>Solé‐Porta, Anna</creatorcontrib><creatorcontrib>Areny‐Balagueró, Aina</creatorcontrib><creatorcontrib>Camprubí‐Rimblas, Marta</creatorcontrib><creatorcontrib>Fernández Fernández, Elena</creatorcontrib><creatorcontrib>O’Sullivan, Andrew</creatorcontrib><creatorcontrib>Giannoccari, Rossella</creatorcontrib><creatorcontrib>MacLoughlin, Ronan</creatorcontrib><creatorcontrib>Closa, Daniel</creatorcontrib><creatorcontrib>Artigas, Antonio</creatorcontrib><creatorcontrib>Roig, Anna</creatorcontrib><title>Efficient Nebulization and Pulmonary Biodistribution of Polymeric Nanocarriers in an Acute Lung Injury Preclinical Model</title><title>Small science</title><description>Acute respiratory distress syndrome (ARDS) is a clinical syndrome characterized by acute hypoxemic respiratory failure. Pneumonia and sepsis are the most common causes, turning ARDS into a critical public health problem. Despite recent advances in pharmacological strategies, clinical trials have not demonstrated a reduction in ARDS‐associated mortality. This is in part connected to the singularity of the pulmonary physiological barrier, which hampers drug delivery, specifically at distal areas. To this aim, the use of polymeric nanocarriers as a platform for the efficient delivery of therapeutics to the lungs by nebulization is introduced. Herein, poly(lactic‐co‐glycolic acid) (PLGA) nanocapsules (NCs) loaded with human serum albumin, as an inhalable nanotherapeutic are prepared. The production of stable NCs aerosols in the inhalable range is achieved using a commercial device, while the nanocarrier's physicochemical parameters are only minimally altered after nebulization. Importantly, in vivo studies with healthy and acute lung injury animals show that after inhalation, the NCs are homogeneously distributed throughout the lungs, arriving at the distal areas. The NCs are internalized by alveolar type II cells, avoiding macrophage‐mediated lung clearance. These features make the PLGA NCs excellent vehicles for noninvasive pulmonary delivery, facilitating a ready‐to‐be‐used nanomedicine.
Poly(lactic‐co‐glycolic acid) nanocapsules (NCs) are investigated as inhalable nanotherapeutics. Stable aerosols can be produced using a commercial nebulizer without any significant alteration of the NCs. In vivo studies with healthy and acute lung injury animals show NCs homogeneously distributed throughout the lungs, arriving at even distal areas. NCs are internalized by alveolar type II cells, avoiding macrophage‐mediated lung clearance.</description><subject>Aerosols</subject><subject>Biodistribution</subject><subject>Drug delivery systems</subject><subject>Drug dosages</subject><subject>Drug therapy</subject><subject>Efficiency</subject><subject>Growth factors</subject><subject>Health care</subject><subject>inhalation</subject><subject>Inhalers</subject><subject>lung</subject><subject>Lungs</subject><subject>Microscopy</subject><subject>Mortality</subject><subject>nanocarriers</subject><subject>Nanomaterials</subject><subject>poly(lactic‐co‐glycolic acid)</subject><subject>Proteins</subject><subject>vibrating mesh nebulizer</subject><issn>2688-4046</issn><issn>2688-4046</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpNUUtPAjEQ3hhNJMrVcxPPYN9sj0hQSUBJ0HPT7YOUlBa7u1H89S5giHOZ1zffzOQrijsEhwhC_FBvaz3EEFMIIecXRQ_zshxQSPnlv_i66Nf1poNghtBI4F7xPXXOa29jA15t1Qb_oxqfIlDRgGUbtimqvAePPhlfN9lX7bGbHFimsN_a7DV4VTFplbO3uQb-MArGum0smLdxDWZx03YMy2x18NFrFcAiGRtuiyunQm37f_6m-Hiavk9eBvO359lkPB8YQjgfoEqUpHSQdmYJc8pQVDqKIUcMlwg6BR02mJWECsoZQZzxkpGKIsK0EpDcFLMTr0lqI3fZb7uHZFJeHgspr6XKjdfBSk201YQ7JBijxKmKj4QTVhDhtKHYdFz3J65dTp-trRu5SW2O3fmSINQthyM06lDihPrywe7PKxGUB6XkQSl5VkquFqvJOSO_QC-JQA</recordid><startdate>202409</startdate><enddate>202409</enddate><creator>Solé‐Porta, Anna</creator><creator>Areny‐Balagueró, Aina</creator><creator>Camprubí‐Rimblas, Marta</creator><creator>Fernández Fernández, Elena</creator><creator>O’Sullivan, Andrew</creator><creator>Giannoccari, Rossella</creator><creator>MacLoughlin, Ronan</creator><creator>Closa, Daniel</creator><creator>Artigas, Antonio</creator><creator>Roig, Anna</creator><general>John Wiley & Sons, Inc</general><general>Wiley-VCH</general><scope>24P</scope><scope>WIN</scope><scope>3V.</scope><scope>7XB</scope><scope>88I</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>M2P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-6464-7573</orcidid><orcidid>https://orcid.org/0000-0002-4085-5324</orcidid><orcidid>https://orcid.org/0000-0002-3164-1607</orcidid><orcidid>https://orcid.org/0000-0002-8029-1017</orcidid><orcidid>https://orcid.org/0000-0003-3797-3095</orcidid><orcidid>https://orcid.org/0000-0002-5823-2731</orcidid><orcidid>https://orcid.org/0000-0002-6129-4087</orcidid><orcidid>https://orcid.org/0000-0001-9611-1781</orcidid><orcidid>https://orcid.org/0000-0002-5434-1260</orcidid></search><sort><creationdate>202409</creationdate><title>Efficient Nebulization and Pulmonary Biodistribution of Polymeric Nanocarriers in an Acute Lung Injury Preclinical Model</title><author>Solé‐Porta, Anna ; Areny‐Balagueró, Aina ; Camprubí‐Rimblas, Marta ; Fernández Fernández, Elena ; O’Sullivan, Andrew ; Giannoccari, Rossella ; MacLoughlin, Ronan ; Closa, Daniel ; Artigas, Antonio ; Roig, Anna</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-d3366-1b9838f04444e35fad418f4206152810fa0f2d25834946531656853b4135ca903</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Aerosols</topic><topic>Biodistribution</topic><topic>Drug delivery systems</topic><topic>Drug dosages</topic><topic>Drug therapy</topic><topic>Efficiency</topic><topic>Growth factors</topic><topic>Health care</topic><topic>inhalation</topic><topic>Inhalers</topic><topic>lung</topic><topic>Lungs</topic><topic>Microscopy</topic><topic>Mortality</topic><topic>nanocarriers</topic><topic>Nanomaterials</topic><topic>poly(lactic‐co‐glycolic acid)</topic><topic>Proteins</topic><topic>vibrating mesh nebulizer</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Solé‐Porta, Anna</creatorcontrib><creatorcontrib>Areny‐Balagueró, Aina</creatorcontrib><creatorcontrib>Camprubí‐Rimblas, Marta</creatorcontrib><creatorcontrib>Fernández Fernández, Elena</creatorcontrib><creatorcontrib>O’Sullivan, Andrew</creatorcontrib><creatorcontrib>Giannoccari, Rossella</creatorcontrib><creatorcontrib>MacLoughlin, Ronan</creatorcontrib><creatorcontrib>Closa, Daniel</creatorcontrib><creatorcontrib>Artigas, Antonio</creatorcontrib><creatorcontrib>Roig, Anna</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Wiley Online Library Free Content</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Science Database</collection><collection>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>Directory of Open Access Journals</collection><jtitle>Small science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Solé‐Porta, Anna</au><au>Areny‐Balagueró, Aina</au><au>Camprubí‐Rimblas, Marta</au><au>Fernández Fernández, Elena</au><au>O’Sullivan, Andrew</au><au>Giannoccari, Rossella</au><au>MacLoughlin, Ronan</au><au>Closa, Daniel</au><au>Artigas, Antonio</au><au>Roig, Anna</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficient Nebulization and Pulmonary Biodistribution of Polymeric Nanocarriers in an Acute Lung Injury Preclinical Model</atitle><jtitle>Small science</jtitle><date>2024-09</date><risdate>2024</risdate><volume>4</volume><issue>9</issue><epage>n/a</epage><issn>2688-4046</issn><eissn>2688-4046</eissn><abstract>Acute respiratory distress syndrome (ARDS) is a clinical syndrome characterized by acute hypoxemic respiratory failure. Pneumonia and sepsis are the most common causes, turning ARDS into a critical public health problem. Despite recent advances in pharmacological strategies, clinical trials have not demonstrated a reduction in ARDS‐associated mortality. This is in part connected to the singularity of the pulmonary physiological barrier, which hampers drug delivery, specifically at distal areas. To this aim, the use of polymeric nanocarriers as a platform for the efficient delivery of therapeutics to the lungs by nebulization is introduced. Herein, poly(lactic‐co‐glycolic acid) (PLGA) nanocapsules (NCs) loaded with human serum albumin, as an inhalable nanotherapeutic are prepared. The production of stable NCs aerosols in the inhalable range is achieved using a commercial device, while the nanocarrier's physicochemical parameters are only minimally altered after nebulization. Importantly, in vivo studies with healthy and acute lung injury animals show that after inhalation, the NCs are homogeneously distributed throughout the lungs, arriving at the distal areas. The NCs are internalized by alveolar type II cells, avoiding macrophage‐mediated lung clearance. These features make the PLGA NCs excellent vehicles for noninvasive pulmonary delivery, facilitating a ready‐to‐be‐used nanomedicine.
Poly(lactic‐co‐glycolic acid) nanocapsules (NCs) are investigated as inhalable nanotherapeutics. Stable aerosols can be produced using a commercial nebulizer without any significant alteration of the NCs. In vivo studies with healthy and acute lung injury animals show NCs homogeneously distributed throughout the lungs, arriving at even distal areas. NCs are internalized by alveolar type II cells, avoiding macrophage‐mediated lung clearance.</abstract><cop>Weinheim</cop><pub>John Wiley & Sons, Inc</pub><doi>10.1002/smsc.202400066</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-6464-7573</orcidid><orcidid>https://orcid.org/0000-0002-4085-5324</orcidid><orcidid>https://orcid.org/0000-0002-3164-1607</orcidid><orcidid>https://orcid.org/0000-0002-8029-1017</orcidid><orcidid>https://orcid.org/0000-0003-3797-3095</orcidid><orcidid>https://orcid.org/0000-0002-5823-2731</orcidid><orcidid>https://orcid.org/0000-0002-6129-4087</orcidid><orcidid>https://orcid.org/0000-0001-9611-1781</orcidid><orcidid>https://orcid.org/0000-0002-5434-1260</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aerosols Biodistribution Drug delivery systems Drug dosages Drug therapy Efficiency Growth factors Health care inhalation Inhalers lung Lungs Microscopy Mortality nanocarriers Nanomaterials poly(lactic‐co‐glycolic acid) Proteins vibrating mesh nebulizer |
title | Efficient Nebulization and Pulmonary Biodistribution of Polymeric Nanocarriers in an Acute Lung Injury Preclinical Model |
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