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Organotropic Targeting of Biomimetic Nanoparticles to Treat Lung Disease
Active targeting strategies aimed at improving drug homing while reducing systemic toxicity are widely being pursued in the growing field of nanomedicine. While they can be effective, these approaches often require the identification of cell-specific targets and in-depth knowledge of receptor bindin...
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Published in: | Bioconjugate chemistry 2022-04, Vol.33 (4), p.586-593 |
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container_issue | 4 |
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container_title | Bioconjugate chemistry |
container_volume | 33 |
creator | Holay, Maya Zhou, Jiarong Park, Joon Ho Landa, Igor Ventura, Christian J Gao, Weiwei Fang, Ronnie H Zhang, Liangfang |
description | Active targeting strategies aimed at improving drug homing while reducing systemic toxicity are widely being pursued in the growing field of nanomedicine. While they can be effective, these approaches often require the identification of cell-specific targets and in-depth knowledge of receptor binding interactions. More recently, there has been significant interest in biomimetic nanoformulations capable of replicating the properties of naturally occurring systems. In particular, the advent of cell membrane coating nanotechnology has enabled researchers to leverage the inherent tropisms displayed by living cells, bypassing many of the challenges associated with traditional bottom-up nanoengineering. In this work, we report on a biomimetic organotropic nanodelivery system for localizing therapeutic payloads to the lungs. Metastatic breast cancer exosomes, which are lung tropic due to their unique surface marker expression profile, are used to coat nanoparticle cores loaded with the anti-inflammatory drug dexamethasone. In vivo, these nanoparticles demonstrate enhanced accumulation in lung tissue and significantly reduce proinflammatory cytokine burden in a lung inflammation model. Overall, this work highlights the potential of using biomimetic organ-level delivery strategies for the management of certain disease conditions. |
doi_str_mv | 10.1021/acs.bioconjchem.1c00599 |
format | article |
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In vivo, these nanoparticles demonstrate enhanced accumulation in lung tissue and significantly reduce proinflammatory cytokine burden in a lung inflammation model. 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While they can be effective, these approaches often require the identification of cell-specific targets and in-depth knowledge of receptor binding interactions. More recently, there has been significant interest in biomimetic nanoformulations capable of replicating the properties of naturally occurring systems. In particular, the advent of cell membrane coating nanotechnology has enabled researchers to leverage the inherent tropisms displayed by living cells, bypassing many of the challenges associated with traditional bottom-up nanoengineering. In this work, we report on a biomimetic organotropic nanodelivery system for localizing therapeutic payloads to the lungs. Metastatic breast cancer exosomes, which are lung tropic due to their unique surface marker expression profile, are used to coat nanoparticle cores loaded with the anti-inflammatory drug dexamethasone. In vivo, these nanoparticles demonstrate enhanced accumulation in lung tissue and significantly reduce proinflammatory cytokine burden in a lung inflammation model. Overall, this work highlights the potential of using biomimetic organ-level delivery strategies for the management of certain disease conditions.</description><subject>Anti-inflammatory agents</subject><subject>Bioaccumulation</subject><subject>Biocompatibility</subject><subject>Biomimetic Materials - chemistry</subject><subject>Biomimetic Materials - therapeutic use</subject><subject>Biomimetics</subject><subject>Breast cancer</subject><subject>Cell membranes</subject><subject>Cytokines</subject><subject>Dexamethasone</subject><subject>Drug Delivery Systems</subject><subject>Exosomes</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Lung cancer</subject><subject>Lung Diseases</subject><subject>Metastases</subject><subject>Nanoengineering</subject><subject>Nanomedicine</subject><subject>Nanoparticles</subject><subject>Nanoparticles - chemistry</subject><subject>Nanotechnology</subject><subject>Payloads</subject><subject>Surface markers</subject><subject>Toxicity</subject><issn>1043-1802</issn><issn>1520-4812</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqFkL1OwzAURi0EolB4BYjEwpJybceJM0L5KVJFlzJHjntTXCVxsJOBt8dVS4VYmHwtnfv58yHkmsKEAqN3SvtJaay27UZ_YDOhGkDk-RE5o4JBnEjKjsMMCY-pBDYi595vACCnkp2SERdMipRmZ2S2cGvV2t7Zzuhoqdwae9OuI1tFD8Y2pglXHb0FpFMujDX6qLfR0qHqo_kQyEfjUXm8ICeVqj1e7s8xeX9-Wk5n8Xzx8jq9n8eKS9HHGSSVzkNHxErqPBMJpwlAUnKWipTxSoi0Cj8RiisEXOXAUGlRhbI0KzXlY3K7y-2c_RzQ90VjvMa6Vi3awRcs5TJPIJdJQG_-oBs7uDa0C5TgQrKUiUBlO0o7673DquicaZT7KigUW9lFkF38kl3sZYfNq33-UDa4Ouz92A0A3wHbhMPb_8V-A9Wlj4I</recordid><startdate>20220420</startdate><enddate>20220420</enddate><creator>Holay, Maya</creator><creator>Zhou, Jiarong</creator><creator>Park, Joon Ho</creator><creator>Landa, Igor</creator><creator>Ventura, Christian J</creator><creator>Gao, Weiwei</creator><creator>Fang, Ronnie H</creator><creator>Zhang, Liangfang</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0637-0654</orcidid></search><sort><creationdate>20220420</creationdate><title>Organotropic Targeting of Biomimetic Nanoparticles to Treat Lung Disease</title><author>Holay, Maya ; 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subjects | Anti-inflammatory agents Bioaccumulation Biocompatibility Biomimetic Materials - chemistry Biomimetic Materials - therapeutic use Biomimetics Breast cancer Cell membranes Cytokines Dexamethasone Drug Delivery Systems Exosomes Humans Inflammation Lung cancer Lung Diseases Metastases Nanoengineering Nanomedicine Nanoparticles Nanoparticles - chemistry Nanotechnology Payloads Surface markers Toxicity |
title | Organotropic Targeting of Biomimetic Nanoparticles to Treat Lung Disease |
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