Lysine-based surfactants in nanovesicle formulations: the role of cationic charge position and hydrophobicity in in vitro cytotoxicity and intracellular delivery
Abstract Understanding nanomaterial interactions within cells is of increasing importance for assessing their toxicity and cellular transport. Here, the authors developed nanovesicles containing bioactive cationic lysine-based amphiphiles and assessed whether these cationic compounds increase the li...
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Veröffentlicht in: | Nanotoxicology 2014-06, Vol.8 (4), p.404-421 |
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creator | Nogueira, Daniele Rubert Carmen Morán, Maria del Mitjans, Montserrat Pérez, Lourdes Ramos, David Lapuente, Joaquín de Pilar Vinardell, Maria |
description | Abstract
Understanding nanomaterial interactions within cells is of increasing importance for assessing their toxicity and cellular transport. Here, the authors developed nanovesicles containing bioactive cationic lysine-based amphiphiles and assessed whether these cationic compounds increase the likelihood of intracellular delivery and modulate toxicity. Different cytotoxic responses were found among the formulations, depending on surfactant, cell line and endpoint assayed. The induction of mitochondrial dysfunction, oxidative stress and apoptosis were the general mechanisms underlying cytotoxicity. Fluorescence microscopy analysis demonstrated that nanovesicles were internalised by HeLa cells and evidenced that their ability to release endocytosed materials into cell cytoplasm depends on the structural parameters of amphiphiles. The cationic charge position and hydrophobicity of surfactants determine the nanovesicle interactions within the cell and, thus, the resulting toxicity and intracellular behaviour after cell uptake of the nanomaterial. The insights into some toxicity mechanisms of these new nanomaterials contribute in reducing the uncertainty surrounding their potential health hazards. |
doi_str_mv | 10.3109/17435390.2013.793779 |
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Understanding nanomaterial interactions within cells is of increasing importance for assessing their toxicity and cellular transport. Here, the authors developed nanovesicles containing bioactive cationic lysine-based amphiphiles and assessed whether these cationic compounds increase the likelihood of intracellular delivery and modulate toxicity. Different cytotoxic responses were found among the formulations, depending on surfactant, cell line and endpoint assayed. The induction of mitochondrial dysfunction, oxidative stress and apoptosis were the general mechanisms underlying cytotoxicity. Fluorescence microscopy analysis demonstrated that nanovesicles were internalised by HeLa cells and evidenced that their ability to release endocytosed materials into cell cytoplasm depends on the structural parameters of amphiphiles. The cationic charge position and hydrophobicity of surfactants determine the nanovesicle interactions within the cell and, thus, the resulting toxicity and intracellular behaviour after cell uptake of the nanomaterial. The insights into some toxicity mechanisms of these new nanomaterials contribute in reducing the uncertainty surrounding their potential health hazards.</description><identifier>ISSN: 1743-5390</identifier><identifier>EISSN: 1743-5404</identifier><identifier>DOI: 10.3109/17435390.2013.793779</identifier><identifier>PMID: 23560805</identifier><language>eng</language><publisher>England: Informa UK, Ltd</publisher><subject>3T3 Cells ; Analysis of Variance ; Animals ; Apoptosis - drug effects ; Cations ; Cell culture ; Cell Cycle - drug effects ; cell internalisation ; Cell Survival - drug effects ; Cell-mediated cytotoxicity ; Citotoxicitat per mediació cel·lular ; Cultiu cel·lular ; DNA Damage - drug effects ; Drug Carriers - chemistry ; drug delivery ; Drug delivery systems ; Erythrocytes ; HeLa Cells ; Hemolysis - drug effects ; Humans ; Hydrophobic and Hydrophilic Interactions ; Intracellular Space - chemistry ; Intracellular Space - metabolism ; Lysine - chemistry ; Lysine - toxicity ; Materials nanoestructurats ; Mice ; Nanostructured materials ; Nanostructures - chemistry ; Nanostructures - toxicity ; nanotoxicity ; pH-sensitivity ; Rats ; Sistemes d'alliberament de medicaments ; Surface-Active Agents - chemistry ; Surface-Active Agents - toxicity ; Toxicologia ; Toxicology</subject><ispartof>Nanotoxicology, 2014-06, Vol.8 (4), p.404-421</ispartof><rights>Informa UK, Ltd. 2013</rights><rights>(c) Informa Healthcare, 2013 info:eu-repo/semantics/openAccess</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c493t-dfdc0390894ad30434e8a0fb0b90364712a3de1d74c78f9bd2995324b81b5e983</citedby><cites>FETCH-LOGICAL-c493t-dfdc0390894ad30434e8a0fb0b90364712a3de1d74c78f9bd2995324b81b5e983</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,782,887,26981</link.rule.ids><linktorsrc>$$Uhttps://recercat.cat/handle/2072/229741$$EView_record_in_Consorci_de_Serveis_Universitaris_de_Catalunya_(CSUC)$$FView_record_in_$$GConsorci_de_Serveis_Universitaris_de_Catalunya_(CSUC)$$Hfree_for_read</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23560805$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nogueira, Daniele Rubert</creatorcontrib><creatorcontrib>Carmen Morán, Maria del</creatorcontrib><creatorcontrib>Mitjans, Montserrat</creatorcontrib><creatorcontrib>Pérez, Lourdes</creatorcontrib><creatorcontrib>Ramos, David</creatorcontrib><creatorcontrib>Lapuente, Joaquín de</creatorcontrib><creatorcontrib>Pilar Vinardell, Maria</creatorcontrib><title>Lysine-based surfactants in nanovesicle formulations: the role of cationic charge position and hydrophobicity in in vitro cytotoxicity and intracellular delivery</title><title>Nanotoxicology</title><addtitle>Nanotoxicology</addtitle><description>Abstract
Understanding nanomaterial interactions within cells is of increasing importance for assessing their toxicity and cellular transport. Here, the authors developed nanovesicles containing bioactive cationic lysine-based amphiphiles and assessed whether these cationic compounds increase the likelihood of intracellular delivery and modulate toxicity. Different cytotoxic responses were found among the formulations, depending on surfactant, cell line and endpoint assayed. The induction of mitochondrial dysfunction, oxidative stress and apoptosis were the general mechanisms underlying cytotoxicity. Fluorescence microscopy analysis demonstrated that nanovesicles were internalised by HeLa cells and evidenced that their ability to release endocytosed materials into cell cytoplasm depends on the structural parameters of amphiphiles. The cationic charge position and hydrophobicity of surfactants determine the nanovesicle interactions within the cell and, thus, the resulting toxicity and intracellular behaviour after cell uptake of the nanomaterial. The insights into some toxicity mechanisms of these new nanomaterials contribute in reducing the uncertainty surrounding their potential health hazards.</description><subject>3T3 Cells</subject><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Apoptosis - drug effects</subject><subject>Cations</subject><subject>Cell culture</subject><subject>Cell Cycle - drug effects</subject><subject>cell internalisation</subject><subject>Cell Survival - drug effects</subject><subject>Cell-mediated cytotoxicity</subject><subject>Citotoxicitat per mediació cel·lular</subject><subject>Cultiu cel·lular</subject><subject>DNA Damage - drug effects</subject><subject>Drug Carriers - chemistry</subject><subject>drug delivery</subject><subject>Drug delivery systems</subject><subject>Erythrocytes</subject><subject>HeLa Cells</subject><subject>Hemolysis - drug effects</subject><subject>Humans</subject><subject>Hydrophobic and Hydrophilic Interactions</subject><subject>Intracellular Space - chemistry</subject><subject>Intracellular Space - metabolism</subject><subject>Lysine - chemistry</subject><subject>Lysine - toxicity</subject><subject>Materials nanoestructurats</subject><subject>Mice</subject><subject>Nanostructured materials</subject><subject>Nanostructures - chemistry</subject><subject>Nanostructures - toxicity</subject><subject>nanotoxicity</subject><subject>pH-sensitivity</subject><subject>Rats</subject><subject>Sistemes d'alliberament de medicaments</subject><subject>Surface-Active Agents - chemistry</subject><subject>Surface-Active Agents - toxicity</subject><subject>Toxicologia</subject><subject>Toxicology</subject><issn>1743-5390</issn><issn>1743-5404</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>XX2</sourceid><recordid>eNp9UU2v1CAUbYzG9xz9B8awdNMRCp0WFxrz4lcyiRtdEwq3lpcOjBc6z_4c_6nUzmjcvAQCHM49h8spiueMbjmj8hVrBK-5pNuKMr5tJG8a-aC4XuCyFlQ8vOwz56p4EuMtpfWu2rHHxVXF6x1taX1d_NrP0XkoOx3Bkjhhr03SPkXiPPHahxNEZ0YgfcDDNOrkgo-vSRqAYMhw6In5AzpDzKDxO5BjiG5BiPaWDLPFcBxC54xL8yKax8klDMTMKaTwc71YuM4n1AbGMfsgsTC6E-D8tHjU6zHCs_O6Kb59eP_15lO5__Lx8827fWmE5Km0vTU0t9pKoS2nggtoNe072knKd6JhleYWmG2EadpedraSsuaV6FrW1SBbvinYqmviZBSCAcydqaDdv8MyK9pUqqpkI1iuebnWHDH8mCAmdXBx6UB7CFNUbMellJRmp00hzvIYYkTo1RHdQeOsGFVLoOoSqFoCVWuguezF2WHqDmD_Fl0SzIS3K8H5JSJ9F3C0Kul5DNij9sbFRf5eizf_KQygxzQYjaBuw4Q-f_r9b_wNf_PHLA</recordid><startdate>201406</startdate><enddate>201406</enddate><creator>Nogueira, Daniele Rubert</creator><creator>Carmen Morán, Maria del</creator><creator>Mitjans, Montserrat</creator><creator>Pérez, Lourdes</creator><creator>Ramos, David</creator><creator>Lapuente, Joaquín de</creator><creator>Pilar Vinardell, Maria</creator><general>Informa UK, Ltd</general><general>Taylor & Francis</general><general>Informa Healthcare</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>7U7</scope><scope>C1K</scope><scope>XX2</scope></search><sort><creationdate>201406</creationdate><title>Lysine-based surfactants in nanovesicle formulations: the role of cationic charge position and hydrophobicity in in vitro cytotoxicity and intracellular delivery</title><author>Nogueira, Daniele Rubert ; Carmen Morán, Maria del ; Mitjans, Montserrat ; Pérez, Lourdes ; Ramos, David ; Lapuente, Joaquín de ; Pilar Vinardell, Maria</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c493t-dfdc0390894ad30434e8a0fb0b90364712a3de1d74c78f9bd2995324b81b5e983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>3T3 Cells</topic><topic>Analysis of Variance</topic><topic>Animals</topic><topic>Apoptosis - drug effects</topic><topic>Cations</topic><topic>Cell culture</topic><topic>Cell Cycle - drug effects</topic><topic>cell internalisation</topic><topic>Cell Survival - drug effects</topic><topic>Cell-mediated cytotoxicity</topic><topic>Citotoxicitat per mediació cel·lular</topic><topic>Cultiu cel·lular</topic><topic>DNA Damage - drug effects</topic><topic>Drug Carriers - chemistry</topic><topic>drug delivery</topic><topic>Drug delivery systems</topic><topic>Erythrocytes</topic><topic>HeLa Cells</topic><topic>Hemolysis - drug effects</topic><topic>Humans</topic><topic>Hydrophobic and Hydrophilic Interactions</topic><topic>Intracellular Space - chemistry</topic><topic>Intracellular Space - metabolism</topic><topic>Lysine - chemistry</topic><topic>Lysine - toxicity</topic><topic>Materials nanoestructurats</topic><topic>Mice</topic><topic>Nanostructured materials</topic><topic>Nanostructures - chemistry</topic><topic>Nanostructures - toxicity</topic><topic>nanotoxicity</topic><topic>pH-sensitivity</topic><topic>Rats</topic><topic>Sistemes d'alliberament de medicaments</topic><topic>Surface-Active Agents - chemistry</topic><topic>Surface-Active Agents - toxicity</topic><topic>Toxicologia</topic><topic>Toxicology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nogueira, Daniele Rubert</creatorcontrib><creatorcontrib>Carmen Morán, Maria del</creatorcontrib><creatorcontrib>Mitjans, Montserrat</creatorcontrib><creatorcontrib>Pérez, Lourdes</creatorcontrib><creatorcontrib>Ramos, David</creatorcontrib><creatorcontrib>Lapuente, Joaquín de</creatorcontrib><creatorcontrib>Pilar Vinardell, Maria</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Recercat</collection><jtitle>Nanotoxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Nogueira, Daniele Rubert</au><au>Carmen Morán, Maria del</au><au>Mitjans, Montserrat</au><au>Pérez, Lourdes</au><au>Ramos, David</au><au>Lapuente, Joaquín de</au><au>Pilar Vinardell, Maria</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Lysine-based surfactants in nanovesicle formulations: the role of cationic charge position and hydrophobicity in in vitro cytotoxicity and intracellular delivery</atitle><jtitle>Nanotoxicology</jtitle><addtitle>Nanotoxicology</addtitle><date>2014-06</date><risdate>2014</risdate><volume>8</volume><issue>4</issue><spage>404</spage><epage>421</epage><pages>404-421</pages><issn>1743-5390</issn><eissn>1743-5404</eissn><abstract>Abstract
Understanding nanomaterial interactions within cells is of increasing importance for assessing their toxicity and cellular transport. Here, the authors developed nanovesicles containing bioactive cationic lysine-based amphiphiles and assessed whether these cationic compounds increase the likelihood of intracellular delivery and modulate toxicity. Different cytotoxic responses were found among the formulations, depending on surfactant, cell line and endpoint assayed. The induction of mitochondrial dysfunction, oxidative stress and apoptosis were the general mechanisms underlying cytotoxicity. Fluorescence microscopy analysis demonstrated that nanovesicles were internalised by HeLa cells and evidenced that their ability to release endocytosed materials into cell cytoplasm depends on the structural parameters of amphiphiles. The cationic charge position and hydrophobicity of surfactants determine the nanovesicle interactions within the cell and, thus, the resulting toxicity and intracellular behaviour after cell uptake of the nanomaterial. The insights into some toxicity mechanisms of these new nanomaterials contribute in reducing the uncertainty surrounding their potential health hazards.</abstract><cop>England</cop><pub>Informa UK, Ltd</pub><pmid>23560805</pmid><doi>10.3109/17435390.2013.793779</doi><tpages>18</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 3T3 Cells Analysis of Variance Animals Apoptosis - drug effects Cations Cell culture Cell Cycle - drug effects cell internalisation Cell Survival - drug effects Cell-mediated cytotoxicity Citotoxicitat per mediació cel·lular Cultiu cel·lular DNA Damage - drug effects Drug Carriers - chemistry drug delivery Drug delivery systems Erythrocytes HeLa Cells Hemolysis - drug effects Humans Hydrophobic and Hydrophilic Interactions Intracellular Space - chemistry Intracellular Space - metabolism Lysine - chemistry Lysine - toxicity Materials nanoestructurats Mice Nanostructured materials Nanostructures - chemistry Nanostructures - toxicity nanotoxicity pH-sensitivity Rats Sistemes d'alliberament de medicaments Surface-Active Agents - chemistry Surface-Active Agents - toxicity Toxicologia Toxicology |
title | Lysine-based surfactants in nanovesicle formulations: the role of cationic charge position and hydrophobicity in in vitro cytotoxicity and intracellular delivery |
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