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Ferritin Decorated PLGA/Paclitaxel Loaded Nanoparticles Endowed with an Enhanced Toxicity Toward MCF‑7 Breast Tumor Cells
Polylactic and glycolic acid nanoparticles (PLGA-NPs), coated with L-ferritin, are exploited for the simultaneous delivery of paclitaxel and an amphiphilic Gd based MRI contrast agent into breast cancer cells (MCF7). L-ferritin has been covalently conjugated to the external surface of PLGA-NPs explo...
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Published in: | Bioconjugate chemistry 2017-04, Vol.28 (4), p.1283-1290 |
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creator | Turino, Ludmila N Ruggiero, Maria R Stefanìa, Rachele Cutrin, Juan C Aime, Silvio Geninatti Crich, Simonetta |
description | Polylactic and glycolic acid nanoparticles (PLGA-NPs), coated with L-ferritin, are exploited for the simultaneous delivery of paclitaxel and an amphiphilic Gd based MRI contrast agent into breast cancer cells (MCF7). L-ferritin has been covalently conjugated to the external surface of PLGA-NPs exploiting NHS activated carboxylic groups. The results confirmed that nanoparticles decorated with L-ferritin have many advantages with respect to both albumin-decorated and nondecorated particles. Ferritin moieties endow PLGA-NPs with targeting capability, exploiting SCARA5 receptors overexpressed by these tumor cells, that results in an increased paclitaxel cytotoxicity. Moreover, protein coating increased nanoparticle stability, thus reducing the fast and aspecific drug release before reaching the target. The theranostic potential of the nanoparticles has been demonstrated by evaluating the signal intensity enhancement on T1-weighted MRI images of labeled MCF7 cells. The results were compared with that obtained with MDA cells used as negative control due to their lower SCARA5 expression. |
doi_str_mv | 10.1021/acs.bioconjchem.7b00096 |
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L-ferritin has been covalently conjugated to the external surface of PLGA-NPs exploiting NHS activated carboxylic groups. The results confirmed that nanoparticles decorated with L-ferritin have many advantages with respect to both albumin-decorated and nondecorated particles. Ferritin moieties endow PLGA-NPs with targeting capability, exploiting SCARA5 receptors overexpressed by these tumor cells, that results in an increased paclitaxel cytotoxicity. Moreover, protein coating increased nanoparticle stability, thus reducing the fast and aspecific drug release before reaching the target. The theranostic potential of the nanoparticles has been demonstrated by evaluating the signal intensity enhancement on T1-weighted MRI images of labeled MCF7 cells. The results were compared with that obtained with MDA cells used as negative control due to their lower SCARA5 expression.</description><identifier>ISSN: 1043-1802</identifier><identifier>EISSN: 1520-4812</identifier><identifier>DOI: 10.1021/acs.bioconjchem.7b00096</identifier><identifier>PMID: 28301933</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Albumin ; Antineoplastic Agents, Phytogenic - administration & dosage ; Breast cancer ; Breast Neoplasms - diagnostic imaging ; Breast Neoplasms - drug therapy ; Breast Neoplasms - pathology ; Cells ; Contrast agents ; Contrast Media - administration & dosage ; Contrast Media - pharmacokinetics ; Cytotoxicity ; Decoration ; Drug Carriers - chemistry ; Drug Delivery Systems - methods ; Ferritin ; Ferritins - chemistry ; Gadolinium ; Glycolic acid ; Humans ; Image enhancement ; Magnetic Resonance Imaging ; MCF-7 Cells ; Nanoparticles ; Nanoparticles - chemistry ; Nanoparticles - therapeutic use ; Paclitaxel ; Paclitaxel - administration & dosage ; Paclitaxel - pharmacokinetics ; Polyglycolic Acid - chemistry ; Polylactide-co-glycolide ; Proteins ; Scavenger Receptors, Class A ; Toxicity ; Tumor cells ; Tumors</subject><ispartof>Bioconjugate chemistry, 2017-04, Vol.28 (4), p.1283-1290</ispartof><rights>Copyright © 2017 American Chemical Society</rights><rights>Copyright American Chemical Society Apr 19, 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a434t-1390f591e769da1fbda531e9efbf887e99a668b66a9283bbe51a281d855049a13</citedby><cites>FETCH-LOGICAL-a434t-1390f591e769da1fbda531e9efbf887e99a668b66a9283bbe51a281d855049a13</cites><orcidid>0000-0003-2998-5424 ; 0000-0003-2374-6692</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28301933$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Turino, Ludmila N</creatorcontrib><creatorcontrib>Ruggiero, Maria R</creatorcontrib><creatorcontrib>Stefanìa, Rachele</creatorcontrib><creatorcontrib>Cutrin, Juan C</creatorcontrib><creatorcontrib>Aime, Silvio</creatorcontrib><creatorcontrib>Geninatti Crich, Simonetta</creatorcontrib><title>Ferritin Decorated PLGA/Paclitaxel Loaded Nanoparticles Endowed with an Enhanced Toxicity Toward MCF‑7 Breast Tumor Cells</title><title>Bioconjugate chemistry</title><addtitle>Bioconjugate Chem</addtitle><description>Polylactic and glycolic acid nanoparticles (PLGA-NPs), coated with L-ferritin, are exploited for the simultaneous delivery of paclitaxel and an amphiphilic Gd based MRI contrast agent into breast cancer cells (MCF7). L-ferritin has been covalently conjugated to the external surface of PLGA-NPs exploiting NHS activated carboxylic groups. The results confirmed that nanoparticles decorated with L-ferritin have many advantages with respect to both albumin-decorated and nondecorated particles. Ferritin moieties endow PLGA-NPs with targeting capability, exploiting SCARA5 receptors overexpressed by these tumor cells, that results in an increased paclitaxel cytotoxicity. Moreover, protein coating increased nanoparticle stability, thus reducing the fast and aspecific drug release before reaching the target. The theranostic potential of the nanoparticles has been demonstrated by evaluating the signal intensity enhancement on T1-weighted MRI images of labeled MCF7 cells. The results were compared with that obtained with MDA cells used as negative control due to their lower SCARA5 expression.</description><subject>Albumin</subject><subject>Antineoplastic Agents, Phytogenic - administration & dosage</subject><subject>Breast cancer</subject><subject>Breast Neoplasms - diagnostic imaging</subject><subject>Breast Neoplasms - drug therapy</subject><subject>Breast Neoplasms - pathology</subject><subject>Cells</subject><subject>Contrast agents</subject><subject>Contrast Media - administration & dosage</subject><subject>Contrast Media - pharmacokinetics</subject><subject>Cytotoxicity</subject><subject>Decoration</subject><subject>Drug Carriers - chemistry</subject><subject>Drug Delivery Systems - methods</subject><subject>Ferritin</subject><subject>Ferritins - chemistry</subject><subject>Gadolinium</subject><subject>Glycolic acid</subject><subject>Humans</subject><subject>Image enhancement</subject><subject>Magnetic Resonance Imaging</subject><subject>MCF-7 Cells</subject><subject>Nanoparticles</subject><subject>Nanoparticles - chemistry</subject><subject>Nanoparticles - therapeutic use</subject><subject>Paclitaxel</subject><subject>Paclitaxel - administration & dosage</subject><subject>Paclitaxel - pharmacokinetics</subject><subject>Polyglycolic Acid - chemistry</subject><subject>Polylactide-co-glycolide</subject><subject>Proteins</subject><subject>Scavenger Receptors, Class A</subject><subject>Toxicity</subject><subject>Tumor cells</subject><subject>Tumors</subject><issn>1043-1802</issn><issn>1520-4812</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqFkM9uEzEQxi0EoqXwCmCJ86ae9f6xjyVt2kop9BDOq1nvrOJosw62o7TiwivwijwJjpK23DjNzKfffKP5GPsEYgIih3M0YdJaZ9y4MktaT-pWCKGrV-wUylxkhYL8depFITNQIj9h70JY7RFQ-Vt2kispQEt5yn7OyHsb7cgvyTiPkTp-P7--OL9HM9iIDzTwucMuyV9xdBv00ZqBAr8aO7dL6s7GJccxzUscTRIW7sEaGx9Ts0Pf8bvp7M-v3zX_4glD5Ivt2nk-pWEI79mbHodAH471jH2fXS2mN9n82_Xt9GKeYSGLmIHUoi81UF3pDqFvOywlkKa-7ZWqSWusKtVWFer0V9tSCZgr6FRZikIjyDP2-eC78e7HlkJsVm7rx3SyAS2EAigKnaj6QBnvQvDUNxtv1-gfGxDNPvQmhd78E3pzDD1tfjz6b9s1dc97TyknQB6AvcPL7f_Y_gVzM5Sb</recordid><startdate>20170419</startdate><enddate>20170419</enddate><creator>Turino, Ludmila N</creator><creator>Ruggiero, Maria R</creator><creator>Stefanìa, Rachele</creator><creator>Cutrin, Juan C</creator><creator>Aime, Silvio</creator><creator>Geninatti Crich, Simonetta</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><orcidid>https://orcid.org/0000-0003-2998-5424</orcidid><orcidid>https://orcid.org/0000-0003-2374-6692</orcidid></search><sort><creationdate>20170419</creationdate><title>Ferritin Decorated PLGA/Paclitaxel Loaded Nanoparticles Endowed with an Enhanced Toxicity Toward MCF‑7 Breast Tumor Cells</title><author>Turino, Ludmila N ; Ruggiero, Maria R ; Stefanìa, Rachele ; Cutrin, Juan C ; Aime, Silvio ; Geninatti Crich, Simonetta</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a434t-1390f591e769da1fbda531e9efbf887e99a668b66a9283bbe51a281d855049a13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Albumin</topic><topic>Antineoplastic Agents, Phytogenic - administration & dosage</topic><topic>Breast cancer</topic><topic>Breast Neoplasms - diagnostic imaging</topic><topic>Breast Neoplasms - drug therapy</topic><topic>Breast Neoplasms - pathology</topic><topic>Cells</topic><topic>Contrast agents</topic><topic>Contrast Media - administration & dosage</topic><topic>Contrast Media - pharmacokinetics</topic><topic>Cytotoxicity</topic><topic>Decoration</topic><topic>Drug Carriers - chemistry</topic><topic>Drug Delivery Systems - methods</topic><topic>Ferritin</topic><topic>Ferritins - chemistry</topic><topic>Gadolinium</topic><topic>Glycolic acid</topic><topic>Humans</topic><topic>Image enhancement</topic><topic>Magnetic Resonance Imaging</topic><topic>MCF-7 Cells</topic><topic>Nanoparticles</topic><topic>Nanoparticles - chemistry</topic><topic>Nanoparticles - therapeutic use</topic><topic>Paclitaxel</topic><topic>Paclitaxel - administration & dosage</topic><topic>Paclitaxel - pharmacokinetics</topic><topic>Polyglycolic Acid - chemistry</topic><topic>Polylactide-co-glycolide</topic><topic>Proteins</topic><topic>Scavenger Receptors, Class A</topic><topic>Toxicity</topic><topic>Tumor cells</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Turino, Ludmila N</creatorcontrib><creatorcontrib>Ruggiero, Maria R</creatorcontrib><creatorcontrib>Stefanìa, Rachele</creatorcontrib><creatorcontrib>Cutrin, Juan C</creatorcontrib><creatorcontrib>Aime, Silvio</creatorcontrib><creatorcontrib>Geninatti Crich, Simonetta</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Bioconjugate chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Turino, Ludmila N</au><au>Ruggiero, Maria R</au><au>Stefanìa, Rachele</au><au>Cutrin, Juan C</au><au>Aime, Silvio</au><au>Geninatti Crich, Simonetta</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ferritin Decorated PLGA/Paclitaxel Loaded Nanoparticles Endowed with an Enhanced Toxicity Toward MCF‑7 Breast Tumor Cells</atitle><jtitle>Bioconjugate chemistry</jtitle><addtitle>Bioconjugate Chem</addtitle><date>2017-04-19</date><risdate>2017</risdate><volume>28</volume><issue>4</issue><spage>1283</spage><epage>1290</epage><pages>1283-1290</pages><issn>1043-1802</issn><eissn>1520-4812</eissn><abstract>Polylactic and glycolic acid nanoparticles (PLGA-NPs), coated with L-ferritin, are exploited for the simultaneous delivery of paclitaxel and an amphiphilic Gd based MRI contrast agent into breast cancer cells (MCF7). L-ferritin has been covalently conjugated to the external surface of PLGA-NPs exploiting NHS activated carboxylic groups. The results confirmed that nanoparticles decorated with L-ferritin have many advantages with respect to both albumin-decorated and nondecorated particles. Ferritin moieties endow PLGA-NPs with targeting capability, exploiting SCARA5 receptors overexpressed by these tumor cells, that results in an increased paclitaxel cytotoxicity. Moreover, protein coating increased nanoparticle stability, thus reducing the fast and aspecific drug release before reaching the target. The theranostic potential of the nanoparticles has been demonstrated by evaluating the signal intensity enhancement on T1-weighted MRI images of labeled MCF7 cells. The results were compared with that obtained with MDA cells used as negative control due to their lower SCARA5 expression.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>28301933</pmid><doi>10.1021/acs.bioconjchem.7b00096</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-2998-5424</orcidid><orcidid>https://orcid.org/0000-0003-2374-6692</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Albumin Antineoplastic Agents, Phytogenic - administration & dosage Breast cancer Breast Neoplasms - diagnostic imaging Breast Neoplasms - drug therapy Breast Neoplasms - pathology Cells Contrast agents Contrast Media - administration & dosage Contrast Media - pharmacokinetics Cytotoxicity Decoration Drug Carriers - chemistry Drug Delivery Systems - methods Ferritin Ferritins - chemistry Gadolinium Glycolic acid Humans Image enhancement Magnetic Resonance Imaging MCF-7 Cells Nanoparticles Nanoparticles - chemistry Nanoparticles - therapeutic use Paclitaxel Paclitaxel - administration & dosage Paclitaxel - pharmacokinetics Polyglycolic Acid - chemistry Polylactide-co-glycolide Proteins Scavenger Receptors, Class A Toxicity Tumor cells Tumors |
title | Ferritin Decorated PLGA/Paclitaxel Loaded Nanoparticles Endowed with an Enhanced Toxicity Toward MCF‑7 Breast Tumor Cells |
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