Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:Bioconjugate chemistry 2017-04, Vol.28 (4), p.1283-1290
Main Authors: Turino, Ludmila N, Ruggiero, Maria R, Stefanìa, Rachele, Cutrin, Juan C, Aime, Silvio, Geninatti Crich, Simonetta
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-a434t-1390f591e769da1fbda531e9efbf887e99a668b66a9283bbe51a281d855049a13
cites cdi_FETCH-LOGICAL-a434t-1390f591e769da1fbda531e9efbf887e99a668b66a9283bbe51a281d855049a13
container_end_page 1290
container_issue 4
container_start_page 1283
container_title Bioconjugate chemistry
container_volume 28
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
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1900811449</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1900811449</sourcerecordid><originalsourceid>FETCH-LOGICAL-a434t-1390f591e769da1fbda531e9efbf887e99a668b66a9283bbe51a281d855049a13</originalsourceid><addsrcrecordid>eNqFkM9uEzEQxi0EoqXwCmCJ86ae9f6xjyVt2kop9BDOq1nvrOJosw62o7TiwivwijwJjpK23DjNzKfffKP5GPsEYgIih3M0YdJaZ9y4MktaT-pWCKGrV-wUylxkhYL8depFITNQIj9h70JY7RFQ-Vt2kispQEt5yn7OyHsb7cgvyTiPkTp-P7--OL9HM9iIDzTwucMuyV9xdBv00ZqBAr8aO7dL6s7GJccxzUscTRIW7sEaGx9Ts0Pf8bvp7M-v3zX_4glD5Ivt2nk-pWEI79mbHodAH471jH2fXS2mN9n82_Xt9GKeYSGLmIHUoi81UF3pDqFvOywlkKa-7ZWqSWusKtVWFer0V9tSCZgr6FRZikIjyDP2-eC78e7HlkJsVm7rx3SyAS2EAigKnaj6QBnvQvDUNxtv1-gfGxDNPvQmhd78E3pzDD1tfjz6b9s1dc97TyknQB6AvcPL7f_Y_gVzM5Sb</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1900811449</pqid></control><display><type>article</type><title>Ferritin Decorated PLGA/Paclitaxel Loaded Nanoparticles Endowed with an Enhanced Toxicity Toward MCF‑7 Breast Tumor Cells</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read &amp; Publish Agreement 2022-2024 (Reading list)</source><creator>Turino, Ludmila N ; Ruggiero, Maria R ; Stefanìa, Rachele ; Cutrin, Juan C ; Aime, Silvio ; Geninatti Crich, Simonetta</creator><creatorcontrib>Turino, Ludmila N ; Ruggiero, Maria R ; Stefanìa, Rachele ; Cutrin, Juan C ; Aime, Silvio ; Geninatti Crich, Simonetta</creatorcontrib><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><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 &amp; dosage ; Breast cancer ; Breast Neoplasms - diagnostic imaging ; Breast Neoplasms - drug therapy ; Breast Neoplasms - pathology ; Cells ; Contrast agents ; Contrast Media - administration &amp; 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 &amp; 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 &amp; 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 &amp; 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 &amp; 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 &amp; 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 &amp; 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 &amp; 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>
fulltext fulltext
identifier ISSN: 1043-1802
ispartof Bioconjugate chemistry, 2017-04, Vol.28 (4), p.1283-1290
issn 1043-1802
1520-4812
language eng
recordid cdi_proquest_journals_1900811449
source American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T08%3A42%3A50IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Ferritin%20Decorated%20PLGA/Paclitaxel%20Loaded%20Nanoparticles%20Endowed%20with%20an%20Enhanced%20Toxicity%20Toward%20MCF%E2%80%917%20Breast%20Tumor%20Cells&rft.jtitle=Bioconjugate%20chemistry&rft.au=Turino,%20Ludmila%20N&rft.date=2017-04-19&rft.volume=28&rft.issue=4&rft.spage=1283&rft.epage=1290&rft.pages=1283-1290&rft.issn=1043-1802&rft.eissn=1520-4812&rft_id=info:doi/10.1021/acs.bioconjchem.7b00096&rft_dat=%3Cproquest_cross%3E1900811449%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a434t-1390f591e769da1fbda531e9efbf887e99a668b66a9283bbe51a281d855049a13%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1900811449&rft_id=info:pmid/28301933&rfr_iscdi=true