Perlecan-targeted nanoparticles for drug delivery to triple-negative breast cancer.

antibody perlecan polymeric nanoparticles targeted drug delivery triple-negative breast cancer

Journal

Future drug discovery
ISSN: 2631-3316
Titre abrégé: Future Drug Discov
Pays: England
ID NLM: 101752189

Informations de publication

Date de publication:
Jul 2019
Historique:
received: 18 01 2019
accepted: 07 05 2019
pmc-release: 01 07 2020
entrez: 27 8 2019
pubmed: 27 8 2019
medline: 27 8 2019
Statut: epublish

Résumé

We previously developed two antibodies that bind to a cell surface protein, perlecan, overexpressed in triple-negative breast cancer (TNBC). The goal of this study was to investigate these antibodies as targeting ligands for nanoparticle-mediated drug delivery. Paclitaxel-loaded poly(D,L-lactide-co-glycolide) nanoparticles were functionalized with antibodies using thiol-maleimide chemistry. Effect of antibody functionalization on therapeutic efficacy of drug-loaded nanoparticles was investigated using The antibodies were covalently conjugated to nanoparticles without affecting antibody binding affinity or nanoparticle properties. Perlecan-targeted nanoparticles showed improved cell uptake, retention, cytotoxicity The data presented here indicates that perlecan-targeted nanoparticles can improve tumor drug delivery to TNBC.

Identifiants

pubmed: 31448368
doi: 10.4155/fdd-2019-0005
pmc: PMC6700713
doi:

Types de publication

Journal Article

Langues

eng

Pagination

FDD8

Subventions

Organisme : NIBIB NIH HHS
ID : R01 EB019893
Pays : United States

Déclaration de conflit d'intérêts

Financial & competing interests disclosure J Panyam, V Khanna and S Kalscheuer have a US patent application disclosing the composition of the antibody reagents and their use described in this manuscript. Funding was provided by the Community of Pharmaceutical Development (to J Panyam) and NIH EB 019893 (to J Panyam). The authors have no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed. No writing assistance was utilized in the production of this manuscript.

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Auteurs

Vidhi Khanna (V)

Department of Pharmaceutics, University of Minnesota, Minneapolis, MN 55455, USA.

Stephen Kalscheuer (S)

Department of Pharmaceutics, University of Minnesota, Minneapolis, MN 55455, USA.

Ameya Kirtane (A)

Department of Pharmaceutics, University of Minnesota, Minneapolis, MN 55455, USA.

Wenqiu Zhang (W)

Department of Pharmaceutics, University of Minnesota, Minneapolis, MN 55455, USA.

Jayanth Panyam (J)

Department of Pharmaceutics, University of Minnesota, Minneapolis, MN 55455, USA.
Masonic Cancer Center, University of Minnesota, Minneapolis, MN 55455, USA.

Classifications MeSH