Targeted Doxorubicin-Loaded Dendronized Gold Nanoparticles

dc.contributor.authorDockery, Lance
dc.contributor.authorDaniel, Marie-Christine
dc.date.accessioned2023-08-30T14:50:58Z
dc.date.available2023-08-30T14:50:58Z
dc.date.issued2023-08-09
dc.description.abstractDendronized nanoparticles, also called nanoparticle-cored dendrimers, combine the advantages of nanoparticles and dendrimers. These very stable and polyvalent nanoparticles can be used for diverse applications. One such application is drug delivery, because the dendrons can enhance the density of the payload. In this report, we describe the design of multifunctional gold nanoparticles (AuNPs) coated with poly(propylene imine) (PPI) dendrons that contain both prostate cancer active targeting and chemotherapeutic drugs. The PPI dendron is a good candidate for the design of drug delivery vehicles because of its ability to induce a proton sponge effect that will enhance lysosomal escape and intracellular therapeutic delivery. The chemotherapeutic drug used is doxorubicin (DOX), and it was linked to the dendron through a hydrazone acid-sensitive bond. Subsequent acidification of the AuNP system to a pH of 4–5 resulted in the release of 140 DOX drugs per nanoparticles. In addition, the PPI dendron was conjugated via “click” chemistry to an EphA2-targeting antibody fragment that has been shown to target prostate cancer cells. In vitro cell viability assays revealed an IC50 of 0.9 nM for the targeted DOX-bearing AuNPs after 48 h incubation with PC3 cells. These results are very promising upon optimization of the system.en_US
dc.description.sponsorshipThis research was funded by the NSF (CBET-1705538). L.T.D. was also supported by the NIH (TT32GM066706-19). The APC was funded by the University of Maryland, Baltimore County (PRFEXC02). The authors thank John Strong (Electron Microscopy Core Imaging Facility (EMCIF), University of Maryland, Baltimore) for the TEM imaging of the PC3 cells. This work utilized an EM sample preparation instrument that was purchased with funding from a National Institutes of Health SIG grant (1S10RR26870-1) awarded to the University of Maryland Baltimore. The authors are also grateful to Charles Bieberich’s group for providing the PC3 cells as well as for training L.T.D. for the in vitro assays.en_US
dc.description.urihttps://www.mdpi.com/1999-4923/15/8/2103en_US
dc.format.extent14 pagesen_US
dc.genrejournal articlesen_US
dc.identifierdoi:10.13016/m2g2gx-51c5
dc.identifier.citationDockery, Lance T., and Marie-Christine Daniel. 2023. "Targeted Doxorubicin-Loaded Dendronized Gold Nanoparticles" Pharmaceutics 15, no. 8: 2103. https://doi.org/10.3390/pharmaceutics15082103en_US
dc.identifier.urihttps://doi.org/10.3390/pharmaceutics15082103
dc.identifier.urihttp://hdl.handle.net/11603/29434
dc.language.isoen_USen_US
dc.publisherMDPIen_US
dc.relation.isAvailableAtThe University of Maryland, Baltimore County (UMBC)
dc.relation.ispartofUMBC Chemistry & Biochemistry Department Collection
dc.relation.ispartofUMBC Faculty Collection
dc.relation.ispartofUMBC Student Collection
dc.rightsThis item is likely protected under Title 17 of the U.S. Copyright Law. Unless on a Creative Commons license, for uses protected by Copyright Law, contact the copyright holder or the author.en_US
dc.rightsAttribution 4.0 International (CC BY 4.0)*
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.titleTargeted Doxorubicin-Loaded Dendronized Gold Nanoparticlesen_US
dc.typeTexten_US
dcterms.creatorhttps://orcid.org/0000-0002-1964-4135en_US
dcterms.creatorhttps://orcid.org/0000-0002-7336-5655en_US

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