| Literature DB >> 31675204 |
Feng Chen, Kai Ma1, Li Zhang, Brian Madajewski, Melik Z Turker1, Fabio Gallazzi, Kiara Cruickshank, Xiuli Zhang, Pocharapong Jenjitranant, Karim A Touijer, Thomas P Quinn2, Pat Zanzonico, Ulrich Wiesner1, Michelle S Bradbury.
Abstract
Although important advances have been achieved in the development of radiolabeled prostate-specific membrane antigen (PSMA)-targeting ligand constructs for both diagnosis and therapy of prostate cancer (PCa) over the past decade, challenges related to off-target effects and limited treatment responses persist. In this study, which builds upon the successful clinical translation of a series of ultrasmall, dye-encapsulating core-shell silica nanoparticles, or Cornell Prime Dots (C' dots), for cancer management, we sought to address these limitations by designing a dual-modality, PSMA-targeting platform that evades undesirable accumulations in the salivary glands, kidneys, and reticuloendothelial system, while exhibiting bulk renal clearance. This versatile PCa-targeted particle imaging probe offers significant clinical potential to improve future theranostic applications in a variety of patient care settings.Entities:
Keywords: C′ dots; PSMA; prostate cancer; targeting; ultrasmall
Mesh:
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Year: 2019 PMID: 31675204 PMCID: PMC7199444 DOI: 10.1021/acsami.9b15195
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229