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.
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Authors | Feng Chen, Kai Ma, Li Zhang, Brian Madajewski, Melik Z Turker, Fabio Gallazzi, Kiara Cruickshank, Xiuli Zhang, Pocharapong Jenjitranant, Karim A Touijer, Thomas P Quinn, Pat Zanzonico, Ulrich Wiesner, Michelle S Bradbury |
Journal | ACS applied materials & interfaces
(ACS Appl Mater Interfaces)
Vol. 11
Issue 47
Pg. 43879-43887
(Nov 27 2019)
ISSN: 1944-8252 [Electronic] United States |
PMID | 31675204
(Publication Type: Journal Article)
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Chemical References |
- Silicon Dioxide
- Prostate-Specific Antigen
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Topics |
- Animals
- Humans
- Kidney
(metabolism)
- Liver
(metabolism)
- Male
- Mice
- Mice, Inbred NOD
- Nanoparticles
(chemistry, metabolism)
- Positron-Emission Tomography
(instrumentation)
- Prostate-Specific Antigen
(antagonists & inhibitors, metabolism)
- Prostatic Neoplasms
(diagnostic imaging, metabolism)
- Silicon Dioxide
(chemistry, metabolism)
- Theranostic Nanomedicine
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