Near-Infrared Luminescent Nanoparticles Enable Olaparib Delivery for Radiosensitized Image-Guided Theranostics

High Resolution Image Download MS PowerPoint Slide This work presents the design of near-infrared (NIR) luminescent nanoparticles codoped with rare-earth and transition-metal ions as a multifunctional materials platform for imaging-guided cancer therapy and radiological treatment assistance. Germanium oxide-based nanoparticles codoped with La 3+ and Cr 3+ (GeO 2:La 3+, Cr 3+; GOLC) were engineered to generate long-lasting NIR emission through a stable oxide host lattice and Cr 3+ -mediated charge-trapping states. The resulting NIR luminescence enables high-contrast, background-suppressed optical imaging without continuous external excitation, addressing key challenges associated with tissue autofluorescence and photobleaching in biological environments. To integrate therapeutic functionality, GOLC nanoparticles were loaded with the poly(ADP-ribose) polymerase (PARP) inhibitor olaparib, yielding GOLC@OLA nanostructures. These nanostructures effectively suppress oral cancer cell proliferation and induce apoptosis, combining optical tracking capability with drug delivery within a single materials system. Beyond chemical delivery, the high atomic number (high- Z ) the GOLC carrier confers an inherent radiosensitizing effect, significantly enhancing the efficacy of radiotherapy (RT) by increasing local photoelectric absorption. From a radiological perspective, La 3+ was incorporated primarily as a structural and electronic modulator rather than a conventional high- Z radiosensitizer. Although La 3+ does not strongly enhance photoelectric absorption, its incorporation may indirectly influence radiation responses through lattice defect modulation, defect-assisted charge dynamics, and radiation-induced apoptosis. This integration enables precise spatial correlation among nanoparticle localization, imaging readout, and therapeutic payload delivery, thereby supporting image-guided chemo-radiotherapy strategies in oral cancer models. Overall, this study establishes a versatile NIR luminescent nanoparticle framework that bridges optical imaging, drug delivery system, and imaging-guided radiological therapy, providing a materials-centric foundation for advanced oncological nanomedicine research.

Authors

Institutions

Publication Details

Journal
ACS Applied Nano Materials
Published
2026-07-17
DOI
https://doi.org/10.1021/acsanm.6c01735
Primary Topic
Nanoparticle-Based Drug Delivery
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Near-Infrared Luminescent Nanoparticles Enable Olaparib Delivery for Radiosensitized Image-Guided Theranostics

Fei‐Ting Hsu, Ming‐Hsien Chan, Hsi‐Feng Tu, Tsai-Lan Liao et al.
ACS Applied Nano Materials
Nanoparticle-Based Drug Delivery
article

Near-Infrared Luminescent Nanoparticles Enable Olaparib Delivery for Radiosensitized Image-Guided Theranostics

Fei‐Ting Hsu, Ming‐Hsien Chan, Hsi‐Feng Tu, Tsai-Lan Liao, Chia-Ying Lee
article en

Abstract

High Resolution Image Download MS PowerPoint Slide This work presents the design of near-infrared (NIR) luminescent nanoparticles codoped with rare-earth and transition-metal ions as a multifunctional materials platform for imaging-guided cancer therapy and radiological treatment assistance. Germanium oxide-based nanoparticles codoped with La 3+ and Cr 3+ (GeO 2:La 3+, Cr 3+; GOLC) were engineered to generate long-lasting NIR emission through a stable oxide host lattice and Cr 3+ -mediated charge-trapping states. The resulting NIR luminescence enables high-contrast, background-suppressed optical imaging without continuous external excitation, addressing key challenges associated with tissue autofluorescence and photobleaching in biological environments. To integrate therapeutic functionality, GOLC nanoparticles were loaded with the poly(ADP-ribose) polymerase (PARP) inhibitor olaparib, yielding GOLC@OLA nanostructures. These nanostructures effectively suppress oral cancer cell proliferation and induce apoptosis, combining optical tracking capability with drug delivery within a single materials system. Beyond chemical delivery, the high atomic number (high- Z ) the GOLC carrier confers an inherent radiosensitizing effect, significantly enhancing the efficacy of radiotherapy (RT) by increasing local photoelectric absorption. From a radiological perspective, La 3+ was incorporated primarily as a structural and electronic modulator rather than a conventional high- Z radiosensitizer. Although La 3+ does not strongly enhance photoelectric absorption, its incorporation may indirectly influence radiation responses through lattice defect modulation, defect-assisted charge dynamics, and radiation-induced apoptosis. This integration enables precise spatial correlation among nanoparticle localization, imaging readout, and therapeutic payload delivery, thereby supporting image-guided chemo-radiotherapy strategies in oral cancer models. Overall, this study establishes a versatile NIR luminescent nanoparticle framework that bridges optical imaging, drug delivery system, and imaging-guided radiological therapy, providing a materials-centric foundation for advanced oncological nanomedicine research.

ACS Applied Nano Materials
National Yang Ming Chiao Tung University (TW), National Central University (TW), Far Eastern Memorial Hospital (TW)
National Science and Technology Council
Openalex Percentile: Top 15%
Nanoparticle-Based Drug Delivery
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.