Evidence map›Paper›PMID 40034443›Full record

ArticleResearch square2025

Quantitative Fluorescence Imaging of Porphyrin Phospholipid Photobleaching and Light Activated Liposomal Doxorubicin Release Using Wide-field and Laparoscopic SFDI in an Ovarian Cancer Model.

Rasel Ahmmed, Elias Kluiszo, Semra Aygun-Sunar, Matthew Willadsen, Hilliard L Kutscher, Jonathan F Lovell, Ulas Sunar

Abstract readPreprint
In one paragraph

Article in Research square, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Rasel AhmmedDepartment of Biomedical, Engineering, Stony Brook University, Stony Brook, NY 11794, USA.
Elias KluiszoDepartment of Biomedical, Engineering, Stony Brook University, Stony Brook, NY 11794, USA.
Semra Aygun-SunarDepartment of Biomedical, Engineering, Stony Brook University, Stony Brook, NY 11794, USA.
Matthew WilladsenPOP Biotechnologies, Buffalo, NY 14228, USA.
Hilliard L KutscherPOP Biotechnologies, Buffalo, NY 14228, USA.
Jonathan F LovellDepartment of Biomedical Engineering, University at Buffalo, Buffalo, NY 14260, USA.
Ulas SunarDepartment of Biomedical, Engineering, Stony Brook University, Stony Brook, NY 11794, USA.

Funding

Quantitative Fluorescence Imaging-Guided Detection and Targeted Therapy Monitoring Platform for Ovarian Cancer MicrometastasesR01CA243164 · NCI · WRIGHT STATE UNIVERSITY · PI Ulas Sunar · 2020 to 2026
$1.7M
NCI NIH HHS R01 CA243164
6 · The paper itself

Abstract

Chemophototherapy (CPT) is an emerging cancer treatment that leverages the synergistic effects of photodynamic therapy (PDT) and chemotherapy. This approach utilizes photosensitizers like Porphyrin Phospholipid (PoP) and Doxorubicin (Dox) to enable phototriggered drug release and targeted tumor destruction. In this study, we present the development and validation of a wide-field laparoscopic spatial frequency domain imaging (SFDI) system, designed to improve intraoperative quantitative fluorescence imaging and monitoring of PoP photobleaching, a PDT-driven effect for tumor destruction, and light-activated Dox release, which facilitates targeted chemotherapeutic drug delivery in an ovarian cancer model. Compared to previous flexible endoscopic imaging methods, our laparoscopic SFDI system offers enhanced spatial coverage, enabling accurate wide-field optical property quantification in minimally invasive surgical settings. Using this system, we performed quantitative fluorescence imaging in vivo to obtain absolute concentrations of PoP and Dox fluorescence, correcting for tissue absorption and scattering effects. This capability allows for precise assessment of PoP photobleaching and Dox release kinetics with improved spatial resolution. Fluorescence imaging revealed a significant reduction in PoP concentration in tumor regions post-illumination, demonstrating the PDT-mediated photobleaching effect and successful light-triggered drug release activation for chemo-induced tumor destruction. The ability to differentiate PoP and Dox fluorescence in a laparoscopic system underscores its potential for real-time intraoperative monitoring of CPT efficacy. These findings establish wide-field laparoscopic SFDI as a promising tool for guiding minimally invasive photodynamic therapy and targeted drug delivery in clinical settings.

Indexed as

doxorubicin drug concentrationlaparoscopelight-triggered releasephotodynamic therapyporphyrinsquantitative fluorescence imagingspatial frequency domain imaging

Identifiers

PMID40034443
PMCPMC11875292

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.