Evidence map›Paper›PMID 39899458›Full record

ReviewAngewandte Chemie (International ed. in English)2025

Activatable Photosensitizers: From Fundamental Principles to Advanced Designs.

Nahyun Kwon, Hanyi Weng, Maneesha A Rajora, Gang Zheng

Abstract readReview
In one paragraph

Review in Angewandte Chemie (International ed. in English), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

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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

4 authors.

Nahyun KwonPrincess Margaret Cancer Centre, University Health Network, 101 College Street, PMCRT 5-354, Toronto, ON, M5G1L7, Canada.
Hanyi WengPrincess Margaret Cancer Centre, University Health Network, 101 College Street, PMCRT 5-354, Toronto, ON, M5G1L7, Canada.
Maneesha A RajoraPrincess Margaret Cancer Centre, University Health Network, 101 College Street, PMCRT 5-354, Toronto, ON, M5G1L7, Canada.
Gang ZhengPrincess Margaret Cancer Centre, University Health Network, 101 College Street, PMCRT 5-354, Toronto, ON, M5G1L7, Canada.ORCID 0000-0002-0705-7398

Funding

Canada Excellence Research Chairs, Government of Canada 950-232468CIHR PJT190047 and 190093Princess Margaret Cancer FoundationTerry Fox Research Institute PPG1137
6 · The paper itself

Abstract

Photodynamic therapy (PDT) is a promising treatment that uses light to excite photosensitizers in target tissue, producing reactive oxygen species and localized cell death. It is recognized as a minimally invasive, clinically approved cancer therapy with additional preclinical applications in arthritis, atherosclerosis, and infection control. A hallmark of ideal PDT is delivering disease-specific cytotoxicity while sparing healthy tissue. However, conventional photosensitizers often suffer from non-specific photoactivation, causing off-target toxicity. Activatable photosensitizers (aPS) have emerged as more precise alternatives, offering controlled activation. Unlike traditional photosensitizers, they remain inert and photoinactive during circulation and off-target accumulation, minimizing collateral damage. These photosensitizers are designed to "turn on" in response to disease-specific biostimuli, enhancing therapeutic selectivity and reducing off-target effects. This review explores the principles of aPS, including quenching mechanisms stemming from activatable fluorescent probes and applied to activatable photosensitizers (RET, PeT, ICT, ACQ, AIE), as well as pathological biostimuli (pH, enzymes, redox conditions, cellular internalization), and bioresponsive constructs enabling quenching and activation. We also provide a critical assessment of unresolved challenges in aPS development, including limitations in targeting precision, selectivity under real-world conditions, and potential solutions to persistent issues (dual-lock, targeting moieties, biorthogonal chemistry and artificial receptors). Additionally, it provides an in-depth discussion of essential research design considerations needed to develop translationally relevant aPS with improved therapeutic outcomes and specificity.

Indexed as

Drug DesignPhotosensitizing AgentsAnimalsHumansNeoplasmsPhotochemotherapyReactive Oxygen SpeciesPhotosensitizing AgentsReactive Oxygen Speciesactivationfluorescencephotodynamic therapyphotosensitizerquenching

Identifiers

PMID39899458
PMCPMC11976215

What OpenQuestion holds

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Registered trials

None linked

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.