Photochemical Generation and Regulation of Reactive Oxygen Species: From Molecular Mechanisms to Health and Environmental Impacts

A special issue of Photochem (ISSN 2673-7256).

Deadline for manuscript submissions: 31 December 2026 | Viewed by 3551

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Guest Editor
Department of Chemistry, College of William & Mary, Williamsburg, VA 23185, USA
Interests: reactive oxygen species; photochemical reactions; catechols; quinones

Special Issue Information

Dear Colleagues,

This Special Issue of Photochem seeks to assemble cutting-edge research and comprehensive reviews that address the role of reactive oxygen species (ROS) in photochemistry. Photochemical processes that generate ROS are numerous in biological settings, especially photodynamic therapy (PDT). Light-activated photosensitizers transfer energy or electrons to nearby molecules to create ROS in PDT. These processes, known as Type I (electron transfer) and Type II (energy transfer), may occur concurrently and are modulated by molecular oxygen concentration. For example, photo-oxidation and photoreduction of benzoquinones and catechols by methylene blue and chlorophyll metabolites generate ROS [1].

Photodynamic therapy targets tissues for ROS-mediated cell death by the combination of molecular oxygen, photosensitizer uptake, and light exposure. A recent review in Photochem highlights the range of PDT applications, including treatment of solid tumors, bacterial infections, and skin conditions [2]. Furthermore, this review article highlights challenges of tissue light penetration, uptake of photosensitizers and ROS production.

ROS are also generated in environmental settings because photosynthesis is the most widely occurring photochemical process on Earth. Photoexcitation of chlorophyll initiates electron transfer to plastoquinone in chloroplasts. Yet, when light is excessive, ROS are produced. Plants have evolved mechanisms to mitigate damage by ROS using antioxidants. Aquatic ecosystems that contain chlorophyll as part of phytoplankton are also susceptible to ROS-mediated pathways and oxygen depletion.

We seek contributions that delve into the photochemical generation of ROS and their intentional use in health and environmental settings.

1. Phan, K.; Lessard, E.E.; Reed, J.A.; Warsen, M.G.; Zimmer, S.; Landino, L.M. Concurrent Photooxidation and Photoreduction of Catechols and Para-Quinones by Chlorophyll Metabolites. Photochem 20244, 346-360. https://doi.org/10.3390/photochem4030021

2. Allamyradov, Y.; ben Yosef, J.; Annamuradov, B.; Ateyeh, M.; Street, C.; Whipple, H.; Er, A.O. Photodynamic Therapy Review: Past, Present, Future, Opportunities and Challenges. Photochem 20244, 434-461. https://doi.org/10.3390/photochem4040027

Prof. Dr. Lisa Landino
Guest Editor

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Keywords

  • reactive oxygen species
  • singlet oxygen
  • chlorophyll
  • photosensitizer
  • photodynamic therapy
  • electron transfer

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Published Papers (2 papers)

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Research

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18 pages, 2086 KB  
Article
Photochemical Redox Reactions of Catecholamines: Detection of Cyclized Oxidation Products and Boronate Esters
by Lisa M. Landino, Antonios Tsompanidis, Hannah McMinn, Andrew Mooney and Brandon Yu
Photochem 2026, 6(1), 11; https://doi.org/10.3390/photochem6010011 - 9 Mar 2026
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Abstract
Our recent work has focused on red light-mediated photoreduction of p-benzoquinones and both o-, and p-naphthoquinones using methylene blue and the chlorophyll metabolite, pheophorbide A as photosensitizers. Photoreduction of biologically relevant quinones mimics photoreduction of plastoquinone by chlorophyll in photosynthesis. We examined photo-oxidation [...] Read more.
Our recent work has focused on red light-mediated photoreduction of p-benzoquinones and both o-, and p-naphthoquinones using methylene blue and the chlorophyll metabolite, pheophorbide A as photosensitizers. Photoreduction of biologically relevant quinones mimics photoreduction of plastoquinone by chlorophyll in photosynthesis. We examined photo-oxidation and photoreduction reactions of catechols because their oxidation to o-quinones by reactive oxygen species is implicated in protein damage in neurodegeneration. Photo-oxidation of catecholamines including dopamine, epinephrine and norepinephrine required red light, methylene blue or pheophorbide A, and molecular oxygen. Their cyclized oxidation products, aminochrome, adrenochrome and noradrenochrome, were detected by UV/visible spectroscopy. Hydrogen peroxide was generated during photo-oxidation by singlet oxygen-dependent oxidation of catecholamines. Inclusion of tertiary amine electron donors decreased cyclized products but did not affect hydrogen peroxide yield consistent with concurrent photo-oxidation followed by photoreduction of the o-quinone intermediate. Unreacted dopamine and norepinephrine were quantified using 3-hydroxyphenyl boronic acid following photochemical reactions. Dopamine and norepinephrine boronate esters absorb at 417 and 550 nm. Photo-oxidation of dihydroxycaffeic acid and dihydroxyphenyl acetic acid was also evaluated by detecting their boronate esters at 475 nm. We hypothesize that photoreduction of transient o-quinones by the combination of red light and dietary chlorophyll metabolites may be a path to limit protein damage and to recycle catechol antioxidants. Full article
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Review

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28 pages, 1013 KB  
Review
Plant-Derived Photosensitizers in Antimicrobial Photodynamic Therapy: Mechanisms, Advances, and Emerging Applications
by Edith Dube
Photochem 2026, 6(2), 17; https://doi.org/10.3390/photochem6020017 - 17 Apr 2026
Cited by 2 | Viewed by 1485
Abstract
The increasing prevalence of antimicrobial resistance, together with recurring infectious disease outbreaks, has intensified the need for alternative strategies to control microbial infections beyond conventional antibiotic therapies. Antimicrobial photodynamic therapy has emerged as a promising non-antibiotic approach in which light-activated photosensitising compounds generate [...] Read more.
The increasing prevalence of antimicrobial resistance, together with recurring infectious disease outbreaks, has intensified the need for alternative strategies to control microbial infections beyond conventional antibiotic therapies. Antimicrobial photodynamic therapy has emerged as a promising non-antibiotic approach in which light-activated photosensitising compounds generate reactive oxygen species that induce oxidative damage to microbial cells. Plant-derived photosensitisers have attracted increasing attention due to their structural diversity, biocompatibility, natural abundance, and potential for sustainability. Natural compounds such as curcumin, hypericin, chlorophyll derivatives, flavonoids, anthraquinones, and riboflavin exhibit favourable photochemical properties that enable efficient production of reactive oxygen species upon irradiation with visible light. Through radical- and singlet-oxygen-mediated photochemical pathways, these molecules exhibit broad-spectrum antimicrobial activity against bacteria, fungi, viruses, and biofilm-associated microorganisms. This review examines the photophysical properties and mechanisms of reactive oxygen species generation associated with plant-derived photosensitisers, together with key factors influencing their antimicrobial performance. Recent advances in nanocarrier-based delivery systems, dual-wavelength activation strategies, and synergistic combination therapies are also discussed for their potential to improve photostability, enhance reactive oxygen species generation, and increase microbial inactivation efficiency. Finally, current progress, challenges, and future research directions for advancing plant-derived photosensitisers in antimicrobial photodynamic therapy are discussed. Full article
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