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Recent Advances in Photolysis and Photodegradation

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Physical Chemistry and Chemical Physics".

Deadline for manuscript submissions: 30 September 2024 | Viewed by 3287

Special Issue Editor


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Guest Editor
1. Faculty of Physics, St. Peterburg State University, 199034 St. Petersburg, Russia
2. Institute of Physics, Kazan Federal University, 420008 Kazan, Russia
Interests: photochemistry; molecur biophysics; photosensitization; pterins; aromatic amino acids; metal nanoclusters; density functional theory; QSAR/QSPR

Special Issue Information

Dear Colleagues,

Photolysis is a chemical process that occurs when molecules absorb photons and degrade into smaller units. This Special Issue aims to cover the photodissociation/photofragmention topic for biomolecular and non-biomolecular systems. A particular example of such a bioprocess is the photolysis of water during photosynthesis, the biophotolysis production of hydogen, etc. Another important point is the photosensitized degradation of chemical substances which do not absorb light themselves, but become subjected to photolytic degradation. Photodegradation is a process associated with the turnover of colored photolabile compounds in ecosystems. For this reason, the photodegradation of chemical compounds and its effect on the environment are explored in this Special Issue, particularly the photodegrdation of drug substances and their negative effect on organism. The process of photolysis is not restricted to visible light only, but may occur under ultraviolet and X-ray radiation, as well as infrared multiphoton irradiation. Both theoretical and experimental studies are welcomed to be published in the Special Issue.

Dr. Andrey А. Buglak
Guest Editor

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Keywords

  • indirect photolysis
  • photosensitized oxidation
  • biophotolysis
  • photodissociation
  • photofragmentation
  • ultraviolet radiation
  • photoactive drugs

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Published Papers (4 papers)

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Research

7 pages, 1922 KiB  
Communication
Far-Ultraviolet Light at 222 nm Affects Membrane Integrity in Monolayered DLD1 Colon Cancer Cells
by Jun Nishikawa, Yuta Tamura, Tomohiro Fujii, Soichiro Fukuda, Shoma Yoneda, Nanami Yamaura, Shinichi Takahashi, Takeshi Yamamoto, Junzo Nojima, Yutaka Suehiro, Takahiro Yamasaki and Taro Takami
Int. J. Mol. Sci. 2024, 25(13), 7051; https://doi.org/10.3390/ijms25137051 - 27 Jun 2024
Viewed by 453
Abstract
222 nm far-ultraviolet (F-UV) light has a bactericidal effect similar to deep-ultraviolet (D-UV) light of about a 260 nm wavelength. The cytotoxic effect of 222 nm F-UV has not been fully investigated. DLD-1 cells were cultured in a monolayer and irradiated with 222 [...] Read more.
222 nm far-ultraviolet (F-UV) light has a bactericidal effect similar to deep-ultraviolet (D-UV) light of about a 260 nm wavelength. The cytotoxic effect of 222 nm F-UV has not been fully investigated. DLD-1 cells were cultured in a monolayer and irradiated with 222 nm F-UV or 254 nm D-UV. The cytotoxicity of the two different wavelengths of UV light was compared. Changes in cell morphology after F-UV irradiation were observed by time-lapse imaging. Differences in the staining images of DNA-binding agents Syto9 and propidium iodide (PI) and the amount of cyclobutane pyrimidine dimer (CPD) were examined after UV irradiation. F-UV was cytotoxic to the monolayer culture of DLD-1 cells in a radiant energy-dependent manner. When radiant energy was set to 30 mJ/cm2, F-UV and D-UV showed comparable cytotoxicity. DLD-1 cells began to expand immediately after 222 nm F-UV light irradiation, and many cells incorporated PI; in contrast, PI uptake was at a low level after D-UV irradiation. The amount of CPD, an indicator of DNA damage, was higher in cells irradiated with D-UV than in cells irradiated with F-UV. This study proved that D-UV induced apoptosis from DNA damage, whereas F-UV affected membrane integrity in monolayer cells. Full article
(This article belongs to the Special Issue Recent Advances in Photolysis and Photodegradation)
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14 pages, 2885 KiB  
Article
Photodegradation of a Broad-Spectrum Antibiotic Azithromycin Using H2O2 under Ultraviolet Irradiation
by Nasser Ibrahim Zouli
Int. J. Mol. Sci. 2024, 25(12), 6702; https://doi.org/10.3390/ijms25126702 - 18 Jun 2024
Viewed by 469
Abstract
The photodegradation of azithromycin present was carried out in water using H2O2 under UV irradiation. The reaction variables considered in this study were the amount of H2O2 solution and the initial concentration of azithromycin to evaluate the [...] Read more.
The photodegradation of azithromycin present was carried out in water using H2O2 under UV irradiation. The reaction variables considered in this study were the amount of H2O2 solution and the initial concentration of azithromycin to evaluate the performance of the photodegradation process. The azithromycin degradation was not observed in the dark during stirring for 20 min. The study showed an efficient photodegradation of azithromycin using H2O2 as an oxidant in the presence of UV irradiation. The azithromycin degradation was altered significantly by the pH of the irradiated solution. The degradation was low at an acidic pH and showed an increasing trend as the pH changed to basic. The azithromycin degradation increased with a higher amount (higher concentration) of H2O2. The degradation of azithromycin decreased with a higher concentration of azithromycin in the reacting solution. The highest degradation of AZT was achieved in 1 h using a 1.0 ppm AZT solution containing 3 mL of H2O2. The experimental data obtained were well-fitted to zero-order reaction kinetics. The results of this study were found quite excellent. They showed 100% degradation in 1 h when compared with those reported in the literature, both with photocatalysis using nanomaterials and photolysis using light irradiation and/or H2O2. The UV/H2O2 system was found to be quite efficient for the photodegradation of azithromycin, and this system can be applied to degrade other organic pollutants present in industrial wastewater. Full article
(This article belongs to the Special Issue Recent Advances in Photolysis and Photodegradation)
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15 pages, 2855 KiB  
Article
Hydrophilicity and Pore Structure Enhancement in Polyurethane/Silk Protein–Bismuth Halide Oxide Composite Films for Photocatalytic Degradation of Dye
by Lingxi Meng, Jian Jian, Dexing Yang, Yixiao Dan, Weijie Sun, Qiuhong Ai, Yusheng Zhang and Hu Zhou
Int. J. Mol. Sci. 2024, 25(12), 6653; https://doi.org/10.3390/ijms25126653 - 17 Jun 2024
Cited by 1 | Viewed by 428
Abstract
Polyurethane/silk protein–bismuth halide oxide composite films were fabricated using a blending-wet phase transformationin situsynthesis method. The crystal structure, micromorphology, and optical properties were conducted using XRD, SEM, and UV-Vis DRS characterize techniques. The results indicated that loaded silk protein enhanced the hydrophilicity and [...] Read more.
Polyurethane/silk protein–bismuth halide oxide composite films were fabricated using a blending-wet phase transformationin situsynthesis method. The crystal structure, micromorphology, and optical properties were conducted using XRD, SEM, and UV-Vis DRS characterize techniques. The results indicated that loaded silk protein enhanced the hydrophilicity and pore structure of the polyurethane composite films. The active species BiOX were observed to grow as nanosheets with high dispersion on the internal skeleton and silk protein surface of the polyurethane–silk protein film. The photocatalytic efficiency of BiOX/PU-SF composite films was assessed through the degradation of Rhodamine B under visible light irradiation. Among the tested films, the BiOBr/PU-SF composite exhibited the highest removal rate of RhB at 98.9%, surpassing the removal rates of 93.7% for the BiOCl/PU-SF composite and 85.6% for the BiOI/PU-SF composite. Furthermore, an active species capture test indicated that superoxide radical (•O2) and hole (h+) species played a predominant role in the photodegradation process. Full article
(This article belongs to the Special Issue Recent Advances in Photolysis and Photodegradation)
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18 pages, 2691 KiB  
Article
Tetrahydrobiopterin as a Trigger for Vitiligo: Phototransformation during UV Irradiation
by Taisiya A. Telegina, Yuliya L. Vechtomova, Vera A. Borzova and Andrey A. Buglak
Int. J. Mol. Sci. 2023, 24(17), 13586; https://doi.org/10.3390/ijms241713586 - 1 Sep 2023
Cited by 3 | Viewed by 1271
Abstract
Vitiligo is a type of hypomelanosis. Tetrahydrobiopterin (H4Bip), the coenzyme of the initial stage of melanogenesis, appears to be a trigger for vitiligo. H4Bip is present in vitiligo in 3–5-fold excess and causes oxidative stress by triggering an autocatalytic [...] Read more.
Vitiligo is a type of hypomelanosis. Tetrahydrobiopterin (H4Bip), the coenzyme of the initial stage of melanogenesis, appears to be a trigger for vitiligo. H4Bip is present in vitiligo in 3–5-fold excess and causes oxidative stress by triggering an autocatalytic cycle of excess hydrogen peroxide synthesis. Using quantum-chemical calculations, we have evaluated the possibility of H4Bip reactions occurring in the dark and under ultraviolet (UV) irradiation, including the formation of dihydropterin dimers. In order to simulate the oxidative stress, oxidative modification of human serum albumin (HSA) has been carried out in the presence of excessive H4Bip using the fluorescence method. The fraction of oxidized protein (FOP) has been calculated. It has been established that there is a strong oxidative modification of amino acids chromophores (tryptophan and tyrosine) in the protein (FOP 0.64). Under UV irradiation of the system (HSA + H4Bip), FOP is reduced to 0.39. Apparently, a part of H4Bip transforms into dihydropterin dimers and does not participate in the oxidative modification of the protein. The data on oxidative modification of HSA are consistent with dynamic light scattering: H4Bip promotes HSA aggregation with the formation of particles with a hydrodynamic radius Rh ≥ 2000 nm, which can become immunogenic. Full article
(This article belongs to the Special Issue Recent Advances in Photolysis and Photodegradation)
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