Photoaging Process Research Articles

Molecular properties of dissolved organic matter leached from microplastics during photoaging process

The occurrence of dissolved organic matter (DOM) derived from microplastics (MPs) and its effect on aquatic systems has attracted great interest recently. However, the photoaging effect on the molecular structure of MP-derived DOM (MP-DOM) remains unclear. This paper presents the characteristics of DOM leached from three commercial MPs, i.e., polyethylene (PE), polypropylene (PP) and polyethylene terephthalate (PET) under UV irradiation. With prolonged aging periods, the surface roughness and oxygen-containing groups on the surface of MPs increase as more DOM leachate is generated. Moreover, the dissolved organic carbon (DOC) content of the leached DOM from PET MPs varies from 0.52 mg/L to 2.25 mg/L, which is higher than PE and PP MPs, due to the larger increased surface reaction area and the cleavage of the benzene ring. According to the excitation-emission matrix and parallel factor analysis (EEM-PARAFAC), the plastic-derived protein/phenolic-like components (C1 and C3) in MP-DOM were changed into photo-induced humic-like components (C2), which were closely related to the intermediates during photo-oxidation. High-performance liquid chromatography-mass spectrometry (HPLC−MS) analysis further identified that the highest proportion of antioxidants (24.8 %∼34.6 %) was contained in MP-DOM. Plasticizers, intermediate additives, and antimicrobial agents were also detected in DOM leachate. Correlation analysis identified that the composition of leached DOM was positively correlated with the surface roughness, the carbonyl index (CI), and the chemical groups of MPs. Moreover, a partial least square structural equation model (PLS−SEM) analysis further verified that the change of morphology and the chemical structure of MPs could affect the DOM structures and fractions directly. This study provides an in-depth understanding of the composition of MP-derived DOM during the aging process, as well as a comprehensive environmental impact assessment of MPs.

Succinylated Type I Collagen Regulates Ferroptosis to Attenuate Skin Photoaging.

During the process of photoaging in the skin, Succinylated type I collagen has a significant effect on reversing the damage caused by UVB radiation, with the regulation of cellular ferroptosis being one of its important pathophysiological mechanisms. Specifically, Succinylated type I collagen reduces the expression of key cell cycle regulators P16, P21, and P53, as well as the ferroptosis-related factor Acyl-CoA Synthetase Long Chain Family Member 4 (ACSL4), induced by UVB radiation in cells and tissues. Meanwhile, it increases the expression of key factors Glutathione Peroxidase 4 (GPX4) and Solute Carrier Family 7 Member 11 (SLC7A11), which inhibit ferroptosis. Additionally, our study also reveals the impact of Succinylated type I collagen on the levels of malondialdehyde (MDA), glutathione (GSH), and reactive oxygen species (ROS) in cells and tissues, directly affecting the cells' ability to cope with oxidative stress. This further suggests that Succinylated type I collagen may improve skin photoaging through various pathways, including regulating ferroptosis, antioxidation, promoting collagen synthesis, protecting the skin barrier, reducing pigmentation, and inhibiting inflammatory responses, contributing to maintaining healthy and youthful skin.

Caenorhabditis elegans as a Model to Study Aging and Photoaging.

Caenorhabditis elegans (C. elegans) has emerged as an outstanding model organism for investigating the aging process due to its shortened lifespan, well-defined genome, and accessibility of potent genetic tools. This review presents the current findings on chronological aging and photoaging in C. elegans, exploring the elaborate molecular pathways that control these processes. The progression of chronological aging is characterized by a gradual deterioration of physiological functions and is influenced by an interaction of genetic and environmental factors, including the insulin/insulin-like signaling (IIS) pathway. In contrast, photoaging is characterized by increased oxidative stress, DNA damage, and activation of stress response pathways induced by UV exposure. Although the genetic mechanisms of chronological aging in C. elegans have been characterized by extensive research, the pathways regulating photoaging are comparatively less well-studied. Here, we provide an overview of the current understanding of aging research, including the crucial genes and genetic pathways involved in the aging and photoaging processes of C. elegans. Understanding the complex interactions between these factors will provide invaluable insights into the molecular mechanisms underlying chronological aging and photoaging and may lead to novel therapeutic approaches and further studies for promoting healthy aging in humans.

The effect of aging on mast cell density in human skin: a comparative analysis of photoexposed and photoprotected regions.

Mast cells are mononuclear cells originating from bone marrow. They produce various biologically active substances, which allow them to actively participate in immune and inflammatory processes associated with intrinsic and extrinsic skin aging. This research focused on distribution and density of mast cells in healthy skin in different stages of skin aging. This project included samples of photoexposed and photoprotected skin, obtained from 90 cadavers aged 0-82 years. The samples were classified into five age groups: newborns, young age, middle age, senior age and the oldest age. In order to visualize the mast cells, we have employed several histochemical staining protocols. The number of mast cells of the photoexposed skin significantly correlated to the individual's age. The number of mast cells of the photoprotected skin was in general statistically significantly lower in younger compared to older groups; however, the correlation of the mast cell density in photoprotected skin and the age did not reach statistical significance. In middle age, senior age and the oldest age groups, a significantly higher number of mast cells was recorded in the skin of the photoexposed compared to photoprotected region. The increase in mast cell density correlated with age only in photoexposed skin. Age-related higher accumulation of dermal mast cells in photoexposed skin can be an important factor in the photoaging process, as well as the contributing factor in the occurrence of skin cancer.

Advanced understanding of the natural forces accelerating aging and release of black microplastics (tire wear particles) based on mechanism and toxicity analysis

Currently, tire wear particles (TWPs), a typical type of black microplastics (MPs), are frequently overlooked as the major source of MPs in aquatic environments. TWPs are widely distributed and exhibit complex environmental behaviors. However, how natural forces affect the aging and release behavior of TWPs at the nano(micro)scale remains inadequately explored. This study systematically investigated the aging behavior and mechanism of TWPs under the action of simulated natural light and high-temperature in both dry and wet environments, as well as the effect of aging treatment on the released leachate. The findings demonstrated that aging treatment significantly altered the physicochemical properties of TWPs, including chain scission and surface oxidation, and facilitated the release of heavy metals and organic additives in the meantime. In particular, the leaching concentration of Zn exhibited a positive linear relationship with exposure time. In the thermal-aging process, the oxidation of TWPs was primarily caused by superoxide anion (O2•−). During the photo-aging exposure, TWPs exhibited heightened electron-donating capacity, resulting in the formation of more O2•− and singlet oxygen (1O2) to attack TWPs. Moreover, the analysis of leachate produced under light and high-temperature conditions suggested that heavy metals exerted low ecological risks in water. Nonetheless, the photo-aging process enhanced the toxicity of released leachate to L929 cells, which could be attributed to highly toxic additive transformation products (such as HMMM-411 and 6PPD-Q) and more heavy metals. These findings shed light on the fate of TWPs and the ecological risks posed by aged TWPs in aquatic environments.

Bottom-Up Defect Modification Through Oily-Allicin Modified Buried Interface Achieving Highly Efficient and Stable Perovskite Solar Cells.

The buried interface properties of the perovskite solar cells (PSCs) play a crucial role in the power conversion efficiency (PCE) and operational stability. The metal-oxide/perovskite heterogeneous interfaces are highly defective and cause serious ion migration. However, the buried and unexposed bottom interface and simultaneous stabilization of grain boundaries receive less attention and effective solutions. To tackle this problem, a solid-liquid strategy is employed by introducing oily-additive allicin at the buried interface to passivate the shallow (VI and Vo) and deep traps (VPb and PbI). Interestingly, oily status allicin fills the pinholes at the heterointerface and wraps the perovskite grains, suppressing the ion migration during the photoaging process. As a result, an outstanding PCE of 25.07% is achieved with a remarkable fill factor (FF) of 84.03%. The modified devices can maintain 94.51% of the original PCE after light soaking under 1-sun illumination for 1000h. This work demonstrates a buried interface modification method that employs an eco-friendly additive, which helps promote the development of PSCs with high performance and stability.

High-altitude aquatic ecosystems offer faster aging rate of plastics

While research on the aging behavior of plastics in aquatic systems is extensive, studies focusing on high-altitude ecosystems, characterized by higher solar radiation and lower temperatures, remain limited. This study investigated the long-term aging behavior of non-biodegradable plastics (non-BPs), namely polyethylene terephthalate (PET) and polypropylene (PP) and biodegradable plastics (BPs), specifically polylactic acid plus polybutylene adipate-co-terephthalate (PLA + PBAT) and starch-based plastic (SBP), in a tributary of the Yarlung Zangbo River on the high-altitude Tibetan Plateau. Over 84 days of field aging, all four types of plastics exhibited initial rapid aging followed by deceleration. This aging process can be divided into two phases: rapid surface oxidation aging and an aging plateau phase. Notably, PP aged at a rate comparable to BPs, contrary to expectations of faster aging for BPs. Compared to low-altitude aquatic ecosystems, plastics in this study showed a faster aging rate. This was primarily due to intense ultraviolet radiation causing severe photoaging. Furthermore, the lower temperatures contributed to the formation of thinner biofilms. These thinner biofilms exhibited a reduced capacity to block light, further exacerbating the photoaging process of plastics. Statistical analysis results indicated that temperature, total nitrogen TN, and total phosphorus TP were likely the main water quality parameters influencing plastic aging. The varying effects of water properties and nutrients underscore the complex interaction of water quality parameters in high-altitude environments. Given the delicate nature of the high-altitude environment, the environmental impact of plastics, especially BPs, warrants careful consideration.

The Protective Effects of Silkworm (Bombyx mori) Pupae Peptides on UV-Induced Skin Photoaging in Mice.

Silkworm (Bombyx mori) pupae are popular edible insects with high nutritional and therapeutic value. Currently, there is growing interest in the comprehensive application of silkworm pupae. In this study, peptides that exhibited anti-photoaging activity were obtained from silkworm pupae protein, aiming to investigate the protective effects and potential mechanisms of silkworm pupae peptides (SPPs) on skin photoaging. The results showed that SPPs were composed of 900 short peptides and could effectively alleviate skin photoaging progression. They significantly eliminated excessive production of ROS and MDA; meanwhile, they also renovated the antioxidant enzyme activities. The biomarkers related to collagen synthesis and degradation, including hydroxyproline, interstitial collagenase, and gelatinase, demonstrated that SPPs could suppress collagen degradation. Histopathological results showed that SPPs could reduce the inflammatory infiltrate and the thickness of the dermis and epidermis, as well as increase the collagen bundles and muscle fibers. The histopathological and biochemical results confirmed that SPPs could alleviate photoaging by inhibiting abnormal skin changes, reducing oxidative stress, and immune suppression. Overall, these data prove the protective effects of SPPs against the photoaging process, suggesting their potential as an active ingredient in skin photoaging prevention and therapy.

Photoaging processes and mechanisms of polyolefin microplastics

The photoaging processes of microplastics (MPs) under various conditions, including environmental factors and soluble organic matter, have been extensively investigated. However, a notable gap exists in the literature regarding comparative experiments on the photoaging of polyolefin-type MPs, and research on different light sources is particularly scarce. This research involved exposing representative MPs (polystyrene (PS), polyvinyl chloride (PVC), and polyethylene (PE)) to light with different wavelength ranges (200–2000 nm and 320–780 nm). Results indicated that PS and PVC, with benzene rings and C-Cl chains, exhibited higher susceptibility to photoaging compared to PE, leading to changes in physicochemical properties. In 200–2000 nm, including UVC (200–280 nm) and UVB (280–315 nm), a pronounced PS and PVC photoaging process was observed due to their higher energy, which resulted in noticeable yellowing of the morphology. PE showed less pronounced effects, except for noticeable aging in the 320–780 nm range within 6 h (UV–vis spectrum), with a slow depolymerization rate over 72 h. Furthermore, a limited aging of polyolefins was observed under dark conditions. In summary, this study provides crucial insight into the accelerated photoaging of polyolefin-type MPs under different light source, which offers novel perspectives and references for future research directions.

Releasing characteristics of toxic chemicals from polystyrene microplastics in the aqueous environment during photoaging process

Microplastics (MPs) are pervasive in the environment and inevitably undergo photoaging due to UV irradiation. This study delved into the dynamic releasing and transformation process of toxic chemicals from polystyrene microplastics (PS MPs) during photoaging, a subject that remains underexplored. It was revealed that photoaging led to substantial alterations in the physicochemical properties of PS MPs, initiating polymer chain scission and facilitating the release of a large number of toxic chemicals, including numerous organic compounds and several inorganic compounds. The kinetic analysis revealed a dynamic release pattern for PS MPs, where under varying UV intensities (2, 5, and 10 mW/cm2), the release rate (kDOC) initially increased and then decreased, peaking at a total irradiation energy of approximately 7 kW·h/m2. Furthermore, chemicals in leachate were transformed into compounds with smaller molecular weight, higher oxidized and greater unsaturated state over the prolonged photoaging. This transformation was primarily attributed to two reasons. Firstly, the aged PS MPs released chemicals with higher oxidized state compared to the pristine MPs. Secondly, the chemicals previously released underwent further reactions. Besides, among the complex leachate generated by aged PS MPs, the organic chemicals characterized by small molecular weight and high oxidized state exhibited notable acute toxicity, whereas heavy metal ions showed lesser toxicity, and anions were non-toxic. This study shed more light on the photoaging process of PS MPs, releasing characteristics of organic chemicals, and the potential environmental risks associated with plastic wastes.

Interactions between methyl octabromo ether flame retardant and expanded polystyrene microplastics in the photoaging process

Expanded polystyrene (EPS) plastic is widely used because of its low density and lightweight properties, enabling it to float on water and increase its exposure to sunlight. In this study, we simulated the photoaging process of flame retardant-added EPS (FR-EPS) and common original EPS (OR-EPS) microplastic (MP) particles with and without methyl octabromoether flame retardant (MOBE) in the laboratory to explore the effect of MOBE on the photodegradation of EPS. Results showed that MOBE accelerated size reduction and surface hole formation on the particles, hastening the shedding and replacement of particle surfaces. FR-EPS particles exhibited a weight loss exceeding that of OR-EPS, reaching 40.85 ± 3.72% after 36 days of irradiation. Moreover, rapid physical peeling of the FR-EPS surface was accompanied by continuous chemical oxidation and fluctuations of the carbonyl index and O/C ratio. A diffusion model based on Fick's second law fitted well for the concentration of MOBE remaining in FR-EPS particles. MOBE's sensitivity to direct photochemical reactions inhibited the early-stage photoaging of EPS MP particles by competing for photons. However, MOBE as chromophores could absorb photons and produce •OH to promote the aging of EPS. Moreover, the capacity of EPS to absorb light energy also accelerated MOBE degradation. These findings suggested that the photoaging behavior of commercial EPS products containing flame retardants in the environment is quite different from that of pure EPS, indicating that additive-plastic interactions significantly alter MP fate and environmental risks.

New Insights into Aggregation Behaviors of the UV-Irradiated Dissolved Biochars (DBioCs) in Aqueous Environments: Effects of Water Chemistries and Variation in the Hamaker Constant.

The aggregation behavior of ubiquitous dissolved black carbon (DBC) largely affects the fate and transport of its own contaminants and the attached contaminants. However, the photoaging processes and resulting effects on its colloidal stability remain yet unknown. Herein, dissolved biochars (DBioCs) were extracted from common wheat straw biochar as a proxy for an anthropogenic DBC. The influences of UV radiation on their aggregation kinetics were systematically investigated under various water chemistries (pH, electrolytes, and protein). The environmental stability of the DBioCs before and after radiation was further verified in two natural water samples. Hamaker constants of pristine and photoaged DBioCs were derived according to Derjaguin-Landau-Verwey-Overbeek (DLVO) prediction, and its attenuation (3.19 ± 0.15 × 10-21 J to 1.55 ± 0.07 × 10-21 J after 7 days of radiation) was described with decay kinetic models. Pearson correlation analysis revealed that the surface properties and aggregation behaviors of DBioCs were significantly correlated with radiation time (p < 0.05), indicating its profound effects. Based on characterization and experimental results, we proposed a three-stage mechanism (contended by photodecarboxylation, photo-oxidation, and mineral exposure) that DBioCs might experience under UV radiation. These findings would provide an important reference for potential phototransformation processes and relevant behavioral changes that DBC may encounter.

Ferulic acid in synergy with retinol alleviates oxidative injury of HaCaT cells during UVB-induced photoaging.

Application of retinol (Vitamin A, VA) in skincare is limited for instability, poor water solubility, and skin intolerance that combats skin aging. We employed computer-aided virtual screening and cell experiments with transcriptomics, thereby unveiling the comprehensive gene expression and regulation pathway of photoaging HaCaT cell treated with ferulic acid (FA) in synergizing with VA. Through network pharmacology analysis, the combined use of VA and FA exhibited highly correlated cross-targets with skin aging acting on EGFR, PTPN1, ESR2, GSK3B, BACE1, PYGL, PTGS2 and APP. The indicators of oxidative stress, such as SOD, GSH, MDA, CAT and ROS in HaCaT cells after co-administration, were significantly improved from those in photoaging group (p<0.0001). 155 differential expressed genes (DEGs) were specific between groups, while reducing the expression of PTGS2 was identified as an important regulatory factor in photoaging HaCaT cells by VA and FA. Those DEGs of co-administration group focused on oxidative-reduction enzyme activity, skin growth, keratinization, and steroid biosynthesis. Apparently, the co-administration of VA and FA effectively mitigated the process of UVB-induced photoaging by reducing oxidative stress injury, inflammation responses, and regulating cell growth. This synergistic approach significantly slowed down the photoaging progression and improved the applied performance of VA in HaCaT cells.

The therapeutic effects of ADSCs on photoaging of skin induced by UVB irradiation.

Skin photoaging affects appearance and is associated with a variety of skin diseases, even skin cancer. Therefore, the prevention and treatment of skin photoaging is very important. However, there is a lack of effective evaluation methods, so it is an urgent problem to explore a comprehensive, non-invasive and in vivo evaluation method. Adipose-derived mesenchymal stem cells (ADSCs) are widely used to improve skin conditions as easier to obtain and positive effects. Recently, as the development of ultrasound technology, skin ultrasound has been widely used. Changes in skin layer and structure can be observed by high-frequency ultrasound (HFUS). In addition, Shear wave elastography (SWE) technology can be used to monitor the change of skin hardness. However, it is necessary to further explore the ultrasound parameters in interpreting histological changes. We simulate the progression and treatment process of human skin photoaging by using UVB-induced nude mice skin photoaging model and ADSCs injection. The analysis of the degree and therapeutic effect of skin photoaging was conducted by HFUS, SWE and to verify with histopathology. Our study aims to clarify the value of HFUS combined SWE techniques in evaluating the degree and therapeutic efficacy of skin photoaging, which provides theoretical basis for diagnosis and treatment evaluation systems.

Co-existing inorganic anions influenced the Norrish I and Norrish II type photoaging mechanism of biodegradable microplastics

The degradation of biodegradable plastics (BPs) in natural environments is constrained, and the mechanisms underlying their photoaging in aquatic settings remain inadequately understood. In view of this, this study systematically investigated the photoaging process of biodegradable Poly (butyleneadipate-co-terephthalate) microplastics (PBAT-MPs), which are more widely used. The investigation was carried out in the presence of common inorganic anions (Br−, Cl− and NO3−). The results of EPR, FTIR and FESEM tests, along with pseudo-first-order kinetics analyses, showed that the presence of NO3− promoted the photoaging of PBAT-MPs, while the presence of Br− and Cl− inhibited the photoaging of PBAT-MPs. In addition, the results of the Two-Dimensional Correlation Spectroscopy (2D-COS) analysis determined the order of the changes in the functional groups, revealing that the Norrish I and Norrish II reaction mechanisms are presented by PBAT-MPs during the aging process, and the process is closely related to the ion concentration and UV irradiation time. This study provides valuable insights for understanding the phototransformation process of BPs in natural aqueous environments.

Marine Bioactive Peptides: Anti-Photoaging Mechanisms and Potential Skin Protective Effects.

Skin photoaging, resulting from prolonged exposure to ultraviolet radiation, is a form of exogenous aging that not only impacts the aesthetic aspect of the skin but also exhibits a strong correlation with the onset of skin cancer. Nonetheless, the safety profile of non-natural anti-photoaging medications and the underlying physiological alterations during the process of photoaging remain inadequately elucidated. Consequently, there exists a pressing necessity to devise more secure interventions involving anti-photoaging drugs. Multiple studies have demonstrated the noteworthy significance of marine biomolecules in addressing safety concerns related to anti-photoaging and safeguarding the skin. Notably, bioactive peptides have gained considerable attention in anti-photoaging research due to their capacity to mitigate the physiological alterations associated with photoaging, including oxidative stress; inflammatory response; the abnormal expression of matrix metalloproteinase, hyaluronidase, and elastase; and excessive melanin synthesis. This review provides a systematic description of the research progress on the anti-photoaging and skin protection mechanism of marine bioactive peptides. The focus is on the utilization of marine bioactive peptides as anti-photoaging agents, aiming to offer theoretical references for the development of novel anti-photoaging drugs and methodologies. Additionally, the future prospects of anti-aging drugs are discussed, providing an initial reference for further research in this field.

Self-motivated photoaging of microplastics by biochar-dissolved organic matter under different pyrolysis temperatures

Dissolved organic matter (DOM) released from biochar (BDOM) can interact with microplastics (MPs) in the environment, inevitably affecting their environmental behaviour. Information regarding the influence of BDOM on MPs during photoaging and associated variations in the MP aging mechanism remains unclear. This study evaluated the effect of BDOM on the aging of polystyrene (PS) MPs. The results showed that among three pyrolysis temperatures, low-temperature BDOM significantly enhanced the photoaging process of PS MPs, with the smallest average particle size and highest carbonyl index value after 15 days of aging under light conditions. The DOM level decreased after 5 days, increased after 5–10 days, and stabilised after 15 d. BDOM accelerates PS MPs aging, leading to more DOM released from PS, which can be transformed into 1O2 via triplet-excited state (3DOM⁎ and 3PS⁎) to further enhance PS MPs aging, resulting in the realisation of the self-accelerated aging process of PS MPs. 1O2 plays a crucial role in the self-motivated accelerated aging process of PS MPs. These findings provide new insights into the effects of the DOM structure and composition on reactive oxygen species generation during MPs aging.

Photo-aging of brominated epoxy microplastics in water under simulated solar irradiation.

Microplastics have become an increasingly concerning pollutant in aquatic environments, and photodegradation is their main degradation pathway in water. Gaining insight into the transformation process of microplastics will enhance our understanding of their behavior and destiny in natural environments. This paper studied the aging process of BER microplastics in aquatic environments under simulated sunlight and investigated the changes in the physical and chemical properties of microplastics and the changes in the leachate. During the photodegradation process, BER-MPs underwent extensive oxidation and reduction in particle size, and the originally smooth surface developed numerous voids, accompanied by yellowing. Introduction of O atoms in the molecular chains increased their hydrophilicity, resulting in the polymer chains breaking away from the plastic particles and dissolving in water. Also, once BER was excited by light, environmentally persistent free radicals are produced on its surface. Moreover, the breaking of C-Br bonds occurred during the photodegradation process of BER-MPs, which suggested that tetrabromobisphenol A would be transformed during the photoaging process of BER even if it was covalently bound to BER.

Aging kinetics and mechanisms of polystyrene microplastic in water under sunlight irradiation: Effects of inorganic cations

The effects of chemical components in water on the photochemical transformation of microplastics (MPs) have been well documented, but inorganic cations are often considered inert and ignored. This work studied the photoaging kinetics and mechanisms of polystyrene microplastic (PS-MP) in natural water bodies when common inorganic cations were present at ambient concentrations, including Fe(Ⅲ), NH4+, Ca2+, and Na+. Unlike previous understanding, Fe(Ⅲ) inhibited the photodegradation of MPs by mediating the direct photodegradation of MPs rather than the indirect pathway. Also, NH4+ inhibited PS-MP photoaging, while Ca2+ and Na+ had no effect. Specifically, Fe(Ⅲ) (5 μmol/L) and NH4+ (0.1 mmol/L) reduced the photoaging rate constant (k) to 0.00618 d-1 and 0.00644 d-1, respectively, compared with PS-H2O (k = 0.00705 d-1). With increasing cations’ concentration, the inhibitory effect of Fe(Ⅲ) and NH4+ on PS-MP photoaging was strengthened. According to the results of the reactive oxygen species quenching experiment and ultraviolet–visible spectrum, it was found that light shielding by Fe(Ⅲ) and depletion of hydroxyl radical (•OH) by NH4+ were responsible for the inhibition of photoaging of PS-MP. This work provides new theoretical support for further research on the photoaging process of MPs in the natural water environment.

Anticorrosive and antimicrobial efficiency of photopolymerizable phosphorus (meth)acrylate oligomers-based coating materials

Novel photopolymerizable phosphorus (meth)acrylate oligomers were verified as anticorrosive and antimicrobial coating materials. Oligomers containing P-atoms were prepared by a solution-free UV-initiated telomerization process of aliphatic (meth)acrylates and styrene in the presence of different organic phosphorus compounds (P-telogens). The influence of the P-telogen structure on the photoaging process of coatings, as well as their anticorrosion and antibacterial properties was investigated. Relatively the highest anticorrosive efficiency was revealed for a varnish based on a telomers syrup containing dibutyl phosphite (DBPh) and dibutyl phosphate (DBP) due to the relatively long alkyl chain. In turn, UV-photocurable coatings exhibited moderate antibacterial and good anti-yeast activity but the best properties were found for the coating with dimethyl phosphite (DMPh). The higher resistance to photodegradation was observed in the case of the diphenyl phosphite (DPPh) due to the large phenyl substituent. Regardless of the structure of the organophosphorus compound, all coatings showed excellent adhesion to the glass substrate.