4.6 Article

Diabetic skin and UV light: Protection by antioxidants

Journal

EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES
Volume 127, Issue -, Pages 1-8

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.ejps.2018.10.010

Keywords

Diabetes; Mouse; Skin; Dehydration; Antioxidants; UV radiation

Ask authors/readers for more resources

Non-invasive biophysical methods were used to study the effect of antioxidant gels, which were prepared from Pinus halepensis bark extracts, vitamin C and water, on the skin of diabetic hairless mice irradiated with UV radiation of 1 and 2 minimal erythemal doses (MEDs). The calculated transepidermal water loss (TEWL) for diabetic mice was found to be fivefold higher on day 11 after irradiation, and in all cases, the TEWL values converged to their initial values on day 21. Both pinus and vitamin C gels inhibited the dehydration of the skin, while water gels did not show similar protection. At low dose of UV-irradiation (1 MED), vitamin C gels showed the best hydration, while by doubling the UV dose, pinus gels induced significant skin-protective effects. Upon irradiation, the mice treatment with pinus gel showed diminished inflammation in comparison with the other gels. Pinus also inhibited the hyperkeratosis of skin. As expected, 2 MEDs caused greater skin damage, such as inflammation, dryness, oxidative stress and rides (aging) compared to the damage induced by 1 MED.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

Article Chemistry, Applied

Catalytic transformation of the marine polysaccharide ulvan into rare sugars, tartaric and succinic acids

Iunia Podolean, Simona M. Coman, Cristina Bucur, Cristian Teodorescu, Stefanos Kikionis, Efstathia Ioannou, Vassilios Roussis, Ana Primo, Hermenegildo Garcia, Vasile Parvulescu

Summary: Ulva rigida, a green macroalga, is considered a promising feedstock for biorefinary due to its fast growth and widespread distribution. The cell walls of U. rigida contain a sulfated glucuronorhamnan polysaccharide called ulvan, which, due to its high sulfate content, can be efficiently recovered as rhamnose through hydrothermal autohydrolysis at 130 degrees C. Under different catalytic conditions, including triflate-based graphene oxide, significant amounts of tartaric acid and succinic acid can also be obtained. The catalyst shows good reusability, maintaining its activity for at least five consecutive cycles.

CATALYSIS TODAY (2022)

Article Chemistry, Medicinal

Aerophobin-1 from the Marine Sponge Aplysina aerophoba Modulates Osteogenesis in Zebrafish Larvae

Marta Carnovali, Maria Letizia Ciavatta, Ernesto Mollo, Vassilios Roussis, Giuseppe Banfi, Marianna Carbone, Massimo Mariotti

Summary: With longer life expectancy, there has been an increased focus on discovering new healing agents for age-related disorders, including bone diseases. Marine organisms, known for their diverse bioactive metabolites, are being recognized as potential sources for therapeutic options. Additionally, the zebrafish model has proven to be an efficient and cost-effective platform for screening molecules that regulate bone development. In this study, the effects of the crude acetonic extract from the marine sponge Aplysina aerophoba and its bromotyrosine components on bone development were evaluated using zebrafish larvae. The results led to the identification of aerophobin-1 as a promising candidate for regenerative medicine and a potential novel therapeutic option for osteoporosis treatment.

MARINE DRUGS (2022)

Article Chemistry, Medicinal

Synthesis and Antifouling Activity Evaluation of Analogs of Bromosphaerol, a Brominated Diterpene Isolated from the Red Alga Sphaerococcus coronopifolius

Kyriakos C. Prousis, Stefanos Kikionis, Efstathia Ioannou, Silvia Morgana, Marco Faimali, Veronica Piazza, Theodora Calogeropoulou, Vassilios Roussis

Summary: Marine biofouling is a global issue that causes significant economic problems for the shipping industry and aquaculture companies, and its prevention often leads to adverse environmental effects. In this study, bromosphaerol and its derivatives were found to have strong antifouling activity and low toxicity, making them potential candidates for the development of effective antifouling agents.

MARINE DRUGS (2022)

Article Chemistry, Medicinal

Antifouling Activity of Halogenated Compounds Derived from the Red Alga Sphaerococcus coronopifolius: Potential for the Development of Environmentally Friendly Solutions

Maxence Quemener, Stefanos Kikionis, Marilyne Fauchon, Yannick Toueix, Fanny Aulanier, Antonios M. Makris, Vassilios Roussis, Efstathia Ioannou, Claire Hellio

Summary: This study identified two active compounds against key biofoulers, which can be produced by cultivable algae, showing great potential. This research approach is beneficial for discovering new environmentally friendly antifouling compounds.

MARINE DRUGS (2022)

Review Chemistry, Medicinal

What Was Old Is New Again: The Pennate Diatom Haslea ostrearia (Gaillon) Simonsen in the Multi-Omic Age

Noujoud Gabed, Frederic Verret, Aurelie Peticca, Igor Kryvoruchko, Romain Gastineau, Orlane Bosson, Julie Seveno, Olga Davidovich, Nikolai Davidovich, Andrzej Witkowski, Jon Bent Kristoffersen, Amel Benali, Efstathia Ioannou, Aikaterini Koutsaviti, Vassilios Roussis, Helene Gateau, Suliya Phimmaha, Vincent Leignel, Myriam Badawi, Feriel Khiar, Nellie Francezon, Mostefa Fodil, Pamela Pasetto, Jean-Luc Mouget

Summary: The marine pennate diatom Haslea ostrearia, known for its blue pigment marennine, has potential applications in various industries. The discovery of a new blue Haslea species revealed previously unknown biodiversity. This study advocates for establishing H. ostrearia as a new model organism, highlighting its advantages and the challenges involved.

MARINE DRUGS (2022)

Article Biochemistry & Molecular Biology

Losartan Interactions with 2-Hydroxypropyl-β-CD

Vasiliki Palli, Georgios Leonis, Nikoletta Zoupanou, Nikitas Georgiou, Maria Chountoulesi, Nikolaos Naziris, Demeter Tzeli, Costas Demetzos, Georgia Valsami, Konstantinos D. Marousis, Georgios A. Spyroulias, Thomas Mavromoustakos

Summary: In this study, the molecular interactions between losartan potassium salt and 2-hydroxypropyl-beta-cyclodextrin were investigated using experimental methods including Differential Scanning Calorimetry, Nuclear Magnetic Resonance, and Molecular Dynamics. The results demonstrated the complexation of losartan potassium salt with 2-hydroxypropyl-beta-cyclodextrin, suggesting the potential for further biological experiments.

MOLECULES (2022)

Article Chemistry, Medicinal

Valorization of Fish Waste: Isolation and Characterization of Acid- and Pepsin-Soluble Collagen from the Scales of Mediterranean Fish and Fabrication of Collagen-Based Nanofibrous Scaffolds

Leto-Aikaterini Tziveleka, Stefanos Kikionis, Labros Karkatzoulis, Kostas Bethanis, Vassilios Roussis, Efstathia Ioannou

Summary: By comparing the collagen content of fish scales from five Mediterranean fish species and Atlantic salmon, it was found that fish scales could be efficiently utilized for the production of high added-value biomaterials. The isolated collagenous materials showed typical electrophoretic patterns of type I collagen, and were morphologically and physicochemically characterized for potential applications in the biomedical sector.

MARINE DRUGS (2022)

Article Chemistry, Medicinal

Secondary Metabolites with Anti-Inflammatory Activity from Laurencia majuscula Collected in the Red Sea

Mohamed A. A. Tammam, Maria G. G. Daskalaki, Nikolaos Tsoureas, Ourania Kolliniati, Aldoushy Mahdy, Sotirios C. C. Kampranis, Christos Tsatsanis, Vassilios Roussis, Efstathia Ioannou

Summary: The chemical investigation of the organic extract of the red alga Laurencia majuscula resulted in the isolation of several new natural products with significant anti-inflammatory activity. The structures and configurations of these natural products were determined through NMR, MS, and single-crystal X-ray diffraction analysis. The most prominent anti-inflammatory activity was exhibited by compounds 5 and 18.

MARINE DRUGS (2023)

Article Chemistry, Medicinal

Development of Novel Pharmaceutical Forms of the Marine Bioactive Pigment Echinochrome A Enabling Alternative Routes of Administration

Stefanos Kikionis, Paraskevi Papakyriakopoulou, Panagiotis Mavrogiorgis, Elena A. A. Vasileva, Natalia P. P. Mishchenko, Sergey A. A. Fedoreyev, Georgia Valsami, Efstathia Ioannou, Vassilios Roussis

Summary: By incorporating Echinochrome A (EchA) isolated from sea urchins into electrospun micro-/nanofibrous matrices composed of polycaprolactone and polyvinylpyrrolidone, the dissolution and bioavailability of EchA can be improved, making it suitable for oral administration, while also increasing its stability and solubility.

MARINE DRUGS (2023)

Article Chemistry, Medicinal

Development of Bi- and Tri-Layer Nanofibrous Membranes Based on the Sulfated Polysaccharide Carrageenan for Periodontal Tissue Regeneration

Stefanos Kikionis, Konstantina Iliou, Aikaterini G. Karra, Georgios Polychronis, Ioannis Choinopoulos, Hermis Iatrou, George Eliades, Efthymia Kitraki, Ioulia Tseti, Spiros Zinelis, Efstathia Ioannou, Vassilios Roussis

Summary: Nanofibrous GTR/GBR membranes based on carrageenans and other biocompatible polymers were developed for the regeneration of periodontal tissue. The membranes exhibited favorable morphological, thermal, and mechanical properties, and demonstrated the potential for periodontal tissue regeneration through evaluation of cell attachment, biocompatibility, and osteogenic differentiation.

MARINE DRUGS (2023)

Article Chemistry, Medicinal

Butanolides and Butenolides from a Marine-Derived Streptomyces sp. Exert Neuroprotective Activity through Activation of the TrkB Neurotrophin Receptor

Paolo Giaccio, Despoina Charou, Dafni-Ioanna Diakaki, Anna Chita, Achille Gravanis, Ioannis Charalampopoulos, Vassilios Roussis, Efstathia Ioannou

Summary: Neurodegenerative diseases are incurable and debilitating conditions. Currently, effective therapies for most neurodegenerative disorders are lacking. A study evaluated the activity of various extracts on TrkB-expressing cells and found that a certain strain of actinobacteria called Streptomyces sp. BI0788 exhibited neuroprotective activity. Further chemical analysis resulted in the identification of new and previously known compounds, some of which showed protective effects on cells through the activation of TrkB.

MARINE DRUGS (2023)

Article Biochemistry & Molecular Biology

Widespread biosynthesis of 16-carbon terpenoids in bacteria

Yao-Tao Duan, Aikaterini Koutsaviti, Maria Harizani, Codruta Ignea, Vassilios Roussis, Yong Zhao, Efstathia Ioannou, Sotirios C. Kampranis

Summary: By combining gene mining, biochemical characterization, and chemical structure analysis, this study reveals the existence of an extensive class of terpenoids with 16 carbon atoms in bacteria.

NATURE CHEMICAL BIOLOGY (2023)

Article Engineering, Biomedical

Development of Ulvan-Containing Liposomes as Antibacterial Drug Delivery Platforms

Leto-Aikaterini Tziveleka, Natassa Pippa, Efstathia Ioannou, Costas Demetzos, Vassilios Roussis

Summary: Liposomes, as nanocarriers for antimicrobial delivery, have been extensively studied due to their safety and targeting ability. However, their use is limited by lack of stability and non-specific interaction with cells and proteins. To overcome these limitations, ulvan, a marine sulfated polysaccharide, was incorporated into liposomes to improve their physicochemical properties and stability. Interactions between ulvan and neutral, negatively, and positively charged lipids were studied using Differential Scanning Calorimetry. Ulvan-containing liposomes were prepared based on the results, with ulvan interacting with lipid chains and polar groups in the liposomal bilayer. Fusidic acid, a model antibacterial drug, was entrapped in the liposomes and the antibacterial activity against Staphylococcus aureus was evaluated. The physicochemical properties, stability, morphology, and entrapment efficiency of the liposomal formulations were determined.

JOURNAL OF FUNCTIONAL BIOMATERIALS (2022)

Article Pharmacology & Pharmacy

Analysis of stabilization mechanisms in β-lactoglobulin-based amorphous solid dispersions by experimental and computational approaches

Xuezhi Zhuo, Vito Fodera, Per Larsson, Zarah Schaal, Christel A. S. Bergstrom, Korbinian Lobmann, Aleksei Kabedev

Summary: Our previous work demonstrated that beta-lactoglobulin-stabilized amorphous solid dispersion (ASD) loaded with 70 % indomethacin remains stable for over 12 months. We further investigated the stabilization mechanisms by testing five other drug molecules and using experimental techniques and molecular dynamics simulations. The results showed that steric confinement, hydrogen bonding, and the glass transition temperature of the drug molecule play important roles in stabilizing ASDs with high drug loadings.

EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2024)

Article Pharmacology & Pharmacy

Do the enantiomers of ketamine bind enantioselectively to human serum albumin?

Sebastian Schmidt, Ulrike Holzgrabe

Summary: The binding of drugs to plasma proteins, such as human serum albumin (HSA), is crucial for determining pharmacokinetic parameters. This study investigated the enantioselective binding of S- and R-ketamine to HSA. It was found that ketamine has weak affinity to HSA, with no significant differences in binding behavior between the individual enantiomers and the racemate. The aromatic ring and N-methyl group were identified as the most strongly involved structural moieties in the binding of ketamine to HSA.

EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2024)

Article Pharmacology & Pharmacy

Targeting fusion proteins of the interleukin family: A promising new strategy for the treatment of autoinflammatory diseases

Yuchen Zhao, Han Wang, Lin Jin, Ziwei Zhang, Lianghu Liu, Mengqi Zhou, Xianzheng Zhang, Lingling Zhang

Summary: Interleukins (ILs) are important for communication between immune cells and non-immune cells, but dysregulation of ILs expression is a characteristic of autoinflammatory diseases. Drugs targeting ILs have significant clinical benefits, but may also cause adverse reactions. Fusion protein technology, with its ability to enhance therapeutic efficacy, has been explored for developing anti-inflammatory drugs. This review discusses the efficacy of fusion protein drugs developed with ILs or their receptors in treating autoinflammatory diseases, highlighting the potential of this technology in future anti-inflammatory drug development.

EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2024)

Article Pharmacology & Pharmacy

The use of polymorphic state modifiers in solid lipid microparticles: The role of structural modifications on drug release performance

Serena Bertoni, Elena Simone, Stefano Sangiorgi, Beatrice Albertini, Nadia Passerini

Summary: This study investigated the correlation between the structure and release properties of solid lipid microparticles (MPs) with different liquid additives. The additives accelerated the conversion of the unstable alpha-form of tristearin to the stable beta-polymorph and caused structural modifications in the MPs. The presence of additives prolonged the drug release in water and resulted in higher release profiles in biorelevant media. The findings suggest that the release behavior can be influenced by the polymorphism and supramolecular-level structural modification of lipid formulations containing crystal modifiers.

EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2024)

Article Pharmacology & Pharmacy

Altering distribution profile of palbociclib by its prodrugs

Juulia Jarvinen, Ahmed B. Montaser, Santosh Kumar Adla, Jukka Leppanen, Marko Lehtonen, Kati-Sisko Vellonen, Tuomo Laitinen, Aaro Jalkanen, William F. Elmquist, Juri Timonen, Kristiina M. Huttunen, Jarkko Rautio

Summary: This study attempted to alter the brain distribution pattern of Palbociclib by creating and assessing two novel prodrugs. Although the prodrug design did not significantly improve Palbociclib brain delivery, the study provides valuable insights for future prodrug development and drug delivery strategies targeting specific transporters.

EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2024)

Review Pharmacology & Pharmacy

The prescription design and key properties of nasal gel for CNS drug delivery: A review

Miao Wang, Xinyu Ma, Shiyu Zong, Yaqiong Su, Rui Su, Hong Zhang, Yang Liu, Chunliu Wang, Ye Li

Summary: This article discusses the potential and limitations of nasal administration in central nervous system drug delivery. Nasal gel viscosity can alleviate the impact of nasal mucociliary clearance on drug delivery, and materials such as gellan gum, chitosan, carbomer, cellulose, and poloxamer can be used to prepare nasal gels.

EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2024)

Article Pharmacology & Pharmacy

Impact of drug load and polymer molecular weight on the 3D microstructure of printed tablets

Bjarke Strom Larsen, Eric Kissi, Liebert Parreiras Nogueira, Natalja Genina, Ingunn Tho

Summary: This study investigates the influence of drug load and polymer molecular weight on the structure of 3D printed tablets. The results show that drug load and polymer molecular weight have a significant impact on the porosity and size of the tablets, while the effect of drug load on the total porosity of the tablets is minimal.

EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2024)

Article Pharmacology & Pharmacy

Ultrasound-guided periadventitial administration of rapamycin-fibrin glue attenuates neointimal hyperplasia in the rat carotid artery injury model

Zhentao Qiao, Fuhang Wang, Dongjian Han, Yuansong Zhuang, Qingjiao Jiang, Yi Zhang, Miaomiao Liu, Quanxu An, Zhiwei Wang, Deliang Shen

Summary: In this study, it was demonstrated that periadventitial delivery of rapamycin-fibrin glue (RPM-FG) can inhibit intimal hyperplasia (IH) in a rat carotid artery injury model without compromising re-endothelialization. This provides a promising direction for the future development of a safe, effective, and minimally invasive perivascular drug delivery method to treat vascular disease.

EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2024)

Article Pharmacology & Pharmacy

Designing greener active pharmaceutical ingredients: Insights from pharmaceutical industry into drug discovery and development

Neele Puhlmann, Rodrigo Vidaurre, Klaus Kuemmerer

Summary: Active pharmaceutical ingredients and their metabolites and transformation products are pollutants that can harm human and environmental health. Designing greener APIs is an effective strategy to address this issue. The drug discovery and development process can incorporate environmental parameters to achieve this design, and this process is highly flexible.

EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES (2024)