Anna Sukhanova

Dr. Anna Sukhanova


Research Focus & Metrics

Academic Career Length

4Years (2023-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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15 May 2023 in Molecules
Verified
Journal Article
Open access
PDF file
MGMakar Gerasimov
Makar Gerasimov
IPIrina Perova
Irina Perova
KEKonstantin I Eller
Konstantin I Eller
MAMichail Y. Akimov
Michail Y. Akimov
ASAnna Sukhanova
Anna Sukhanova
GRGalina Ramenskaya
Galina Ramenskaya
The purpose of this work was to study the qualitative and quantitative composition of the main groups of biologically active substances in the fresh fruits of five different varieties of black chokeberry (Aronia melanocarpa (Michx.) Elliot), carried out within the framework of the search for available and cost-effective raw materials for food product fortification. Samples of aronia chokeberry were grown at the Federal Scientific Center named after I.V. Michurin in the Tambov region of Russia. Using a modern chemical–analytical methodology, the contents and profiles of anthocyanin pigments, proanthocyanidins, flavonoids, hydroxycinnamic acids, organic acids (malic, quinic, succinic, and citric), monosaccharides, disaccharides, and sorbitol were determined in detail. Based on the results of the study, the most promising varieties were determined in terms of the content of the main biologically active substances.

1 December 2024 in Current Rheumatology Reviews
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Journal Article
Open access
PDF file
ASAnna Sukhanova
Anna Sukhanova
MGMariam A. Gilavian
Mariam A. Gilavian
EMElizaveta V. Melnik
Elizaveta V. Melnik
ESEvgenia V. Shikh
Evgenia V. Shikh
APAlexey E. Petukhov
Alexey E. Petukhov
GRGalina V. Ramenskaya
Galina V. Ramenskaya
Background: Ankylosing spondylitis (AS) is a chronic inflammatory disease known for causing pain, stiffness, and reduced mobility in the axial skeleton. Adalimumab, a tumor necrosis factor (TNF) inhibitor, has emerged as a promising therapeutic option for AS. Methods: This systematic review involved a comprehensive search of randomized controlled trials related to AS treatment, conducted in major databases such as MEDLINE, Google Scholar, and PubMed. The search terms encompassed ankylosing spondylitis, adalimumab, methotrexate, other non-biologic DMARDs, glucocorticoids, NSAIDs, and analgesics. A total of 14 randomized controlled trials with 4,500 participants were included in the review. Results: The review's results revealed that adalimumab demonstrated notable superiority when compared to a placebo. It effectively reduced disease activity, improved physical function, and lowered inflammatory markers such as C-reactive protein and erythrocyte sedimentation rate. Adalimumab demonstrated a favorable safety profile, with adverse events comparable to those observed with placebo. Conclusion: Based on the results, adalimumab is deemed an effective treatment for AS, showcasing its potential as a first-line therapeutic option. Notably, no significant increase in adverse events was observed compared to placebo. However, the conclusion emphasizes the need for further studies with extended follow-up durations to ascertain the long-term efficacy and safety of adalimumab in AS management. This systematic review provides valuable insights supporting the use of adalimumab in the treatment of AS and underscores the importance of ongoing investigations into its long-term effects to optimize its clinical utilization in AS patients.

29 October 2026 in Molbank
Verified
Journal Article
Open access
PDF file
VKVladimir Khodonov
Vladimir Khodonov
SUStanislava R. Usova
Stanislava R. Usova
NGNatalia V. Vasil'evna Gorphinchenko
Natalia V. Vasil'evna Gorphinchenko
ASAnna Sukhanova
Anna Sukhanova
VKVladimir Kokorekin
Vladimir Kokorekin
A two-stage synthesis of the novel compound 1-(1-methyl-5-thiocyanato-1H-pyrrol-2-yl)-3-nitro-1H-1,2,4-triazole utilizing electrochemistry as an environmentally benign tool is reported. The structure of the target molecule was confirmed by 1H and 13C NMR spectroscopy and HRMS. The compound exhibits antibacterial and antifungal activity comparable to chloramphenicol, ciprofloxacin, and fluconazole.