Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Irina A. Doroshenko"'
Autor:
Arseniy A. Pypin, Anna V. Shik, Irina A. Stepanova, Irina A. Doroshenko, Tatyana A. Podrugina, Mikhail K. Beklemishev
Publikováno v:
Sensors, Vol 23, Iss 18, p 7682 (2023)
Optical “fingerprints” are widely used for chemometrics-assisted recognition of samples of different types. An emerging trend in this area is the transition from obtaining “static” spectral data to reactions analyzed over time. Indicator reac
Externí odkaz:
https://doaj.org/article/becf14f462934d3d9ad797233172dd86
Autor:
Anna V. Shik, Irina A. Stepanova, Irina A. Doroshenko, Tatyana A. Podrugina, Mikhail K. Beklemishev
Publikováno v:
Sensors, Vol 23, Iss 9, p 4299 (2023)
Optical sensor arrays are widely used in obtaining fingerprints of samples, allowing for solutions of recognition and identification problems. An approach to extending the functionality of the sensor arrays is using a kinetic factor by conducting ind
Externí odkaz:
https://doaj.org/article/663d49228dbc439eb5719237a706f9e4
Autor:
Anna V. Shik, Irina A. Stepanova, Irina A. Doroshenko, Tatyana A. Podrugina, Mikhail K. Beklemishev
Publikováno v:
Chemosensors, Vol 10, Iss 2, p 88 (2022)
Array-based optical sensing is an efficient technique for the determination and discrimination of small organic molecules. This study is aimed at the development of a simple and rapid strategy for obtaining an optical response from a wide range of lo
Externí odkaz:
https://doaj.org/article/18255296b7654a09941cd72c24ab41b0
Autor:
Sofia A. Zakharenkova, Marina I. Lebedeva, Alexandra N. Lebedeva, Irina A. Doroshenko, Ksenya Yu Vlasova, Anastasiya A. Bartoshevich, Vladimir M. Senyavin, Sergey S. Abramchuk, George G. Krivtsov, Alexander A. Ezhov, Tatyana A. Podrugina, Natalia L. Klyachko, Mikhail K. Beklemishev
Publikováno v:
Molecules, Vol 26, Iss 24, p 7426 (2021)
Imaging-guided delivery is developed for hydrophobic drugs, and to a much lesser extent, hydrophilic ones. In this work we have designed a novel strategy for real-time monitoring of hydrophilic drug delivery. Traditionally, the drug and the dye are c
Externí odkaz:
https://doaj.org/article/fb149f8761c444b195dbb937f0a59d4a
Autor:
Anna V. Shik, Evgenii V. Skorobogatov, Ulyana A. Bliznyuk, Alexander P. Chernyaev, Valentina M. Avdyukhina, Polina Yu. Borschegovskaya, Sergey A. Zolotov, Maksim O. Baytler, Irina A. Doroshenko, Tatyana A. Podrugina, Mikhail K. Beklemishev
Publikováno v:
Food Chemistry. 414:135668
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d839009bc35cf10e427e711329fff4f2
https://doi.org/10.1016/j.foodchem.2023.135668
https://doi.org/10.1016/j.foodchem.2023.135668
Autor:
Tatiana M. Kulinich, Irina A. Doroshenko, Viatcheslav N. Azev, Tatyana A. Podrugina, Kamilla G. Aminulla, Alexander A. Shtila, Vladislav A. Vasilichin
Publikováno v:
Mendeleev Communications. 31:615-617
New βββ-alanine modified tricarbocyanines containing various substituents at quaternized nitrogen atoms were obtained. The peptide synthesis method has been utilized for further conjugation thus giving promising tricarbocyanines containing two sul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::debbe036dbe011036ccd04fff957f909
https://doi.org/10.1016/j.mencom.2021.09.008
https://doi.org/10.1016/j.mencom.2021.09.008
Autor:
Dmitry A. Veryutin, Irina A. Doroshenko, Ekaterina A. Martynova, Ksenia A. Sapozhnikova, Elena V. Svirshchevskaya, Anna V. Shibaeva, Alina A. Markova, Alexey A. Chistov, Natalya E. Borisova, Maxim V. Shuvalov, Vladimir A. Korshun, Vera A. Alferova, Tatyana A. Podrugina
Publikováno v:
Biochimie.
Along with bright fluorescence in the near-IR range, heptamethine carbocyanine dyes possess affinity to cancer cells. Thus, these dyes could be utilized as fluorescent labels and vectors for drug delivery as covalent conjugates with cytotoxic compoun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e78d07272b61f9853c75f8c8b3b9b2c7
https://pubmed.ncbi.nlm.nih.gov/36179940
https://pubmed.ncbi.nlm.nih.gov/36179940
Autor:
Vera Alferova, Ekaterina A. Martynova, Anna Shibaeva, Alexey A. Chistov, Dmitriy Veriutin, Elena V. Svirshchevskaya, Ksenya Sapozhnikova, Maxim V. Shuvalov, Irina A. Doroshenko, Natalya E. Borisova, Alina A. Markova, Vladimir A. Korshun, Tatyana A. Podrugina
Heptamethine carbocyanine dyes possess bright fluorescence in the near IR range and affinity to cancer cells. Thus, these dyes could be utilized as fluorescent labels and vectors for drug delivery in their covalent conjugates with cytotoxic compounds
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ecae40728859abf92417ce7b73416ef0
https://doi.org/10.33774/chemrxiv-2021-xqprl
https://doi.org/10.33774/chemrxiv-2021-xqprl
Autor:
Sofia A. Zakharenkova, Mikhail K. Beklemishev, Anna S. Kriveleva, Nikolai Yu. Polovkov, Irina A. Doroshenko, Ekaterina A. Katkova, Tatyana A. Podrugina
Publikováno v:
Methods and applications in fluorescence. 9(1)
The work is aimed at the search of selective fluorescent sensors without using specific artificial receptors, antibodies, enzymes etc. With this end in view, methods based on non-covalent binding of target analytes are sought. We observed dramatic ch
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f83b8263bdc8be6f739d7f1255769f3
https://pubmed.ncbi.nlm.nih.gov/33053517
https://pubmed.ncbi.nlm.nih.gov/33053517
Autor:
Irina A. Doroshenko, Sergei S. Abramchuk, Sofia A. Zakharenkova, Anna S. Kriveleva, Tatyana A. Vidinchuk, Mikhail K. Beklemishev, Tatyana A. Podrugina, Aleksandra N. Lebedeva, Ekaterina A. Katkova, Anna V. Shik
Publikováno v:
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy. 247
This study is aimed at developing sensing schemes without obtaining selective receptors. A series of simple carbocyanine dyes was synthesized, whose emission was quenched in water with formation of nanoparticles in the range of 20-100 nm. Fluorescenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41fe65d4d0ab090212ae142ec0fffa67
https://pubmed.ncbi.nlm.nih.gov/33147554
https://pubmed.ncbi.nlm.nih.gov/33147554