Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Natalia R. Onishchenko"'
Autor:
Natalia R. Onishchenko, Alexey A. Moskovtsev, Maria K. Kobanenko, Daria S. Tretiakova, Anna S. Alekseeva, Dmitry V. Kolesov, Anna A. Mikryukova, Ivan A. Boldyrev, Marina R. Kapkaeva, Olga N. Shcheglovitova, Nicolai V. Bovin, Aslan A. Kubatiev, Olga V. Tikhonova, Elena L. Vodovozova
Publikováno v:
Pharmaceutics, Vol 15, Iss 6, p 1754 (2023)
Previously, we showed in the human umbilical vein endothelial cells (HUVECs) model that a liposome formulation of melphalan lipophilic prodrug (MlphDG) decorated with selectin ligand tetrasaccharide Sialyl Lewis X (SiaLeX) undergoes specific uptake b
Externí odkaz:
https://doaj.org/article/f7f68554b7634b1e86713e7a8d0e8ddb
Autor:
Maria K. Kobanenko, Daria S. Tretiakova, Ekaterina S. Shchegravina, Nadezhda V. Antipova, Ivan A. Boldyrev, Alexey Yu. Fedorov, Elena L. Vodovozova, Natalia R. Onishchenko
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 3, p 1034 (2022)
To assess the stability and efficiency of liposomes carrying a phospholipase A2-sensitive phospholipid-allocolchicinoid conjugate (aC-PC) in the bilayer, egg phosphatidylcholine and 1-palmitoyl-2-oleoylphosphatidylglycerol-based formulations were tes
Externí odkaz:
https://doaj.org/article/04466fae14a64e3ca184935ff4e9ec6b
Autor:
Vodovozova, Natalia R. Onishchenko, Alexey A. Moskovtsev, Maria K. Kobanenko, Daria S. Tretiakova, Anna S. Alekseeva, Dmitry V. Kolesov, Anna A. Mikryukova, Ivan A. Boldyrev, Marina R. Kapkaeva, Olga N. Shcheglovitova, Nicolai V. Bovin, Aslan A. Kubatiev, Olga V. Tikhonova, Elena L.
Publikováno v:
Pharmaceutics; Volume 15; Issue 6; Pages: 1754
Previously, we showed in the human umbilical vein endothelial cells (HUVECs) model that a liposome formulation of melphalan lipophilic prodrug (MlphDG) decorated with selectin ligand tetrasaccharide Sialyl Lewis X (SiaLeX) undergoes specific uptake b
Publikováno v:
Acta Biomaterialia. 134:57-78
Although an established drug delivery platform, liposomes have not fulfilled their true potential. In the body, interactions of liposomes are mediated by the layer of plasma proteins adsorbed on the surface, the protein corona. The review aims to col
Autor:
Alexey Natykan, Elena L. Vodovozova, Natalia R. Onishchenko, Diana Arantseva, Anton Lokhmotov, Ivan A. Boldyrev, Dmitry Shobolov, Elena V. Svirshchevskaya, Daria Tretiakova, Anna Alekseeva, Roman Kamyshinsky
Publikováno v:
Current Drug Delivery. 17:312-323
Background:: Recently we developed a scalable scheme of synthesis of melphalan ester conjugate with 1,2-dioleoyl-sn-glycerol (MlphDG) and a protocol for the fabrication of its lyophilized liposomal formulation. Objective: Herein we compared this new
Autor:
Timur R. Galimzyanov, Andrey Yu. Chernyadyev, Ivan A. Boldyrev, Oleg V. Batishchev, Natalia R. Onishchenko, Daria Tretiakova, Pavel E. Volynsky, A. S. Alekseeva
Publikováno v:
Soft Matter. 16:3216-3223
Archaeal lipids ensure unprecedented stability of archaea membranes in extreme environments. Here, we incorporate a characteristic structural feature of an archaeal lipid, the cyclopentane ring, into hydrocarbon chains of a short-chain (C12) phosphat
Autor:
Elena L. Vodovozova, Daria Tretiakova, Judith Kuntsche, Natalia R. Onishchenko, Elena V. Kudryashova, Irina M. Le-Deigen
Publikováno v:
Pharmaceutics, Vol 13, Iss 473, p 473 (2021)
Pharmaceutics
Volume 13
Issue 4
Tretiakova, D, Le-Deigen, I, Onishchenko, N, Kuntsche, J, Kudryashova, E & Vodovozova, E 2021, ' Phosphatidylinositol stabilizes fluid-phase liposomes loaded with a melphalan lipophilic prodrug ', Pharmaceutics, vol. 13, no. 4, 473 . https://doi.org/10.3390/pharmaceutics13040473
Pharmaceutics
Volume 13
Issue 4
Tretiakova, D, Le-Deigen, I, Onishchenko, N, Kuntsche, J, Kudryashova, E & Vodovozova, E 2021, ' Phosphatidylinositol stabilizes fluid-phase liposomes loaded with a melphalan lipophilic prodrug ', Pharmaceutics, vol. 13, no. 4, 473 . https://doi.org/10.3390/pharmaceutics13040473
Previously, a liposomal formulation of a chemotherapeutic agent melphalan (Mlph) incorporated in a fluid lipid bilayer of natural phospholipids in the form of dioleoylglyceride ester (MlphDG) was developed and the antitumor effect was confirmed in mo
Autor:
Elena L. Vodovozova, Natalia R. Onishchenko, D. C. Tretiakova, I. S. Frolova, O. N. Shcheglovitova, A. A. Babayants, S. V. Khaidukov
Publikováno v:
Acta Naturae
Previously, we showed that incorporation of methotrexate (MTX) in the form of a lipophilic prodrug (MTXDG) in 100-nm lipid bilayer liposomes of egg phosphatidylcholine can allow one to reduce toxicity and improve the antitumor efficiency of MTX in a
Autor:
Elena L. Vodovozova, Julian G. Molotkovsky, Roman G. Efremov, Anton O. Chugunov, Ivan A. Boldyrev, Natalia R. Onishchenko, A. S. Alekseeva, Pavel E. Volynsky
Publikováno v:
Russian Journal of Bioorganic Chemistry. 44:732-739
Preparation of liposomal formulations containing water-soluble drugs in the form of lipophilic prodrugs in their lipid bilayer is of considerable interest. Previously, we synthesized doxorubicin dioleoyl glyceride and oleoyl conjugates intended for i
Publikováno v:
Russian Journal of Bioorganic Chemistry. 43:678-689
Interactions of 100-nm liposomes prepared from egg yolk phosphatidylcholine and baker’s yeast phosphatidylinositol carrying diglyceride ester conjugates of melphalan (Mlph-liposomes) and methotrexate (MTX-liposomes) in the bilayer with blood plasma