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Mendeleev Communications, 2017, Volume 27, Issue 1, Pages 47–49
DOI: https://doi.org/10.1016/j.mencom.2017.01.014
(Mi mendc1891)
 

This article is cited in 9 scientific papers (total in 9 papers)

Communications

A pH-controllable protein container for the delivery of hydrophobic porphyrins

N. Sh. Lebedevaa, E. S. Yurinaa, Yu. A. Gubareva, O. I. Koifmanb

a G.A. Krestov Institute of Solution Chemistry, Russian Academy of Sciences, Ivanovo, Russian Federation
b Research Institute of Macroheterocycles, Ivanovo State University of Chemistry and Technology, Ivanovo, Russian Federation
Full-text PDF (744 kB) Citations (9)
Abstract: The possibility of creating a pH-controllable protein container for the delivery of hydrophobic porphyrins as photosensitizers in cancer cells has been demonstrated.
Document Type: Article
Language: English


Citation: N. Sh. Lebedeva, E. S. Yurina, Yu. A. Gubarev, O. I. Koifman, “A pH-controllable protein container for the delivery of hydrophobic porphyrins”, Mendeleev Commun., 27:1 (2017), 47–49
Linking options:
  • https://www.mathnet.ru/eng/mendc1891
  • https://www.mathnet.ru/eng/mendc/v27/i1/p47
  • This publication is cited in the following 9 articles:
    1. O. I. Koifman, N. Sh. Lebedeva, E. S. Yurina, Yu. A. Gubarev, S. A. Syrbu, A. N. Kiselev, M. A. Lebedev, “Interaction of Lyophilic Zinc(II) Porphyrins with Bovine Serum Albumin”, Russ J Coord Chem, 50:5 (2024), 326  crossref
    2. O. I. Koifman, N. S. Lebedeva, E. S. Yurina, Yu. A. Gubarev, S. A. Syrbu, A. N. Kiselev, M. A. Lebedev, “Interaction of Lyophilic Zinc(II) Porphyrins with Bovine Serum Albumin”, Koordinacionnaâ himiâ, 50:6 (2024), 374  crossref
    3. Yu. A. Gubarev, E. S. Yurina, N. Sh. Lebedeva, “Detection of green fluorescence in serum albumin upon excitation with 375 nm light: revealing new fluorescent properties”, Mendeleev Commun., 34:3 (2024), 421–423  mathnet  crossref
    4. N. Sh. Lebedeva, O. I. Koifman, “Supramolecular Systems Based on Macrocyclic Compounds with Proteins: Application Prospects”, Russ J Bioorg Chem, 48:1 (2022), 1  crossref
    5. Lin Li, Yan Wang, Tao Huang, Xiaodong He, Kai Zhang, En-Tang Kang, Liqun Xu, “Cationic porphyrin-based nanoparticles for photodynamic inactivation and identification of bacteria strains”, Biomater. Sci., 10:11 (2022), 3006  crossref
    6. Natalya Sh Lebedeva, Elena S. Yurina, Sabir S. Guseinov, Yury A. Gubarev, Sergey A. Syrbu, “The interaction of 5,10,15,20-tetrakis [4- (2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl) phenyl] porphine with biopolymers”, Dyes and Pigments, 162 (2019), 266  crossref
    7. T. S. Lyubova, N. S. Zakharycheva, E. A. Zakharychev, S. A. Lermontova, E. Yu. Ladilina, L. G. Klapshina, “Polysiloxane based on hydroxyl-containing monomer. Preparation, properties and biomedical application”, Russ Chem Bull, 68:5 (2019), 1075  crossref
    8. S. V. Blagodarov, G. A. Zheltukhina, A. S. Urban, E. E. Shishkina, V. E. Nebolsin, “Synthesis of cyclic norspermidine derivative of protohemin IX”, Mendeleev Commun., 29:2 (2019), 209–211  mathnet  crossref
    9. K. A. Zhdanova, A. V. Ezhov, N. A. Bragina, A. F. Mironov, “Synthesis of new binary porphyrin–cyanine conjugates and their self-aggregation in organic-aqueous media”, Mendeleev Commun., 28:6 (2018), 626–628  mathnet  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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