Please use this identifier to cite or link to this item: https://elar.urfu.ru/handle/10995/131234
Title: Carborane-Containing Folic Acid bis-Amides: Synthesis and In Vitro Evaluation of Novel Promising Agents for Boron Delivery to Tumour Cells
Authors: Gruzdev, D. A.
Telegina, A. A.
Levit, G. L.
Solovieva, O. I.
Gusel’nikova, T. Y.
Razumov, I. A.
Krasnov, V. P.
Charushin, V. N.
Issue Date: 2022
Publisher: MDPI
Citation: Gruzdev, DA, Telegina, AA, Levit, GL, Solovieva, OI, Gusel’nikova, TY, Razumov, IA, Krasnov, VP & Charushin, VN 2022, 'Carborane-Containing Folic Acid bis-Amides: Synthesis and In Vitro Evaluation of Novel Promising Agents for Boron Delivery to Tumour Cells', International Journal of Molecular Sciences, Том. 23, № 22, 13726. https://doi.org/10.3390/ijms232213726
Gruzdev, D. A., Telegina, A. A., Levit, G. L., Solovieva, O. I., Gusel’nikova, T. Y., Razumov, I. A., Krasnov, V. P., & Charushin, V. N. (2022). Carborane-Containing Folic Acid bis-Amides: Synthesis and In Vitro Evaluation of Novel Promising Agents for Boron Delivery to Tumour Cells. International Journal of Molecular Sciences, 23(22), [13726]. https://doi.org/10.3390/ijms232213726
Abstract: The design of highly selective low-toxic, low-molecular weight agents for boron delivery to tumour cells is of decisive importance for the development of boron neutron capture therapy (BNCT), a modern efficient combined method for cancer treatment. In this work, we developed a simple method for the preparation of new closo- and nido-carborane-containing folic acid bis-amides containing 18–20 boron atoms per molecule. Folic acid derivatives containing nido-carborane residues were characterised by high water solubility, low cytotoxicity, and demonstrated a good ability to deliver boron to tumour cells in in vitro experiments (up to 7.0 µg B/106 cells in the case of U87 MG human glioblastoma cells). The results obtained demonstrate the high potential of folic acid–nido-carborane conjugates as boron delivery agents to tumour cells for application in BNCT. © 2022 by the authors.
Keywords: AMIDES
BNCT
BORON ACCUMULATION
CARBORANES
CYTOTOXICITY
FOLIC ACID
MTT ASSAY
TUMOUR CELLS
AMIDES
BORON
FOLIC ACID
GLIOBLASTOMA
HUMANS
THINNESS
2 [[4 [[(2 AMINO 4 HYDROXYPTERIDIN 6 YL)METHYL]AMINO]PHENYL] FORMAMIDO] N 1 N 5 BIS [2 [(7,8 DICARBA NIDO UNDECARBORAN 3 YL)AMINOCARBONYL]PENTYL]PENTANEDIAMIDE
2 [[4 [[(2 AMINO 4 HYDROXYPTERIDIN 6 YL)METHYL]AMINO]PHENYL] FORMAMIDO] N 1 N 5 BIS [2 [(7,8 DICARBA NIDO UNDECARBORAN 7 YL)ACETYLAMINO]ETHYL]PENTANEDIAMIDE SEMIHYDRATE
2 [[4 [[(2 AMINO 4 HYDROXYPTERIDIN 6 YL)METHYL]AMINO]PHENYL] FORMAMIDO] N 1 N 5 BIS [5 [(1,2 DICARBA CLOSO DODECARBORAN 3 YL)AMINOCARBONYL]PENTYL]PENTANEDIAMIDE
AMIDE
BORON DERIVATIVE
CARBORANE DERIVATIVE
CISPLATIN
FOLIC ACID DERIVATIVE
UNCLASSIFIED DRUG
AMIDE
BORON
FOLIC ACID
NIDO-CARBORANE
ARTICLE
BORON NEUTRON CAPTURE THERAPY
CELL VIABILITY
CONTROLLED STUDY
CYTOTOXICITY
DRUG SYNTHESIS
DU145 CELL LINE
ELEMENTAL ANALYSIS
FEMALE
GLIOBLASTOMA
HUMAN
HUMAN CELL
IN VITRO STUDY
MALE
MDA-MB-231 CELL LINE
MTT ASSAY
PRECIPITATION
PROTON NUCLEAR MAGNETIC RESONANCE
SK-MEL-28 CELL LINE
SYNTHESIS
THIN LAYER CHROMATOGRAPHY
TUMOR CELL
U-87MG-LUC CELL LINE
GLIOBLASTOMA
UNDERWEIGHT
URI: http://elar.urfu.ru/handle/10995/131234
Access: info:eu-repo/semantics/openAccess
cc-by
License text: https://creativecommons.org/licenses/by/4.0/
SCOPUS ID: 85142607924
WOS ID: 000887544500001
PURE ID: 32802407
99e840be-b260-48b7-be72-835f4c6a2245
ISSN: 1661-6596
DOI: 10.3390/ijms232213726
Sponsorship: Russian Science Foundation, RSF, (21-73-10073)
This research was funded by the Russian Science Foundation, grant number 21-73-10073.
RSCF project card: 21-73-10073
Appears in Collections:Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

Files in This Item:
File Description SizeFormat 
2-s2.0-85142607924.pdf1,69 MBAdobe PDFView/Open


This item is licensed under a Creative Commons License Creative Commons