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Hydrazides of glycine-containing decasubstituted pillar[5]arenes: Synthesis and encapsulation of Floxuridine

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dc.contributor.author Shurpik D.
dc.contributor.author Sevastyanov D.
dc.contributor.author Zelenikhin P.
dc.contributor.author Subakaeva E.
dc.contributor.author Evtugyn V.
dc.contributor.author Osin Y.
dc.contributor.author Cragg P.
dc.contributor.author Stoikov I.
dc.date.accessioned 2019-01-22T20:34:52Z
dc.date.available 2019-01-22T20:34:52Z
dc.date.issued 2018
dc.identifier.issn 0040-4039
dc.identifier.uri https://dspace.kpfu.ru/xmlui/handle/net/147802
dc.description.abstract © 2018 Elsevier Ltd Hydrazides of glycine-containing decasubstituted pillar[5]arenes were synthesized and characterized. Dynamic light scattering (DLS) and transmission electron microscopy (TEM) showed that self-assembly into monodisperse spherical nanoparticles (28 nm) was typical in water for pillarene hydrazides containing glycylglycide fragments (1 × 10−3 M). Binding of the antitumor drug Floxuridine in water by the substituents of the macrocycle was established by NMR spectroscopy. It was shown by DLS and TEM, that heating the macrocycle-Floxuridine system in a 1:1 ratio at 1 × 10−4 M led to its self-organization into monodisperse spherical particles 132 nm in diameter.
dc.relation.ispartofseries Tetrahedron Letters
dc.subject Floxuridine
dc.subject Macrocyclic receptors
dc.subject Pillar[5]arene
dc.subject Self-assembly
dc.subject TEM
dc.title Hydrazides of glycine-containing decasubstituted pillar[5]arenes: Synthesis and encapsulation of Floxuridine
dc.type Article
dc.relation.ispartofseries-issue 50
dc.relation.ispartofseries-volume 59
dc.collection Публикации сотрудников КФУ
dc.relation.startpage 4410
dc.source.id SCOPUS00404039-2018-59-50-SID85055910428


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  • Публикации сотрудников КФУ Scopus [24551]
    Коллекция содержит публикации сотрудников Казанского федерального (до 2010 года Казанского государственного) университета, проиндексированные в БД Scopus, начиная с 1970г.

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