-
Je něco špatně v tomto záznamu ?
Cobalt bis(dicarbollide) derivatives: solubilization and self-assembly suppression
J. Rak, M. Jakubek, R. Kaplánek, P. Matějíček, V. Král
Jazyk angličtina Země Francie
Typ dokumentu časopisecké články, práce podpořená grantem
- MeSH
- biologická dostupnost MeSH
- hydrodynamika MeSH
- kobalt chemie MeSH
- molekulární konformace MeSH
- molekulární modely MeSH
- organokovové sloučeniny chemie farmakokinetika MeSH
- radiační rozptyl MeSH
- rozpustnost MeSH
- světlo MeSH
- voda chemie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Cobalt bis(dicarbollide) derivatives are promising therapeutic agents however their utilization is complicated due to their low solubility and self-assembling in water. Earlier we have shown that their solubility can be increased by using of suitable biocompatible excipients--carriers of pharmaceutically active compounds. Expected mechanism of solubilization was disassembling of self-assemblies and complexation of unimers. Newly our results of time-dependent light scattering study correct this presumption. Poor solubility of all derivatives can be easily improved by using various excipients, however only heptakis(2,6-di-O-methyl)-β-cyclodextrin displays ability to disassemble self-assemblies of all derivatives and suppress their self-assembling. Surprisingly, the other excipients participate on formation of mixed assemblies of derivative/excipient complex or cover assemblies to make them more soluble without decreasing their size.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc12027058
- 003
- CZ-PrNML
- 005
- 20160502071711.0
- 007
- ta
- 008
- 120816s2011 fr f 000 0#eng||
- 009
- AR
- 024 7_
- $a 10.1016/j.ejmech.2011.01.032 $2 doi
- 035 __
- $a (PubMed)21315496
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a fr
- 100 1_
- $a Rak, Jakub $7 xx0125850 $u Department of Analytical Chemistry, Faculty of Chemical Engineering, Institute of Chemical Technology, Technická 5, 166 28 Prague 6, Czech Republic
- 245 10
- $a Cobalt bis(dicarbollide) derivatives: solubilization and self-assembly suppression / $c J. Rak, M. Jakubek, R. Kaplánek, P. Matějíček, V. Král
- 520 9_
- $a Cobalt bis(dicarbollide) derivatives are promising therapeutic agents however their utilization is complicated due to their low solubility and self-assembling in water. Earlier we have shown that their solubility can be increased by using of suitable biocompatible excipients--carriers of pharmaceutically active compounds. Expected mechanism of solubilization was disassembling of self-assemblies and complexation of unimers. Newly our results of time-dependent light scattering study correct this presumption. Poor solubility of all derivatives can be easily improved by using various excipients, however only heptakis(2,6-di-O-methyl)-β-cyclodextrin displays ability to disassemble self-assemblies of all derivatives and suppress their self-assembling. Surprisingly, the other excipients participate on formation of mixed assemblies of derivative/excipient complex or cover assemblies to make them more soluble without decreasing their size.
- 650 _2
- $a biologická dostupnost $7 D001682
- 650 _2
- $a kobalt $x chemie $7 D003035
- 650 _2
- $a hydrodynamika $7 D057446
- 650 _2
- $a světlo $7 D008027
- 650 _2
- $a molekulární modely $7 D008958
- 650 _2
- $a molekulární konformace $7 D008968
- 650 _2
- $a organokovové sloučeniny $x chemie $x farmakokinetika $7 D009942
- 650 _2
- $a radiační rozptyl $7 D012542
- 650 _2
- $a rozpustnost $7 D012995
- 650 _2
- $a voda $x chemie $7 D014867
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Jakubek, Milan $u Department of Analytical Chemistry, Faculty of Chemical Engineering, Institute of Chemical Technology, Technická 5, 166 28 Prague 6, Czech Republic
- 700 1_
- $a Kaplánek, Robert $7 _AN061422 $u Department of Analytical Chemistry, Faculty of Chemical Engineering, Institute of Chemical Technology, Technická 5, 166 28 Prague 6, Czech Republic
- 700 1_
- $a Matějíček, Pavel $7 _AN058789 $u Department of Physical and Macromolecular Chemistry, Faculty of Science, Charles University in Prague, Hlavova 2030, 128 40 Prague 2, Czech Republic
- 700 1_
- $a Král, Vlastimil $7 xx0140517 $u Department of Analytical Chemistry, Faculty of Chemical Engineering, Institute of Chemical Technology, Technická 5, 166 28 Prague 6, Czech Republic; Zentiva R&D, Part of Sanofi-Aventis, U Kabelovny 130, 102 37 Prague 10, Czech Republic
- 773 0_
- $w MED00001628 $t European journal of medicinal chemistry $x 1768-3254 $g Roč. 46, č. 4 (2011), s. 1140-1146
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/21315496 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y m $z 0
- 990 __
- $a 20120816 $b ABA008
- 991 __
- $a 20160502071814 $b ABA008
- 999 __
- $a ok $b bmc $g 949100 $s 784404
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2011 $b 46 $c 4 $d 1140-1146 $e 20110128 $i 1768-3254 $m European journal of medicinal chemistry $n Eur J Med Chem $x MED00001628
- LZP __
- $b NLK122 $a Pubmed-20120816/11/02