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Tricarbonyl M(I) (M = Re, 99mTc) complexes bearing acridine fluorophores: synthesis, characterization, DNA interaction studies and nuclear targetingElectronic supplementary information (ESI) available: Fig. S1-S9. See DOI: 10.1039/c0ob00073f
New pyrazolyl-diamine ligands with acridine derivatives at the 4-position of the pyrazolyl ring were synthesized and characterized ( L1 and L2 ). Coordination towards the fac -[M(CO) 3 ] + (M = Re, 99m Tc) led to complexes fac -[M(CO) 3 (κ 3 -L)] (L = L1 : M = Re1 , Tc1 ; L = L2 : M = Re2 , Tc2 ). T...
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Main Authors: | , , , , , , , , , , |
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Format: | Article |
Language: | English |
Online Access: | Get full text |
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Summary: | New pyrazolyl-diamine ligands with acridine derivatives at the 4-position of the pyrazolyl ring were synthesized and characterized (
L1
and
L2
). Coordination towards the
fac
-[M(CO)
3
]
+
(M = Re,
99m
Tc) led to complexes
fac
-[M(CO)
3
(κ
3
-L)] (L =
L1
: M =
Re1
,
Tc1
; L =
L2
: M =
Re2
,
Tc2
). The interaction of the novel pyrazolyl-diamine ligands (
L1
and
L2
) and rhenium(
i
) complexes (
Re1
and
Re2
) with calf thymus DNA (CT-DNA) was investigated by a variety of techniques, namely UV-visible, fluorescence spectroscopy and circular and linear dichroism. Compounds
L1
and
Re1
have moderate affinity to CT-DNA and bind to DNA by intercalation, while
L2
and
Re2
have a poor affinity for CT-DNA. Moreover, LD measurements showed that
L1
and
Re1
act as perfect intercalators. By confocal fluorescence microscopy we found that
L1
and
Re1
internalize and localize in the nucleus of B16F1 murine melanoma cells. The congener
Tc1
complex also targets the cell nucleus exhibiting a time-dependent cellular uptake and a fast and high nuclear internalization (67.2% of activity after 30 min). Plasmid DNA studies have shown that
Tc1
converts supercoiled (sc) puc19 DNA to the open circular (oc) form.
Nuclear-targeting and DNA intercalation of Re and
99m
Tc-tricarbonyl complexes. |
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ISSN: | 1477-0520 1477-0539 |
DOI: | 10.1039/c0ob00073f |