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1.
Mikrochim Acta ; 190(6): 212, 2023 May 12.
Artigo em Inglês | MEDLINE | ID: mdl-37171627

RESUMO

Novel solid-phase microextraction coatings based on the use of multiwalled carbon nanotube-cyclodextrin (MWCNT-CD) nanocomposites were developed for the determination of 16-priority polycyclic aromatic hydrocarbons at ultratrace levels in snow samples. The performance of both ß- and γ-CD was tested to increase the detection capabilities towards the heaviest and most lipophilic compounds, i.e., five- and six-ring PAHs. To facilitate the interactions of MWCNTs with CDs, an oxidation procedure using both HNO3 and H2O2 was applied, obtaining superior results using MWCNTs-H2O2-γ-CD fiber. Detection and quantitation limits below 0.7 and 2.3 ng/L, RSD lower than 21%, and recoveries of 88(± 2)-119.8(± 0.4)% proved the reliability of the developed method for the determination of PAHs at ultratrace levels. The complexation capability of the γ-CD was also demonstrated in solution by NMR and fluorescence spectroscopy studies and at solid state by XRD analysis. Finally, snow samples collected in the ski area of Dolomiti di Brenta were analyzed, showing a different distribution of the 16 priority PAHs, being naphthalene, phenanthrene, fluoranthene, and pyrene the only compounds detected in all the analyzed samples.

2.
J Inorg Biochem ; 87(3): 137-47, 2001 Dec 01.
Artigo em Inglês | MEDLINE | ID: mdl-11730895

RESUMO

By reacting thiosemicarbazides substituted on the aminic nitrogen with both alkyl or aryl groups, and methyl pyruvate a new group of methylpyruvate thiosemicarbazones (Hmpt) derivatives was obtained. These ligands were then treated with copper and zinc inorganic salts. All isolated compounds were characterized using spectroscopic methods. The single crystal structural analysis of the ligands Me-Hmpt x 0.5H2O 1, Et-Hmpt x H2O 2, Ph-Hmpt 5, Meph-Hmpt 6 showed that only compound 6 presents significant deviation from planarity. The X-ray structure of [Zn(Me-Hmpt)Cl2] x H2O 8 showed that in this complex Me-Hmpt behaves as a neutral ligand SNO terdentate and that the penta coordination is achieved by chloride ions according to spectroscopic and elemental analyses. On the basis of the analytical data the same behavior is proposed for the other zinc complexes. All the ligands in copper complexes seem to be monodeprotonated; nevertheless the same SNO behavior is expected. Tests on cell proliferation of human leukemic cell line U937 showed that the copper complex Cu(Et-mpt)Cl x H2O is the most active compound among those reported even though it is not able to induce apoptosis.


Assuntos
Cobre/química , Tiossemicarbazonas/química , Zinco/química , Apoptose , Divisão Celular/efeitos dos fármacos , Cristalografia , Humanos , Espectroscopia de Ressonância Magnética , Modelos Moleculares , Espectrofotometria Infravermelho , Tiossemicarbazonas/síntese química , Tiossemicarbazonas/farmacologia , Células Tumorais Cultivadas
3.
J Inorg Biochem ; 83(2-3): 169-79, 2001 Jan 15.
Artigo em Inglês | MEDLINE | ID: mdl-11237256

RESUMO

Three new complexes of transition metals as copper, nickel and cobalt with 5-formyluracil thiosemicarbazone (H3ut) have been synthesised and characterised by single-crystal X-ray diffraction. In all compounds the ligand behaves as SNO terdentate. In the copper complex the coordination geometry is square pyramidal with the ligand lying on the basal plane and two water molecules that complete the metal environment, the nickel compound is surrounded by six donor atoms (three of the ligand, two water oxygen atoms and a chlorine atom) in an octahedral fashion, and cobalt also shows an octahedral geometry but determined only by two terdentate ligand molecules. These three compounds have been tested on human leukemic cell lines K562 and CEM. The nickel and cobalt complexes have demonstrated low activity in cell growth, while the copper complex that is more active has been tested also on a third leukemic human cell line (U937), but it was not able to induce apoptosis on all cell lines.


Assuntos
Divisão Celular/efeitos dos fármacos , Tiossemicarbazonas/química , Tiossemicarbazonas/farmacologia , Uracila/análogos & derivados , Uracila/química , Uracila/farmacologia , Apoptose/efeitos dos fármacos , Apoptose/fisiologia , Cobalto/química , Cobalto/farmacologia , Cobre/química , Cobre/farmacologia , Cristalografia por Raios X , Ensaios de Seleção de Medicamentos Antitumorais , Humanos , Ligantes , Estrutura Molecular , Mutagênicos/síntese química , Mutagênicos/química , Mutagênicos/farmacologia , Níquel/química , Níquel/farmacologia , Tiossemicarbazonas/síntese química , Células Tumorais Cultivadas , Uracila/síntese química
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