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1.
Langmuir ; 40(5): 2562-2566, 2024 Feb 06.
Artículo en Inglés | MEDLINE | ID: mdl-38276954

RESUMEN

An electrochemical Langmuir-Blodgett trough that permits an examination of local redox processes in a layer floating on the surface of water with a scanning tunneling microscopy-tip ultramicroelectrode has been constructed and tested on a layer of 1,1'-dicarbooctadecyloxyferrocene.

2.
Anal Chem ; 95(8): 4196-4203, 2023 Feb 28.
Artículo en Inglés | MEDLINE | ID: mdl-36800482

RESUMEN

Electrospray may exhibit inadequate ionization efficiency in some applications. In such cases, atmospheric-pressure chemical ionization (APCI) and photoionization (APPI) can be used. Despite a wide application potential, no APCI and APPI sources dedicated to very low sample flow rates exist on the market. Since the ion source performance depends on the transfer of analytes from the liquid to the gas phase, a nebulizer is a critical component of an ion source. Here, we report on the nebulizer with a gas dynamic virtual nozzle (GDVN) and its applicability in APCI at microliter-per-minute flow rates. Nebulizers differing by geometrical parameters were fabricated and characterized regarding the jet breakup regime, droplet size, droplet velocity, and spray angle for liquid flow rates of 0.75-15.0 µL/min. A micro-APCI source with the GDVN nebulizer behaved as a mass-flow-sensitive detector and provided stable and intense analyte signals. Compared to a classical APCI source, an order of magnitude lower detection limit for verapamil was achieved. Mass spectra recorded with the nebulizer in dripping and jetting modes were almost identical and did not differ from normal APCI spectra. Clogging never occurred during the experiments, indicating the high robustness of the nebulizer. Low-flow-rate APCI and APPI sources with a GDVN sprayer promise new applications for low- and medium-polar analytes.

3.
Angew Chem Int Ed Engl ; 55(10): 3504-8, 2016 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-26845382

RESUMEN

Magnetic Raman optical activity of gases provides unique information about their electric and magnetic properties. Magnetic Raman optical activity has recently been observed in a paramagnetic gas (Angew. Chem. Int. Ed. 2012, 51, 11058; Angew. Chem. 2012, 124, 11220). In diamagnetic molecules, it has been considered too weak to be measurable. However, in chlorine, bromine and iodine vapors, we could detect a significant signal as well. Zeeman splitting of electronic ground-state energy levels cannot rationalize the observed circular intensity difference (CID) values of about 10(-4). These are explicable by participation of paramagnetic excited electronic states. Then a simple model including one electronic excited state provides reasonable spectral intensities. The results suggest that this kind of scattering by diamagnetic molecules is a general event observable under resonance conditions. The phenomenon sheds new light on the role of excited states in the Raman scattering, and may be used to probe molecular geometry and electronic structure.

4.
ACS Omega ; 5(7): 3165-3171, 2020 Feb 25.
Artículo en Inglés | MEDLINE | ID: mdl-32118132

RESUMEN

Successful surgeries involving orthopedic implants depend on the avoidance of biofilm development on the implant surface during the early postoperative period. Here, we investigate the potential of novel antibacterial compounds-second-generation lipophosphonoxins (LPPOs II)-as additives to surgical bone cements. We demonstrate (i) excellent thermostability of LPPOs II, which is essential to withstand elevated temperatures during exothermic cement polymerization; (ii) unchanged tensile strength and elongation at the break properties of the composite cements containing LPPOs II compared to cements without additives; (iii) convenient elution kinetics on the order of days; and (iv) the strong antibiofilm activity of the LPPO II-loaded cements even against bacteria resistant to the medicinally utilized antibiotic, gentamicin. Thus, LPPOs II display promising potential as antimicrobial additives to surgical bone cements.

5.
Arch Biochem Biophys ; 488(2): 153-62, 2009 Aug 15.
Artículo en Inglés | MEDLINE | ID: mdl-19549503

RESUMEN

HIV integrase (IN) catalyzes the insertion of proviral DNA into the host cell chromosome. While IN has strict sequence requirements for the viral cDNA ends, the integration site preference has been shown to be very diverse. Here, we mapped the HIV IN strand transfer reaction requirements using various short oligonucleotides (ON) that mimic the target DNA. Most double stranded DNA dodecamers served as excellent IN targets with variable integration efficiency depending mostly on the ON sequences. The preferred integration was lost with any changes in the geometry of the DNA double helical structures. Various hairpin-loop-forming ONs also served as efficient integration targets. Similar integration preferences were also observed for ONs, in which the nucleotide hairpin loop was replaced with a flexible aliphatic linker. The integration biases with all target DNA structures tested were significantly influenced by changes in the resulting secondary ON structures.


Asunto(s)
Integrasa de VIH/genética , VIH-1/genética , Oligonucleótidos/genética , Secuencia de Bases , Catálisis , ADN Viral/genética , Dimerización , Integrasa de VIH/aislamiento & purificación , Datos de Secuencia Molecular , Conformación de Ácido Nucleico , Relación Estructura-Actividad , Especificidad por Sustrato/genética , Integración Viral/genética
6.
J Enzyme Inhib Med Chem ; 24(1): 241-6, 2009 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-18608742

RESUMEN

Retroviral integrase participates in two catalytic reactions, which require interactions with the two ends of the viral DNA in the 3'processing reaction, and with a targeted host DNA in the strand transfer reaction. The 3'-hydroxyl group of 2'-deoxyadenosine resulting from the specific removing of GT dinucleotide from the viral DNA in the processing reaction provides the attachment site for the host DNA in a transesterification reaction. We synthesized oligonucleotides (ONs) of various lengths that mimic the processed HIV-1 U5 terminus of the proviral long terminal repeat (LTR) and are ended by 2'-deoxyadenosine containing a 3'-O-phosphonomethyl group. The duplex stability of phosphonomethyl ONs was increased by covalent linkage of the modified strand with its complementary strand by a triethylene glycol loop (TEG). Modified ONs containing up to 10 bases inhibited in vitro the strand transfer reaction catalyzed by HIV-1 integrase at nanomolar concentrations.


Asunto(s)
Inhibidores de Integrasa VIH/síntesis química , Duplicado del Terminal Largo de VIH/genética , Oligonucleótidos/farmacología , Integrasa de VIH/efectos de los fármacos , Inhibidores de Integrasa VIH/farmacología , Imitación Molecular , Conformación de Ácido Nucleico , Oligonucleótidos/síntesis química , Ácidos de Fósforo
7.
Org Lett ; 17(14): 3426-9, 2015 Jul 17.
Artículo en Inglés | MEDLINE | ID: mdl-26133076

RESUMEN

Purine and pyrimidine 4'-alkoxy-2'-deoxynucleosides were efficiently prepared from nucleoside 4'-5'-enol acetates in three steps by N-iodosuccinimide promoted alkoxylation, hydrolysis, and reduction followed by conversion to phosphoramidite monomers for the solid-phase synthesis of the oligonucleotides. Fully modified 4'-alkoxyoligodeoxynucleotides, which are characterized by a prevalent N-type (RNA-like) conformation, exhibited superior chemical and nuclease resistance as well as excellent hybridization properties with a strong tendency for RNA-selective hybridization, suggesting a potential application of 4'-alkoxy-oligodeoxynucleotides in antisense technologies.


Asunto(s)
Oligodesoxirribonucleótidos/química , Oligodesoxirribonucleótidos/síntesis química , Oligonucleótidos Antisentido/química , Purinas/química , ARN/química , Conformación Molecular , Estructura Molecular , Conformación de Ácido Nucleico , Hibridación de Ácido Nucleico , Succinimidas/química
8.
Artículo en Inglés | MEDLINE | ID: mdl-18776516

RESUMEN

A novel series of racemic piperidin-3-yl and piperidin-4-yl derivatives of nucleobases and their phosphonate derivatives were prepared.


Asunto(s)
Nucleósidos/síntesis química , Nucleótidos/síntesis química , Piperidinas/química , Nucleósidos/química , Nucleótidos/química
9.
Nucleic Acids Symp Ser (Oxf) ; (52): 665-6, 2008.
Artículo en Inglés | MEDLINE | ID: mdl-18776555

RESUMEN

A number of structurally diverse nucleoside phosphonic acids have been tested against human recombinant thymidine phosphorylase and human platelets supernatant using 2'-deoxy-5-nitrouridine as the substrate. We have selected several inhibitors working at micromolar level as lead structures for further evaluation.


Asunto(s)
Inhibidores Enzimáticos/química , Nucleósidos/química , Nucleósidos/farmacología , Organofosfonatos/química , Timidina Fosforilasa/antagonistas & inhibidores , Animales , Plaquetas/enzimología , Células CHO , Cricetinae , Cricetulus , Inhibidores Enzimáticos/farmacología , Humanos , Relación Estructura-Actividad , Timidina Fosforilasa/química
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