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1.
Langmuir ; 40(5): 2562-2566, 2024 Feb 06.
Article in English | MEDLINE | ID: mdl-38276954

ABSTRACT

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.
Article in English | MEDLINE | ID: mdl-36800482

ABSTRACT

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.
ACS Omega ; 5(7): 3165-3171, 2020 Feb 25.
Article in English | MEDLINE | ID: mdl-32118132

ABSTRACT

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.

4.
Angew Chem Int Ed Engl ; 55(10): 3504-8, 2016 Mar 01.
Article in English | MEDLINE | ID: mdl-26845382

ABSTRACT

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.

5.
Org Lett ; 17(14): 3426-9, 2015 Jul 17.
Article in English | MEDLINE | ID: mdl-26133076

ABSTRACT

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.


Subject(s)
Oligodeoxyribonucleotides/chemistry , Oligodeoxyribonucleotides/chemical synthesis , Oligonucleotides, Antisense/chemistry , Purines/chemistry , RNA/chemistry , Molecular Conformation , Molecular Structure , Nucleic Acid Conformation , Nucleic Acid Hybridization , Succinimides/chemistry
6.
Arch Biochem Biophys ; 488(2): 153-62, 2009 Aug 15.
Article in English | MEDLINE | ID: mdl-19549503

ABSTRACT

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.


Subject(s)
HIV Integrase/genetics , HIV-1/genetics , Oligonucleotides/genetics , Base Sequence , Catalysis , DNA, Viral/genetics , Dimerization , HIV Integrase/isolation & purification , Molecular Sequence Data , Nucleic Acid Conformation , Structure-Activity Relationship , Substrate Specificity/genetics , Virus Integration/genetics
7.
J Enzyme Inhib Med Chem ; 24(1): 241-6, 2009 Feb.
Article in English | MEDLINE | ID: mdl-18608742

ABSTRACT

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.


Subject(s)
HIV Integrase Inhibitors/chemical synthesis , HIV Long Terminal Repeat/genetics , Oligonucleotides/pharmacology , HIV Integrase/drug effects , HIV Integrase Inhibitors/pharmacology , Molecular Mimicry , Nucleic Acid Conformation , Oligonucleotides/chemical synthesis , Phosphorus Acids
8.
Article in English | MEDLINE | ID: mdl-18776516

ABSTRACT

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


Subject(s)
Nucleosides/chemical synthesis , Nucleotides/chemical synthesis , Piperidines/chemistry , Nucleosides/chemistry , Nucleotides/chemistry
9.
Nucleic Acids Symp Ser (Oxf) ; (52): 665-6, 2008.
Article in English | MEDLINE | ID: mdl-18776555

ABSTRACT

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.


Subject(s)
Enzyme Inhibitors/chemistry , Nucleosides/chemistry , Nucleosides/pharmacology , Organophosphonates/chemistry , Thymidine Phosphorylase/antagonists & inhibitors , Animals , Blood Platelets/enzymology , CHO Cells , Cricetinae , Cricetulus , Enzyme Inhibitors/pharmacology , Humans , Structure-Activity Relationship , Thymidine Phosphorylase/chemistry
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