RESUMO
In Leishmania donovani, the causative protozoan of visceral leishmaniasis, nucleoside hydrolase enzyme (NH) is fundamental for the biosynthesis of its DNA and RNA. Therefore, LdNH is considered a potential target for the development of new leishmaniasis chemotherapy. Moringa oleifera Lamarck is a medicinal plant native to northeastern India with numerous pharmacological properties, including antileishmanial activity. Thus, this study aimed to explore the inhibitory activity of different extracts from M. oleifera leaves and flowers on LdNH. Using LdNH covalently immobilized on magnetic particles (LdNH-MPs), a novel activity assay was developed based on the direct quantification of the formed product by HPLC-DAD. This study screened 12 extracts from leaves and flowers of M. oleifera using different extraction methods. The hydroethanolic (70% ethanol) extract from flowers, obtained by infusion (FIEH) or ultrasound-assisted extraction (FUEH), exhibited respectively IC50 values of 26.2 ± 4.63 µg/mL and 4.96 ± 0.52 µg/mL. The most promising extract (FUEH) was investigated by high-resolution LdNH inhibition profiling, which showed different regions of inhibition in the biochromatogram. A ligand fishing assay was attempted to pinpoint the bioactive compounds. Experimental conditions employed in the elution step of the ligand fishing assay did not result in ligands isolation. However, the analyses of the crude extract solution and the supernatants after the incubation with the active and inactive LdNH-MPs indicated missing peaks referring to compounds selectively retained in the active LdNH-MPs incubation. The missing peaks eluted in the same region that exhibits inhibition in the high-resolution LdNH inhibition profiling. The ligands were identified by UHPLC-MS/MS as palatinose, adenosine, 3-p-coumaroylquinic acid, 4-p-coumaroylquinic acid, hyperoside, quercetin-3-O-malonyl glycoside, and kaempferol-3-O-galactoside.
Assuntos
Moringa oleifera , Ligantes , N-Glicosil Hidrolases , Extratos Vegetais/análise , Folhas de Planta/química , Espectrometria de Massas em TandemRESUMO
A SPE-LC-MS/MS method for the determination of ketamine (KET) and norketamine (NKET) was developed and validated. Extensive pulverization (25min at 25Hz) of previously cooled samples (5min in liquid nitrogen) allowed for extraction in a phosphate buffer (pH 6) solution after 10min vortex agitation at room temperature, simplifying the coupling of the extraction to an effective mixed-mode SPE (solid phase extraction) clean-up procedure. The extraction optimization was performed with samples fortified by drug incorporation according to a published procedure involving incubation of blank matrices for 16days. The method was validated for selectivity, matrix effect, linearity, LLQ (lower limit of quantification), precision, accuracy, recovery, carryover and stability after preparation and has proven to be accurate and reliable within a range of 0.02-10ng/mg for KET and 0.04-4ng/mg for NKET, meeting proposed KET cutoffs for discrimination from chronic use. In addition, the method was sensitive enough to detect the drugs after unique small (1mg/kg) intravenous doses received by patients submitted to general anesthesia before surgical procedures. Ketamine levels varied from 0.060 to 0.111ng/mg and norketamine was positive (Assuntos
Cromatografia Líquida/métodos
, Cabelo/química
, Ketamina/análogos & derivados
, Ketamina/administração & dosagem
, Ketamina/análise
, Extração em Fase Sólida/métodos
, Espectrometria de Massas em Tandem/métodos
, Adulto
, Idoso
, Calibragem
, Relação Dose-Resposta a Droga
, Feminino
, Humanos
, Injeções Intravenosas
, Limite de Detecção
, Reprodutibilidade dos Testes
RESUMO
In Brazil more than 90% of the population are not connected to municipal wastewater treatment plants. As a consequence, surface waters receive continuously considerable amounts of untreated domestic sewage containing surfactants as a major constituent. Such polluted waters gave rise to special interest if they are used as a source for the production of drinking water. In this work, the river Rio Macacu (State Rio de Janeiro, Brazil) was monitored for the occurrence of the most widely used anionic surfactant linear alkylbenzene sulfonate (LAS) together with its main degradative product, sulfophenyl carboxylates (SPC). In order to pursue the fate of both compounds after emission into the river, samples were collected at several locations along the river bank, and analyzed applying liquid chromatography-mass spectrometry after enrichment by solid-phase extraction. The LAS concentrations ranged between 14 and 155 microg l(-1) and the levels of their metabolic intermediates were found from 1.2 to 14 microg l(-1). The self-purification capacity of the water was impressively demonstrated in the upper course of the river downstream of a town considered as one major discharge point, whereas in the lower course the relative constant concentrations of both analytes were detected which was explained with an overall increasing level of pollution. Furthermore, a series of drinking water samples from Niterói and São Gonçalo, supplied by the same waterworks treating surface waters from the Rio Macacu, were taken during two sampling periods and examined for the presence of the strongly polar SPC which is suspected of by-passing the purification processes. The levels detected in the drinking water ranged between 1.6 and 3.3 microg l(-1). For the analyses of drinking and surface waters the peak pattern of a selected SPC homologue composed by several positional isomers served as an indicator to describe the progression of SPC degradation occurred in the river and could be used to distinguish drinking waters of different origins.