Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto

About: Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto is a based out in . It is known for research contribution in the topics: Population & Genus. The organization has 2143 authors who have published 3674 publications receiving 71071 citations. The organization is also known as: FFCLRP & FFCLRP-USP.

Enantioseparation of pesticides: A critical review

Abstract: The potential of chiral pesticides to exhibit stereoselective behavior in regards to activity, toxicity, degradation, bioaccumulation, and/or metabolism has inspired numerous studies, e.g., several works have investigated the contamination of water, food, and soil by chiral pesticides and the consequences of non-targeted species (including human) exposure to these chemicals. As these studies typically rely on enantioselective separation methods such as liquid chromatography, supercritical fluid chromatography, gas chromatography, and capillary electromigration techniques, this review aims to provide a critical point of view on these analytical techniques used for the enantioselective analysis of pesticides. Accordingly, we selected papers from different areas and several issues (as chiral stationary phases or chiral selectors, mobile phases, and method detectability) regarding each technique were critically discussed. Finally, we outlined the future trends for each technique in the chiral analysis of pesticides.

Resonance Raman study of polyynes encapsulated in single-wall carbon nanotubes

Abstract: L. M. Malard,1 D. Nishide,2 L. G. Dias,3,4 Rodrigo B. Capaz,3,5 A. P. Gomes,1 A. Jorio,1 C. A. Achete,3,6 R. Saito,7 Y. Achiba,8 H. Shinohara,2 and M. A. Pimenta1 1Departamento de Fisica, Universidade Federal de Minas Gerais, 30123-970 Belo Horizonte, Brazil 2Department of Chemistry, Nagoya University, Nagoya 464-8602, Japan 3Divisao de Metrologia de Materiais, Inmetro, Duque de Caxias, Rio de Janeiro 25245-020, Brazil 4Departamento de Quimica, Faculdade de Filosofia, Ciencias e Letras de Ribeirao Preto, Universidade de Sao Paulo, Ribeirao Preto, Sao Paulo 14040-901, Brazil 5Instituto de Fisica, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Rio de Janeiro 21941-972, Brazil 6Programa de Engenharia Metalurgica e de Materiais, COPPE, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Rio de Janeiro 21941-972, Brazil 7Department of Physics, Tohoku University and CREST JST, Sendai 980-8578, Japan 8Department of Chemistry, Tokyo Metropolitan University, Hachioji 192-0397, Japan Received 10 October 2007; published 28 December 2007

N-Ethyl Pentylone (Ephylone) Intoxications: Quantitative Confirmation and Metabolite Identification in Authentic Human Biological Specimens.

Abstract: N-ethyl pentylone (ephylone) has been identified as the most recent novel stimulant to emerge into the arena of evolving novel psychoactive substances (NPS). Due to its novelty, information regarding case reports with associated quantitative confirmations, biotransformation pathways, and identified unique metabolites will assist the scientific community in understanding the implications of the emergence and risks associated with N-ethyl pentylone use. Authentic blood specimens (n = 26) submitted as part of toxicological death investigations or drugged driving casework tested positive for N-ethyl pentylone, and were quantitatively analyzed by liquid chromatography tandem mass spectrometry (LC-MS-MS). N-ethyl pentylone concentrations ranged from 12 to 1,200 ng/mL, with mean (±standard deviation) and median concentrations of 313 (±366) and 125 ng/mL, respectively, excluding one case measured at 50,000 ng/mL. N-ethyl pentylone was often found in combination with other drugs of abuse and NPS, include a variety of novel opioids including fentanyl analogs. Oral fluid specimens (n = 5), collected from recreational drug users at a dance music festival, were quantitatively analyzed using LC-MS-MS. Concentrations ranged from 12.6 to 1,377 ng/mL. Additional analysis was performed to characterize the metabolic profile of N-ethyl pentylone using human liver microsomes (HLM), followed by confirmation of the presence of the proposed metabolites in a subset of the blood specimens and oral fluid specimens. Metabolomic analysis was performed using a liquid chromatograph quadrupole time-of-flight mass spectrometer (LC-QTOF), followed by data processing using MetabolitePilot™ software. In vivo verification of in vitro HLM-generated metabolites resulted in the confirmation of four metabolites. Reduction of the beta-ketone to an alcohol resulted in the most prominent metabolite found in the authentic specimens, and its uniqueness to N-ethyl pentylone leads to this metabolite being an appropriate biomarker to determine N-ethyl pentylone ingestion. This is the first study to report N-ethyl pentylone concentrations and to characterize the metabolic profile of N-ethyl pentylone.

Cranial anatomy of a new genus of hyperodapedontine rhynchosaur (Diapsida, Archosauromorpha) from the Upper Triassic of southern Brazil

Abstract: Detailed description of the cranial anatomy of the rhynchosaur previously known as Scaphonyx sulcognathus allows its assignment to a new genus Teyumbaita. Two nearly complete skulls and a partial skull have been referred to the taxon, all of which come from the lower part of the Caturrita Formation, Upper Triassic of Rio Grande do Sul, southern Brazil. Cranial autapomorphies of Teyumbaita sulcognathus include anterior margin of nasal concave at midline, prefrontal separated from the ascending process of the maxilla, palatal ramus of pterygoid expanded laterally within palatines, dorsal surface of exoccipital markedly depressed, a single tooth lingually displaced from the main medial tooth-bearing area of the maxilla, and a number of other characters (such as skull broader than long; a protruding orbital anterior margin; anguli oris extending to anterior ramus of the jugal; bar between the orbit and the lower temporal fenestra wider than 0·4 of the total orbital opening; mandibular depth reaching more than 25 of the total length) support its inclusion in Hyperodapedontinae. T. sulcognathus is the only potential Norian rhynchosaur, suggesting that the group survived the end-Carnian extinction event.