Potentiometric Sensor for Furosemide Determination in Pharmaceuticals, Urine, Blood Serum and Bovine Milk

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Farmacocinética pré-clínica e avaliação toxicológica preliminar da nova tiazolidinadiona desenvolvida para o tratamento do diabetes mellitus tipo 2: 5-(4-cloro-benzilideno)-3-(4-metil-benzil)-tiazolidina-2,4-diona (GQ-2)

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Síntese e caracterização de compostos de coordenação do Ácido 4-cloro-2-(2- furilmetilamino)-5- sulfamoil-benzóico com os íons níquel, cobalto e zinco

This work aimed to promote the synthesis, characterization and propose a plausible molecular structure for coordination compounds involving furosemide (4-Chloro-2-(2- furylmethylamino)-5-sulfamoyl-benzoic acid) with the metal ions Ni+2, Zn+2 and Co+2. The compounds were obtained in methanoic medium by evaporation of the solvent after the synthesis procedure. For characterization of coordination compounds determining the levels of metals by EDTA complexometry, infrared spectroscopy (FTIR), solubility of compounds in various solvents, thermogravimetry (TG), differential scanning calorimetry (DSC), differential thermal analysis were made (DTA), determination of the carbon , hydrogen and nitrogen (CHN). The results of infrared spectroscopy in the region suggest that the organic ligand is coordinated in a bidentate fashion to the metal ions, the metal center interactions to occur by the coordination of the nitrogen atom of the amino group and the oxygen atom of the carboxylic acid of the structure of furosemide. With the results of the levels of metal, elemental analysis (CHN) and thermal analysis has been possible to propose the structure of the ligand. The values of the molar conductivity of the complex in acetonitrile behavior suggest the non acetonitrile electrolyte solution. With the solubility tests it was found that the compounds have high solubility in methanol and acetonitrile, as are partially insoluble in water. From the results of thermal analysis (TG, DSC, DTA), it was possible to obtain the thermal behavior of the compounds as stages of dehydration, thermal stability, decomposition and the energies involved.

Synthesis, Antifungal and Antitumor Activity of Novel (Z)-5-Hetarylmethylidene-1,3-thiazol-4-ones and (Z)-5-Ethylidene-1,3-thiazol-4-ones

New hetaryl- and alkylidenerhodanine derivatives 3a-d, 3e, and 4a-d were prepared from heterocyclic aldehydes 1a-d or acetaldehyde 1e. The treatment of several rhodanine derivatives 3a-d and 3e with piperidine or morpholine in THF under reflux, afforded (Z)-5-(hetarylmethylidene)-2-(piperidin-1-yl) thiazol-4(5H)-ones and 2-morpholinothiazol-4(5H)-ones 5a-d, 6a-d, and (Z)-5-ethylidene-2-morpholinothiazol-4(5H)-one (5e), respectively, in good yields. Structures of all compounds were determined by IR, 1D and 2D NMR and mass spectrometry. Several of these compounds were screened by the U.S. National Cancer Institute (NCI) to assess their antitumor activity against 60 different human tumor cell lines. Compound 3c showed high activity against HOP-92 (Non-Small Cell Lung Cancer), which was the most sensitive cell line, with GI(50) = 0.62 mu M and LC50 > 100 mu M from the in vitro assays. In vitro antifungal activity of these compounds was also determined against 10 fungal strains. Compound 3e showed activity against all fungal strains tested, but showed high activity against Saccharomyces cerevisiae (MIC 3.9 mu g/mL).

Silsesquioxane organofunctionalized with 4-amino-3-hydrazino-5-mercapto-1,2,4-triazole: preparation and subsequent reaction with silver and potassium hexacyanoferrate(III) for detection of l-cysteine

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Synthesis, structure and magnetism of the oxalato-bridged chromium(III) complex [NBu4n](4)[Cr-2(ox)(5)]center dot 2CHCl(3)

The binuclear complex [NBu4n](4)[Cr-2(ox)(5)]. 2CHCl(3) has been prepared by an ion-exchange procedure employing Dowex 50WX2 cation-exchange resin in the n-butylammonium form and potassium tris(oxalato)chromate(III). The dimeric complex was characterised by a crystal structure determination: monoclinic, space group C2/c, a = 29.241(7), b = 15.192(2), c = 22.026(5) Angstrom, beta = 94.07(1)degrees, Z = 4. The magnetic susceptibility (300-4.2 K) indicated that the chromium(III) sites were antiferromagnetically coupled (J = -3.1 cm(-1)).

Transient disruption of liver gap junctional intercellular communication and induction of apoptosis after administration of 1,4-bis[2-(3,5 dichloropyridyloxy)]benzene in mice

Gap junctional intercellular communication (GJIC) and connexin expression (Cx26 and Cx32) in mouse liver were studied after administration of 4-bis[2-(3,5 dichloropyridyloxy)]benzene (TCPOBOP), a phenobarbital-like enzyme inducer. Female C57BI/6 mice were administered TCPOBOP (5.8 mg/kg BW) and euthanized 0, 24, 48 and 72 hours later. Liver samples were snap frozen, or fixed in formalin, or submitted to GJIC analysis. The proliferating cell nuclear antigen (PCNA) immunohistochemistry and the Western blotting for Cx26 and Cx32 were performed. After 48 and 72 h of drug administration the liver-to-body weight ratio was increased 70% and 117% (p < 0.0001), respectively. There were temporal-dependent alterations in liver histopathology and a significant increase in cell proliferation was noted after 48h and sustained after 72h, though to a lesser extent (p < 0.0001). In addition. TCPOBOP administration induced apoptosis, which appeared to be time-dependent showing statistical significance only after 72h (p < 0.0001). Interestingly, a transient disruption by nearly 50% of GJIC capacity was detected after 48 h of drug ingestion, which recovered after 72 h (p = 0.003). These GJIC changes were due to altered levels of Cx26 and Cx32 in the livers of TCPOBOP-treated mice. We concluded that a single administration of TCPOBOP transiently disrupted the levels of GJIC due to decreased expression of connexins and increased apoptotic cell death in mouse liver. (C) 2009 Elsevier GmbH. All rights reserved.

A comparison of the clinical anesthetic efficacy of 4% articaine and 0.5% bupivacaine (both with 1 : 200,000 epinephrine) for lower third molar removal

Objective: This study compared the clinical efficacy of 4% articaine (A200) and 0.5% bupivacaine (B200), both with 1: 200,000 epinephrine, for lower third molar removal. Study design: Fifty patients underwent removal of symmetrically positioned lower third molars, in 2 separate appointments, under local anesthesia either with A200 or B200, in a double-blind, randomized, and crossover manner. Time to onset, duration of postoperative analgesia, duration of anesthetic action on soft tissues, intraoperative bleeding, and hemodynamic parameters were evaluated. Results: A statistically significant difference between the time to onset of A200 (1.66 +/- 0.13 minutes) and B200 (2.51 +/- 0.21 minutes) was found (P < .05). There was no statistically significant difference in the duration of analgesia, whether the patient was subjected to osteotomy or not, regardless of the local anesthetic used (3 to 4 hours; P < .05). However, when patients received B200 they experienced a statistically significant longer period of anesthesia on the soft tissues as compared with when they had received A200 (around 5 hours and 4 hours, respectively, P < .05). The surgeon`s rating of intraoperative bleeding was considered very close to minimal for both anesthetics. In the surgeries with osteotomy, the comparison between A200 and B200 showed statistically significant differences in the diastolic (64 mm Hg and 68 mm Hg, respectively, P = .001) and mean arterial pressure (86 mm Hg and 89 mm Hg, respectively, P = .031) when data from all the surgical phases were pooled. Additionally, the mouth opening at the suture removal was statistically different for A200 and B200 solutions (91.90% +/- 3.00% and 88.57% +/- 2.38% of the preoperative measure, respectively) when surgeries required bone removal (P < .05). Conclusions: In comparison with 0.5% bupivacaine, 4% articaine (both with 1: 200,000 epinephrine) provided a shorter time to onset and comparable hemostasis and postoperative pain control with a shorter duration of soft tissue anesthesia in lower third molar removal.

1.° Waztalkora, sive tractatus de utilitatibus astrolabii. — 2.° Tractatus de horologio secundùm Alchoram, id est, sphaeram rotundam ; inprimìs de horis diei. — 3.° Evangelium sancti Matthaei, cum glossis. — 4.° Anonymi quaestiones physicae. — 5.° Isidori Hispalensis etymologiarum fragmenta : praemittuntur ejusdem epistolae ad Braulionem, cum hujus responsis. — 6.° Sancti Bernardi, Abbatis Claraevallensis, epistola ad Innocentium Papam, contra Petrum Abailardum. — Hujusce codicis pars duodecimo, pars decimo tertio saeculo videtur exarata.

nuper comparatus

1.° Abstractiones è libris Senecae. — 2.° Marbodi, Rhedonensis, carmen de lapidibus pretiosis, cum anonymi commentario. — 3.° Nonnulla ad historiam naturalem pertinentia. — 4.° Anonymus de Sacramentis. — 5.° Fragmenta ad opticam pertinentia.

Mazarinaeus

Áreas de pesca de la flota artesanal de la zona norte del Perú (3,4° S A 6,5° S) 1996-1999

Analiza los resultados del procesamiento de la información relacionada a la potencialidad y dinámica extractiva de los pescadores artesanales, del área litoral comprendida entre los paralelos 3,4° y 6,5° de latitud sur (S) y los meridianos 80,0°-82,5°de longitud oeste (W) que conforman la zona de más alta diversidad y producción pesquera artesanal en el litoral peruano, frete a las costas de los departamentos de Tumbes y Piura.

Novas cultivares de algodoeiro para Minas Gerais: EPAMIG-4 (Redenção) E EPAMIG-5 (Precoce-1)

São apresentadas duas cultivares de algodoeiro anual (Gossypium hirsutum L.), EPAMIG-4 (Redenção) e EPAMIG-5 (Precoce-1) lançadas pela Empresa de Pesquisa Agropecuária de Minas Gerais (EPAMIG) para o plantio nas regiões algodoeiras do mesmo Estado. Suas características agronômicas e de fibra são descritas em valores absolutos e em comparação com a cultivar-testemunha utilizada. A primeira originou-se de seleção em campo de produção da cultivar IAC-17, e é recomendada para plantio em todo o Estado de Minas Gerais, enquanto a segunda foi originada de seleção sobre a linhagem introduzida "C-25-1-80", e é recomendada para o plantio na região norte de Minas Gerais. As cultivares em questão são altamente produtivas, tanto em condições de sequeiro quanto sob irrigação, e apresentam excelentes características agronômicas e de qualidade de fibra.

Novas cultivares de acerola (Malpighia emarginata DC): UEL 3 -- Dominga, UEL 4 -- Lígia e UEL 5 -- Natália

O programa de melhoramento genético de acerola, na Universidade Estadual de Londrina, iniciou-se em 1992, com a implatação de um pomar clonal constituído de genótipos selecionados no Norte do Paraná. As cultivares UEL 3-Dominga , UEL 4-Lígia, UEL 5-Natália são resultados de 5 ciclos de avaliações, onde foram considerados: precocidade, produtividade, conteúdo de vitamina C nos frutos, tolerância a pragas e doenças, tamanho e aparência dos frutos. As cultivares UEL 3-Dominga e UEL 5- Natália, destacam-se pela produtividade das plantas, conteúdo de vitamina C e pelo tamanho do fruto. Em Londrina, a frutificação dessas cultivares concentra-se nos meses de novembro a março. A cultivar UEL 4-Lígia destaca-se pela precocidade e produtividade que, em Londrina, se concentra nos meses de outubro a março. A cultivar UEL 3-Dominga apresenta peso médio de frutos igual a 6,31g, Vitamina C igual a 2906 e 1250 mg/100g em frutos verdes e maduros, respectivamente, acidez igual a 694,34 mg/100g e Brix igual a 9,2º. A cultivar UEL 4-Lígia apresenta peso médio dos frutos igual a 7,85g, vitamina C igual a 3579 e 1458 mg/100g em frutos verdes e maduros, respectivamente, acidez igual a 1110 mg/100g e Brix igual a 7,85º. A cultivar UEL 5-Natália apresenta peso médio dos frutos igual a 7,47g, Vitamina C igual a 3134,5 e 1098 mg/100g em frutos verdes e maduros, respectivamente, acidez igual a 725 mg/100g e Brix igual a 7,6º. Estas três cultivares são indicadas para plantio no Norte do Estado do Paraná.