Suspected Brazilian Purpuric Fever, Brazilian Amazon Region

Ministry of Health. Brasília. DF, Brazil.Ministry of Health. Brasília. DF, Brazil.Municipal Secretary of Health. Anajás, PA, Brazil.Secretary of Health of Pará State. Belém, PA, Brazil.Ministério da Saúde. Secretaria de Vigilância em Saúde. Instituto Evandro Chagas. Belém, PA, Brasil.Ministério da Saúde. Secretaria de Vigilância em Saúde. Instituto Evandro Chagas. Belém, PA, Brasil.Secretary of Health of São Paulo State. Instituto Adolfo Lutz. São Paulo, SP, Brazil.Secretary of Health of São Paulo State. Instituto Adolfo Lutz. São Paulo, SP, Brazil.Ministry of Health. Brasília, DF, Brazil.Centers for Disease Control and Prevention. Atlanta, GA, USA

Quantitative determination of amlodipine besylate in tablets by high performance liquid chromatography and UV spectrophotometry

The purpose of this study was to develop and validate analytical methods for determination of amlodipine besylate in tablets. Simple, accurate and precise liquid chromatographic and spectrophotometric methods are proposed. For the chromatographic method, the conditions were: a LiChrospher®100 RP-18 Merck® (125 mm x 4.6 mm, 5 µm) column; methanol/water containing 1 % of trietylamine adjusted to pH 5.0 with phosphoric acid (35:65) as mobile phase; a flow rate of 1.0 mL/min and UV detector at 238 nm. Linearity was in the range of 50.0 - 350.0 µg/mL with a correlation coefficient (r) = 0.9999. For the spectrophotometric method, the first dilutions of samples were performed in methanol and the consecutives in ultrapure water. The quantitation was made at 364.4 nm. Linearity was determined within the range of 41.0 - 61.0 µg/mL with a correlation coefficient (r) = 0.9996. Our results demonstrate that both methods can be used in routine analysis for quality control of tablets containing amlodipine besylate.Colegio de Farmacéuticos de la Provincia de Buenos Aire

Fusion and Binary-Decay Mechanisms in the 35^{35}Cl+24^{24}Mg System at E/A ≈\approx 8 MeV/Nucleon

Compound-nucleus fusion and binary-reaction mechanisms have been investigated for the $^{35}$Cl+$^{24}$Mg system at an incident beam energy of E$_{Lab}$= 282 MeV. Charge distributions, inclusive energy spectra, and angular distributions have been obtained for the evaporation residues and the binary fragments. Angle-integrated cross sections have been determined for evaporation residues from both the complete and incomplete fusion mechanisms. Energy spectra for binary fragment channels near to the entrance-channel mass partition are characterized by an inelastic contribution that is in addition to a fully energy damped component. The fully damped component which is observed in all the binary mass channels can be associated with decay times that are comparable to, or longer than the rotation period. The observed mass-dependent cross sections for the fully damped component are well reproduced by the fission transition-state model, suggesting a fusion followed by fission origin. The present data cannot, however, rule out the possibility that a long-lived orbiting mechanism accounts for part or all of this yield.Comment: 41 pages standard REVTeX file, 14 Figures available upon request -