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ABSTRACT African mahogany is a species preferred by many entrepreneurs as an investment in the forestry sector. However, there are few studies or research on the species, especially in Brazil. The aim of this work was to study the efficiency of nutrient uptake, accumulation, distribution and use in Khaya ivorensis and Khaya senegalensis, in addition to aspects of growth variables and of dry matter partitioning as a function of mineral fertilisation. Morphological, physiological and nutritional parameters were determined in the African mahogany plants 140 days after transplanting (DAT). The greatest zinc (Zn) content was detected in the shoots of both the Khaya ivorensis and Khaya senegalensis plants, accounting for more than 50% of the accumulated total of the plants with added nutrient solution. Maintaining the plants of Khaya senegalensis and Khaya ivorensis with the use of nutrient solution provides the best conditions for nutrient use, and allows plants with excellent morphological and nutritional characteristics to be ready for the field within five months after transplanting in a shaded nursery. The most efficient uptake, transport and use of macro and micronutrients is found in the species Khaya senegalensis with the addition of nutrient solution.

Due to the shortage of information on both mineral fertilizer and organic substrate in Khaya senegalensis, it was proposed in the current study to verify the potential of the use or not of addition of nutrient solution in the production of high quality seedlings of K. senegalensis as well as to obtain the total accumulation of macro and micronutrients in the seedlings. The experimental design was completely randomized in a factorial 2x6, being the first factor constituted by the presence and nutritious solution absence of and the second factor for times evaluation (0, 60, 80, 100, 120 and 140 days after transplanting) repetitions with four seedlings. The following growth traits (height, stem diameter and shoot and root dry mass) and seedling quality parameters (total dry mass and Dickson quality index). The addition of nutrient solution supported the increase of the determined morphological characteristics of the seedlings of K. senegalensis as well as the total accumulation of macro and micronutrients. The nutrient solution modifies the absorption dynamics of nutrients in K. senegalensis and the amount absorbed at 140 days after transplantation obeys according to the order: N>K>P>Ca>S>Mg> Fe>B>Mn>Zn>Cu.

Dapagliflozin was the first of its class (inhibitors of sodium-glucose cotransporter) to be approved in Europe, USA, and Brazil. As the drug was recently approved, there is the need for research on analytical methods, including dissolution studies for the quality evaluation and assurance of tablets. The dissolution methodology was developed with apparatus II (paddle) in 900 mL of medium (simulated gastric fluid, pH 1.2), temperature set at 37±0.5°C, and stirring speed of 50 rpm. For the quantification, a spectrophotometric (λ=224 nm) method was developed and validated. In validation studies, the method proved to be specific and linear in the range from 0.5 to 15 μg·mL−1 (r2=0.998). The precision showed results with RSD values lower than 2%. The recovery of 80.72, 98.47, and 119.41% proved the accuracy of the method. Through a systematic approach by applying Factorial 23, the robustness of the method was confirmed (p>0.05). The studies of commercial tablets containing 5 or 10 mg demonstrated that they could be considered similar through f1, f2, and dissolution efficiency analyses. Also, the developed method can be used for the quality evaluation of dapagliflozin tablets and can be considered as a scientific basis for future official pharmacopoeial methods.

A sinvastatina, pertencente à classe das estatinas, é um importante fármaco redutor do colesterol e é encontrada comercialmente como medicamentos referência, genéricos e similares em diferentes dosagens, sendo a de 10 mg a mais comum. Este trabalho tem como objetivo avaliar a qualidade e a equivalência entre comprimidos de sinvastatina 10 mg comercializados no mercado brasileiro. Foram selecionados dois medicamentos similares, um genérico e referência. Os ensaios de controle de qualidade aplicados foram: determinação do peso médio, dureza, friabilidade, desintegração, teor de princípio ativo, uniformidade de conteúdo e dissolução in vitro. Para tanto, foi necessário desenvolvimento e validação de metodologia por espectrofotometria na região do ultravioleta (UV). As formulações apresentaram-se dentro dos limites preconizados para todas as análises. No entanto, quando analisou-se estatisticamente os perfis de dissolução, verificou-se a não equivalência entre os medicamentos similares e o de referência. Porém, através dos resultados obtidos, podemos evidenciar a equivalência entre o genérico e o de referência, sugerindo sua intercambialidade.

A liquid chromatography-tandem mass spectrometry method with atmospheric pressure chemical ionization (LC-APCI/MS/MS) was validated for the determination of etoricoxib in human plasma using antipyrin as internal standard, followed by on-line solid-phase extraction. The method was performed on a Luna C18 column and the mobile phase consisted of acetonitrile:water (95:5, v/v)/ammonium acetate (pH 4.0; 10 mM), run at a flow rate of 0.6 mL/min. The method was linear in the range of 1-5000 ng/mL (r²>0.99). The lower limit of quantitation was 1 ng/mL. The recoveries were within 93.72-96.18%. Moreover, method validation demonstrated acceptable results for the precision, accuracy and stability studies.