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Etude thermoanalytique de substances medicamenteuses

II-Détermination de la pureté de l'aminophénazone (I) par analyse thermique

Journal of Thermal Analysis and Calorimetry
Authors: J. Masse and A. Chauvet

The authors have determined the degree of purity on different samples of aminophenazone (I) containing very small quantities of phenazone and amino-4-phenazone. The advantages of differential scanning calorimetry and the of transparency recording in the change from the solid to the liquid state during the fusion is shown.

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Etude thermo analytique de substances medicamenteuses

I — Etude des mélanges binaires aminophénazone (I) — Phénazone, aminophénazone (I) — Amino-4 phénazone

Journal of Thermal Analysis and Calorimetry
Authors: J. Masse and A. Chauvet

After studying the thermal behaviour of the reactants the authors have established the diagrams of state of binary systems of aminophenazone form (I) with phenazone and with amino-4-phenazone by thermomicroscopy, differential scanning calorimetry and differential thermal analysis. Only one eutectic point is observed for each binary system, the fusion temperature and the composition of which have been determined.

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Résumé  

The solubility and rate of dissolution of a poorly-soluble active principle are of importance when substances are destined for oral administration. Physical blends in wich drug and carrier are able to form particular compositions, such as a eutectic, may exibit an increased rate of dissolution. In this work the interactions lorazepam and PEG 6000, were examined, the particular thermal behaviour of lorazepam being taken into account. An eutectic was obtained and its composition was studied by means of differential scanning calorimetry, thermomicroscopy, infrared spectroscopy and X-ray methods.

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The thermal behaviour of khellin has been studied by thermomicroscopy, differential scanning calorimetry, differential thermal analysis and measurement of transparency. The polymorphism of this drug has been established; the commercial form (I) melting at 153.3° and the form (II) melting at 150.3° have been identified, and their enthalpies (7725±166 cal·mole−1, 6668±230 cal·Mol−1) and entropies (18.17±0.41,15.76± 0.54) of fusion evaluated, while the degree of purity of form (I) has been determined.

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We have determined the eutectic composition nordazépam (NDZ) polyoxyethylene glycol 6000 (PEG): 4% NDZ, 96% PEG (T f=59,0±0,5°C ΔH f=155,9±2,4 J·g−1; NDZ succinic acid: 0,32n (NDZ) and 0,68n (succinic acid) (T f=163,8±0,4°C and ΔH f=119,34±2,1 J·g−1). No solid solution has been found. The negative and high absolute value of mixing enthalpy indicates that the eutectic composition is formed by interactions between OH, CO, NH groups of carrier and drug with hydrogene bonds formation, confirmed by X-ray diffraction.

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