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Biomedical subjects

R Bouche

Publications and source records attributed to R Bouche.

18 recordsLinked to original sources

[*calcium-oxalate lithogenesis: crystallization in the presence of urine from healthy subjects].

In the present study we aim at describing the influence of urine of non-lithiasic subjects on the different crystallization stages of calcium oxalates. The experimental method consists in comparing the turbidimetric curves obtained by crystallization in pure synthetic urine to the curves obtained after addition of natural urine to the solution. Natural urine plays an important role on nucleation, crystal growth and agglomeration even if only small amounts (4% v/v) are added to the mother solution. Nucleation is favoured (decrease of the induction period and increase of the crystal number) by the presence of solid particles, such as cellular fragments, which play the role of substrates for heterogeneous nucleation. On the other hand, both the growth rate of the crystals and their degree of agglomeration are reduced. Moreover, the physical nature of the crystals which precipitate is different from that of the crystals which nucleate in synthetic urine. Under our conditions of high super-saturation, natural urine favours the nucleation of calcium oxalate dihydrate at the expenses of calcium oxalate trihydrate which forms in pure synthetic urine. A hypothesis on the origin of the lithogenesis process is made and a correlation between the localization of the calcium oxalate stones in the urinary tracts and their main constituents is proposed.

Adult

[Model of calcium oxalate lithogenesis by kinetic turbidimetry].

The crystallization process of calcium oxalates in synthetic urine at 37 degrees C is followed by turbidimetry. As the solution absorbance is very sensitive to the number of particles in suspension, it is possible to distinguish nucleation and growth from agglomeration. In the former case, the slopes of the turbidimetric curves are positive whereas in the latter case, they are negative. Poisoning the solutions by some active additives induces changes of the slopes so that it becomes possible to know whether the additive is a promotor or an inhibitor of nucleation, growth or agglomeration. As an example, the model is tested for checking the influence of human urine on the crystallization process. It is shown that urine fractions of non stone-formers inhibit agglomeration when they contain macromolecules of high molecular weight (> 30,000 Da).

Calcium Oxalate

Polymorphism of butyrophenones related to haloperidol.

A comparison of X-ray powder diffraction patterns, IR spectra, and crystal structures of structurally related compounds belonging to the butyrophenone family has been undertaken to obtain information about the elements of chemical structure which predispose a substance to exhibit polymorphism. Five butyrophenones, differing by the nature of only one substituent, were selected. After crystallization from 15 solvents, it appears that two compounds of the group exhibit more than one crystalline form. An explanation of the absence of polymorphism in the other compounds of the group is proposed and discussed.

Butyrophenones

Conformational study of two polymorphs of spiperone: possible consequences on the interpretation of pharmacological activity.

A second polymorph of spiperone, 8-[3-(p-fluorobenzoyl)-propyl]-1-phenyl-1,3,8-triazaspiro[4,5] decan-4-one, has been isolated and characterized by thermal analysis and IR spectrometry. Its structure was solved by X-ray diffraction analysis. The results are compared with those previously obtained on spiperone, the main difference being in the conformation of the side chain and in the nature of the hydrogen bonding.

Butyrophenones

Ketonic oxidation products of cyclobarbital.

Chemical or biochemical oxidation of cyclobarbital yielded 5-(3-oxo-1-cyclohexen-1-yl)-5-ethyl -2,4,6,- (1H,3H,5H)-pyrimidinetrione, and photochemical oxidation gave 5-(6-oxo-1-cyclohexen-1-yl)-5-ethyl-2,4,6-(1H,3H,3H)-pyrimidinetrione. These compounds were isolated and purified by TLC, and their structures were determined by UV, IR, NMR, and mass spectral data; the crystalline structure was determined by X-ray diffraction.

Barbiturates

IR spectroscopic characterization of 2-thiohydantoins and 2-thiobarbiturates.

A characterization of 2-thiohydantoins and 2-thiobarbiturates by IR spectra is proposed, using three characteristic group frequencies: the "thioureide band" around 1500 cm-1 and the antisymmetric-symmetric stretching modes of NCS bonds around 1400 and 1200 cm-1. The general characteristic absorption areas are found by comparison with N-phenylthioureas and thioanilides.

Chemical Phenomena