[Gallstone biochemical characteristics using Fourier transform infrared spectroscopy method]. / Caractéristiques biochimiques des lithiases vésiculaires par spectrométrie infrarouge à Abidjan.

This study reports biochemical composition and morphological aspect of gallstones as investigated by spectroscopy IR method. Participants were 24 patients composed of 12 males and 12 females who underwent cholecystectomy with age mean of 44.8 years. The gallstones were classified either as pigments stones (n = 12), cholesterol stones (n = 8) or as mixed stones (n = 4) according to analysis by Fourier transform infrared spectroscopy. The infrared spectroscopy quantification reported eight stones contained 100% of cholesterol, eight of 100% of calcium bilirubinate, four stones were composed of 65% calcium bilirubinate phosphate and 35% calcium carbonate, and four stones contained 65% cholesterol, 30% neutral calcium bilirubinate, 5% protein and traces of calcium bilirubinate acid. Our findings showed that most gallstones were composed of pigment stones with relative large proportion of cholesterol stones, whereas previous study in Caucasian reported predominance of cholesterol stones. These findings indicate the influence of diet and chronic haemolysis in the stones formation in regard to biochemical composition differences between those found in European area and our results. Therefore, Fourier transform infrared spectroscopy method allowed to determine quality and quantity of biochemical components of gallstones. Therefore, a careful survey must allow knowing the nutritional and environmental factors in the occurrence of gallstones to Côte d'Ivoire, in order to prevent this disease.

[Purification and characterization of protease inhibitors from urine during pregnancy (author's transl)]. / Purification et caracterisation des inhibiteurs de protéases de l'urine humaine.

Two forms of urinary trypsin inhibitor, A and B, were purified from the pooled urine from pregnant women using non-denaturing methods. The inhibitor B arose from the inhibitor A and was not present in native urine. Electrophoresis on polyacrylamide gel in the presence of sodium dodecyl sulfate indicated a new heterogeneity of the inhibitor B with molecular weights of 33 000 and 24 000; the molecular weight obtained for the inhibitor A was 50 000. Inhibitors A and B were acidic proteins with an isoelectric pH of about 2.6 for A and about 4.2 for B. Inhibitor A and inter-alpha-trypsin inhibitor formed a precipitate with an antiserum to purified inhibitor B. But neither inhibitor A nor inhibitor B formed a precipitate with anti whole human serum or anti-inter-alpha-trypsin inhibitor antiserum. Measurements of specific activity of inhibitor A were consistent with two active sites in the molecule.