PubMed Health⌕ Search

Biomedical subjects

M Ebihara

Publications and source records attributed to M Ebihara.

22 records · Page 2Linked to original sources

CCXVII. Separation and characterization of bile acid 3-glucuronides in human urine by high-performance liquid chromatography.

The separation and characterization of unconjugated and conjugated bile acid 3-glucuronides in biological fluids without prior deconjugation by high-performance liquid chromatography (HPLC) are described. A urine sample from a patient with obstructive jaundice was passed through a Sep-Pak C18 cartridge and was separated into groups by ion-exchange chromatography on a lipophilic gel, piperidinohydroxypropyl Sephadex LH-20, providing the glucuronide fraction. Subsequent resolution into individual 3-glucuronides was attained by HPLC on muBondapak C18 and Shodex ODS Pak F-411 columns. The 3-glucuronides of cholate, deoxycholate, chenodeoxycholate, glycocholate, glycochenodeoxycholate and taurochenodeoxycholate were identified on the basis of their behaviour in HPLC using mobile phases of different pH. The enzymatic hydrolysis of these glucuronides and derivatization of deconjugated bile acids with 1-anthroyl nitrile followed by chromatographic separation on a Cosmosil 5C18 column with fluorescence detection were carried out for unequivocal characterization. The ratio of unconjugated, glyco- and tauro-conjugated bile acid 3-glucuronides excreted in urine was found to be ca. 2:3:1.

Bile Acids and Salts↗

[Studies on the application of apatite to dental materials. (I) --Apatite ceramics-- (author's transl)].

Apatite ceramics is composed of hydroxyapatite [Ca10(PO4)6(OH)2] sintered at high temperature. It is known that hydroxyapatite is the main component of bone and tooth minerals. There are two synthetic methods for the apatite powder. One is so called wet synthetic method: Synthesis by the reaction of Ca++ and PO4--- in the aqueous solution of approximately pH 7.0, the other is dry method: Synthesis by the solid state reaction at high temperature. The apatite powder stable below 1400 degrees C was prepared by the latter method in this work. After passing through a sieve, this powder was cold-pressed and then sintered at 1000 degrees C to 1300 degrees C in air. Biological apatite powders were also perpared as a reference. It was found that any apatite ceramics having porosity in the range of 5 to 50% could be obtained under the various sintering conditions. Compressive strength of these apatite ceramics increased with the reduction of the porosity, and those with porosity less than 20% were more than 100 kg/cm2. Vickers hardness was measured. This result showed the same tendency as that of compressibility. Hardness of the apatite ceramics with 90% relative density was almost the same or more as that of enamel. Solubility of the synthetic apatite powder in distilled water and aqueous solution of lactic acid (pH 4.0) was nearly the same as biological apatites. The dissolution rate decreased with the reduction of porosity of the ceramics. It was certified that hot pressing technique was extremely effective to obtain high density ceramics (more than 95% of density) and thus low parosity apatite ceramics. From the facts as described above, it is understood that sintered pure hydroxy-apatite is an excellent ceramics of high mechanical strength.

Apatites↗