Bile analysis

This method is applicable to urine, serum and bile. Analysis is performed with 200 pi of sample. 

Parasher VK, Romain K, Sukumar R, Jordan J. Can ERCP contrast agents cause pseudomicrolithiasis Their effect on the final outcome of bile analysis in patients with suspected microhthiasis. Gastrointest Endosc 2000 51(4 Pt 1) 401. ... 

The bile contained the glucuronides of two metabolites, tefluthrin alcohol (CAS no. 79538-03-7) and tetrafluoro-1, 4-benzenediol (CAS no. 142209-31-2). No parent compound was found in the bile. Analysis of fecal extracts from the rats administered the [ " C]-alcohol label contained mostly unchanged or unabsorbed tefluthrin. Metabolites consisted of 4-OH methyl tefluthrin (CAS no. 120851-77-6), 2-OH methyl tefluthrin (CAS no. 120808-42-6) and 2-OH methyl, 4-OH methyl tefluthrin (CAS no. NA). Several minor metabolites were found, two of which were tetrafluoro-4-OH methyl benzoic acid (CAS no. 107900-84-5) and tetrafluoro-4-methyl benzoic acid (CAS no. 652-32-4). 

Two nucleation processes important to many people (including some surface scientists ) occur in the formation of gallstones in human bile and kidney stones in urine. Cholesterol crystallization in bile causes the formation of gallstones. Cryotransmission microscopy (Chapter VIII) studies of human bile reveal vesicles, micelles, and potential early crystallites indicating that the cholesterol crystallization in bile is not cooperative and the true nucleation time may be much shorter than that found by standard clinical analysis by light microscopy [75]. Kidney stones often form from crystals of calcium oxalates in urine. Inhibitors can prevent nucleation and influence the solid phase and intercrystallite interactions [76, 77]. Citrate, for example, is an important physiological inhibitor to the formation of calcium renal stones. Electrokinetic studies (see Section V-6) have shown the effect of various inhibitors on the surface potential and colloidal stability of micrometer-sized dispersions of calcium oxalate crystals formed in synthetic urine [78, 79]. 

Clinical Analysis. A wide range of clinically important substances can be detected and quantitated using chemiluminescence or bioluminescence methods. Coupled enzyme assay protocols permit the measurement of kinase, dehydrogenase, and oxidases or the substrates of these enzymes as exemplified by reactions of glucose, creatine phosphate, and bile acid in the following ... 

Thermal neutron activation analysis has been used for archeological samples, such as amber, coins, ceramics, and glass biological samples and forensic samples (see Forensic chemistry) as weU as human tissues, including bile, blood, bone, teeth, and urine laboratory animals geological samples, such as meteorites and ores and a variety of industrial products (166). 

FATP5 KO mice have been characterized in two studies focusing on the role of FATP5 in hepatic lipid and bile metabolism. LCFA uptake in primary hepato-cytes isolated from FATP5 KO mice was reduced by 50% and hepatic lipid content in the KO mice was significantly reduced despite an increased fatty acid de novo biosynthesis. Detailed analysis of the hepatic lipidome of FATP5 KO mice revealed significant... 

Swaan PW, Szoka FC, Jr. and Oie S. Molecular modeling of the intestinal bile acid carrier a comparative molecular field analysis study. J Comput Aided Mol Des 1997 11 581-8. 

Several sample preparation techniques are performed inside the inlet system. Large-volume injection can be carried out by a number of methods including programmed temperature vaporisation (PTV). Automated SPE may be interfaced to GC using a PTV injector for large volume injection. SPE-PTV-GC with on-column injection is suited to analysis of thermola-bile compounds. 

Fate. Preliminary investigations directed at adapting the method of Averell and Norris (2) to the analysis of animal tissues indicated that if precautions were taken to avoid emulsions the method could be used satisfactorily. Tissue samples of about 5 grams were most convenient, and the usual reagent and tissue blanks were run simultaneously. Following the administration of an acutely lethal intravenous dose to a dog it was found that parathion could be recovered from the urine, liver, bile, kidney, spleen, and lung. 

Christie, D. M., et al. Comparative analysis of the ontogeny of a sodium-dependent bile acid transporter in rat kidney and ileum. Am. J. Physiol. 

MDCK II cells (Fig. 12.3) [93], Kinetic analysis revealed that the Km value for transcellular transport (24 pM) was similar to the Km for OATP2 (34 pM) [93], Moreover, the efflux across the bile canalicular membrane was not saturated under these experimental conditions. These in vitro observations are consistent with in vivo experimental results in rats which showed that the rate-determining process for the biliary excretion of pravastatin is uptake across the sinusoidal membrane. By normalizing the expression level between the double transfectant and human hepatocytes, it might be possible to predict in vivo hepatobiliary excretion. 

If the unbound drug concentrations in plasma are higher than their K values on the transporters, then transporter function may be significantly affected [106], Following a pharmacokinetic analysis of the effect of probenecid on the hepatobiliary excretion of methotrexate, it has been shown the extent of an in vivo drug-drug interaction can be quantitatively predicted from the kinetic parameters for transport across the sinusoidal and bile canalicular membranes determined in vitro [107]. 

Baker et al. [138] studied the excretion of metabolites in bile following the administration of primaquine in rats. Six metabolites of primaquine were found in the bile of rats. Quantitative high performance liquid chromatography analysis of the metabolites revealed that the sum of the six metabolites excreted in the bile represented quantitative recovery of the dose of primaquine. 

Baldini F., Bechi P., Cianchi F., Falai A., Fiorillo C., Francalanci M., Nassi P., Analysis of the optical properties of the bile, J. Biomedical Optics 2000 5 321. 

Bifunctional protein deficiency. The enzyme defect involves the D-bifunctional protein. This enzyme contains two catalytic sites, one with enoyl-CoA hydratase activity, the other with 3-hydroxyacyl-CoA activity [13]. Defects may involve both catalytic sites or each separately. The severity of clinical manifestations varies from that of a very severe disorder that resembles Zellweger s syndrome clinically and pathologically, to somewhat milder forms. Table 41-6 shows that biochemical abnormalities involve straight chain, branched chain fatty acids and bile acids. Bifunctional deficiency is often misdiagnosed as Zellweger s syndrome. Approximately 15% of patients initially thought to have a PBD have D-bifunctional enzyme deficiency. Differential diagnosis is achieved by the biochemical studies listed in Table 41-7 and by mutation analysis. 

More recently, Smith et al. have developed another model based on spontaneous curvature.163 Their analysis is motivated by a remarkable experimental study of the elastic properties of individual helical ribbons formed in model biles. As mentioned in Section 5.2, they measure the change in pitch angle and radius for helical ribbons stretched between a rigid rod and a movable cantilever. They find that the results are inconsistent with the following set of three assumptions (a) The helix is in equilibrium, so that the number of helical turns between the contacts is free to relax, (b) The tilt direction is uniform, as will be discussed below in Section 6.3. (c) The free energy is given by the chiral model of Eq. (5). For that reason, they eliminate assumption (c) and consider an alternative model in which the curvature is favored not by a chiral asymmetry but by an asymmetry between the two sides of the bilayer membrane, that is, by a spontaneous curvature of the bilayer. With this assumption, they are able to explain the measurements of elastic properties. 

There are medical tests to determine whether you have been exposed to chlordecone and/or its breakdown product, chlordecone alcohol. Levels of chlordecone and/or chlordecone alcohol can be measured in blood, saliva, feces, or bile. Chlordecone levels in blood are the best indicator of exposure to chlordecone. Since chlordecone remains in the blood for a long time, the test is useful for a long time after exposure has stopped. Chlordecone can be detected in saliva only within the first 24 hours after exposure therefore, this test has limited use. Blood levels of chlordecone are a good reflection of total body content of chlordecone. However, the test is an unsatisfactory indicator of the amount of chlordecone to which you have been exposed because you cannot be sure how much chlordecone left your body between the time you were exposed and the time the test is performed. These tests cannot predict how your health may be affected after exposure. The tests are not done in routine medical examinations, but doctors can collect body fluid samples and send them to a university medical center or a medical laboratory for analysis. Refer to Chapters 2 and 6 for more information. 

Chlordecone, which is excreted mainly in the feces, appears to undergo enterohepatic recirculation, which limits its excretion (Boylan et al. 1978). Analysis of the amount of chlordecone excreted in the bile compared to the amount found in the stool has indicated that only 5-10% of the bile level of the pesticide is eliminated in the feces (Boylan et al. 1978). Approximately equal fractions of... 

An RP-HPLC technique was employed for the analysis of bilirubin, one of the main components of pigment gallstones. The aim of the study was the determination of the inhibition of chlolesterol crytallization under bilirubin deconjugation. Bilirubin in rat bile was measured in an ODS column (250 X 4.5 mm. i.d. particle size 5 pm). Separation was... 

Table III summarizes the results of tissue residue analysis. It is evident that the amount of radioactivity in tissues was not directly related to the length of chemical exposure. The average accumulation in fish exposed from 1 to 14 days was 1.35%. In general, liver, kidney, intestine, and bile contained the most 1 C. C-labeled materials accumulated in the liver at levels 3 to 5 times greater than [111C]molinate concentration in the water. The maximum radiocarbon level in the bile was 14.5 ppm and was reached by the 7th day. On the 14th day, the radiocarbon decreased to 6.09 ppm which was 30-fold higher than the [ 1 C]molinate water concentration. Blood contained negligible amounts of radioactivity, and little of that was associated with the plasma. Twenty percent of total blood radioactivity was detected in the erythrocytes within 4 days after treatment and by the 14th day, 69% of the radiocarbon in whole blood was present in the erythrocytes.

Batta AK, Salen G, Rapole KR, Batta M, Earnest D, et al. 1998. Capillary gas chromatographic analysis of serum bile acids as the fi-butyl ester—trimethylsilyi ether derivatives. J Chromatogr B 706 337. 

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