2 research outputs found

    Acute and chronic effects of cadmium on blood homeostasis of an estuarine crab, Chasmagnathus granulata, and the modifying effect of salinity

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    Whole body oxygen consumption and some hemolymph parameters such as pH, partial pressure of gases, level of ions and lactate were measured in the estuarine crab Chasmagnathus granulata after both acute (96 h) and chronic (2 weeks) exposure to cadmium at concentrations ranging from 0.4 to 6.3 mg/l. In all instances, the crabs developed hemolymph acidosis, but no respiratory (increased PCO2) or lactate increases were evident. Hemolymph levels of sodium and calcium were always increased by cadmium exposure. The chronic toxicity of cadmium was enhanced at 12‰ salinity, even causing a significantly higher mortality in comparison with the higher salinity (30‰) used. A general metabolic arrest took place at 12‰ salinity in the crabs chronically exposed to cadmium, as indicated by decreases of oxygen consumption and PCO2, an increase of PO2, along with no changes in lactate levels. These imbalances were associated with severe necrosis and telangiectasia in the respiratory gills, probably leading to respiratory impairment and finally histotoxic hypoxia and death of the animals

    Cyproterone Acetate Quantification In Human Plasma By High-performance Liquid Chromatography Coupled To Atmospheric Pressure Photoionization Tandem Mass Spectrometry

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    A specific, fast and sensitive high performance liquid chromatography (HPLC) coupled to atmospheric pressure photoionization (APPI) tandem mass spectrometric (LC-MS/MS) assay was developed for the determination of cyproterone (CYP) acetate (CAS 427-51-0) in human plasma. The retention times were 3.26 and 2.90 min for CYP acetate and its internal standard (I. S.) finasteride (FIN), respectively. The overall mean recovery, using liquid/liquid extraction, was found to be 109.0, 107.7 and 100.3%, for low, mediumand high concentrations, respectively. Calibration curves were linear in the concentration range of 0.1 - 50.0 ng/ml, and the lower limit of quantification (LLOQ) was 0.1 ng/ml. The LLOQ, 0.1 ng/ml, was sensitive enough for detecting terminal phase concentrations of the drug. Inter-batch precision of the method ranged from 2.2 to 5.55%, while Inter-batch accuracy ranged from 95.5 to 100.0%. Intra-batch precision ranged from 1.8 to 5.6%, while Intra-batch accuracy ranged from 92.0 to 99.4% at concentrations of 0.3 ng/ml, 20.0 and 40.0 ng/ml. The developed method was applied to a bioequivalenc study of CYP acetate in a group of 44 female volunteers at a single oral dose of a 2 mg tablet, in a combination of ethinylestradiol/CYP acetate (0.25/2 mg). The plasma concentration of CYP acetate did not differ significantly after administration of both formulations (test formulation and the reference one). The geometric mean and respective 90% CI of CYP acetate test/reference percent ratios were 90.66 % (84.39-97.40%) for Cmax and 96.20 % (90.45-102.33 %) for AUC0-t. © ECV Editio Cantor Verlag.597335344Baumann, A., Kulmann, H., Gorkov, V., Mahler, M., Kuhnz, W., Radioimmunological analysis of cyproterone acetate in human serum. Comparison with a gas chromatographic/ mass spectrometric method and influence of each method on the outcome of a bioequivalence trial (1996) Arzneimittelforschung, 46, pp. 412-418Speck, U., Wendt, H., Schulze, P.E., Jentsch, D., Bio-availability and pharmacokinetics of cyproterone acetate-14C and ethinyloestradiol-3H after oral administration as a coated tablet (SH B 209 AB) (1976) Contraception, 14, pp. 151-163Dusterberg, B., Plasma levels of levonorgestrel, gestodene, norethisterone and cyproterone acetate on single-dose subcutaneous administration in oily solution in the rat, beagle and rhesus monkey (1984) Steroids, 43 (1), pp. 43-56. , DOI 10.1016/0039-128X(84)90057-6Fiet, J., Giton, F., Boudi, A., Boudou, P., Vexiau, P., Galons, H., Raynaud, J.-P., Highly sensitive and specific time-resolved fluoroimmunoassay (TR-FIA) of cyproterone acetate and free cyproterone (2000) Journal of Steroid Biochemistry and Molecular Biology, 75 (4-5), pp. 315-322. , DOI 10.1016/S0960-0760(00)00189-8, PII S0960076000001898Kuhnz, W., Kulmann, H., Fuhrmeister, A., Investigation into the age-dependence of the pharmacokinetics of cyproterone acetate in healthy male volunteers (1997) European Journal of Clinical Pharmacology, 53 (1), pp. 75-80. , DOI 10.1007/s002280050340Nieuweboer, B., Lubke, K., Radioimmunological determination of cyproterone acetate (1977) HormRes, 8, pp. 210-218Bebawy, L.I., Mostafa, A.A., Refaat, H.H., Different methods for the determination of gestodene, and cyproterone acetate in raw material and dosage forms (2001) J Pharm Biomed Anal, 25, pp. 425-436Cannell, G.R., Mortimer, R.H., Thomas, M.J., High-performance liquid chromatographic estimation of cyproterone acetate in human plasma (1981) J Chromatogr, 226, pp. 492-497Christiaens, B., Fillet, M., Chiap, P., Rbeida, O., Ceccato, A., Streel, B., Graeve, J.D., Hubert, P., Fully automated method for the liquid chromatographic-tandem mass spectrometric determination of cyproterone acetate in human plasma using restricted access material for on-line sample clean-up (2004) Journal of Chromatography a, 1056 (1-2 SPEC.ISS), pp. 105-110. , DOI 10.1016/j.chroma.2004.06.107, PII S0021967304010787Dikkeschei, L.D., Wolthers, B.G., De Ruyter-Buitenhuis, A.W., Nagel, G.T., Sleijfer, D.T., Willemse, P.H., Determination of megestrol acetate and cyproterone acetate in serum of patients with advanced breast cancer by high-performance liquid chromatography (1990) J Chromatogr, 529, pp. 145-154Frith, R.G., Phillipou, G., 15-Hydroxycyproterone acetate and cyproterone acetate levels in plasma and urine (1985) Journal of Chromatography - Biomedical Applications, 338 (1), pp. 179-186Yodo, K., Saisho, S., Shimozawa, K., Yata, J., A reversed-phase high-performance liquid chromatographic method for the simultaneous determination of serum concentrations of cyproterone acetate and 15 beta-hydroxycyproterone acetate (1988) Endocrinologia Japonica, 35 (1), pp. 143-148Matejicek, D., Kuban, V., High performance liquid chromatography/ion-trap mass spectrometry for separation and simultaneous determination of ethynylestradiol, gestodene, levonorgestrel, cyproterone acetate and desogestrel (2007) Analytica Chimica Acta, 588 (2), pp. 304-315. , DOI 10.1016/j.aca.2007.02.028, PII S0003267007003273Viswanathan, C.T., Bansal, S., Booth, B., Destefano, A.J., Rose, M.J., Sailstad, J., Shah, V.P., Weiner, R., Quantitative bioanalytical methods validation and implementation: Best practices for chromatographic and ligand binding assays (2007) Pharmaceutical Research, 24 (10), pp. 1962-1973. , DOI 10.1007/s11095-007-9291-7Pereira, A.S., Mendes, G.D., Oliveira, L.S., Valle, H.F., De Nucci, G., Atmospheric pressure photoionization applied to quantitation of cyproterone acetate in human plasma (2005) J Chromatogr Sci, 43, pp. 513-517Robb, D.B., Covey, T.R., Bruins, A.P., Atmospheric pressure photoionization: An ionization method for liquid chromatography - Mass spectrometry (2000) Analytical Chemistry, 72 (15), pp. 3653-3659. , DOI 10.1021/ac0001636Leinonen, A., Kuuranne, T., Kostiainen, R., Liquid chromatography/mass spectrometry in anabolic steroid analysis - Optimization and comparison of three ionization techniques: Electrospray ionization, atmospheric pressure chemical ionization and atmospheric pressure photoionization (2002) Journal of Mass Spectrometry, 37 (7), pp. 693-698. , DOI 10.1002/jms.328Cai, Y., Kingery, D., McConnell, O., Bach II, A.C., Advantages of atmospheric pressure photoionization mass spectrometry in support of drug discovery (2005) Rapid Commun Mass Spectrom, 19, pp. 1717-172
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