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  • 1
    ISSN: 1432-0827
    Keywords: Bone formation ; Osteoblasts ; Osteoclasts ; Bone Induction ; Alkaline Phosphatase ; Cell Culture
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine , Physics
    Notes: Summary Osteoblast-like and osteoclast-like cells freed from neonatal calvaria by sequential enzymatic digestion after 6–7 days in culture were placed in diffusion chambers and implanted in the peritoneal cavities of CD-1 mice. About half of the chambers also contained a dead calvarium to test for the need of an “inducer.” After 20 days, 11 of 18 chambers containing the osteoblast-like cells formed large foci of mineralized bone that corresponded to alkaline phosphatase activity throughout the chambers. Moreover, only type I (i.e., bone) collagen was formed. Occasional deposits of bone were found in only 3 of 22 chambers containing the osteoclast-like cells. The presence of dead bone did not affect any of the results. These data confirm the osteoblast-like nature of the isolated cell populations and demonstrate that these cells retain their differentiated function in culture.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ephedrine and methamphetamine standards were separately derivatized with heptafluorobutyric anhydride (HFBA) and carbethoxyhexafluorobutyryl chloride (CB) and analyzed by full-scan gas chromatography/ion trap mass spectrometry with electron ionization (EI) and chemical ionization (CI). Using EI, a high-concentration ephedrine standard produced a total ion gas chromatogram containing several minor HFB derivatives in addition to ephedrine. One of these had the same retention time as the derivative of methamphetamine, while another eluted 3 s later. Both contained the same major mass fragmentation ions that could be erroneously used in targeted selected ion monitoring gas chromatographic/mass spectrometric analysis for methamphetamine. The full-scan EI and CI spectra showed that these derivatives were not methamphetamine. CI mass spectrometric studies of ephedrine scanning up to m/z 700 demonstrated that reaction with HFBA caused acylation of both the hydroxyl and secondary amino groups. The HFBA used in this study was contaminated with pentafluoropropionic anhydride and tri-fluoroacetic anhydride and produced mixtures of derivatives, some with retention times near or identical to that of methamphetamine. In contrast, CB derivatization of ephedrine produces a single methamphetamine-like compound that has the same retention time and mass spectra as methamphetamine, and is produced only when high gas chromatograph injector temperatures are used ( 〉 260°C). Collision-induced decomposition tandem mass spectrometric studies for the CB derivative verified that methamphetamine is produced from ephedrine at elevated GC injection port temperatures. In view of these findings, substance abuse testing for methamphetamine in urine must proceed with caution when ephedrine and other sympathomimetic amines are present. Definitive analyses can be accomplished by full-scan CI gas chromatographic/mass spectrometric analysis with HFB derivatives, or by lowering gas chromatograph injector temperatures with CB derivatives.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1052-9306
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Oral (44Ca: 0.13-0.20 mmol) and intravenous (42Ca: 0.02-0.037 mmol) isotopically enriched stable calcium (Ca) tracers were given together with an oral dose of 2.5 mmol of natural Ca to normal subjects. Blood and urine samples were collected up to 24 h after the tracer doses and atom fractions (AFs) of these tracers (relative to natural Ca) were measured by high-precision thermal ionization mass spectrometry (TIMS). The time(dependent fractional rate of oral dose absorbed and true fractional intestinal Ca absorption (α) were derived from the AFs by mathematical deconvolution. After 6 h, the ratio AF oral tracer/AF intravenous tracer in blood equalled that in urine and did not change thereafter. Reproducibility of the combination of chemical precipitation of Ca (from a urine standard) and subsequent TIMS measurements, in nine runs over 13 months, was 1.2% (coefficient of variation). This was in accord with the within-run reproducibility. An estimate of α derived from a single blood or urine measurement was 6-10% higher than the reference value obtained by deconvolution. This discrepancy could be explained by a correction factor depending, in part, on the elapsed time for peak Ca intestinal absorption rate. Instrumentally induced mass fractionation, as well as contributions from radiogenic Ca, had a significant effect on the accuracy and reproducibility of the ratio of AFs of tracers in blood and urine.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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