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11.
526例儿童指血微量元素检测结果分析 总被引:8,自引:0,他引:8
为了解吐哈油区婴幼儿体内钙、铁、锌、铜、镁的含量,使用多通道原子吸收光谱仪对门诊体查的526例0~7岁幼儿指血检测了钙、铁、锌、铜、镁。结果表明,各个年龄组中缺铁均居第一位,缺钙居第二位,缺锌居第三位,年龄越小,这3种元素含量越低。提示婴幼儿生长发育快,易缺钙,铁,锌元素,年龄越小,越易缺乏。 相似文献
12.
A new chemical method is reported for the determination of total fluoride in complex liquids and suspensions, such as fruit juices, urine, serum and blood. It is based on the formation of the A1F radical in a graphite furnace afterin situ oxygen-assisted ashing of the untreated sample. The absorbance of this radical is measured at 227.45 nm. The method is relatively easy to use and provides a low detection limit (14 ng/ml) and reasonable reproducibility (5–10%). 相似文献
13.
An extract of crystal violet-tetrachloroferrate(III) in nitrobenzene was used to prepare a tetrachloroferrate(III)-selective liquid membrane electrode with a poly(vinyl chloride) support. The optimal conditions to determine 2.5 × 10–5 – 5.0 × 10–2
M iron(III) as tetrachloroferrate(III) (anionic slope 56 mV/decade, detection limit 7.9 × 10–6
M) were found to be 4.0–5.5.M total chloride in 0.75–1.5M hydrochloric acid. The electrode was reliably applied to determine iron in human blood, haematite and mineralized vitamin syrup by direct potentiometry, standard and sample additions as well as standard subtraction techniques. 相似文献
14.
15.
慢性支气管炎急性发作期病人血中微量元素的变化分析 总被引:2,自引:1,他引:2
韦民 《广东微量元素科学》1997,4(2):35-38
为观察慢性支气管炎急性女作期血液中微量元素的变化,对101例慢性支气管炎急性发作期病人和30例正常人全血中锌、铁、铜及钙进行检测。结果显示:慢性支气管炎急性发作期病人锌、铁、铜和钙4种元素均明显于正常人。提示患者血中微量元素总量减少,可能是慢性支气官炎易反复感染、加剧病变发展的原因之一。认为合理补充缺乏的微量元素,有助于疾病的防治。 相似文献
16.
《Electroanalysis》2004,16(3):224-230
The 3′‐azido‐3′‐deoxythymidine (AZT, Zidovudine) is an antiproliferative and virostatic drug widely used in human immunodeficiency virus type 1 (HIV‐1) infection treatment. With respect to side effects of high doses and a short half‐life of AZT, a fast and simple detection method for this agent could be helpful. The aim of our study was to determine AZT levels in natural samples (urine, serum, whole blood, and cell cultures, such as the HaCaT line of keratinocytes) without their mineralization and/or purification, by means of electrochemical methods using hanging mercury drop electrode (HMDE). On this electrode, AZT undergoes irreversible reduction at the peak potential near Ep?1.1 V (vs. Ag/AgCl/3 M KCl). Reduction AZT signals were measured by cyclic voltammetry (CV), differential pulse voltammetry (DPV), square‐wave voltammetry (SWV), and constant current chronopotentiometric stripping analysis (CPSA). In phosphate buffer (pH 8) the SWV yielded the best AZT signal with the detection limit of 1 nM. The determination of AZT concentration in biological materials is affected by electroactive components, such as proteins and DNA. For monitoring the influence of these compounds, AZT reduction was performed in the presence of 10 μg/mL calf thymus ssDNA and/or 100 μg/mL bovine serum albumin. In these cases, the detection limit increased to 0.25 μM. Also studied was the AZT concentration in keratinocyte cells (HaCaT line) during cell cultivation. It has been shown that the SWV may be considered as a useful tool for the determination of AZT concentration in cell cultures, and for monitoring AZT pharmacokinetics. 相似文献
17.
18.
Arsenic Speciation in Urine and Blood Reference Materials 总被引:1,自引:0,他引:1
Todor I. Todorov John W. Ejnik Florabel G. Mullick Jose A. Centeno 《Mikrochimica acta》2005,151(3-4):263-268
Acute and chronic exposure to arsenic is a growing problem in the industrialized world. Arsenic is a potent carcinogen and
toxin in humans. In the body, arsenic is metabolized to produce several species, including inorganic forms, such as trivalent
(AsIII) and pentavalent (AsV), and the methylated metabolites such as monomethylarsonic acid, (MMAV), and dimethylarsinic acid (DMAV), in addition to arsenobetaine (AsB) which is ingested and excreted from the body in the same form. Each of these species
has been reported to possess a specific but different degree of toxicity. Thus, not only is the measurement of total As required,
but also quantification of the individual metabolites is necessary to evaluate the toxicity and risk assessment of this element.
There are a large number of reference materials that are used to validate methodology for the analysis of As in blood and
urine, but they are limited to total As concentrations. In this study, the speciation of five arsenic metabolites is reported
in blood and urine from commercial available control materials certified for total arsenic levels. The separation was performed
with an anion exchange column using inductively coupled plasma mass spectrometry as a detector. Baseline separation was achieved
for AsIII, AsV, MMAV, DMAV, and AsB, allowing us to quantify all five species. Excellent agreement between the total arsenic levels and the sum of the
speciated As levels was obtained. 相似文献
19.
Burchard Franck 《Angewandte Chemie (International ed. in English)》1982,21(5):343-353
Uroporphyrinogen III plays a key role in the biosynthesis of heme, the red pigment of blood. In vivo studies with specifically 14C- and 3H-labeled precursors have revealed that the formation uroporphyrinogen III in the organism follows several primary and subsidiary pathways. Model experiments on the pattern of biosynthesis have led to simple and effective methods of synthesizing uroporphyrin analogs and have shown that their production is strongly favored thermodynamically. The biologically porphyrins important thus available permit a mechanistic explanation of the light-induced dermatoses in porphyria diseases and suggest promising medical applications in diagnosis and therapy. 相似文献
20.
A total of seven pesticides and eight alkylphenols were monitored using this method for the determination of their trace levels in human cord blood. The pesticides are lindane, diazinon, α-endosulfan, β-endosulfan, endosulfan sulfate, chlorpyrifos and endrin; while the alkylphenols are 4-n-butylphenol, 4-n-pentylphenol, 4-n-hexylphenol, 4-t-octylphenol, 4-n-heptylphenol, nonylphenol, 4-n-octylphenol and bisphenol A. The pesticides and alkylphenols in the cord blood samples were extracted with solid phase extraction IST C18 cartridges and analyzed by selected ion monitoring mode using quadrapole detector in Shimadzu QP-5000 gas chromatograph-mass spectrometer. Trace levels of pesticide and alkylphenols in the range of non-detectable to 15.17 ng ml−1, were detected in the human cord blood samples. This technique of monitoring the levels of endocrine-disruptors in blood samples is consistent, reliable and cost effective while reducing wastage of time and solvents. 相似文献