共查询到20条相似文献,搜索用时 297 毫秒
1.
2.
介绍了氯化钾电导率溶液标准物质的研制方法,采用与一级标准物质比较定值的方法对该标准物质进行了定值,利用高精度电导率仪对定值结果进行了验证,同时对该标准物质进行了均匀性检验和稳定性考察。氯化钾电导率溶液标准物质的定值结果为1408μS/cm,扩展不确定度为:Urel=0.6%,k=2。其均匀性和稳定性检验结果表明,该标准物质符合国家二级标准物质的技术要求。 相似文献
3.
4.
5.
6.
龚维姚旭霞田平吕辉刘新 《计量学报》2023,(12):1912-1918
余氯是水质监测的一个重要指标,是评判水质好坏的重要参数。为此,研制了国家二级总余氯标准物质GBW(E)084725、GBW(E)084726。针对常用的总余氯测量方法,从中选取适合标准物质定值的测试方法,并对测试方法进行方法学研究。分别对2种浓度总余氯标准物质进行了均匀性和稳定性检验。方差检验F值均小于列表临界值,表明该标准物质均匀性良好。在6个月的稳定性考察期内,2种含量的标准物质在统计学上无明显变化,进行10天短期高低温模拟实验,2种含量的标准物质在统计学上也无明显变化,说明2种标准物质稳定性良好。采用氧化还原滴定法进行标准物质定值,量值分别为50 mg/L和500 mg/L,相对扩展不确定度分别为0.9%和0.5%。 相似文献
7.
8.
采用专用的白细胞、红细胞和血小板3类生物粒子合成模拟人的血液,按照国家一级标准物质研制规范制备血细胞计数标准物质,采用显微图像分析法为血细胞计数标准物质定值,对该血细胞计数标准物质的定值结果及不确定度评定、均匀性检验、稳定性检验过程进行分析,将该血细胞标准物质定值结果与国际参考方法的测定结果进行比对。结果证明:本血细胞计数标准物质适于血细胞分析仪的校准与计量检定。 相似文献
9.
采用二甲基亚砜(DMSO)作为冻干标准物质的溶剂,以重量法准确配制维生素K_1/DMSO溶液,再进行分装、冷冻干燥,经定性分析、定值分析、均匀性检验、稳定性考察和不确定度评定,研制了维生素K_1冻干标准物质。以维生素K_1纯度标准物质溶液为校准品,对得到的冻干物质进行了高效液相色谱法定值分析,冻干标准物质的准确定值结果为0.96 mg/mL,相对扩展不确定度为7%。建立的维生素K_1冻干标准物质研制方法,对于临床检验中维生素K_1的准确测定和相关疾病的正确诊断治疗以及维生素K_1长期保存具有重要意义。 相似文献
10.
文章以氟化钠标准物质为原料,超纯水为溶剂,采用重量-容量法制备水中氟离子溶液标准物质,介绍了水中氟离子溶液标准物质的研制方法。研制的水中氟离子溶液标准物质利用离子色谱法进行检测,分别采用F检验和回归曲线法进行均匀性和稳定性检验,方差分析和线性拟合结果表明该标准物质具有良好的均匀性和稳定性。选择国家二级标准物质采用同样的检测方法进行验证,结果表明制备的标准物质的方法准确度满足要求。研制的水中氟离子溶液标准物质的定值结果为1 000 mg/L,相对扩展不确定度Urel=1%(k=2)。该标准物质量值准确,且具有溯源性,可用于水中氟离子测量过程的质量控制及分析方法的确认和评价。 相似文献
11.
12.
血糖是诊断和判别糖尿病的直接指标,标准物质是血糖检测结果准确可比的重要保障。研制人血清中6个不同浓度水平的葡萄糖标准物质的过程包括标准物质的制备、定值、均匀性、稳定性检验、不确定度评定以及互通性评价等内容。其中标准物质定值采用了两种不同原理的方法即同位素稀释-液相色谱-串联质谱法及同位素稀释-气相色谱-质谱法,准确测定人血清中葡萄糖的浓度,并重点分析了两种方法测试结果的差异及成因。人血清中葡萄糖标准物质的量值覆盖1.70~28.12 mmol/L,具有良好的均匀性和稳定性,已获得国家二级标准物质定级证书,编号为GBW(E)091140~GBW(E)091145,有望用于临床检验及相关领域对血清葡萄糖项目测量的质量评价等方面。 相似文献
13.
14.
Progesterone is a steroid hormone that is involved in regulating female reproductive processes. Its concentration in blood is measured to determine ovarian function. A candidate reference measurement procedure for progesterone in human serum involving isotope dilution coupled with liquid chromatography/tandem mass spectrometry (LC/MS/MS) has been developed and critically evaluated. The progesterone along with its internal standard (progesterone-13C2) was extracted from the serum matrix using liquid-liquid extraction prior to reversed-phase LC/MS/MS. The accuracy of the measurement was evaluated by a comparison of results of this method on a lyophilized human serum reference material for progesterone [Certified Reference Material (CRM) 347] with the certified values determined by gas chromatography/mass spectrometry (GC/MS) reference methods and by a recovery study for the added progesterone. The results of this method for progesterone agreed with the certified value within the uncertainty of the measurements for the CRM 347. The recovery of the added progesterone ranged from 100.1 to 100.9%. This method was applied to the determination of progesterone in frozen serum samples from three individual female donors with the progesterone concentrations ranging from 0.151 to 24.42 ng/g. Excellent reproducibility was obtained with within-set coefficients of variation (CVs) ranging from 0.1 to 1.4%, and between-set CVs ranging from 0.3 to 0.5%. Excellent linearity was also obtained with correlation coefficients of all linear regression lines (measured intensity ratios vs mass ratios) ranging from 0.9998 to 1.0000. The detection limit at a signal-to-noise ratio of approximately 3 was 1.8 pg of progesterone. This well-characterized LC/MS/MS method for serum progesterone, which demonstrates good accuracy and precision, low susceptibility to interferences, and comparability with GC/MS reference methods, qualifies as a reference measurement procedure that can be used to provide an accuracy base to which routine methods for progesterone can be compared and that will serve as a standard of higher order for measurement traceability. 相似文献
15.
采用了以高一级标准物质为标准进行比较定值的方式,进而分析了火药爆热标准物质标准值的误差来源和影响因素,并评估了标准物质标准值的合成标准不确定度和扩展不确定度。 相似文献
16.
17.
18.
19.