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使用新型羟基磷灰石-胶原蛋白校准标准品,通过激光烧蚀电感耦合等离子体质谱法对骨中局部锌和钨沉积物进行定量分析。

Quantification of local zinc and tungsten deposits in bone with LA-ICP-MS using novel hydroxyapatite-collagen calibration standards.

作者信息

VanderSchee Cassidy R, Frier David, Kuter David, Mann Koren K, Jackson Brian P, Bohle D Scott

机构信息

Department of Chemistry, McGill University, Montreal, H3A 0B8, Canada.

Department of Chemistry, The King's University, Edmonton, T6H 2H3, Canada.

出版信息

J Anal At Spectrom. 2021 Nov;36(11):2431-2438. doi: 10.1039/d1ja00211b. Epub 2021 Sep 20.

Abstract

Tungsten has recently emerged as a potential toxicant and is known to heterogeneously deposit in bone as reactive polytungstates. Zinc, which accumulates in regions of bone remodeling, also has a heterogenous distribution in bone. Determining the local concentrations of these metals will provide valuable information about their mechanisms of uptake and action. A series of bone (BN), 7:3 hydroxyapatite:collagen (HC), and hydroxyapatite (HA) standards were spiked with tungsten and zinc and used as calibration standards for laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) analysis of bone tissue. The analytical performance of these standards was studied and validated at different step sizes using NIST SRM 1486 Bone Meal. The effect of matrix-matched calibration was assessed by comparing the calibration with BN and HC standards, which incorporate both inorganic and organic components of bone, to that of HA standards. HC standards were found to be more homogenous (RSD < 10%) and provide a linear calibration with better accuracy (R > 0.994) compared to other standards. The limits of detection for HC at a 15 μm step size were determined to be 0.24 and 0.012 μg g for zinc and tungsten, respectively. Using this approach, we quantitatively measured zinc and tungsten deposits in the femoral bone of a mouse exposed to 15 μg mL tungsten for four weeks. Localized concentrations of zinc (942 μg g) and tungsten (15.7 μg g) at selected regions of enrichment were substantially higher than indicated by bulk measurements of these metals.

摘要

钨最近已成为一种潜在的有毒物质,已知它会以活性多钨酸盐的形式非均匀地沉积在骨骼中。锌在骨骼重塑区域积累,在骨骼中也具有非均匀分布。确定这些金属的局部浓度将为它们的摄取和作用机制提供有价值的信息。一系列骨(BN)、7:3羟基磷灰石:胶原蛋白(HC)和羟基磷灰石(HA)标准品用钨和锌进行加标,并用作骨组织激光烧蚀电感耦合等离子体质谱(LA-ICP-MS)分析的校准标准品。使用NIST SRM 1486骨粉在不同步长下研究并验证了这些标准品的分析性能。通过比较使用包含骨骼无机和有机成分的BN和HC标准品进行校准与使用HA标准品进行校准的效果,评估了基体匹配校准的影响。发现HC标准品比其他标准品更均匀(相对标准偏差<10%),并提供具有更高准确度(R>0.994)的线性校准。在15μm步长下,HC对锌和钨的检测限分别确定为0.24和0.012μg/g。使用这种方法,我们定量测量了暴露于15μg/mL钨四周的小鼠股骨中锌和钨的沉积量。在选定的富集区域,锌(942μg/g)和钨(15.7μg/g)的局部浓度明显高于这些金属的整体测量值。

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