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Alcoholic beverages from araçá-boi fruit: quantification of antioxidant compounds by NMR ERETIC2.阿拉萨博伊果制成的酒精饮料:通过核磁共振ERE TIC2对抗氧化化合物进行定量分析。
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A feasible and practical H NMR analytical method for the quality control and quantification of bioactive principles in Lycii Fructus.一种可行且实用的~1H NMR 分析方法,用于控制和定量枸杞中生物活性成分的质量。
J Food Drug Anal. 2018 Jul;26(3):1105-1112. doi: 10.1016/j.jfda.2018.01.001. Epub 2018 Jan 17.
3
Evolution of Quantitative Measures in NMR: Quantum Mechanical qHNMR Advances Chemical Standardization of a Red Clover (Trifolium pratense) Extract.核磁共振定量测量的发展:量子力学qHNMR推动红三叶草(Trifolium pratense)提取物的化学标准化。
J Nat Prod. 2017 Mar 24;80(3):634-647. doi: 10.1021/acs.jnatprod.6b00923. Epub 2017 Jan 9.
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Quantitative Nuclear Magnetic Resonance Spectroscopy Based on PULCON Methodology: Application to Quantification of Invaluable Marine Toxin, Okadaic Acid.基于PULCON方法的定量核磁共振波谱法:在珍贵海洋毒素——冈田酸定量分析中的应用
Toxins (Basel). 2016 Oct 13;8(10):294. doi: 10.3390/toxins8100294.
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6
Determination of the purity of pharmaceutical reference materials by 1H NMR using the standardless PULCON methodology.采用无标准物PULCON方法通过¹H NMR测定药物标准物质的纯度。
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Accurate determination of reference materials and natural isolates by means of quantitative (1)h NMR spectroscopy.通过定量 (1)h NMR 光谱法准确测定参考物质和天然分离物。
J Agric Food Chem. 2014 Mar 26;62(12):2506-15. doi: 10.1021/jf405529b. Epub 2014 Mar 11.
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Improving the efficiency of quantitative (1)H NMR: an innovative external standard-internal reference approach.提高定量 (1)H NMR 效率:一种创新的外标-内标方法。
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10
Validation of a generic quantitative (1)H NMR method for natural products analysis.一种用于天然产物分析的通用定量(1)H NMR 方法的验证。
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准确而精确的外部校准增强了定量 NMR(qNMR)的多功能性。

Accurate and Precise External Calibration Enhances the Versatility of Quantitative NMR (qNMR).

机构信息

Division of Food Additives, National Institute of Health Sciences (NIHS), Kawasaki-ku, Kawasaki, Kanagawa 210-9501, Japan.

出版信息

Anal Chem. 2021 Feb 9;93(5):2733-2741. doi: 10.1021/acs.analchem.0c02967. Epub 2021 Jan 22.

DOI:10.1021/acs.analchem.0c02967
PMID:33481571
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8046598/
Abstract

Quantitative H nuclear magnetic resonance (qHNMR) is a highly regarded analytical methodology for purity determination as it balances metrological rigor, practicality, and versatility well. While ideal for intrinsically mass-limited samples, external calibration (EC) qHNMR is overshadowed by the prevalence of internal calibration and perceived rather than real practical limitations. To overcome this hurdle, this study applied the principle of reciprocity, certified reference materials (caffeine as analyte, dimethyl sulfone as calibrant), and a systematic evaluation of data acquisition workflows to extract key factors for the achievement of accuracy and precision in EC-qHNMR. Automatic calibration of the 90° pulse width (90 PW) formed the foundation for the principle of reciprocity and used optimized nutation experiments, showing good agreement with values derived from manual high-precision measurement of 360 PW. Employing the automatic 90 PW calibration, EC-qHNMR with automatic vs manual tuning and matching (T&M) yielded the certified purity value within 1% error. The timing of T&M (before vs after shimming) turned out to be critically important: sufficient time is required to achieve full-temperature equilibrium relative to thermal gradients in the air inside the probe and the sample. Achievable accuracy across different NMR solvents varies with differences in thermal conductivity and leads to 2% or greater errors. With matching solvents, the demonstrated accuracy of ∼1.0% underscores the feasibility of EC-qHNMR as a highly practical research tool.

摘要

定量氢核磁共振(qHNMR)是一种备受推崇的纯度分析方法,因为它很好地平衡了计量学的严格性、实用性和多功能性。虽然它非常适合本质上质量有限的样品,但外部校准(EC)qHNMR 由于内部校准的普及以及感知到的而不是实际的实用限制而黯然失色。为了克服这一障碍,本研究应用了互易原理、认证参考物质(咖啡因作为分析物,二甲亚砜作为校准剂),以及对数据采集工作流程的系统评估,以提取在 EC-qHNMR 中实现准确性和精密度的关键因素。90°脉冲宽度(90PW)的自动校准为互易原理奠定了基础,并使用了优化的旋进实验,与手动高精度测量 360PW 得出的值具有良好的一致性。采用自动 90PW 校准,自动与手动调谐和匹配(T&M)的 EC-qHNMR 在 1%的误差范围内产生了认证的纯度值。T&M 的时间(在调谐之前与之后)非常重要:相对于探头和样品内部空气中的热梯度,需要足够的时间来实现全温度平衡。不同 NMR 溶剂的可实现精度因热导率的差异而有所不同,导致误差为 2%或更高。使用匹配的溶剂,所证明的约 1.0%的精度突出了 EC-qHNMR 作为一种高度实用的研究工具的可行性。