Yin Tianpeng, Lu Jingguang, Liu Qinghua, Zhu Guoyuan, Zhang Wei, Jiang Zhihong
State Key Laboratory of Quality Research in Chinese Medicines, Macau Institute for Applied Research in Medicine and Health, Macau University of Science and Technology, Taipa 999078, Macau, China.
Faculty of Bioengineering, Zunyi Medical University, Zhuhai Campus, Zhuhai 519041, China.
ACS Omega. 2021 Nov 16;6(47):31810-31817. doi: 10.1021/acsomega.1c04464. eCollection 2021 Nov 30.
Uncariae Ramulus Cum Uncis, known as "Gou-Teng" in Chinese, is derived mainly from the dried hook-bearing stems of . Quantitative determination of monoterpenoid indole alkaloids is critical for controlling its quality. In the present study, a rapid, accurate, and precise method was developed for the simultaneous quantitation of four characteristic components, namely, rhynchophylline (), isorhynchophylline (), corynoxeine (), and isocorynoxeine (), through H NMR spectrometry techniques. This method was performed on a 600 MHz NMR spectrometer with optimized acquisition parameters for performing quantitative experiments within 14 min. The highly deshielded signal of NH was at δ 10-11 in the aprotic solvent DMSO- , which enables satisfactory separation of the signals to be integrated. Validation of the quantitative method was also performed in terms of specificity, linearity, sensitivity, accuracy, and precision. The method is linear in the concentration range of 25-400 μg/mL. The lower limit of quantification is 25 μg/mL. The intra- and interday relative standard deviation across three validation runs over the entire concentration range is less than 2.51%. The accuracy determined at three concentrations was within ±4.4% in terms of relative error. The proposed qNMR method was demonstrated to be a powerful tool for quantifying the alkaloids in traditional Chinese medicines (TCMs) due to its unique advantages of high precision, rapid analysis, and nonrequirement of standard compounds for calibration curve preparation. Moreover, qNMR represents a feasible alternative to high-performance liquid chromatography-based methods for the quality control of TCMs.
钩藤,中药名为“钩藤”,主要来源于带钩茎枝的干燥品。单萜吲哚生物碱的定量测定对其质量控制至关重要。在本研究中,开发了一种快速、准确且精密的方法,通过1H NMR光谱技术同时定量四种特征成分,即钩藤碱、异钩藤碱、柯诺辛碱和异柯诺辛碱。该方法在600 MHz NMR光谱仪上进行,采用优化的采集参数,可在14分钟内完成定量实验。在非质子溶剂DMSO-d6中,NH的高去屏蔽信号位于δ 10 - 11处,这使得待积分信号能够得到满意的分离。还从特异性、线性、灵敏度、准确度和精密度方面对定量方法进行了验证。该方法在25 - 400 μg/mL浓度范围内呈线性。定量下限为25 μg/mL。在整个浓度范围内,三次验证运行的日内和日间相对标准偏差均小于2.51%。在三个浓度下测定的准确度,相对误差在±4.4%以内。所提出的定量核磁共振方法因其具有高精度、快速分析以及无需标准化合物制备校准曲线的独特优势,被证明是定量中药中生物碱的有力工具。此外,定量核磁共振是基于高效液相色谱法进行中药质量控制的一种可行替代方法。