Qiu Zi-Dong, Wei Xu-Ya, Sun Rui-Qi, Chen Jin-Long, Tan Ting, Xu Jia-Quan, Cui Guang-Hong, Chen Tong, Guo Juan, Lai Chang-Jiang-Sheng, Huang Lu-Qi
State Key Laboratory Breeding Base of Dao-di Herbs, National Resource Center for Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China.
State Key Laboratory of Natural Medicines, China Pharmaceutical University, Nanjing 210009, China.
Acta Pharm Sin B. 2020 Aug;10(8):1511-1520. doi: 10.1016/j.apsb.2019.12.009. Epub 2019 Dec 19.
Development of rapid analytical methods and establishment of toxic component limitation standards are of great importance in quality control of traditional Chinese medicine. Herein, an on-line extraction electrospray ionization mass spectrometry (oEESI-MS) coupled with a novel whole process integral quantification strategy was developed and applied to direct determination of nine key aconitine-type alkaloids in 20 proprietary Chinese medicines (APCMs). Multi-type dosage forms (, tablets, capsules, pills, granules, and liquid preparation) of APCM could be determined directly with excellent versatility. The strategy has the characteristics of high throughput, good tolerance of matrix interference, small amount of sample (∼0.5 mg) and reagent (∼240 μL) consumption, and short analysis time for single sample (<15 min). The results were proved to be credible by high performance liquid chromatography-mass spectrometry (LC-MS) and electrospray ionization mass spectrometry, respectively. Moreover, the limitation standard for the toxic aconitines in 20 APCMs was established based on the holistic weight toxicity (HWT) evaluation and the severally, and turned out that HWT-based toxicity evaluation results were closer to the real clinical applications. Hence, a more accurate and reliable APCM toxicity limitation was established and expected to play an important guiding role in clinics. The current study extended the power of ambient MS as a method for the direct quantification of molecules in complex samples, which is commonly required in pharmaceutical analysis, food safety control, public security, and many other disciplines.
快速分析方法的开发以及有毒成分限量标准的建立在中药质量控制中至关重要。在此,开发了一种在线萃取电喷雾电离质谱(oEESI-MS)并结合一种新型的全过程积分定量策略,并将其应用于直接测定20种中成药中的9种关键乌头碱型生物碱。中成药的多种剂型(片剂、胶囊、丸剂、颗粒剂和液体制剂)均可直接测定,通用性极佳。该策略具有高通量、对基质干扰耐受性好、样品用量少(约0.5毫克)和试剂用量少(约240微升)以及单一样品分析时间短(<15分钟)的特点。分别通过高效液相色谱-质谱(LC-MS)和电喷雾电离质谱证明结果可靠。此外,基于整体重量毒性(HWT)评估分别建立了20种中成药中有毒乌头碱的限量标准,结果表明基于HWT的毒性评估结果更接近实际临床应用。因此,建立了更准确可靠的中成药毒性限量标准,有望在临床上发挥重要的指导作用。当前的研究扩展了常压质谱作为直接定量复杂样品中分子的方法的能力,这在药物分析、食品安全控制、公共安全以及许多其他学科中是普遍需要的。