Yang Hua, Liu Lei, Gao Wen, Liu Ke, Qi Lian-Wen, Li Ping
State Key Laboratory of Natural Medicines, China Pharmaceutical University, No. 24 Tongjia Lane, Nanjing 210009, China.
State Key Laboratory of Natural Medicines, China Pharmaceutical University, No. 24 Tongjia Lane, Nanjing 210009, China.
J Pharm Biomed Anal. 2014 Apr;92:13-21. doi: 10.1016/j.jpba.2013.12.041. Epub 2014 Jan 7.
Shenfu injection (SFI) is a widely used Chinese herbal formulation for cardiac diseases prepared from red ginseng and processed aconite root. Clinical observations and pharmacological effects on SFI have been well investigated. Chemical analysis and quality control studies of this formulation, however, are relatively limited, especially regarding toxic aconite alkaloids. In this work, a high-performance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (HPLC-QTOF MS) method was applied to comprehensive analysis of constituents in SFI. Highly sensitive MS allows direct analysis of injections without additional sample pretreatment required. Using diagnostic ions and fragmentation rules, we identified 23 trace diterpene alkaloids, nineteen ginseng saponins, one panaxytriol, and one 5-hydroxymethylfurfural in SFI. A LC-MS method with selected ion monitoring was then used to quantify 24 major alkaloids and ginsenosides. The method was validated in terms of linearity, accuracy and precision. Especially, the limits of quantification were low to 0.4-18ng/mL for diterpene alkaloids. The total concentrations of saponins and alkaloids were about 676-742μg/mL and 3-7μg/mL in five batches of SFI samples, respectively. Finally, cosine ratio and euclidean distance were introduced to evaluate the batch-to-batch reproducibility of SFI samples, and the results demonstrated high quality consistency. Global identification and quantification of complex constituents based on LC-MS promises wide applications in quality control and batch monitoring for herbal products.
参附注射液(SFI)是一种广泛用于治疗心脏病的中药制剂,由红参和制附子制备而成。对参附注射液的临床观察和药理作用已进行了充分研究。然而,该制剂的化学分析和质量控制研究相对有限,尤其是关于有毒乌头生物碱方面。在本研究中,采用高效液相色谱-四极杆飞行时间质谱联用(HPLC-QTOF MS)方法对参附注射液中的成分进行全面分析。高灵敏度质谱可直接分析注射液,无需额外的样品预处理。利用诊断离子和裂解规则,我们在参附注射液中鉴定出23种痕量二萜生物碱、19种人参皂苷、1种人参三醇和1种5-羟甲基糠醛。然后采用选择性离子监测的液相色谱-质谱法对24种主要生物碱和人参皂苷进行定量分析。该方法在线性、准确度和精密度方面均得到验证。特别是,二萜生物碱的定量限低至0.4-18ng/mL。五批参附注射液样品中皂苷和生物碱的总浓度分别约为676-742μg/mL和3-7μg/mL。最后,引入余弦比和欧氏距离来评估参附注射液样品批次间的重现性,结果表明其具有高质量的一致性。基于液相色谱-质谱的复杂成分的全面鉴定和定量有望在草药产品的质量控制和批次监测中得到广泛应用。