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. 2012 Aug 27;17(9):10242-57.
doi: 10.3390/molecules170910242.

Identification and determination of Aconitum alkaloids in Aconitum herbs and Xiaohuoluo pill using UPLC-ESI-MS

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Identification and determination of Aconitum alkaloids in Aconitum herbs and Xiaohuoluo pill using UPLC-ESI-MS

Ping Cui et al. Molecules. .

Abstract

A rapid, specific, and sensitive ultra-performance liquid chromatography-electrospray ionization-mass spectrometry (UPLC-ESI-MS) method to examine the chemical differences between Aconitum herbs and processed products has been developed and validated. Combined with chemometrics analysis of principal component analysis (PCA) and orthogonal projection to latent structural discriminate analysis, diester-diterpenoid and monoester-type alkaloids, especially the five alkaloids which contributed to the chemical distinction between Aconitum herbs and processed products, namely mesaconitine (MA), aconitine (AC), hypaconitine (HA), benzoylmesaconitine (BMA), and benzoylhypaconitine (BHA), were picked out. Further, the five alkaloids and benzoylaconitine (BAC) have been simultaneously determined in the Xiaohuoluo pill. Chromatographic separations were achieved on a C₁₈ column and peaks were detected by mass spectrometry in positive ion mode and selected ion recording (SIR) mode. In quantitative analysis, the six alkaloids showed good regression, (r) > 0.9984, within the test ranges. The lower limit quantifications (LLOQs) for MA, AC, HA, BMA, BAC, and BHA were 1.41, 1.20, 1.92, 4.28, 1.99 and 2.02 ng·mL⁻¹, respectively. Recoveries ranged from 99.7% to 101.7%. The validated method was applied successfully in the analysis of the six alkaloids from different samples, in which significant variations were revealed. Results indicated that the developed assay can be used as an appropriate quality control assay for Xiaohuoluo pill and other herbal preparations containing Aconitum roots.

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Figures

Figure 1
Figure 1
(A) UPLC-ESI-MS total ion chromatogram (B) and extracted ion chromatogram from Aconitum herbs and processed products. (A1, B1) Radix Aconiti kusnezoffii, (A2, B2) Radix Aconiti Kusnezoffii Praeparata, (A3, B3) Radix Aconiti, and (A4, B4) Radix Aconiti Praeparata. Peaks 1 to 16 are shown in Table 1.
Figure 2
Figure 2
PCA score plot: (1) Radix Aconiti (RA); (2) Radix Aconiti Praeparata (RAP); (3) Radix Aconiti Kusnezoffii (RAK); and (4) Radix Aconiti Kusnezoffii Praeparata (RAKP).
Figure 3
Figure 3
(A) OPLS-DA score plot and (B) S-plot obtained from the groups of RAK and RAKP (I) Radix Aconiti Kusnezoffii and (II) Radix Aconiti Kusnezoffii Praeparata.
Figure 4
Figure 4
(A) UPLC-MS total ion chromatogram and (B) extracted ion chromatogram from the Xiaohuoluo pill. (A1, B1) Concentrated pill and (A2, B2) honey pill (1-delcosine, 2-isotalatizidine, 3-talatizamine, 4-benzoylmesaconitine, 5-aconosine, 6-benzoylaconine, 7-foresticine, 8-benzoylhypaconitine, 9-songorine).
Figure 5
Figure 5
Typical SIR chromatograms of (a) HA, (b) AC, (c) MA, (d) BHA, (e) BAC, and (f) BMA. (A) Mixed standards; (B) samples of Xiaohuoluo pill.

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