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Bacopa |
(previous URL: http://wakandb.u-toyama.ac.jp/wiki/LCMS:Bacopa_INM-484)
試料情報
Voucher No. INM-484
ダウンロード
TIC, MC, and Compounds
Analytical conditions 1 (Fig. 1)
Instrument | Shimadzu LC-IT-TOF MS ESI |
Column | Waters Atlantis T3 (2.1 mm x 150 mm) |
Column Temperature | 40 °C |
Solvent A | 5 mM Ammonium acetate solution |
Solvent B | acetonitrile |
Gradient | 10% to 100% Solvent B (0-30 min), 100% Solvent B (30-40 min) |
Source voltage | 4.5 kV (Positive ion mode), -3.5 kV (Negative ion mode) |
Capillary temperature | 200 °C |
Nebulizer gas | 1.5 l/min |
Analytical conditions 2 (Fig. 2)
Instrument | TSQ7000 ESI |
Column | Waters Atlantis T3 (2.1 mm x 100 mm, 3 μm) |
Column Temperature | 40 °C |
Solvent A | 5 mM Ammonium acetate solution |
Solvent B | acetonitrile |
Flow rate: | 0.15 ml/min |
Gradient | 10% to 100% Solvent B (0-30 min), 100% Solvent B (30-40 min) |
Source voltage | -3.5 kV (Negative ion mode) |
Analytical conditions 3 (Figs. 3-5)
Instrument | TSQ7000 ESI |
Column | Waters Atlantis T3 (2.1 mm x 100 mm, 3 μm) |
Column Temperature | 40 °C |
Solvent A | 0.1% HCOOH |
Solvent B | acetonitrile |
Flow rate: | 0.15 ml/min |
Gradient | 10% to 100% Solvent B (0-30 min), 100% Solvent B (30-40 min) |
Source voltage | -3.5 kV (Negative ion mode) |
Remarks
Figs. 2 and 3 show effect of chromatographic conditions on separation of bacopasides. When CH3COONH4 was used as solvent A (Fig. 2), the order of elution was: Bacopaside I → Bacoside A3 → Bacoside A2 → Bacopaside N1 → Bacopaside N2. In contrast, when HCOOH was used as solvent A (Fig. 3), the order of elution was: Bacoside A3 → Bacoside A2 → Bacopaside N1 → Bacopaside N2 → Bacopaside I. Figs. 4 and 5 show Quantitation of bacopasides. Fig. 4: Standard compounds. Fig. 5: Extract (10 mg/ml solution, 1 μl injection).
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