A: Thin-Layer Chromatographic Identification Test 201
Test solution
Transfer 1.0 g of finely powdered Asian Ginseng to a 25-mL flask fitted with a reflux condenser. Add 10.0 mL of a mixture of methanol and water (7:3), and heat under reflux for 15 minutes. Cool, filter, and dilute the filtrate with methanol to 10.0 mL.
Standard solution:
about 5 mg per mL each of arbutin and escin, in methanol.
Application volume:
20 µL, as bands.
Developing solvent system:
the upper layer of a mixture of butyl alcohol, water, and ethyl acetate (10:5:2.5) in an unsaturated chamber.
Spray reagent
Dissolve 0.5 mL of anisaldehyde in 10 mL of glacial acetic acid, add 85 mL of methanol, and mix. Carefully add 5 mL of sulfuric acid to this mixture, and mix.
Procedure
Proceed as directed in the chapter. Remove the plate from the developing chamber, and allow it to dry. Spray with
Spray reagent. Heat the plate at 105
to 110
for about 10 minutes, and examine the plate. The chromatogram of the
Standard solution shows, in the upper third, a brown zone corresponding to arbutin and, in the lower third, a gray zone corresponding to escin. Between these two zones, the chromatogram of the
Test solution exhibits violet-gray zones corresponding to ginsenoside Rg
1 in the upper portion and to ginsenoside Re in the middle. A violet-gray zone corresponding to ginsenoside Rb
1 is located at the same
RF value as the gray zone corresponding to escin in the chromatogram of the
Standard solution. Other, less intense bands may be observed between the zones due to ginsenosides Rb
1 and Re, and the zone closest to the origin corresponds to ginsenoside Rc. Other spots may be visible in the lower third of the chromatogram.