Abutili Semen (Qingmazi)

Abutili Semen (Qingmazi)

Chingma Abutilon Seed

Chingma Abutilon Seed is the dried ripe seed of Abutilon theophrastii Medic. (Fam. Malvaceae). The fruit is collected in autumn when ripe, dried in the sun, and the seed is trapped out, removed from foreign matter.

Description:

Triangular reniform, 3. 5-6 mm long, 2. 54. 5 mm wide, 1-2 mm thick. Externally greyish-black or dark brown, bearing sparse white tomenta, a subelliptical hilum at the dented part, pale brown, radially striated around the edges. Testa hard, cotyledons 2, folded, oily. Odour, slight; taste, weak.

Identification:

(1) Transverse section: Epidermal cells 1 layer, flattened-rectangular, sometimes differentiated to unicellu-lar non-glandular hairs; hypodermal cells 1 layer, slightly radially prolated. Palisade cells 1 row, cylindrical, up to about 88 µm long, heavily thick-walled, linear lumina visible at the upper part, the terminal end expended, containing small globular crystals. Pigment cells 4-5 layers, containing yellowish-brown or reddish-brown contents. Cells of endosperm and cotyledons, containing fatty oil droplets and aleurone grains, cells of cotyledons also containing a few of fine clusters of calcium oxalate. :
(2) Add 2 g of the powder to a Soxhlet’s extractor, and add appropriate quantity of petroleum ether (60-90oC), heat under reflux to the extract colourless, cool, discard the petroleum ether. Evaporate the residue to dryness, add 30 ml of ethanol, ultrasonicate for 30 minutes, cool, filter, concentrate the filtrate to 2 ml as the test solution. Prepare a solution of 2 g of Abutili Semen in the same manner as the reference drug solution Carry out the method for thin layer chromatography (Appendix VI B ) , using silica gel G as the coating substance and a mixture of chloroform, acetone, methanol and formic acid (3 : 1 : 0. 5 : 0.1) as the mobile phase. Apply separately 5 µl of each of the above two solutions to the plate. After developing and removal of the plate, dry it in air, spray with a 10% solution of sulfuric acid in ethanol, heat at 110°C to the spots clear. Examine under ultraviolet light at 365 nm, the fluorescent spots in the chromatogram obtained with the test solution correspond in position and colour to the fluorescent spots in the chromatogram obtained with the reference drug solution.

Foreign matter:

Not more than 1 percent (Appendix IX A).

Water:

Not more than 10.0 percent (Appendix IX H, method 2).

Total ash :

Not more than 7. 0 percent (Appendix IX K).

Extractives:

Carry out the hot extraction method for determination of ethanol-soluble extractives (Appendix X A), using anhydrous ethanol as solvent, not less than 17. 0 percent

Property and Flavor:

Neutral; bitter.

Meridian tropism:

Large intestine, small intestine and bladder meridians.

Actions:

To clear heat and remove toxin, drain dampness, relieve nebula.

Indications:

Red or white dysentery, stranguria with slow pain, swelling abscess, sore and toxin, nebula.

Administration and dosage:

3-9 g.

Storage:

Preserve in a cool and dry place.

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