鼻炎丸的制备及临床应用(Preparation and clinical application of Biyan Wan).docVIP

鼻炎丸的制备及临床应用(Preparation and clinical application of Biyan Wan).doc

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鼻炎丸的制备及临床应用(Preparation and clinical application of Biyan Wan)

鼻炎丸的制备及临床应用(Preparation and clinical application of Biyan Wan) Preparation and clinical application of Biyan Wan Update Date: 2011-05-18 Click: Song rainbow Rhinitis is a common and frequently occurring disease in clinic. However, it is still rare to treat the rhinitis at present. In recent years, our hospital has applied self developed rhinitis pills to treat rhinitis, sinusitis, allergic rhinitis and intractable headache caused by rhinitis. It is reported as follows: 1 Prescription By rhinitis pills angelica, Xanthium, parsnip, isatis root, magnolia flower, chuanxiong, mint, Herba Centipedae and Radix Scutellariae etc.. 2 preparation The above herbs washed, dried, crushed through 100 mesh sieve, in coating pan with cold distilled water pills, to a certain size, set out, oven temperature drying, sieving, selection of a certain size of pellets re set the coating pot, with talcum powder, activated carbon, gelatin coating liquid syrup Sichuan wax, polishing to the surface of black and shiny, removed, low temperature drying, with a bottle of G packaging is 70. 3 quality control 3.1 dissolution time limit check: take pills and 6 pieces of finished products, set 78X -2 type tablets, four with the tester (Shanghai the Yellow Sea test equipment factory) in accordance with the provisions of the Chinese Pharmacopoeia, determine its dissolution time limit. Results: the average time of dissolution of the pellets was (32 + 3.5) min, and the finished product was (45 + 2) min, which met the requirements of the Chinese pharmacopoeia. 3.2 Angelica identification test: This product is 10 g, cut into pieces, add an equal amount of diatomaceous earth research uniform, 20 ml 24 h impregnated with ether, divided in centrifugal supernatant, evaporation of volatile ether, ethyl acetate and residue 1 ml dissolved, as the testsolution. A mixed solution containing 1 mg per 1 ml was added to the control substance, which was taken as the control substance. Thin-layer chromatography experiment,

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