Sanwei sandalwood granule and quality control method of preparation thereof
A technology of sandalwood and granules, which is applied in the field of medicine, can solve problems such as poor quality controllability, simple control standards, and simple quality standards, and achieve the effects of quality control, product quality safety, and improved identification
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Embodiment 1
[0102] Embodiment 1: the quality control method of Sanwei Sandalwood Granules
[0103] Identification:
[0104] a. Identification of sandalwood
[0105] Take 5g of sanwei sandalwood granules, grind them finely, add 30ml of petroleum ether with a boiling range of 30-60°C, ultrasonically treat for 15 minutes, filter, evaporate the filtrate to dryness, add 2ml of petroleum ether with a boiling range of 60-90°C to dissolve the residue, and use it as the test sample Solution; take another 2g of sandalwood reference medicinal material, add 30ml of petroleum ether with a boiling range of 30-60°C, ultrasonically treat for 15min, filter, evaporate the filtrate to dryness, add 2ml of petroleum ether with a boiling range of 60-90°C to dissolve the residue, and use it as the reference medicinal material solution ; According to the test of thin-layer chromatography (Appendix VI B of "Pharmacopoeia of the People's Republic of China" in 2010), draw 4 μL of each of the above solutions, and p...
Embodiment 2
[0117] Embodiment 2: the quality control method of Sanwei Sandalwood Dropping Pills
[0118] Identification:
[0119] a. Identification of sandalwood
[0120] Take 7g of Sanwei Sandalwood Dropping Pills, grind finely, add 50ml of petroleum ether with a boiling range of 30-60°C, ultrasonically treat for 25min, filter, evaporate the filtrate to dryness, add 2ml of petroleum ether with a boiling range of 60-90°C to dissolve the residue, and use it as a test product. product solution; take another 2 g of sandalwood reference medicinal material, add 50 ml of petroleum ether with a boiling range of 30 to 60 ° C, ultrasonically treat for 15 to 25 minutes, filter, evaporate the filtrate to dryness, and add 2 ml of petroleum ether with a boiling range of 60 to 90 ° C to dissolve the residue as Control medicinal material solution; test according to thin-layer chromatography (Appendix VI B of "Pharmacopoeia of the People's Republic of China" 2010 Edition), draw 2-15 μL of each of the ab...
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