Qianliexin capsule quality evaluation method based on multi-index active ingredient measurement
An active ingredient, the technology of Qianliexin, applied in the field of quality evaluation of Qianliexin capsules based on the determination of multi-index active ingredients, can solve the problem of inability to fully reflect the multi-components and multi-target points of traditional Chinese medicine prescriptions, unable to meet the quality control of finished medicines, and unable to reflect the overall medicine Quality and other issues, to achieve the effects of sensitive and reliable detection methods, guaranteed effectiveness and safety, and more comprehensive analysis capabilities
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[0032] 1 Instruments and materials
[0033] Agilent 1260 high performance liquid chromatography (autosampler, gradient pump, column thermostat, diode array detector); 1 / 100,000 electronic analytical balance (SARTOURIUS BSA), fingerprint similarity evaluation software is "TCM Chromatographic Fingerprint Similarity Evaluation System" (National Pharmacopoeia Commission 2004A); SB-5200D High Power Digital Control Ultrasonic Instrument (Ningbo Xinzhi Biotechnology Co., Ltd.).
[0034] Chromatographic column: American Agilent ZORBAX SB-C 18 (4.6mm×250mm, 5μm), Swedish Kromasil 100-5C 18(4.6mm×250mm, 5μm). Gallic Acid (Lot No. 149-91-7), Chlorogenic Acid (Lot No. 327-97-9), Caffeic Acid (Lot No. 331-39-5), Braciferin (Lot No. 53452-16-7), Iso Quercitrin (batch number 482-35-9), salvianolic acid B (batch number 115939-25-8), salvianolic acid A (batch number 96574-01-5), cryptotanshinone (batch number 35825-57-1), standard The purity of the products were all ≥98%, and they were all...
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