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An easy, quick, and sensitive approach adopting ultra-performance liquid chromatography (UPLC) equipped with diode array detector was used to analyze and systematically evaluate the quality of Pudilan tablets manufactured by 12 distinct pharmaceutical companies. In this research, 15 peaks were chosen as the common peaks to assess the similarities for different batches (S1–S43) of Pudilan tablet samples. In comparison with the control fingerprint, similarity values for 43 batches of samples exceeded 0.922. In addition, by analyzing the reference substances of epigoitrin, caffeic acid, chlorogenic acid, acetylcorynoline, baicalin and baicanshialein, the chromatogram of the 6 reference substances was established. The recoveries for the reference substances which demonstrated good regression in the linear range (r2 > 0.999) were in the range of 98.3–101.1%. The results demonstrated that the established method was highly accurate, efficient and reliable. This study provides a valid, dependable and pragmatic method to evaluate the quality of Pudilan tablet.
Czasopismo
Rocznik
Tom
Strony
338--346
Opis fizyczny
Bibliogr. 36 poz., rys., tab., wykr.
Twórcy
autor
- School of Pharmacy, Anhui University of Chinese Medicine, Hefei 230012, China
autor
- School of Pharmacy, Anhui University of Chinese Medicine, Hefei 230012, China
autor
- School of Pharmacy, Anhui University of Chinese Medicine, Hefei 230012, China
autor
- School of Pharmacy, Anhui University of Chinese Medicine, Hefei 230012, China
autor
- Medical Department, Taihe Hospital of Chinese Medicine, Taihe 236600, China
autor
- Department of Research and Development, Anhui Jiren Pharmaceutical Company, Bozhou 236800, China
autor
- School of Pharmacy, Anhui University of Chinese Medicine, Hefei 230012, China
autor
- School of Life Sciences, Anhui University of Chinese Medicine, Hefei 230012, China
Bibliografia
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Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-572a627b-f230-4eea-93df-826e167b34ef