[1]
Nestler, G. Traditional Chinese medicine. Med. Clin. North Am., 2002, 86(1), 63-73.
[2]
Zhang, X.; Sang, D.; Zhang, Z.; Kong, S. Analysis and study on 47 cases of adverse reactions of Chinese medicine injection. Afr. J. Tradit. Complement. Altern. Med., 2014, 11(2), 363-364.
[3]
Gui, L.; Liu, J.; Zhang, C.; Liu, D.; Pharmacy, D. Analysis on 561 cases of clinical adverse drug reaction/event caused by Danshen injection. Chin. J. Pharmacoepidemiolo, 2017, 26(8), 547-550.
[4]
Zhu, S.; Xing, B.; Mei, D.; Wang, L.; Feng, L.; Zhang, X. Analysis on adverse drug reaction reports induced by Ginkgo biloba leaves extract injection from 2003 to 2013 in beijing. Chin. J. Pharmacoepidemiolo., 2017, 26(1), 50-53.
[5]
Deyama, T.; Nishibe, S.; Nakazawa, Y. Constituents and pharmacological effects of Eucommia and Siberian ginseng. Acta Pharmacol. Sin., 2001, 22, 1057-1070.
[6]
Lee, S.; Park, H.J.; Jeon, S.J.; Kim, E.; Lee, H.E.; Kim, H.; Kwon, Y.; Zhang, J.; Jung, I.H.; Ryu, J.H. Cognitive ameliorating effect of Acanthopanax koreanum against scopolamine-induced memory impairment in mice. Phytother. Res., 2017, 31(3), 425-432.
[7]
Kuźniewski, R.; Załuski, D.; Olech, M.; Banaszczak, P.; Nowak, R. LC-ESI-MS/MS profiling of phenolics in the leaves of Eleutherococcus senticosus cultivated in the West Europe and anti-hyaluronidase and anti-acetylcholinestarase activities. Nat. Prod. Res., 2018, 32(4), 448-452.
[8]
Song, Y.; Yang, C.J.; Wang, Z.B.; Zhao, N.; Feng, X.S.; Meng, F.H. Chemical constituents of Eleutherococcus sessiliflorus extract and its sedative-hypnotic effect. Nat. Prod. Res., 2017, 31(17), 1-6.
[9]
Li, F.; Zhang, N.; Wu, Q.; Yuan, Y.; Yang, Z.; Zhou, M.; Zhu, J.; Tang, Q. Syringin prevents cardiac hypertrophy induced by pressure overload through the attenuation of autophagy. Int. J. Mol. Med., 2016, 39(1), 199-207.
[10]
Wang, X.; Zhou, G.; Liu, C. Acanthopanax versus 3-methyladenine ameliorates sodium taurocholate-induced severe acute pancreatitis by inhibiting the autophagic pathway in rats. Mediators Inflamm., 2016, 2, 8369704.
[11]
Fang, J.N.; Proksch, A.; Wagner, H. Immunologically active polysaccharides of Acanthopanax senticosus. Phytochemistry, 1985, 24(11), 2619-2622.
[12]
Hu, H.B.; Zhu, J.H. Flavonoid constituents from the roots of Acanthopanax brachypus. Chem. Pharm. Bull., 2011, 59(1), 135-139.
[13]
Huang, L.; Zhao, H.; Huang, B.; Zheng, C.; Peng, W.; Qin, L. Acanthopanax senticosus: Review of botany, chemistry and pharmacology. Pharmazie, 2011, 66, 83-97.
[14]
Huang, J.; Shao, Q.; Xiang, Y.H.; Ge, Z.W.; Fan, X.H. Identification of phenylpropanoids in ciwujia injection by HPLC-MS. Zhongguo Zhongyao Zazhi, 2014, 39(13), 2513-2520.
[15]
Zhou, H.; Xing, J.; Liu, S.; Song, F.; Cai, Z.; Pi, Z.; Liu, Z.; Liu, S. Screening and determination for potential α-glucosidase inhibitors from leaves of Acanthopanax senticosus harms by using UF-LC/MS and ESI-MSn. Phytochem. Anal., 2012, 23(4), 315-323.
[16]
Li, Q.; Jia, Y.; Xu, L.; Wang, X.; Zhen, Z.; Liu, Y.; Bi, K. Simultaneous determination of protocatechuic acid, syringin, chlorogenic acid, caffeic acid, liriodendrin and isofraxidin in Acanthopanax senticosus Harms by HPLC-DAD. Biol. Pharm. Bull., 2006, 29(3), 532-534.
[17]
Liu, S.P.; An, J.T.; Wang, R.; Li, Q. Simultaneous quantification of five bioactive compounds of Acanthopanax senticosus and its extract by ultra performance liquid chromatography with electrospray ionization time-of-flight mass spectrometry. Molecules, 2012, 17(7), 7903-7913.
[18]
Yang, S.X.; Zhao, G.Z.; Zhang, S.M. Determination of syringin in Ciwujia injection by HPLC. Chinese J. Pharmaceut. Anal., 2001, 1, 16-17.
[19]
Chen, Y.C.; Song, W.; Liu, Q.S. Determination of quercetin in Acanthopanax and Acanthopanax injection by high performance capillary electrophoresis (HPCE). China Pharm., 2002, 3, 37-38.
[20]
Yu, F.P.; Lian, C.B. Determination of syringin and chlorogenic acid in Ciwujia injection by UFLC. China Pharmacist., 2010, 13(12), 1769-1770.
[21]
D’Archivio, A.A.; Maggi, M.A. Geographical identification of saffron (Crocus sativus l.) by linear discriminant analysis applied to the UV-visible spectra of aqueous extracts. Food Chem., 2017, 219(15), 408-413.
[22]
Hua, L.; Yang, M.H.; Miao, J.H.; Ma, X.J. Simultaneous chromatographic fingerprinting and quantitative analysis of Flemingia philippinensis by LC-DAD. Chromatographia, 2009, 70(3-4), 447-454.
[23]
Liu, Y.Y.; Hu, X.L.; Bao, Y.F.; Yin, D.Q. Simultaneous determination of 29 pharmaceuticals in fish muscle and plasma by ultrasonic extraction followed by SPE-UHPLC-MS/MS. J. Sep. Sci., 2018, 41(10), 2139-2150.
[24]
Flamini, R. Mass spectrometry in grape and wine chemistry. Part I: polyphenols. Mass Spectrom. Rev., 2003, 2, 218-250.
[25]
Mawatari, S.; Hazeyama, S.; Fujino, T. Measurement of ether phospholipids in human plasma with HPLC-ELSD and LC/ESI-MS after hydrolysis of plasma with phospholipase A1. Lipids, 2016, 51(8), 997-1006.
[26]
Kang, S.W.; Kang, K.; Kim, M.A.; Jeon, N.R.; Kim, S.M.; Jeon, J.S.; Nho, C.W.; Um, B.H. Phytoestrogenic activity of Aceriphyllum rossii and rapid identification of phytoestrogens by LC-NMR/MS and bioassay-guided isolation. Eur. Food Res. Technol., 2014, 239(2), 237-246.
[27]
Mochizuki, A.; Nakazawa, H.; Adachi, N.; Takekawa, K.; Shojo, H. Identification and quantification of mepirapim and acetyl fentanyl in authentic human whole blood and urine samples by GC-MS/MS and LC-MS/MS. Forensic Toxicol., 2018, 36(1), 81-87.
[28]
Steinmann, D.; Ganzera, M. Recent advances on HPLC/MS in medicinal plant analysis. J. Pharm. Biomed. Anal., 2011, 55(4), 744-757.
[29]
D’Archivio, A.A.; Di Donato, F.; Foschi, M.; Maggi, M.A.; Ruggieri, F. UHPLC analysis of saffron (Crocus sativus L.): Optimization of separation using chemometrics and detection of minor crocetin esters. Molecules, 2018, 23(8), 1851.
[30]
Díaz-García, M.C.; Obón, J.M.; Castellar, M.R.; Collado, J.; Alacid, M. Quantification by UHPLC of total individual polyphenols in fruit juices. Food Chem., 2013, 138(2-3), 938-949.
[31]
Weisz, G.M.; Kammerer, D.R.; Carle, R. Identification and quantification of phenolic compounds from sunflower (Helianthus annuus L.) kernels and shells by HPLC-DAD/ESI-MSn. Food Chem., 2009, 115(2), 758-765.
[32]
Challice, J.S.; Williams, A.H. Phenolic compounds of the genus Pyrus-I: The occurrence of flavones and phenolic acid derivatives of 3, 4-dihydroxybenzyl alcohol 4-glucoside in Pyrus calleryana. Phytochemistry, 1968, 7(1), 119-130.
[33]
Xu, H.X.; Kadota, S.; Kurokawa, M.; Shiraki, K.; Matsumoto, T.; Namba, T. Isolation and structure of woodorien, a new glucoside having antiviral activity, from Woodwardia orientalis. Chem. Pharm. Bull., 1993, 41(10), 1803-1806.
[34]
Yang, G.E.; Li, W.; Huang, C.; Lin, L.; Zhang, Q.B.; Koike, K.Z. Phenolic Constituents from the stems of Acanthopanax senticosus. Chem. Nat. Compd., 2011, 46(6), 876-879.
[35]
Mcnamara, C.E.; Perry, N.B.; Follett, J.M.; Pharmenter, G.A.; Douglas, J.A. A new glucosyl feruloyl quinic acid as a potential marker for roots and rhizomes of Goldenseal, Hydrastis canadensis. J. Nat. Prod., 2004, 67(11), 1818-1822.
[36]
Niwa, M.; Iwadare, Y.; Wu, Y.C.; Hirata, Y. Two new phenylpropanoid glycosides from Wikstroemia sikokiana. Chem. Pharm. Bull., 1988, 36(3), 1158-1161.
[37]
Singh, I.P.; Bharate, S.B. Phloroglucinol compounds of natural origin. Nat. Prod. Rep., 2006, 23, 558-591.