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CAS:52286-59-6
Purity:HPLC≥98%
Appearance:White to off-white powder
Storage:Store at 2-8℃，2 years.
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UPLC-PDA
The levels of the main active ingredients of MSJZT were detected using a UPLC-PDA method. Chromatographic separation was performed on a UPLC system with a photodiode array detector (PDA) and C18 (100 mm×2.1 mm, 1.7μm ) column. The column temperature was set at 30℃. The mobile phase was composed of 0.1% phosphoric acid (A) and acetonitrile (B). The optimum adsorption and elution conditions were set as follows: 0–1.5 min, 95% B; 1.5–6 min, 95–80% B; 7–10 min, 80–60% B; 10–10.5 min, 50–35% B; 10.5–12 min, 35–30% B; 12–12.5 min, 30–20% B; 12.5–16 min, 20–10% B; 16–16.5 min, 10–0% B; and 16.5–18 min, 0–95% B.
来源文献：Nie S, Zhao Y, Qiu X, Wang W, Yao Y, Yi M, Wang D. Metabolomic Study on Nude Mice Models of Gastric Cancer Treated with Modified Si Jun Zi Tang via HILIC UHPLC-Q-TOF/MS Analysis. Evid Based Complement Alternat Med. 2019 Jun 23;2019:3817879. doi: 10.1155/2019/3817879. PMID: 31341492; PMCID: PMC6612382.
UPLC
The experimental conditions were as follows: 1) Column: Waters Acquity BEH C18 column (100 mmX2.1 mm, 1.7 mm); 2) chromatographic conditions were: flow rate 0.3 mL/ min; detection wavelength (k) ? 203 nm; sample volume 5 mL; column temperature 30 ℃. With acetonitrile (B) and 0.1% phosphoric acid solution (D) as mobile phase, gradient elution: 0–3 min, 19% B; 3–5 min, 20% B; 5–12 min, 21% B; 12–13 min, 29% B; 13–25 min, 31% B; 25–32 min, 35% B; 32–35 min, 19% B; 35–41 min, 19% B
来源文献：Wu SH, Li HB, Li GL, Qi YJ, Zhang J, Wang BY. Panax ginseng root, not leaf, can enhance thermogenic capacity and mitochondrial function in mice. Pharm Biol. 2020 Dec;58(1):374-384. doi: 10.1080/13880209.2020.1756348. PMID: 32366153; PMCID: PMC7241452.
UPLC
Concentration analysis of ginsenoside was conducted on ACQUITY UPLC system (Waters, Milford, MA) equipped with diode array detector (190 to 800 nm) and a reversed-phase C18 column (2.1 × 50 mm; inner diameter 1.7 μm; Acquity UPLC BEH; Waters). The mobile phase consisted of ACN (A) and 0.00005‰ (v/v) phosphoric acid (B) with the following separation program based on Zhang et al (2018): 0 to 3 min, 17 to 19% A; 3 to 4 min, 19 to 21% A; 4 to 4.5 min, 21 to 24% A; 4.5 to 5 min, 24 to 28% A; 5 to 6.5 min, 28% A; 6.5 to 7.5 min, 28 to 30% A; 7.5 to 9.5 min, 30 to 36% A; 9.5 to 11 min, 36 to 40% A.The injection volume was 2 μL at a flow rate of 0.5 mL min?1 . The column temperature and the detection wavelength were respectively set up at 35℃ and 203 nm.
来源文献：[1] Lei X , Wang Q , Yang H ,et al.Vitrification and proteomic analysis of embryogenic callus ofPanax ginsengC. A. Meyer[J].In Vitro Cellular and Development Biology. Plant: Journal of the Tissue Culture Association, 2021(1):57.
