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引用本文:张文婷,徐靖,程夏倩,李明焱,黄琴伟,郭增喜,赵维良.灵芝孢子粉质量标准提高研究[J].中国现代应用药学,2016,33(6):799-803.
ZHANG Wenting,XU Jing,CHENG Xiaqian,LI Mingyan,HUANG Qinwei,GUO Zengxi,ZHAO Weiliang.Studies on Improving Quality Standard of Ganoderma Lucidum Spore[J].Chin J Mod Appl Pharm(中国现代应用药学),2016,33(6):799-803.
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灵芝孢子粉质量标准提高研究
张文婷1, 徐靖2, 程夏倩3, 李明焱4, 黄琴伟1, 郭增喜1, 赵维良1
1.浙江省食品药品检验研究院,杭州 310052;2.浙江省珍稀植物药工程技术研究中心,浙江 武义 321200;3.浙江省儿童医院,杭州 310052;4.武义寿仙谷中药饮片有限公司,浙江 武义 321200
摘要:
目的 建立灵芝孢子粉的HPLC特征图谱及三油酸甘油酯的含量测定方法。方法 采用ACCHROM Unitary-C18(250 mm×4.6 mm,5 μm)色谱柱,流动相为乙腈-异丙醇(51∶49),流速为1.0 mL·min-1,柱温为30 ℃,检测器为蒸发光散射检测器。结果 建立了灵芝孢子粉HPLC特征图谱,确定了10个共有峰,指认了其中8个共有峰的成分分别为三亚油酸甘油酯、二亚油酸油酸甘油酯、二亚油酸棕榈酸甘油酯、二油酸亚油酸甘油酯、棕榈酸油酸亚油酸甘油酯、三油酸甘油酯、二油酸棕榈酸甘油酯和二油酸硬脂酸甘油酯。三油酸甘油酯进样量在0.613 2~18.40 μg(r=0.998 9)内与峰面积线性关系良好,平均加样回收率为104.1%(RSD=1.8%)。结论 特征图谱结合三油酸甘油酯的含量测定,能更好地控制灵芝孢子粉的质量。
关键词:  灵芝孢子粉  三油酸甘油酯  特征图谱  高效液相色谱法
DOI:
分类号:A
基金项目:
Studies on Improving Quality Standard of Ganoderma Lucidum Spore
ZHANG Wenting1, XU Jing2, CHENG Xiaqian3, LI Mingyan4, HUANG Qinwei1, GUO Zengxi1, ZHAO Weiliang1
1.Zhenjiang Institute for Food and Drug Control, Hangzhou 310052, China;2.Zhejiang Province Rare Plant Medicine Engineering Technology Research Center, Wuyi 321200, China;3.The Children’s Hospital, Zhejiang University School of Medicine, Hangzhou 310052, China;4.Wuyi Shouxiangu Traditional Chinese Medicine Decoction Pieces Co., Ltd., Wuyi 321200, China
Abstract:
OBJECTIVE To establish a specific HPLC chromatogram of Ganoderma lucidum spore and a method for determination of triolein. METHODS The chromatographic separation was performed on an ACCHROM Unitary-C18 column (250 mm×4.6 mm, 5 μm) with the mobile phase of acetonitrile-isopropanol(51∶49). The flow rate was 1.0 mL·min-1 at 30 ℃ with the detection by ELSD. RESULTS The results showed that the chromatographic fingerprint was completed with 10 recognizable peaks, of which 8 peaks kaempferol-3-O-β-D (trilinolein, 1,2-linolein-3-olein, 1,2-linolein-3-palmitin, 1,2-olein-3-linolein, 1-palmitin-2-olein-3-linolein, triolein, 1,2-olein-3-palmitin and 1,2-olein-3-stearin) were determined. The linear range of triolein was 0.613 2-18.40 μg(r=0.998 9), the average recovery was 104.1%(RSD=1.8%). CONCLUSION The combination of specific chromatograms and determination of triolein is suitable for use in the quality control of Ganoderma lucidum spore.
Key words:  Ganoderma lucidum spore  triolein  fingerprint  HPLC
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