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      UPLC-MS/MS法分析旋覆花蜜炙后化學(xué)成分的變化

      2021-10-29 17:34:13呂渭升位翠杰潘曉君楊文惠何民友陳向東孫冬梅魏梅李振雨
      中國(guó)藥房 2021年20期
      關(guān)鍵詞:倍半萜大花酚酸

      呂渭升 位翠杰 潘曉君 楊文惠 何民友 陳向東 孫冬梅 魏梅 李振雨

      中圖分類號(hào) R284 文獻(xiàn)標(biāo)志碼 A 文章編號(hào) 1001-0408(2021)20-2478-07

      DOI 10.6039/j.issn.1001-0408.2021.20.08

      摘 要 目的:比較旋覆花蜜炙前后的化學(xué)成分差異。方法:采用超高效液相色譜-串聯(lián)質(zhì)譜技術(shù)(UPLC-MS/MS)。色譜柱為Waters ACQUITY UPLC BEH C18,流動(dòng)相為0.1%甲酸溶液-乙腈(梯度洗脫),流速為0.3 mL/min,柱溫為30 ℃,進(jìn)樣量為5 ?L。采用電噴霧離子源,以正離子模式掃描,一級(jí)質(zhì)譜掃描范圍為m/z 70~1 050,二級(jí)質(zhì)譜掃描范圍為m/z 50~1 050,歸一化碰撞能量為40、60 eV,質(zhì)譜圖類型為峰形圖,鞘氣流速為35 arb,輔助氣流速為10 arb,噴霧電壓為3.80 kV,透鏡電壓為50 V,加熱溫度為350 ℃,毛細(xì)管溫度為350 ℃。采用Qual Browser 4.1.39.1軟件并參考在線高分辨數(shù)據(jù)庫(kù)mzCloud、中藥成分高分辨質(zhì)譜本地?cái)?shù)據(jù)庫(kù)OTCML,同時(shí)結(jié)合相關(guān)文獻(xiàn)對(duì)化合物進(jìn)行鑒定。采用SIMCA 14.1軟件進(jìn)行主成分分析(PCA)、正交偏最小二乘法-判別分析(OPLS-DA),以變量重要性投影(VIP)值大于1為標(biāo)準(zhǔn)篩選旋覆花蜜炙前后的差異性成分。結(jié)果:從旋覆花及其蜜炙品中共鑒定出29個(gè)共有化學(xué)成分,包括1-咖啡??鼘幩?、綠原酸、3,5-二咖啡??鼘幩岬?個(gè)酚酸類成分,槲皮素、木犀草素、狹葉依瓦菊素等12個(gè)黃酮類成分,以及1-O-乙酰旋覆花內(nèi)酯、二大花旋覆花內(nèi)酯B、1-O-乙酰基-6-O-異丁?;蠡ㄐ不▋?nèi)酯等12個(gè)倍半萜內(nèi)酯類成分。PCA結(jié)果顯示,旋覆花與蜜旋覆花分別位于得分圖的兩側(cè)。OPLS-DA結(jié)果顯示,有7個(gè)成分的VIP值大于1,分別為峰19(大花旋覆花素)、峰6(槲皮萬(wàn)壽菊苷)、峰1(1-咖啡??鼘幩幔?、峰21(紫花牡荊素)、峰20(tomentosin)、峰13(菠葉素)、峰3(瑞香素)。結(jié)論:經(jīng)蜜炙后,旋覆花的化學(xué)成分含量有所改變,且均有一定程度的降低。大花旋覆花素、槲皮萬(wàn)壽菊苷、1-咖啡??鼘幩?、tomentosin、紫花牡荊素、菠葉素、瑞香素可能為旋覆花及其蜜炙品的差異性成分。

      關(guān)鍵詞 旋覆花;蜜旋覆花;超高效液相色譜-串聯(lián)質(zhì)譜法;主成分分析;正交偏最小二乘法-判別分析;化學(xué)成分

      Variations of Chemical Components in Inula japonica by UPLC-MS/MS before and after Honey-frying

      LYU Weisheng1,2,WEI Cuijie1,2,PAN Xiaojun1,2,YANG Wenhui1,2,HE Minyou1,2,CHEN Xiangdong1,2,SUN Dongmei1,2,WEI Mei1,2,LI Zhenyu1,2(1. Guangdong e-fong Pharmaceutical Co., Ltd., Guangdong Foshan 528244, China; 2. Guangdong Provincial Key Laboratory of TCM Formula, Guangdong Foshan 528244, China)

      ABSTRACT? ?OBJECTIVE: To compare the chemical components differences of Inula japonica before and after honey-frying. METHODS: UPLC-MS/MS method was adopted. The determination was performed on Waters ACQUITY UPLC BEH C18 column with mobile phase consisted of 0.1% formic acid-acetonitrile (gradient elution) at the flow rate of 0.3 mL/min. The column temperature was set at 30 ℃, and sample size was 5 ?L. The electrospray ion source was scanned by positive ion mode. The first order mass spectrometry scanning range was m/z 70-1 050, the second order mass spectrometry scanning range was m/z 50-1 050, and the normalized collision energy was 40, 60 eV ; mass spectrum type was the peak figure, the flow rate of sheath gas was 35 arb, the auxiliary airflow speed was 10 arb, the spray voltage was 3.80 kV, the S-lens voltage was 50 V, the heating temperature was 350 ℃, and the capillary temperature was 350 ℃. The components were identified by Qual Browser 4.1.39.1 software, referring to the online high-resolution database mzCloud and local database OTCML of high-resolution mass spectrometry of TCM, and combined with relevant literature. The principal component analysis (PCA) and orthogonal partial least squared-discriminant analysis (OPLS-DA) of I. japonica before and after honey-fried were performed by using SIMCA 14.1 statistical software, and variable importance projection (VIP) value greater than 1 was used as the standard to screen the differential components before and after honey-frying. RESULTS: A total of 29 common chemical components were identified from I. japonica and honey-fried I. japonica, including 5 phenolic acids as 1-caffeoylquinic acid, chlorogenic acid and 3,5-dicaffeoylquinic acid, 12 flavonoids as quercetin, luteolin and evamectin, as well as 12 sesquiterpene lactones as 1-O-acetylinula diester, inula bicolor lactone B and 1-O-acetyl-6-O-isobutyryl inulin. The results of PCA showed that I. japonica and honey-fried I. japonica were located on both sides of the score diagram respectively. The results of OPLS-DA showed that the VIP values of 7 components were greater than 1, which were peak 19 (britanin), peak 6 (quercetagitrin), peak 1 (1-caffeoylquinic acid), peak 21 (vitexicarpin), peak 20 (tomentosin), peak 13 (spinacetin) and peak 3 (daphnetin). CONCLUSIONS: After honey-fried, the content of chemical components of I. japonica changed and decreased to a certain extent. Britanin, quercetagitrin, 1-caffeoylquinic acid, tomentosin,vitexicarpin, spinacetin and daphnetin may be the differential components of I. japonica and honey-fried I. japonica.

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