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首页> 外文期刊>Chromatographia >Isolation of Chlorogenic Acid from Flaveria bidentis (L.) Kuntze by CCC and Synthesis of Chlorogenic Acid-Intercalated Layered Double Hydroxide
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Isolation of Chlorogenic Acid from Flaveria bidentis (L.) Kuntze by CCC and Synthesis of Chlorogenic Acid-Intercalated Layered Double Hydroxide

机译:CCC法分离金盏花中的绿原酸及绿原酸插层双氢氧化物的合成

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Preparative counter-current chromatography (CCC) was successfully used for isolation and purification of chlorogenic acid from Flaveria bidentis (L.) Kuntze with a solvent system composed of ethyl acetate–methanol–water at a volume ratio of 50:1:50, v/v. Using a preparative unit of the CCC centrifuge, about 800?mg of the crude extract was separated, yielding 3.2?mg of chlorogenic acid at a purity of 92.0%. The blood pressure lowering and antivirus chlorogenic acid (C16H18O9) was intercalated into magnesium–aluminum–layered double hydroxides, which was used as host materials for drug-LDH host-guest supermolecular structures by anion exchange under a nitrogen atmosphere. Chlorogenic acid–LDH is a functional and effective drug. The product chlorogenic acid–LDH has been characterized by powder X-ray diffraction (XRD), Fourier transform infrared (FT-IR), thermogravimetric analysis (TGA) and scanning electron micrographs (SEM). The X-ray diffraction patterns of NO3 ? form of LDH and chlorogenic acid–LDH were compared, and the basal d spacing value of NO3 ?-LDH layer was 8.75?? (2θ?=?10.100°); however, the basal reflection (003) of chlorogenic acid–LDH shifts to lower 2θ (for 003 reflection: 2θ?=?5.119°) that is expanded to 17.25??, indicating the intercalation of chlorogenic acid into the interlayer of Mg–Al-LDH. Thermogravimetric analysis showed that chlorogenic acid stability had improved, and scanning electron micrographs showed that the morphology of the chlorogenic acid–LDH was irregular masses of distinctly thicker flakes, which was similar to the morphology of NO3 ? form of LDH.
机译:制备型逆流色谱法(CCC)已成功地用于从黄bid(L.)Kuntze中分离和纯化绿原酸,其溶剂体系为乙酸乙酯-甲醇-水,体积比为50:1:50,v / v。使用CCC离心机的制备单元,分离出约800?mg的粗提物,得到3.2?mg的绿原酸,纯度为92.0%。将降压和抗病毒绿原酸(C16H18O9)插入镁-铝层的双氢氧化物中,在氮气氛下通过阴离子交换将其用作药物-LDH宿主-客体超分子结构的主体材料。绿原酸-LDH是一种功能有效的药物。绿原酸-LDH产品已通过粉末X射线衍射(XRD),傅立叶变换红外(FT-IR),热重分析(TGA)和扫描电子显微照片(SEM)进行了表征。 NO 3的X射线衍射图。比较了LDH的形式和绿原酸-LDH,NO3α-LDH层的基本d间隔值为8.75Ω·m。 (2θ≥10.100°);然而,绿原酸-LDH的基反射(003)移动到较低的2θ(对于003反射:2θ== 5.119°),扩大到17.25°,表明绿原酸插入到Mg-Al的中间层中-LDH。热重分析表明绿原酸的稳定性得到了改善,扫描电子显微镜照片显示绿原酸-LDH的形态是明显不规则的薄片状浓稠的薄片,这类似于NO3的形态。 LDH的形式。

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