Bio-screening and quantification of methyl paraben in vinegar and coconut juice separated by HPTLC

As a widely used food preservative,methyl paraben was experimentally evidenced with serious hormonelike adverse effects.Herein,a high performance thin-layer chromatography platformed bioluminescent bioautography and image analysis for the selective quantification and confirmation of methyl paraben was proposed and validated in vinegar and coconut juice.First,the detectability of the bioautography to the analyte on different layer materials was estimated,revealing that normal silica gel was the best choice.After that,the liquid of sample extract and working solution were separated to overcome the background noises due to co-extracted matrices.The separation result was then coupled to the optimized bioautography,enabling instant and straightforward screening of the targeted conpound.For accurate quantification,bioluninescent inhibition pattern caused by the analyte was processed by image analysis,giving useful sensitivity(LOD>16 mg/kg),precision(RSD<10.1%)and accuracy(spike-recovery rate 76.9%-112.2%).Finally,the suspected result was confirmed by determining its MS fingerprint,further strengthening the reliability of screening.

TLC Identification and Extraction Process of Rubiasin-1-methyl Ether from Yao Medicine Chuanlianzhu

[Objectives]To establish a thin-layer chromatography(TLC)method for the determination of rubiadin-1-methyl ether in Yao Medicine Chuanlianzhu(Damnacanthus giganteus).[Methods]A silica gel G thin-layer plate was adopted for TLC.Petroleum ether(60-90℃)-chloroform-methanol-water(7:15:3:1)was used as the developing solvent and inspected under ultraviolet lamp(365 nm).The content was determined by Inertsil ODS-3 C 18 column(4.60 mm×250 mm,5μm),mobile phase:acetonitrile-0.2%phosphoric acid gradient elution,detection wavelength 277 nm,flow rate 1.0 mL/min,column temperature 30℃,injection volume 10μL.[Results]The spots of 10 Chuanlianzhu samples from different origins showed the same color at the same position as the control,and the spots were clear and specific.The injection volume of rubiadin-1-methyl ether showed a good linear relationship in the range of 2.90-145μg(R=0.9996).The average recovery rate of rubiadin-1-methyl ether in the low,medium and high dose groups of Yao Medicine Chuanlianzhu was 98.72%,and RSD=1.78%.[Conclusions]This method can effectively identify Yao Medicine Chuanlianzhu medicinal materials and accurately determine the content of rubiadin-1-methyl ether in the medicinal materials.It provides a scientific basis for the development and utilization of Yao Medicine Chuanlianzhu medicinal resources.

ANALYSIS OF HUMAN PLACENTA BY ^(31)P NUCLEAR MAGNETIC RESONANCE AND THIN-LAYER CHROMATOGRAPHY SCANNING COMBINED WITH THE CORRECTIVE METHOD OF ABSORBANCE PROPORTIONAL COEFFICIENT

Five phospholipids in human placenta were determined by phosphorus 31 nuclear magnetic resonance(^(31)P NMR)spectroscopy and thin-layer chromatography(TLC) scanning combined with the corrective method of absorbance proportional coefficient. The NMR spectrometer used this investigation was a Bruker AM-500 spectrometer operating at 202.4 MHz for ^(31)P chemical shifts are relative to 85% phosphoric acid. TIC was carried out by silica gel H plate developed in chloroform-methanol-glacial acetic acid-ethanol-water(25:4:6:2:0.5),with Vaskovsky reagent as colour -developing agent of phospholipids.

Quality Evaluation of Leontopodium franchetii Beauv. from Different Localities Based on Moisture,Ash and Extract Contents and Thin-layer Chromatography

[Objectives] The aim was to determine the moisture,ash and extract contents in Leontopodium franchetii Beauv. from different localities. [Methods] The contents of moisture,total ash,acid-insoluble ash and extract in L. franchetii from different localities were determined according to the methods described in Chinese Pharmacopoeia( 2015 Edition). [Results] In the 10 samples,the contents of moisture were all less than or equal to 15. 0%; the contents of total ash were all below 12. 0%; and the contents of acid-insoluble ash were all less than 3. 0%. The contents of water-soluble extract( by cold-soaked extraction method) in the samples were all below 12. 0% except those from Hongyuan Prairie of Sichuan Province and Xinglong Mountain in Lanzhou City,Gansu Province. [Conclusions]The contents of the four indicators measured in this experiment varied by small margins,indicating that the quality was relatively stable. This study provides theoretical data for the revision of the quality standards for L. franchetii.

Separation of Amino Acids Based on Thin-Layer Chromatography by a Novel Quinazoline Based Anti-Microbial Agent

A newly designed quinazoline based compound, 6-pyridin-2-yl-5,6-dihydro-benzo[4,5]imidazo[1,2-c] quinazoline (PDBIQ) has shown the ability for the easy detection of nineteen amino acids on thin-layer chromatography plates as a spray reagent. This new reagent enabled to produce various distinguishable colors with amino acids with different RF values. The detection limits and the binding ability of PDBIQ with amino acids have been calculated. PDBIQ is also able to detect aminoacids from hydrolised seed protein. The title compound also exhibited profound inhibitory action against some gm (+ve) and gm (-ve) bacterial organisms. This paper deals with synthesis, spectroscopic application and biological evaluation of the organic moity.

Preparation Process and Thin Layer Chromatography Identification of Wufang Babu Poultice

[Objectives] To establish the process flow of preparation of Wufang Babu Poultice and the identification method of thin layer chromatography (TLC). [Methods] For the forming process of Wufang Babu Poultice, the preparation method of mixed pharmaceutical powder with suitable pharmaceutical excipients was adopted. Qualitative identification of medicinal materials in Wufang Babu Poultice (Strychni Semen, Rhei Radix Et Rhizoma, Dipsaci Radix, and Angelicae Sinensis Radix) was carried out by TLC. [Results] Mixed pharmaceutical powder mixed with glycerol, gelatin and other pharmaceutical excipients can be prepared for forming. The test solution chromatography of each medicinal material (Strychni Semen, Rhei Radix et Rhizoma, Dipsaci Radix, Angelicae Sinensis Radix) showed pigment spots of the same color at the same position as its corresponding control medicinal materials and reference chromatography, and the display was clear. [Conclusions] The preparation process is simple and feasible, and can be used as the forming process of Wufang Babu Poultice. The TLC determination method is simple to operate, has good specificity, and has no effect on negative results, and can be used for identification of Wufang Babu Poultice.

金水六君煎物质基准中半夏和陈皮的薄层鉴别研究

目的:建立经典名方金水六君煎物质基准中半夏和陈皮的薄层鉴别方法。方法:以半夏对照药材为对照,对金水六君煎中半夏进行薄层鉴别研究,以橙皮苷和陈皮对照药材为对照,对金水六君煎中陈皮进行薄层鉴别研究,并对其进行方法学验证。结果:建立的薄层色谱法能鉴别出半夏和陈皮,斑点对应较好,阴性无干扰,方法学考察结果显示,方法适应性良好。结论:本法简单可行、结果可靠、重复性好,可作为金水六君煎物质基准的质量控制方法。

前列桂芍颗粒质量标准研究

目的制定前列桂芍颗粒质量标准。方法采用薄层色谱法(TLC)对前列桂芍颗粒中熟地黄、赤芍、桃仁、黄芪、黄柏进行定性鉴别;通过使用高效液相色谱法(HPLC)测定盐酸小檗碱在前列桂芍颗粒中的含量。结果前列桂芍颗粒中薄层色谱鉴别专属性强,斑点清晰且阴性无干扰;前列桂芍颗粒中盐酸小檗碱的线性范围是0.0901~1.6215μg(r=0.9998),平均回收率为98.54%,RSD值为0.87%(n=6)。结论薄层色谱鉴别和含量测定方法准确可行,重复性好,可有效控制前列桂芍颗粒质量。

TLC和HPLC法相结合分析盐水鸭中的生物胺

应用薄层层析(TLC)和高效液相色谱(HPLC)两种方法分析盐水鸭中生物胺的组成及含量。薄层层析结果显示,盐水鸭样品中存在着腐胺、尸胺、亚精胺、精胺、酪胺和2-苯乙胺;利用高效液相色谱法也检测到了以上6种生物胺,且各生物胺的含量均在204μg/g以下。两种方法结果相吻合,TLC法可以作为肉制品中生物胺定性分析的一种经济便捷的方法。

应用TLC-FT-SERS对萝芙木中利血平成分的研究

本文报道了应用薄层色谱（ＴＬＣ） 与傅里叶变换表面增强拉曼光谱（ＦＴ－ＳＥＲＳ） 联用技术， 获得了中草药萝芙木有效成分利血平光谱研究的新方法。研究表明：在薄层原位约２ μｇ 的样品即可获得利血平分子的特征振动谱带，并阐述了样品分子在表面增强基底银微粒表面的吸附模式。

TLC-分光光度法测贯叶连翘中金丝桃素含量

:针对贯叶连翘中成分复杂 ,干扰物多的特点 ,采用薄层层析 (TL C)分离出金丝桃素后 ,再进行分光光度测定。薄层层析以石油醚 -乙酸乙酯 -甲醇 (1∶ 4∶ 3)为展开体系展开 ,金丝桃素的 Rf=0 .85。分光光度法测定的回归方程为 A=72 .0 0 C+0 .0 0 3(r=0 .9997) ,平均回收率为 97.9% (RSD=0 .87% )。

TLC-HPLC检测三黄连合剂的有效成分

【目的】以薄层色谱法—高效液相色谱法（TLC-HPLC）检测三黄连合剂的有效成分,为制定其质量标准及后期临床推广应用提供理论依据。【方法】采用TLC对三黄连合剂中的主要组分黄连、黄芩和连翘进行定性鉴别,并以HPLC对其主要有效成分黄芩苷、盐酸小檗碱和连翘苷进行含量测定。【结果】三黄连合剂TLC色谱中的图像斑点清晰,与标准品对照斑点对齐,颜色一致。HPLC测定三黄连合剂中黄芩苷、连翘苷和盐酸小檗碱分别在75.00-1200.00μg/m L（r=0.9997）、4.17-66.67μg/m L（r=0.9998）、9.38-150.00μg/m L（r=0.9999）范围内线性关系良好,平均回收率分别为113.92%、100.18%和100.40%,其含量分别为5.03、0.25和0.27 mg/m L。【结论】TLC-HPLC可作为三黄连合剂的质量控制方法,且操作简便、重现性良好。

基于薄层色谱与一测多评法的沙棘颗粒质量评价方法研究

目的:优化中成药沙棘颗粒的薄层鉴别方法,建立多成分高效液相色谱一测多评方法。方法:采用薄层色谱法对槲皮素、异鼠李素和山柰素进行定性鉴别;采用高效液相色谱法,C18色谱柱(250 mm×4.6 mm,5µm),流动相为乙腈-0.1%磷酸水溶液,梯度洗脱,流速为1.0 mL·min^(–1),柱温为35℃,检测波长为365 nm,以槲皮素为内参物计算异鼠李素和山柰素含量。结果:薄层色谱鉴别方法斑点清晰、专属性好;与外标法对比,一测多评法准确度高、耐用性好。结论:优化的薄层色谱法与建立的一测多评法可靠、准确、重复性好,可为沙棘颗粒的质量标准提升提供参考。

TLC-生物自显影-MTT法检测滇重楼内生真菌中抗菌活性成分

本文采用TLC-生物自显影-MTT法检测了3株滇重楼内生真菌即芬芳镰刀菌、季氏毕赤氏酵母和烟曲霉正丁醇提取物对大肠杆菌、枯草芽孢杆菌、白色念珠菌和稻瘟病菌的抗菌活性成分,以芬芳镰刀菌和季氏毕赤氏酵母菌液提取物中含有的抗菌活性成分为多。同时与打孔药剂扩散法的检测结果进行了比较,为进一步快速分离内生真菌中抗菌活性成分提供了依据。

大蒜中低聚糖的TLC鉴别和HPLC-RID含量测定

目的建立大蒜中低聚糖的薄层色谱(TLC)法和高效液相-示差折光检测器(HPLC-RID)法,用于大蒜中低聚糖的鉴别和含量测定。方法采用TLC法大蒜中果糖、蔗糖、蔗果三糖和蔗果四糖进行鉴别,以冰乙酸-氯仿-水(21/18/4)为展开系统,苯胺-二苯胺溶液为显色剂;采用HPLC-RID法测定大蒜中果糖、蔗糖、蔗果三糖和蔗果四糖的含量,色谱柱为碳水化合物分析柱(4.6×250 mm,4μm);流动相:乙腈-水(75/25),柱温:35℃,流速:1.0 mL/min,进样量:15μL。结果薄层色谱中可以检测到果糖、蔗糖、蔗果三糖和蔗果四糖4种低聚糖。果糖、蔗糖、蔗果三糖和蔗果四糖分别在0.03~0.81、0.5~16.04、0.02~0.65、0.02~0.64 mg/mL范围线性关系良好。4种糖类低、中、高浓度平均回收率(n=3)分别为98.0%、99.7%、100.3%和98.2%;测定新疆5种不同海拔(1733、1680、1250、2800、2300 m)大蒜中果糖、蔗糖、蔗果三糖、蔗果四糖的含量分别为0.34~0.54、6.54~8.74、0.45~0.61、0.04~0.15 mg/g。结论本研究建立的大蒜中低聚糖的定性、定量分析方法准确可靠、重现性好,可用于大蒜中低聚糖的鉴别和含量测定。

蔗渣纤维乳化沥青吸附机制

为了探索蔗渣纤维与沥青吸附机制的问题,通过BET(Brunauer-Emmet-Teller, BET)比表面积检测法、挂篮吸附实验以及棒状薄层色谱-氢火焰离子探测实验(thin-layer chromatography with flame ionization detection, TLC-FID),研究改性前后蔗渣纤维的孔隙结构特性、改性蔗渣纤维对沥青组分的吸附性能的影响,以及不同改性蔗渣纤维掺量对吸附过程的影响,并结合吸附动力学模型进行理论验证分析吸附机理。实验结果表明:蔗渣纤维具有大孔与狭缝孔结构,改性后蔗渣纤维的表面积略有增加,总孔体积、微孔面积与体积增加幅度较大,分别达到241%、170%和276%;达到吸附平衡后,饱和分质量分数降低5.77%、芳香分质量分数增加20.75%、胶质质量分数降低29.37%,以及沥青质质量分数降低5.66%,说明改性蔗渣纤维最易吸附的沥青组分为胶质;随着改性蔗渣纤维掺量的增加,吸附率从15.25%增加至34.16%,而单位平衡吸附量从4.827减小至2.162;实验采用准一级、准二级吸附动力学模型,其中准二级动力学模型拟合效果更好,模型预测单位平衡吸附量q_e(3.247)更接近实验测得的q_e(3.098);胶质的吸附过程是由外向内的,驱动力不足以及吸附点位的数量影响使得吸附达到平衡。

黎药弯柄灵芝质量标准初步研究

目的:初步建立黎药弯柄灵芝的质量标准。方法:对弯柄灵芝药材的性状进行鉴定,对其显微特征进行鉴别;参照《中国药典》2020年版方法,采用薄层色谱法(TLC)对药材进行定性鉴别,采用分光光度法测定药材中的多糖和三萜及甾醇含量。结果:明确了弯柄灵芝的性状及显微特征,建立了专属的TLC定性鉴别法;初步规定了弯柄灵芝多糖含量不得低于0.80%,三萜及甾醇含量不得低于0.90%。结论:本研究建立的弯柄灵芝药材质量标准可为其质量控制及资源可持续利用提供依据。

Identification of Tibetan and Qiang Edible and Medicinal Herbs Cardamine tangutorum and Cardamine macrophylla

[Objectives]To study the original plants,characters,tissue structure,powder characteristics and thin-layer chromatography(TLC)characteristics of Cardamine tangutorum and Cardamine macrophylla as Tibetan and Qiang edible and medicinal herbs,and to provide the basis for the identification of C.tangutorum and C.macrophylla.[Methods]The identification of C.macrophyll and C.tangutorum was carried out by original plant identification,character identification,microscopic identification and TLC identification.[Results]C.tangutorum and C.macrophylla can be distinguished according to the shape of rhizome and stem,the difference of stem leaves and leaflets,and the difference of flower color;there is no obvious difference between the characteristics of the shape and the powder;the thin layer chromatography shows that in the thin layer chromatography of C.tangutorum and C.macrophylla,spots with the same color are shown on the corresponding positions of the ground part and the reference substance quercetin;the underground part and the position corresponding to the reference substanceβ-sitosterol all show the same color spots.[Conclusions]This study provides a reference for the identification of C.tangutorum and C.macrophylla.

关于TLC/FID法测定误差的探讨

TLC/FID法分析重质油中的烃族组成,具有灵敏、快速、用样量少的优点;但过去一直存在着与经典柱色谱法所测数据可比性差的致命缺点。为此,从TLC分离及FID检测的基本原理出发,寻找合适的操作条件,使两种方法具有良好的相关性,完成了TLC/FID法由半定量向定量分析的转变。欲减少误差.提高准确度,关键是要做好以下几点:①严格控制点样量,以保证数据重复性;②选择适宜的TLC展开条件,以保证被测定物质各组分的分高效果;③控制适宜的扫描速度和氢气流量等操作条件;④用被测定物质各组分校正因子的比值进行数据处理,确保测定结果的准确性。

迪娜尔合剂的化学成分预检识及含量测定

目的预检识迪娜尔合剂的化学成分,测定绿原酸和咖啡酸的含量。方法采用化学反应鉴别法对迪娜尔合剂中的化学成分类型进行鉴别检识;采用福林酚法测定迪娜尔合剂中总多酚的含量;采用薄层色谱法(TLC)对迪娜尔合剂进行定性鉴别分析;采用高效液相色谱法(HPLC)对迪娜尔合剂中的绿原酸与咖啡酸含量进行测定。结果迪娜尔合剂富含多种生物活性化合物,包括糖类、香豆素类、生物碱类、酚类化合物和有机酸类化合物。迪娜尔合剂中总多酚含量为(1.57±1.71)mg/mL,绿原酸和咖啡酸两种单体成分的含量分别为(94.17±0.23)μg/mL和(0.27±0.45)μg/mL。结论迪娜尔合剂中含有多种生物活性化合物,其中多分酚类化合物含量较高,本研究为迪娜尔合剂的质量控制和疗效评估提供了科学依据。