固相萃取-超高效液相色谱法测定卷烟主流烟气中丙烯酰胺

建立了一种固相萃取-超高效液相色谱法(SPE-UPLC)快速检测主流烟气中丙烯酰胺的方法。使用剑桥滤片和吸收瓶捕集主流烟气后,蒸馏水做萃取溶剂,采用C18固相萃取小柱对样品液进行纯化,用UPLC检测,外标法定量。UPLC方法采用ACQUITY UPLCTMBEH C181.7μm 2.1×50 mm色谱柱,柱温30℃,流动相为V(乙腈)∶V(水)=6∶94,流速为0.15 mL/min,紫外检测器(TUV)检测波长为202 nm,分析时间为6 min。烤烟型香烟主流烟气中丙烯酰胺的含量为4.75μg/cig。方法的线性范围为0.1~10 mg/mL,线性相关系数为0.9999;平均回收率为98.7%;检出限为10 ng/mL(S/N=3);相对标准偏差为2.3%。该方法适合主流烟气中丙烯酰胺的快速检测。     

Determination of formaldehyde and acetaldehyde in mainstream cigarette smoke by high-performance liquid chromatography

A method is described for the determination of formaldehyde and acetaldehyde in mainstream cigarette smoke. This involved the collection and reaction of the aldehydes with 2,4-dinitrophenylhydrazine in aqueous acetonitrile. The high-performance liquid chromatographic separation and measurement of the various components directly in this reaction solution eliminated the need for a clean-up stage. Cigarette yields of greater than 5 micrograms of formaldehyde and 50 micrograms of acetaldehyde could be determined to estimated relative standard deviations of 0.07 and 0.05, respectively.     

Analysis of formaldehyde in tobacco smoke by high performance liquid chromatography

Formaldehyde in tobacco smoke is allowed to react with 2,4-dinitrophenylhydrazine to form the dinitrophenylhydrazone. This derivative is extracted with chloroform and concentrated. The residue in methylene chloride is separated and analyzed by high performance liquid chromatography. A column packed with 10-micron silica is used for separation. The internal standard is triphenylene. This method can also be used for the analysis of other carbonyl compounds in tobacco smoke that react to form hydrazone derivatives.     

主流烟气中甲胺和乙胺离子色谱法测定

建立了用0.01 mol·L-1盐酸水溶液吸收,离子色谱法测定卷烟主流烟气中甲胺和乙胺的方法。该方法采用Ion Pac CS16(4×250 mm)分离柱和CG16(4×50 mm)保护柱,10mmol·L-1甲烷基磺酸(MSA)水溶液等梯度洗脱,在柱温60℃、流速1.0 m L·min-1的条件下,实现了甲胺和乙胺的有效分离。方法的线性关系良好,RSD均小于5%,甲胺检出限为0.04μg/支,加标平均回收率为92.7%~94.3%,乙胺检出限为0.05μg/支,加标平均回收率为93.5%~103.0%。该方法灵敏度高、准确性好、前处理简单,有良好的可靠性和实用性。     

液相色谱-串联质谱法测定卷烟主流烟气中的四种致癌物

N-亚硝基降烟碱（NNN）、4-（亚硝基甲氨基）-1-（3-吡啶基）-1-丁酮（NNK）、N-亚硝基新烟草碱 （NAT）和N-亚硝基假木贼碱（NAB）是4种广泛存在于烟草和烟气中的致癌物,准确测定其含量对评估其对人体健康的影响有着重要的作用。采用液相色谱-电喷雾串联质谱(LC-ESI MS/MS)技术建立了卷烟主流烟气中NNN、NNK、NAT和NAB的测定方法,并将其用于中国烤烟和混合型卷烟主流烟气的分析。卷烟主流烟气通过剑桥滤片捕集,捕集烟气后的滤片在加入100 μL氘代混合内标后用10 mL 100 mmol/L醋酸铵水溶液萃取,萃取液过水相滤膜后直接进行LC-ESI MS/MS检测。选用Agilent Zorbax Eclipse XDB-C18色谱柱,以流动相0.1%(v/v)乙酸水溶液和0.1%（v/v）乙酸甲醇溶液梯度洗脱,质谱检测采用正离子扫描,多反应监测模式。NNN、NNK、NAT和NAB的检出限分别为0.019、0.002、0.008和0.007 μg/L,回收率为84.9%～104.5%,相对标准偏差(n=8)为2.96%～6.65%。该方法的检出限低,特异性好,适用于卷烟主流烟气中NNN、NNK、NAT和NAB释放量的检测。     

A feasibility study on oxidation state of arsenic in cut tobacco,mainstream cigarette smoke and cigarette ash by X-ray absorption spectroscopy

This work describes the application of synchrotron-based X-ray Absorption Near-Edge Structure spectroscopy to study the oxidation state of arsenic in cigarette mainstream smoke, cut tobacco and cigarette ash. The level of arsenic in the total particulate matter of the smoke is approximately 1 ppm for the standard research reference cigarette 2R4F and its replacement 3R4F. Smoke particulate samples collected by a conventional glass-fiber membrane (commercially known as Cambridge filter pad) and a jet-impaction method were analyzed and compared. In addition smoke particulate samples were aged either at ambient temperature or at 195 K. X-ray Absorption Near-Edge Structure spectroscopy results revealed that the cut tobacco powder and cigarette ash contained almost exclusively As^V. The smoke particulate samples however contained a mixture of As^III and As^V. The As^V in the smoke particulate was reduced to As^III upon aging. Stabilizing the smoke particulate matter at 195 K by solid CO₂ slowed down this aging reaction and revealed a higher percentage of As^V. This behavior is consistent with the redox properties of the arsenic species and the smoke particulate matrix.     

高效液相色谱法同时测定烟用水基胶中的甲醛和乙醛

建立了用高效液相色谱法同时测定卷烟胶中甲醛、乙醛的分析方法。卷烟胶用去离子水提取,在酸性条件下,经2,4-二硝基苯肼(DNPH)衍生后,衍生物直接用HPLC法检测。结果表明:该方法的标准曲线在相关浓度范围内呈良好线性关系,甲醛、乙醛的检出限分别为3.6、6.2μg/L,阶醛、乙醛的样品回收率分别为98.38%~103.11%,89.37%~90.12%,相对标准偏差均小于6%。     

Major- and trace-element distribution in cigarette tobacco,ash and filters

Journal of Radioanalytical and Nuclear Chemistry - To evidence the efficiency of cigarette filter we have determined the content of 27 major and trace elements in two brands of filter and...     

高效液相色谱法同时测定烟草中吡虫啉、啶虫脒、多菌灵和甲基硫菌灵

建立了烟草中吡虫啉、啶虫脒、多菌灵和甲基硫菌灵农药多残留的高效液相色谱检测方法。样品用乙腈提取,PSA固相萃取柱净化,梯度洗脱方式分离,DAD二极管阵列检测器检测。4种农药回收率为82.0%～112.4%,RSD为2.0%～5.3%。     

Determination of seven nitrobenzene compounds in mainstream cigarette smoke with heart-cutting two-dimensional gas chromatography

A heart-cutting two-dimensional gas chromatography (GC) method was developed for the determination of nitrobenzene compounds (NBCs) in mainstream cigarette smoke. For the method, the particulate matter of cigarette smoke was extracted with cyclohexane, purified with a silica solid-phase extraction (SPE) cartridge and analyzed by heart-cutting two-dimensional GC equipped with two electron capture detectors. The heart-cutting two-dimensional GC was achieved by a single-column GC oven equipped with a microfluidic pressure balanced device (Deans switch). Two-dimensional GC was compared to single-dimensional GC and found to be clearly better for the separation of seven NBCs from a complex smoke matrix. The limits of detection ranged from 1.28 to 9.83 ng/mL, spiked recoveries were between 88.3 and 106.8% and relative standard deviation ranged from 2.79 to 12.78%. The NBCs yields of six kinds of Chinese and international cigarettes brands, which were all smoked according to two smoking protocols (International Organization for Standardization and Health Canada Intense smoking regimens), were determined and compared.     

超高效液相色谱β-环糊精流动相添加剂法分析卷烟主流烟气中7种酚类化合物

以β-环糊精(β-CD)作为流动相添加剂,建立了一种超高效液相色谱(UPLC)快速分析卷烟主流烟气中对苯二酚、间苯二酚、邻苯二酚、苯酚、对甲酚、间甲酚、邻甲酚的方法。卷烟主流烟气中7种酚类化合物采用YC/T 255-2008标准方法收集,萃取液经0.22 μm微孔滤膜过滤后直接进行UPLC分析。采用ACQUIT UPLC BEH Shield RP18色谱柱,以含有4 g/L β-CD的流动相进行梯度洗脱,采用优化后的荧光检测条件进行检测,分析时间为10 min。实验结果表明: 与目前国内外普遍应用的HPLC方法相比,该方法实现了间甲酚和对甲酚异构体的有效分离,7种酚类化合物的荧光响应强度显著增加。7种酚类化合物在该方法的线性范围内线性关系良好(r＞0.9999), 3个加标水平上平均回收率为95.5%～103.5%,相对标准偏差(RSD)均小于4%,方法的检出限为4～14 ng/cig。     

Determination of four tobacco-specific nitrosamines in mainstream cigarette smoke by gas chromatography/ion trap mass spectrometry

A specific and sensitive method was developed and validated to quantitatively analyze four tobacco-specific nitrosamines (TSNAs) in the particulate phase of mainstream cigarette smoke. Cigarette smoke particulate matter was collected according to ISO 4387. The particulate matter was extracted with acetic ether, cleaned up with a Supelclean ENVI-Carb silod-phase extraction (SPE) cartridge, concentrated under the protection of nitrogen and analyzed by gas chromatography (GC)/ion trap mass spectrometry (MS) with a very-low-flow-loss column (VF-17 MS) in MS(n) mode using N-nitrosopentyl-3-picolylamine (NNPA) as an internal standard. TSNAs were identified by chromatographic retention time, matching the spectra of the standards and the samples and the consistency of the ratio of the abundance of the ions detected in the standards and the samples. Limits of detection of each TSNA varied from 0.01 to 0.06 ng/cig. A linear calibration range for this method is large enough to measure TSNA levels in cigarette smoke. The recovery of each TSNA was from 91.5 to 102.7%. The method achieved excellent reproducibility (RSD: 1.8-4.8% for intra-assay, 3.4-7.1% for inter-assay). It also shows no evidence of artifact formation. This method is very suitable for the routine detection of TSNAs in mainstream cigarette smoke.     

固相萃取-气相色谱/质谱联用法测定卷烟主流烟气中的香兰素和乙基香兰素

采用固相萃取-气相色谱/质谱联用技术,建立了一种同时测定卷烟主流烟气中香兰素和乙基香兰素的方法。方法优化了萃取条件,考察了萃取溶剂、萃取时间对检测结果的影响。通过硅藻土固相萃取柱净化并浓缩后,选取DB-HeavyWAX毛细管柱进行目标物分离,以香兰素-d3作为内标,对香兰素和乙基香兰素进行定量分析。结果表明,香兰素和乙基香兰素在浓度0.2~20.0 mg/L范围内具有良好的线性关系,其检出限分别为9.1 ng/支和6.5 ng/支,回收率均在96.3%~107.7%之间。     

离子色谱法及聚类分析研究主流烟气中的有机酸

建立了超声辅助萃取-离子色谱法同时测定卷烟主流烟气中主要有机酸的方法.采用20 mL 30 mmol/L J NaOH溶液在50℃下对捕集了卷烟主流烟气的剑桥滤片超声萃取50 min,AS11-HC分离柱、Ion AG11-HC保护柱、ASRS-ULTRAⅡ抑制器,KOH溶液为淋洗液,用电导检测器同时测定了卷烟主流烟气中的乳酸、甲酸、乙酸、丙酸、苹果酸和草酸的含量.方法的线性范围1.0～400 mg/L,相关系数为0.9990～0.9995,相对标准偏差1.4%～4.8%,检出限0.03～0.09 mg/L,回收率为92%～104%.采用此方法测定了19种不同规格卷烟样品主流烟气中6种有机酸的含量,并且以6种有机酸为指标对样品进行了聚类分析.结果表明,6种有机酸的含量分布特征可反映不同等级卷烟产品的特性,可用于不用等级卷烟产品的比较和分类.     

衍生化-高效液相色谱法测定西索米星

采用反相高效液相色谱法，以2，4-二硝基氟苯为衍生化试剂。其线性范围为10mg/L-500mg/L；检出限为5.0mg/L；相对标准偏差为2.3%。方法适用于西索米星的产品质量控制。     

Determination of lysinoalanine by high performance liquid chromatography

This work suggests an HPLC method for qualitative and quantitative determination of N^ε(2-amino-2-carboxyethyl)-L -lysine (LAL). LAL was released from total hydrolysates of various proteins of animal origin and derivatized with dansyl chloride. The performance of two different columns, Spherisorb 3S TG and μ-Bondapack C₁₈, was compared; better resolution and quantitative response were obtained with the former. The mobile phase was a mixture of 0.01 M phosphate buffer (pH 7) and acetonitrile. Linear response and quantitative repeatability were tested for both detectors used (UV-Vis set at 254 nm; fluorimetric set at λ_ex(max) = 360 nm and λ_em(max) = 525 nm). For LAL standard the minimum detectable amount was 0.05 ng, whereas for LAL in actual samples the amount was 0.5 ng (40 μg/g of analyzed proteins). Good analytical repeatability was obtained, resulting in CV % of 4.7 and 3.8 for UV and fluorimetric detectors, respectively. LAL recovery was determined using both detectors; the values obtained were 94 % (fluorimetric) and 92 % (UV). Greater noise levels were observed with the fluorimetric detector and its higher sensitivity could not, therefore, be fully utilized. The highest amounts of LAL were found in the casein (2816 μg/g) and cooked albumin (615 μg/g) samples.     

烟草中水溶性糖的超高效液相色谱分析及聚类分析研究

以ACQUITY UPLC BEH Amide柱为分析柱,乙腈(0.2%TEA)和水作为流动相,采用蒸发光散射检测器,建立了超高效液相色谱分析烟草中鼠李糖、木糖、果糖、甘露糖、葡萄糖、蔗糖、麦芽糖的方法.7种水溶糖的加标回收率在85.2%～105.3%之间,相对标准偏差皆小于5.7%.方法可用于烟草及其制品中水溶性糖含...     

Determination of pyridine, 2-picoline, 4-picoline and quinoline from mainstream cigarette smoke by solid-phase extraction liquid chromatography/electrospray ionization tandem mass spectrometry

The present paper describes the development and validation of a new reversed-phase liquid chromatography–electrospray ionization tandem mass spectrometric method (RP-HPLC–ESI-MS/MS) for simultaneous determination of pyridine, 2-picoline, 4-picoline and quinoline from mainstream cigarette smoke. Liquid–liquid extraction followed by solid-phase extraction was applied to extract the target analytes from cigarette smoke. Baseline chromatographic separation was achieved by utilizing a Zorbax SB-Aq (4.6 × 150 mm, 5 μm) column in gradient chromatographic conditions with acetonitrile and ammonium acetate buffer as mobile phases. Popular commercially available Indian brand filtered and non-filtered cigarettes were analyzed using the same method. The identification of each chemical was established by chromatographic retention times, analyte specific fragmentation patterns and relative peak area ratios of two product/precursor ion pairs. The limit of detection of this method ranged from 1.74 to 14.32 ng/cig using an injection volume of 20 μl. The reproducibility of this method is excellent and better standard deviations were obtained compared to literature reported values for these chemicals. RSD value is less than 9% for all analytes.     

Determination of diphenamide, napropamide and metolachlor in tobacco by gel permeation chromatographic clean-up and high performance liquid chromatography

Diphenamide, napropamide and metolachlor (FIG. 1) are selective, pre-emergence arylamide herbicides used to control the growth of annual grasses and broadleaf weeds in a variety of fields, e.g. fruit trees, nuts, corns, green crops, etc. They possess high activity and moderate toxicity. For food and environment safety, the detailed investigations on their residues and metabolism are very important. Diphenamide, napropamide and metolachlor in the pesticide products, serum, urine, soil, environmental water, fruits and wine have been widely analyzed by ELISA, fluorescence, phosphorescence, capillary electrophoresis, high performance liquid chromatography (HPLC), gas chromatography(GC) and GC mass spectrometry (GC-MS). However, to our knowledge, simultaneous residue analysis of diphenamide, napropamide and metolachlor in tobacco samples has not been extensively documented. Tobacco is greatly consumed by smokers throughout the world. The pesticide residue in tobaccos might be potentially harmful to smokers' health. With this in mind the residue determination and control of diphenamide, napropamide and metolachlor in the tobacco leaves are very important for tobacco products and consumers. For these three herbicides, the tolerable maximum residue limits (MRLs) have been limited ranging from 0.05 (for tobacco products) to 5 mg/kg (for tobacco leaves) in different European countries. For the complex tobacco samples, the GC and HPLC with UV detection suffer from matrix interference making quantification and identification of these herbicides difficult. In such cases the removal of the matrix effects and identification of the target compounds are of great importance. The present work reports the extraction and clean up procedures, as well as, the chromatographic conditions developed for the simultaneous determination of diphenamide, napropamide and metolachlor residues in the fluecured tobacco leaves, from the different sources using HPLC-UV method.