Baizhan Liu

Development of C18-functionalized magnetic silica nanoparticles as sample preparation technique for the determination of ergosterol in cigarettes by microwave-assisted derivatization and gas chromatography/mass spectrometry

Ergosterol is one of the important precursors of tumorigenic polynuclear aromatic hydrocarbons. A large amount of ergosterol is present in mildewy cigarettes, which derives from fungal contaminations. In this paper, a novel approach based on C(18)-functionalized magnetic silica nanoparticles (C(18)-f-MS NPs) coupled with microwave-assisted derivatization and gas chromatography/mass spectrometry (GC/MS) was developed for the rapid enrichment and determination of ergosterol in cigarettes. Due to that, microwave-assisted derivatization requires very short time (several minutes), and the extraction and concentration of ergosterol become the key step in the sample preparation process. In this study, the prepared C(18)-f-MS NPs with its unique properties (high surface area and strong magnetism) provided an efficient way for extraction and concentration of ergosterol in the samples. Additionally, the analyte of ergosterol adsorbed with C(18)-f-MS NPs in cigarettes can be simply and rapidly isolated (only about 2s) through placing a strong magnet on the bottom of container. In this work, different parameters such as added amounts of C(18)-f-MS NPs, extraction temperature, and extraction time were optimized to enhance the extraction efficiency. Method validations (linear range, detection limit, precision, and recovery) were also studied. The results obtained by the optimal conditions showed that the proposed method based on C(18)-f-MS NPs was a simple, high efficient, and had a rapid approach for the enrichment of ergosterol in cigarettes and was successfully applied to the analysis of ergosterol in normal and mildewy cigarettes followed by microwave-assisted derivatization and GC/MS.

Analysis of amino acids in tobacco by derivatization and dispersive liquid–liquid microextraction based on solidification of floating organic droplet method

A new one-step derivatization and microextraction technique was developed for determination of amino acids in tobacco samples. In the proposed method, amino acids were derivatized with isobutyl chloroformate (IBCF) in aqueous solution. The derivatives were extracted by dispersive liquid-liquid microextraction based on solidification of floating organic droplet (DLLME-SFO). Parameters affecting the extraction efficiency were investigated in detail. The optimum conditions were as follows: a mixture of 500μL acetone, containing 40μL 2-dodecanol, was rapidly injected by syringe into the 2mL water sample. After centrifugation, the 2-dodecanol droplets were floated at the top of the tube. Then, the tube was cooled in an ice bath. After 5min the solvent had solidified and was then transferred into a conical vial; it melted quickly at room temperature and it was injected into a gas chromatograph for analysis. Under the optimum conditions, the limits of detection were of the order of 0.12-2.82μg/mL. The calibration curves showed good linearity over the investigated concentration range between 0.5 and 200μg/mL with a coefficient of estimation (R(2))>0.9887 for GC-MS (SIM). The proposed method is an alternative approach to the quantification of amino acids in tobacco samples.

Development of solvent micro-extraction combined with derivatization

Solvent microextraction (SME), such as single-drop microextraction (SDME), hollow-fiber liquid-phase microextraction (HF-LPME) and dispersive liquid-liquid microextraction (DLLME), has been explored for its ability to cover a wide range of analytes. Microextraction, combined microextraction with derivatization can greatly improve separation, detectability and compound identification, expand its scope of application, and improve the effect of analysis. In this view, the article not only highlights the development of the microextraction technology such as SDBE, HF-LPME and DLLME, but also improves the key strategies of microextraction coupled to derivatization in analytical chemistry. In order to encourage further development of microextraction-derivatization, its coupling with different analytical techniques such as GC or GC-MS, HPLC, and the other technique has also been discussed.

Development of single-drop microextraction and simultaneous derivatization followed by GC-MS for the determination of aliphatic amines in tobacco

In this work, for the first time, headspace (HS) single-drop microextraction and simultaneous derivatization followed by GC-MS was developed to determine the aliphatic amines in tobacco samples. In the HS extraction procedure, the mixture of derivatization reagent and organic solvent was employed as the extraction solvent for HS single-drop microextraction and in situ derivatization of aliphatic amine in the samples. Fast extraction and simultaneous derivatization of the analytes were performed in a single step, and the obtained derivatives in the microdrop extraction solvent were analyzed by GC-MS. The optimized experiment conditions were: sample preparation temperature of 80 degrees C and time of 30 min, HS extraction solvent (the mixture of benzyl alcohol and 2,3,4,5,6-pentafluorobenzaldehyde) volume of 2.0 microL, extraction time of 90 s. With the optimal conditions, the method validations were also studied. The method has good linearity (R(2) more than 0.99), accepted precision (RSD less than 13%), good recovery (98-104%) and low limit of detection (0.11-0.97 microg/g). Finally, the proposed technique was successfully applied to the analyses of aliphatic amines in tobacco samples of seven different brands. It was further demonstrated that the proposed method offered a simple, low-cost and reliable approach to determine aliphatic amines in tobacco samples.

Preparation of phenyl group-functionalized magnetic mesoporous silica microspheres for fast extraction and analysis of acetaldehyde in mainstream cigarette smoke by gas chromatography–mass spectrometry

Acetaldehyde is regarded as a toxic mainstream cigarette smoke constituent, and measurement of acetaldehyde in complex real samples is difficult owing to its high volatility and reactivity. In this work, phenyl group-functionalized magnetic mesoporous microspheres were developed as the solid-phase extraction sorbents for enrichment and analysis of acetaldehyde in mainstream cigarette smoke. The functional magnetic microspheres were first synthesized through a facile one-pot co-condensation approach. The prepared nanomaterials possessed abundant silanol groups in the exterior surface and numerous phenyl groups in the interior pore-walls, as well as a large surface area (273.5m(2)/g), strong superparamagnetism and uniform mesopores (3.3 nm). Acetaldehyde in mainstream cigarette smoke was collected in water and derivatizated with O-2,3,4,5,6-(pentafluorobenzyl)hydroxylamine. The formed acetaldehyde oximes were extracted and enriched by the prepared adsorbents via π-π interactions and subsequently analyzed using GC-MS. Extraction conditions such as amounts of sorbents, eluting solvent, adsorption and desorption time were investigated and optimized to achieve the best efficiency. Method validations including linearity, recovery, repeatability, and limit of detection were also studied. It was found that the suggested methodology provided low detection limit of 0.04 mg/mL, good recovery of 88-92%, intra-day and inter-day RSD values of 4.5% and 10.1%, and linear range of 0.25-4 mg/mL (R(2)=0.999). The results indicated that the proposed method based on phenyl-functionalized magnetic mesoporous microspheres was rapid, efficient and convenient for the enrichment and analysis of acetaldehyde in tobacco.

A novel fully automated on-line coupled liquid chromatography-gas chromatography technique used for the determination of organochlorine pesticide residues in tobacco and tobacco products.

In this study, a novel fully automated on-line coupled liquid chromatography-gas chromatography (LC-GC) technique was reported and applied for the determination of organochlorine pesticide residues (OCPs) in tobacco and tobacco products. Using a switching valve to isolate the capillary pre-column and the analytical column during the solvent evaporation period, the LC solvent can be completely removed and prevented from reaching the GC column and the detector. The established method was used to determinate the OCPs in tobacco samples. By using Florisil SPE column and employing GPC technique, polarity impurities and large molecule impurities were removed. A dynamic range 1-100ng/mL was achieved with detection limits from 1.5 to 3.3μg/kg. The method exhibited good repeatability and recoveries. This technology may provide an alternative way for trace analysis of complex samples.

Microwave-assisted silylation followed by gas chromatography/mass spectrometry for rapid determination of ergosterol in cigarettes

Ergosterol is one of the important precursors of tumorigenic polynuclear aromatic hydrocarbons. To the best of our knowledge, a large amount of ergosterol is present in moldy cigarettes, which derives from fungal contaminations. Thus, the development of a simple, fast, and efficient method for the analysis of ergosterol is in great demand. In this paper, GC/MS following microwave-assisted silylation (MAS) was developed for the rapid quantitative analysis of ergosterol in cigarettes for the first time. In our work, total ergosterol in cigarettes after NaOH saponification was extracted with hexane, and then was fast derivatized with bis(trimethylsilyl)trifluoroacetamide (BSTFA) under microwave irradiation. Finally, the ergosterol trimethylsilyl derivative was analyzed by GC/MS. Derivatization conditions including microwave reaction solvent, irradiation time, and power were investigated. Method validations (linear range, LOD, precision, and recovery) were also studied. The results showed that the proposed method provided a fast, simple, and sensitive approach for the determination of ergosterol in cigarettes. Finally it was successfully applied to the analysis of ergosterol in normal and mildewy cigarettes.

Surface properties of solid materials measured by modified inverse gas chromatography.

A novel modified inverse gas chromatography (IGC) method has been developed to investigate the surface properties of solid materials. On the modified IGC system, the every adjusted retention time of miscellaneous probe molecules can be rapidly calculated within only one sample injection through wisely induction a capillary column and two detectors, i.e., flame ionization detector (FID) and thermal conductivity detector (TCD). In the system, the relative dead time can be acquired from FID detector while the retention time can be obtained from TCD detector simultaneously. The significant advantage of our design is that, experimental time is greatly saved compared to the traditional IGC. In addition, the new system is capable of distinguishing variety surface properties of porous materials. Two types of active carbon samples were tested, and the results showed that their thermodynamic parameters were quite different, indicating that the samples have opposite acidic/basic properties. The use of IGC would be an effective tool to evaluate the physiochemical data of solid materials.

Quantitative method for analysis of tobacco-specific N-nitrosamines in mainstream cigarette smoke by using heart-cutting two dimensional liquid chromatography with tandem mass spectrometry

A heart-cutting two dimensional liquid chromatography coupled with tandem mass spectrometry method was developed for the analysis of tobacco-specific N-nitrosamines (TSNAs) at low concentration level in Virginia-type cigarette smoke. A strong cation exchange column was utilized for the first dimensional separation, which effectively removed acidic and neutral components in the smoke, followed by a reversed phase liquid chromatography coupled with tandem mass spectrometric analysis. To capture components of the TSNAs in the effluent on the trapping column, a compensating pump was applied for online dilution and pH adjustment during the period of the TSNAs fraction transferring and enrichment. Highly sensitive determination of the TSNAs in mainstream cigarette smoke was achieved by isotope deuterated internal standards under the multiple reaction monitoring mode. Compared with traditional methodologies, the method was almost no matrix interference. Limits of quantity for the TSNAs were within 0.027-0.094xa0ng/mL, and the results showed good reproducibility and accuracy. Finally, the new method was applied for analysis of the Kentucky reference cigarettes and the results agreed well with joint experiments of Cooperation Centre for Scientific Research Relative to Tobacco.

Development of Multiple Heart-Cutting Two-Dimensional Liquid Chromatography Coupled to Quadrupole-Orbitrap High Resolution Mass Spectrometry for Simultaneous Determination of Aflatoxin B1, B2, G1, G2, and Ochratoxin A in Snus, a Smokeless Tobacco Product

The combination of multiple heart-cutting two-dimensional liquid chromatography (MHC-LC/LC) and quadrupole-orbitrap high-resolution mass spectrometry (HRMS) for simultaneous determination of the aflatoxins and ochratoxin A in snus is presented in this work. A C18 capillary column was used as the first dimension (1D) to isolate the aflatoxins and ochratoxin A from the complex matrices; then, a 2-position/10-port high-pressure valve equipped with two 60 μL loops was employed to transfer the heart-cuts of 1D-LC into a pentafluorophenyl (PFP) column for the second dimension (2D) separation. With the better separation of the MHC-LC/LC system, the sensitivity of the method was improved, which is essential for the trace mycotoxins analysis. Furthermore, HRMS performed in parallel reaction monitoring mode was employed to eliminate the interferences, and the sample pretreatment procedure was simplified. A new approach utilizing ethyl acetate with 1% formic acid/water solution was adopted to extract aflatoxins and ochratoxin A in snus, which provided parallel recoveries for aflatoxins and ochratoxin A with higher responses in comparison with the QuEChERS method. A dynamic range between 0.2 and 20 μg/kg was achieved with LOQs of 0.05 μg/kg for aflatoxin B1, 0.1 μg/kg for aflatoxin B2, G1, G2, and 1.0 μg/kg for ochratoxin A in dry mass of product. The results revealed that the established method exhibited good repeatability and recovery and could be used as a rapid and reliable approach for routine analysis of aflatoxins and ochratoxin A in snus.