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Stressed plants and polymer production can emit many unsaturated volatile organic esters (UVOEs). However, secondary organic aerosol (SOA) formation of UVOEs remains unclear, especially under complex ambient conditions. In this study, we mainly investigated ethyl methacrylate (EM) ozonolysis. Results showed that a substantial increase in secondary H2SO4 particles promoted SOA formation with increasing SO2. An important reason was that the homogeneous nucleation of more H2SO4 at high SO2 level provided greater surface area and volume for SOA condensation. However, increased primary H2SO4 with seed acidity enhanced EM uptake but reduced SOA formation. This was ascribed to the fact that the ozonolysis of more adsorbed EM was hampered with the formation of surface H2SO4 at higher particle acidity. Moreover, the increase in secondary H2SO4 particle via homogeneous nucleation favored to the oligomerization of oxidation products, whereas the increasing of primary H2SO4 with acidity in the presence of seed tended to promote the functionalization conversion products. This study indicated that the role of increased H2SO4 to EM-derived SOA may not be the same under different ambient conditions, which helps to advance our understanding of the complicated roles of H2SO4 in the formation of EM-derived SOA.

To enrich structural chemistry and widen the application prospects of MOFs (metal-organic frameworks), the development of a synthetic strategy to realize structural and functional modulation is highly demanded. By implementation of the linker bent-angle engineering strategy, three banana-like diisophthalate linkers with distinct bent angles were designed and synthesized. The inclusion of the targeted linkers into MOFs through solvothermal assembly with CuCl2·2H2O under identical conditions yielded three crystalline solids featuring diversified topological structures as revealed by X-ray crystallographic studies. Furthermore, functional explorations indicated that they are promising solid adsorbents for acetylene (C2H2) purification application with structurally dependent separation potentials. The results reported in this study illustrated a rare example of modulating the topological structures and separation efficiencies of MOFs by engineering the ligand bent angles.

Biosynthesis of fatty alcohol holds great promise as substitute to replace petroleum-derived fatty alcohols to mitigate environmental concerns and reduce earth's carbon footprint. In this protocol, we detail the procedures of how to use the YaliBrick gene assembly platform to achieve modular assembly of fatty alcohol pathway in Y. lipolytica. To limit fatty alcohol oxidation, we will also describe the hydroxyurea-based protocols for the efficient disruption of POX1 gene, encoding the fatty acyl coenzyme A in Y. lipolytica, with the homologous arm about 500 bp. We envision that this chapter would improve our ability to engineer microbial cell factories for oleochemical and fatty alcohol production in oleaginous yeast species.

Stressed plants and polymer production can emit many unsaturated volatile organic esters (UVOEs). However, secondary organic aerosol (SOA) formation of UVOEs remain unclear, especially under complex ambient conditions. In this study, we mainly investigated ethyl methacrylate (EM) ozonolysis. Results showed that a substantial increase in secondary H2SO4 particles promoted SOA formation with increasing SO2. An important reason was that the homogeneous nucleation of more H2SO4 at high SO2 level provided greater surface area and volume for SOA condensation. However, increased primary H2SO4 with seed acidity enhanced EM uptake, but reduced SOA formation. This was ascribed to the fact that the ozonolysis of more adsorbed EM was hampered with the formation of surface H2SO4 at higher particle acidity. Moreover, the increase in secondary H2SO4 particle via homogeneous nucleation favored to the oligomerization of oxidation products, whereas the increasing of primary H2SO4 with acidity in the presence of seed tended to promote the functionalization conversion products. This study indicated that the role of increased H2SO4 to EM-derived SOA maybe not the same under different ambient conditions, which helps to advance our understanding of the complicated roles of H2SO4 in the formation of EM-derived SOA.

The theophylline aptamer was isolated from an oligonucleotide library in 1994. Since that time, the aptamer has found wide utility, particularly in synthetic biology, cellular engineering, and diagnostic applications. The primary application of the theophylline aptamer is in the construction and characterization of synthetic riboswitches for regulation of gene expression. These riboswitches have been used to control cellular motility, regulate carbon metabolism, construct logic gates, screen for mutant enzymes, and control apoptosis. Other applications of the theophylline aptamer in cellular engineering include regulation of RNA interference and genome editing through CRISPR systems. Here we describe the uses of the theophylline aptamer for cellular engineering over the past 25 years. In so doing, we also highlight important synthetic biology applications to control gene expression in a ligand-dependent manner.

Interactions of Zn2+ with amyloid β-protein (Aβ) and the subsequent induction of Aβ aggregation have been implicated in the pathogenesis of Alzheimer's disease (AD). The development of small-compound inhibitors against Zn2+-mediated Aβ aggregation is therefore greatly desired. In this study, brazilin was used to inhibit Zn2+-mediated Aβ aggregation and alleviate its cytotoxicity. The binding properties of brazilin and Zn2+ were first probed using Fourier transform infrared (FTIR) spectroscopy and isothermal titration calorimetry (ITC) assays. Both the FTIR and ITC results have shown that brazilin is able to bind Zn2+ in a physiologically suitable range of concentrations. The dissociation constant (Kd) between brazilin and Zn2+ was about 46.0±6.8μM, which makes brazilin a potential drug model for the chelation of free Zn2+. Moreover, the higher affinity of brazilin for Aβ42 (Kd=2.5±1.6μM) than that of Zn2+ (Kd=6.2±0. 9μM), enables brazilin to sequester Zn2+ from the Aβ42-Zn2+ complex. In addition, the inhibitory effects of brazilin on Zn2+-mediated Aβ aggregation were examined using the Thioflavin T fluorescence assay, transmission electron microscopy and cytotoxicity assays. It was found that brazilin showed remarkable inhibitory capability against Zn2+-induced aggregation of Aβ42. Furthermore, the Zn2+-mediated cytotoxicity of Aβ42 was also largely mitigated under the influence of brazilin. This study therefore provides further insights into the role of Zn2+ in the Aβ42 aggregation pathway, indicating potential new strategies for the design of small compounds with therapeutic potential for AD.

A closo-dodecaborate [B12H12]2- functionalized metal organic framework (MOF), BSF-3, constructed by the self-assembly of the Cu(II) cation, 1,4-di(pyridin-4-yl)benzene linker and cluster [B12H12]2- pillar was investigated for the adsorption separation of light hydrocarbons. The activated MOF exhibited efficient uptake of CO2 and C2–C3 hydrocarbons with high separation selectivity of C3H8 (138), C2H2 (205), C2H4 (23), C2H6 (13) and CO2 (9) over CH4, outperforming many popular MOFs. The practical gas separation ability for C2H2/CH4, CO2/CH4 and C3H8/C2H6/CH4 was confirmed by mixed gas breakthrough experiments with no capacity loss after 7 cycles, indicating its potential for purification of methane from natural gas and pyrolysis gas. The gas bonding sites within the framework were further studied by modelling studies, which indicated that the anionic [B12H12]2- pillar contributed the most to capturing hydrocarbon molecules by multiple B-Hδ-···Hδ+-C interactions.

Fibrillogenesis of human islet amyloid polypeptide (hIAPP) is a pathological hallmark of type II diabetes mellitus (T2DM), and the inhibition of hIAPP fibrillogenesis is an important strategy for the prevention and treatment of T2DM. In this study, the inhibitory effects of brazilin on the fibrillization and cytotoxicity of hIAPP were examined using the thioflavin T fluorescence (ThT) assay, transmission electron microscopy (TEM), circular dichroism (CD) spectroscopy, cytotoxicity assays, and molecular dynamics simulations. Both the ThT and TEM results have shown that brazilin inhibits hIAPP fibrillogenesis in a dose-dependent manner. CD studies revealed that brazilin delays the conformational transition of hIAPP from its initial α-helical to the β-sheet form. As a result, brazilin greatly alleviates hIAPP-induced cytotoxicity. Moreover, we also found that brazilin disassembles preexisting hIAPP fibrils, and alleviates the cytotoxicity of hIAPP aggregates. The results of free energy decomposition studies calculated using molecular mechanics-Poisson–Boltzmann surface area analysis revealed that hydrophobic interactions contribute more than 75% of the free energy of binding in the brazilin–hIAPP complex, while electrostatic interactions (i.e., hydrogen bonds) play a secondary role (

Methoxyphenols, lignin pyrolysis products, are major biomass combustion components and are considered potential tracers for wood smoke emissions. Their atmospheric reactivity, however, has not been well characterized. Guaiacol, creosol, and syringol are three typical methoxyphenols generated in relatively high concentrations in fresh wood smoke. In this study, the gas-phase reactions of NO3 radicals with these methoxyphenols were investigated using a laboratory-built vacuum ultraviolet photoionization gas time-of-flight mass spectrometer (VUV-GTOFMS) and off-line GC-MS. By combining experimental and theoretical methods, 4-nitroguaiacol, 6-nitroguaiacol, and 4,6-dinitroguaiacol were determined as the primary degradation products for guaiacol; similarly, 6-nitrocreosol and 3-nitrosyringol were identified for creosol and syringol, respectively. Using the relative rate method, rate constants at 298 K and 1 atm for the gas-phase reactions of guaiacol, creosol, and syringol with NO3 radicals were measured to be 3.2 × 10−12, 2.4 × 10−13, and 4.0 × 10−13 cm3 molecule−1 s−1, respectively. At a typical tropospheric concentration of NO3 radicals (5 × 108 molecule cm−3), atmospheric lifetimes for guaiacol, creosol, and syringol toward NO3 radicals were 0.2, 2.3, and 1.4 h, respectively. These results indicate that the reaction with NO3 radicals can be a major sink for methoxyphenols at night.

To clarify whether the blocking reaction sites problem has a significant impact on heterogeneous reactions, experiments contrasting the order of pyrene (PY) particles' exposure to N2O5–O3 or O3–N2O5 in a heterogeneous process were conducted. Additionally, PY particles were exposed to N2O5 (∼8 ppm) in the presence of O3 (2.5–30 ppm) in a reaction chamber at ambient pressure and room temperature. Our results show that the phenomenon of blocking reaction sites may be ubiquitous on the surfaces of atmospheric aerosol particles, and the N2O5-initiated ionic electrophilic nitration may be promoted by NO3 radical-initiated heterogeneous reactions on the aerosol particle surface. We also found that the operative reaction mechanism strongly depends on the concentrations of the nitric oxides in the atmosphere. Our results provide an explanation as to why 2-nitropyrene (2-NPY), one of the most ubiquitous nitro-polyaromatic hydrocarbon pollutants that exists in both the gas and particle phases, was not observed in previous experiments on the heterogeneous reactions of PY and N2O5/NO3/NO2.

In this study, we report on the development of a lamp-based vacuum ultraviolet photoionization mass spectrometer (VUV-PIMS) in our laboratory; it is composed of a radio-frequency-powered VUV lamp, a VUV photoionizer, an ion-migration lens assembly, and a reflection time-of-flight mass spectrometer. By utilizing the novel photoionizer consisting of a photoionization cavity and a VUV light baffle, the baselines of the mass spectra decreased from 263.6 ± 15.7 counts to 4.1 ± 1.8 counts. A detection limit (2σ) of 3 pptv was achieved for benzene after an acquisition time of 10 s. To examine its potential for real-time monitoring applications of samples, the developed VUV-PIMS was employed for the continuous measurement of urban air for 6 days in Beijing, China. Strong signals of trace-level volatile organic compounds, such as benzene and its alkylated derivatives, were observed in the mass spectra. These initial experimental results reveal that the instrument can be used for the online monitoring of trace-level species in the atmosphere.

Pirimiphos-methyl (PMM) is a widely used organophosphorus pesticide that can be released into the atmosphere in gas and condensed phases. It possesses a PS bond and an N,N-dialkyl group adjacent to pyrimidine, which are common functional groups for pesticides. Currently, the reaction mechanisms of O3 with these functional groups are poorly understood. In this study, the mechanisms and possible degradation products for O3-initiated atmospheric oxidation of PMM were investigated using the Density Functional Theory (DFT) method. The results show that H abstraction from the alpha carbon of the N,N-diethyl group and its subsequent reactions (hydroxylation, N-dealkylation, and carbonylation reactions), as well as the transformation of the PS bond to the PO oxone form, are the most favorable reaction pathways for PMM and O3. The Gibbs free energy (ΔG) indicates that the subsequent reactions tend to take place more spontaneously once the initial reaction occurs. In addition, theoretical calculations indicate that water can serve as an effective catalyst in the N-dealkylation reaction process. Water-assisted reactions lead to the activation energy decreasing by 20.2 kcal mol(-1) compared with direct reactions, and thus may represent a dominant reaction pathway for the N-dealkylation process in the atmosphere. These theoretical results provide new insights into O3-initiated degradation of PMM and its analogues.

It is complex to assign the products obtained from the gas-phase reactions of PAHs with NO3/NO2 and N2O5. For this purpose, theoretical calculations are performed. Results show that 2-nitrofluoranthene and 2-nitropyrene are the dominant products for reactions of fluoranthene and pyrene with NO3/NO2, while 3-nitrofluoranthene and 1-nitropyrene are the major nitration products of N2O5. S(N)2 reaction mechanisms are elucidated and homolytic mechanisms are calculated for the first time. Rate constants for reactions of fluoranthene and pyrene with N2O5 are deduced for the first time, which are 2.50 x 10(-27) and 2.16 x 10(-24) cm(3) molecule(-1) s(-1), respectively at 298 K. (C) 2015 Elsevier B.V. All rights reserved.

Online matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) is reported with in situ matrix/analyte aerosol mixing. The analyte and matrix were dissolved in separate solvents and pneumatically atomized into particles. Continuous flows of analyte particles and matrix droplets in nitrogen were mixed in a tee. The resulting particles were sampled using a nozzle, focused into a beam with an aerodynamic lens system, and vertically deposited continuously on a movable target. The matrix/analyte mixture was desorbed/ionized using a 266 nanometers pulsed laser at an incident angle of 45 degrees. The nascent ions were analyzed using reflectron TOF MS. The performance of online MALDI-TOF MS was evaluated by the analysis of palmityl palmitate with the lithium salt of 2, 4-dihydroxybenzoic acid as the matrix. Strong and stable MALDI signals of palmityl palmitate were obtained. The matrix solvent mixture and the analyte concentration were optimized and the results demonstrate the development of an alternative for online MALDI analysis.

Over 60% of herbicides are capable of disrupting the endocrine and/or reproductive systems of animals. These herbicides may be released into the atmosphere in both gas and particulate phases, but most of their degradation processes in the atmosphere are not well known. In this study, the heterogeneous reactions of suspended isopropalin, trifluralin, and alachlor particles with NO3 radicals were investigated using an online vacuum ultraviolet photoionization aerosol time-of-flight mass spectrometer. The reaction products for the three herbicides were determined by the assistance of the gas chromatography–mass spectrometer analysis. Mono-dealkylated derivatives were detected as the main reaction products of isopropalin and trifluralin. In addition, an α-amino alcohol product was detected for isopropalin. The carbonylation derivative and the nitro-substituted derivative were the main reaction products observed for alachlor. The reaction mechanism of NO3 radical-induced N-dealkylation for isopropalin was clarified by density functional theory calculations. It began with the H-abstraction from the N-propyl group, followed by the formation of the α-peroxypropyl radical, α-propyloxy radical, and α-amino alcohol, as well as by the collapse of the α-amino alcohol. The oxidation mechanism for trifluralin is similar to that of isopropalin, whereas the mechanism for alachlor involves carbonylation and nitro-substitution. These results provided insights on the chemical transformation of these herbicides in the atmosphere. The data generated from this study can be used as fundamental information for future studies on their toxic effects to the environment.

Summary Sophorolipids (SLs) are biosurfactants with widespread applications. The yield and purity of SLs are two important factors to be considered during their commercial large‐scale production. Notably, SL accumulation causes an increase in viscosity, decrease in dissolved oxygen and product inhibition in the fermentation medium. This inhibits the further production and purification of SLs. This describes the development of a novel integrated system for SL production using Candida albicans O‐13‐1. Semicontinuous fermentation was performed using a novel bioreactor with dual ventilation pipes and dual sieve‐plates (DVDSB). SLs were separated and recovered using a newly designed two‐stage separation system. After SL recovery, the fermentation broth containing residual glucose and oleic acid was recycled back into the bioreactor. This novel approach considerably alleviated the problem of product inhibition and accelerated the rate of substrate utilization. Production of SLs achieved was 477 g l−1, while their productivity was 1.59 g l−1 h−1. Purity of SLs improved by 23.3%, from 60% to 74%, using DVDSB with the separation system. The conversion rate of carbon source increased from 0.5 g g−1 (in the batch fermentation) to 0.6 g g−1. These results indicated that the integrated system could improve the efficiency of production and purity of SLs.

In order to understand the seasonal levels, formation mechanism and atmospheric chemical behaviours of water-soluble ions of PM10 in the Yangtze River Delta (YRD) region, aerosol samples were collected from January 2nd to December 28th, 2017 at a WMO/GAW regional background station in Lin’an. The concentrations of PM mass and nine water-soluble inorganic ions were obtained. The annual average concentration of PM10 was 59.9±33.9 μg m−3, lower than those reported in previous studies, indicating air quality of YRD region was improved. Nine water-soluble inorganic ions was accounted for 30.2-45.1% of the total PM mass, while ammonium (NH4+), sulfate (SO42+), as well as nitrate (NO3-) were the major ions which contributed 86.3% to total ions. The NO3- concentration was lowest in summer but highest in winter, suggesting it was likely influenced by thermodynamics. The levels of SO42- in spring and winter were related to photochemical reaction and regional transportation. Except for the SNA, Ca2+ was highest in four seasons likely due to sand storm and road fugitive dust. The annual mean ratio of [NO3-]/[SO42-] was nearly to 1, indicating mobile and stationary sources were equally important in Lin’an. The mean nitrogen oxidation ratio (NOR) and sulfur oxidation ratio (SOR) were 0.22±0.13 and 0.41±0.13, respectively, suggesting secondary formation was significant in the atmosphere at the background station of YRD region.

Chlorpyrifos is a typical chlorinated organophosphorus pesticide. The heterogeneous reaction of chlorpyrifos particles with NO3 radicals was investigated using a vacuum ultraviolet photoionization aerosol time-of-flight mass spectrometer (VUV-ATOFMS) and a real-time atmospheric gas analysis mass spectrometer. Chlorpyrifos oxon, 3,5,6-trichloro-2-pyridinol, O,O-diethyl O-hydrogen phosphorothioate, O,O-diethyl ester thiophosphoric acid, diethyl hydrogen phosphate and a phosphinyl disulfide compound were identified as the main degradation products. The heterogeneous reaction pathways were proposed and their kinetic processes were investigated via a mixed-phase relative rate method. The observed effective rate constant is 3.4 +/- 0.2 x 10(-12) cm(3) molecule(-1) s(-1). (C) 2014 Elsevier B.V. All rights reserved.

Doping has been used to enhance the ionization efficiency of analytes in atmospheric pressure photoionization, which is based on charge exchange. Compounds with excellent ionization efficiencies are usually chosen as dopants. In this paper, we report a new phenomenon observed in low-pressure photoionization: Protonation enhancement by dichloromethane (CH2Cl2) doping. CH2Cl2 is not a common dopant due to its high ionization energy (11.33 eV). The low-pressure photoionization source was built using a krypton VUV lamp that emits photons with energies of 10.0 and 10.6 eV and was operated at 500-1000 Pa. Protonation of water, methanol, ethanol, and acetaldehyde was respectively enhanced by 481.7 +/- 122.4, 197.8 +/- 18.8, 87.3 +/- 7.8, and 93.5 +/- 35.5 times after doping 291 ppmv CH2Cl2, meanwhile CH2Cl2 almost does not generate noticeable ions itself. This phenomenon has not been documented in the literature. A new protonation process involving in ion-pair and H-bond formations was proposed to expound the phenomenon. The observed phenomenon opens a new prospect for the improvement of the detection efficiency of VUV photoionization., Comment: 12 pages, 5 figures, 1 table, and under submission

Background Identifying endogenous volatile organic compounds (VOCs) as markers for different cancers currently requires time-consuming procedures and specialized operators. Objective The objective of this study was to develop a rapid and simple method for measuring VOCs at trace levels. Methods A simple vacuum ultraviolet photoionization mass spectrometer (VUV-PIMS) was used to detect trace levels of dimethyl trisulfide (DMTS), dimethyl sulfide (DMS), and 2-butanone, which correspond to volatile biomarker candidates present in the exhaled breath of patients with breast, liver, and lung cancers, respectively. The practicality of measuring endogenous VOCs using VUV-PIMS was confirmed by detecting them in cultured cell lines. Results The abovementioned VOCs were detected with high sensitivity by VUV-PIMS. The limits of detection (LODs) for DMTS, DMS, and 2-butanone were 3.1, 3.9, and 23.2 pptv, respectively, under ambient conditions, which surpass the sensitivity of nearly all other MS-based techniques. Moreover, relatively high concentrations of 2-butanone and DMS were observed in VOCs emitted from the A549 lung cancer cell line and the HepG2 liver cancer cell line, respectively. Conclusions Our results show that VUV-PIMS may serve as a reliable method for real-time measurement of endogenous volatile cancer biomarkers.

On-spot monitoring of threat agents needs high sensitive instrument. In this study, a low-pressure photoionization mass spectrometer (LPPI-MS) was employed to detect trace amounts of vapor-phase explosives and chemical warfare agent mimetics under ambient conditions. Under 10-s detection time, the limits of detection of 2,4-dinitrotoluene, nitrotoluene, nitrobenzene, and dimethyl methyl phosphonate were 30, 0.5, 4, and 1 parts per trillion by volume, respectively. As compared to those obtained previously with PI mass spectrometric techniques, an improvement of 3–4 orders of magnitude was achieved. This study indicates that LPPI-MS will open new opportunities for the sensitive detection of explosives and chemical warfare agents.

Atmospheric 2-nitrofluoranthene (2-NFL) and 2-nitropyrene (2-NPY) were two important nitro-polycyclic aromatic hydrocarbons (NPAHs). Especially, 2-NFL was recognized to be the most abundant particle-associated NPAH (Ramdahl et al., 1986). In previous studies, these two products were observed in the gas-phase reaction between N2O5/NO3/NO2 and their parent polycyclic aromatic hydrocarbons (PAHs), while the heterogeneous reaction generated other nitro-PAH isomers (1, 3, 7, 8-NFL and 1-NPY) (Atkinson et al. 1990). To clarify the possible reasons for this difference, the heterogeneous reactions of suspended fluoranthene (FL) and pyrene (PY) particles under different relative humidity (RH; 0.5%-43%) and [NO3]/[N2O5] ratios were carried out. Under low humidity (0.5% RH) or a relatively high ratio of [NO3]/[N2O5], 2-NFL and 2-NPY were observed as the major nitro-FL isomers for the first time in the heterogeneous reaction. Decreasing the humidity or increasing the [NO3]/[N2O5] ratio in the reaction essentially increases the concentration radio of [NO3(g)]/[NO2(+)(aq)] on the particle surface (NO2(+) is derived from the ionization of N2O5). Thus, it can be concluded that under different atmospheric conditions, the change of [NO3(g)]/[NO2(+)(aq)] in the particle surface has an influence on the product distribution of FL and PY in the atmosphere. The experimental results provide evidence for the heterogeneous formations of particle-bound 2-NFL and 2-NPY. However, relative to the gas-phase formation, they will be negligible in the real atmosphere. 2-NFL and 2-NPY observed in the ambient particles should mainly derive from deposition of gas-phase reactions. Additionally, this study also clarifies the reason for different nitro-PAHs isomers observed between gas and particulate reactions.

beta-Sitosterol is the most abundant phytosterol lipid in plants. This study demonstrates a method for analyzing beta-sitosterol using a laboratory-built MALDI-TOF mass spectrometer. The matrix compound, solvent system, laser intensity, alkali ion, and analyte concentration for sample preparation were optimized to acquire reproducible and informative mass spectra of the analyte. The best MALDI spectrum of beta-sitosterol was obtained by mixing the analyte solution with an equal volume of 2,4-DHB/iPrOH-H2O ( 9 : 1) solution (60 mM) at 13.5 mJ cm(-2) laser intensity. Under the optimized experimental conditions, beta-sitosterol generated intense peaks consisting of the initial lipids and their oxidation products. The former included mass peaks at m/z 396.6, 397.6, 436.9, and 452.6, which corresponded to the [M - H2O](+), [M + H - H2O](+), [M + Na](+), and [M + K](+) ions of beta-sitosterol, respectively. The latter included mass peaks at m/z 412.7, 413.7, and 431.9, which corresponded to the [M' - H2O](+), [M' + H - H2O](+), and [M' + H](+) ions of mono-oxidized beta-sitosterol, respectively. A quantitative analysis of beta-sitosterol was also conducted using a matrix peak. Calibration curves obtained for beta(-)sitosterol show a good linear range of three orders of magnitude with a regression coefficient square of 0.992. The linear ranges were between 12.1 and 1207.5 mu M. The detection limit was 10 nM. These results demonstrate the potential application of MALDI mass spectrometry for analyzing phytosterols.