Publications by authors named "Tenggao Zhu"

Carbon chain elongation (CCE) is normally carried out using either chemical catalysts or bioenzymes. Herein we demonstrate a catalyst-free approach to promote demethylation C-C coupling reactions for advanced CCE constructed with functional groups under ambient conditions. Accelerated by the electric field, two organic cations containing a methyl group (e.

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Protonated water-hydrogen clusters [H(HO)·m(H)] present an interesting model for fundamental water research, but their formation and isolation presents considerable experimental challenges. Here, we report the detection of [H(HO)·m(H)] (2 ≤ ≤ 3, ≤ 2) clusters alongside protonated water clusters H(HO) (2 ≤ ≤ 3) in a linear ion trap mass spectrometer under two different experimental conditions: (1) when water vapor was ionized by +5.5 kV ambient corona discharge in front of the mass spectrometer inlet; (2) when isolated H(HO) clusters were exposed to H gas inside the linear trap.

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Fractionation information on arsenic (As) in complex samples, particularly solid samples, is of immense interest. Herein, selective extraction of various As species adsorbed onto ferrihydrite as the model substrate was online-adapted to inductively coupled plasma-mass spectrometry (ICP-MS) for sensitive detection. The As-adsorbed ferrihydrite sample was loaded into a homemade online sequential elution device using two commercially available micropipette tips, and then, each fraction of As including nonspecifically adsorbed, specifically adsorbed, iron oxide bonded, and residual species was successively extracted for ICP-MS detection, with HO, NHNO, NHHPO, ammonium oxalate, and HF as the eluents, respectively.

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Supercharged protein ions produced by electrospray ionization are extremely efficient proton donors for secondary ionization. Here, by electrospraying the protein solutions containing 5% 1,2-butylene carbonate, the supercharged protein ions with unusually high proton density were produced as the primary ions for the ionization of exhaled breath samples in the extractive electrospray ionization mass spectrometry (EESI-MS), which resulted in the enhanced ionization efficiency for the breath analytes even with relatively low gas phase basicity. Moreover, the total number of metabolites detected in breath increased by about 260% in the mass range of 200-500 Da, owing to the substantial signal enhancement for breath metabolites, providing complementary and additional information to conventional SESI.

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Rapid chemical decoding of bulk alloys to obtain both organic and elemental composition is of sustainable interest in multiple disciplines. Herein, an analytical strategy inherited from electrochemistry and mass spectrometry (MS) was developed for direct molecular characterization of alloys. While the organics on the alloy surface were simply extracted into the solvent for ESI-MS analysis, the components in the bulk alloy were successively converted into metal ions at appropriate electrolysis potentials, which were online chelated with specific ligands for ESI-MS analysis.

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Biological-material-functionalized porous monoliths were prepared with lactoferrin and β-cyclodextrin via a click reaction. With the monolith as an extraction medium, a method combined with ICP-MS was developed for the determination of total gallium originating from metabolic residues of orally bioavailable gallium complexes with tris(8-quinolinolato)gallium (GaQ) as a representative. The method exhibited favorable adsorption behaviors for gallium with high selectivity, low detection limit (2 ng L), and an enrichment factor of 29-fold with the sample throughput of 30 min.

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A facile online method coupling polymer monolithic microextraction (PMME) with mass spectrometry (MS) was developed for the detection of Immunoglobulin G (IgG) galactosylation glycopeptides. A peanut agglutinin-β-cyclodextrin (PNA-β-CD) functionalized poly(hydroxyethyl methylacrylate-ethyleneglycol dimethacrylate) monolith was designed via a click reaction. Thanking to the specificity of PNA-β-CD for the targets, the material exhibited enhanced enrichment selectivity and extraction efficiency for IgG galactosylation glycopeptides.

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Hemoglobin (Hb) present in the blood and meat juice samples was selectively adsorbed by graphene oxide (GO) particles functionalized with amylopectin (AP) and was sensitively detected by direct internal extractive electrospray ionization mass spectrometry (iEESI-MS) analysis for the identification of meat type. Various samples including the whole blood samples of chicken, duck, sheep, mouse, pigeon, turtledove, and meat juice mixtures were successfully identified based on the difference in molecular composition of Hb reflected in MS. The adulteration of sheep blood with only 2% chicken blood could be detected, which demonstrated the high chemical specificity of the approach.

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Direct mass spectrometry analysis of metabolic effects of clenbuterol and salbutamol on pork quality at the molecular level is incredibly beneficial for food regulations, public health and the development of new anti-obesity drugs. With internal extractive electrospray ionization mass spectrometry (iEESI-MS), nutrients including creatine, amino acids, L-carnitine, vitamin B, carnosine and phosphatidylcholines in pork tissue were identified, without sample pretreatment, using collision-induced dissociation (CID) experiments and by comparison with authentic compounds. Furthermore, normal pork samples were clearly differentiated from pork samples with clenbuterol and salbutamol via principal component analysis (PCA).

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Rationale: The deduction of useful information from the mass spectra of a complex mixture like coals remains difficult, which limits the clean and efficient utilization of coals. It is necessary to explore the data interpretation methods for mass spectra and visualize the analytical data of coals for industrial utilization such as feedstock selection.

Methods: Coal sample and methanol were mixed and heated to 310 °C and kept at that temperature for 2 h.

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Article Synopsis
  • - The study analyzed 24 raw propolis samples using a method called surface desorption atmospheric pressure chemical ionization mass spectrometry (SDAPCI-MS) without needing to prepare the samples beforehand.
  • - The most significant signals were found within specific mass ranges (70 to 500 m/z and 200 to 350 m/z), with principal component analyses revealing that color was linked to the first two principal components, while climate zones had no connection to the samples.
  • - Key compounds like chrysin, pinocembrin, and quercetin were identified quickly (within 3 minutes) using advanced mass spectrometry techniques, indicating that SDAPCI-MS is effective for fast and reliable analysis of propolis.
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Tissue spray ionization mass spectrometry (TSI-MS) directly on small tissue samples has been shown to provide highly specific molecular information. In this study, we apply this method to the analysis of 38 pairs of human lung squamous cell carcinoma tissue (cancer) and adjacent normal lung tissue (normal). The main components of pulmonary surfactants, dipalmitoyl phosphatidylcholine (DPPC, m/z 757.

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Synopsis of recent research by authors named "Tenggao Zhu"

  • - Tenggao Zhu's research spans various applications of mass spectrometry, with a focus on innovative methods for analyzing complex biological and environmental samples, such as breath analysis and meat species identification.
  • - A notable recent finding includes a catalyst-free approach for carbon chain elongation that leverages electric field interactions to facilitate demethylation C-C coupling reactions, showcasing a novel avenue for synthetic chemistry.
  • - Zhu's work also emphasizes the development of advanced analytical techniques using functionalized materials, such as polymer monoliths and graphene oxide, to enhance the detection of specific analytes, thus improving sensitivity and selectivity in mass spectrometric analyses.