Laser fluorometric determination of aflatoxin B1 in corn.

A 2-step chromatographic separation, using both thin layer chromatography (TLC) and high pressure liquid chromatography (HPLC), in conjunction with the high sensitivity of laser fluorometry permits extension of the detection limits of aflatoxin contamination in corn to 0.1 ppb (microgram/kg) with a 26% root mean square variation. Aflatoxin B1 is extracted from corn with water-methanol and cleaned up by TLC. The recovery of aflatoxin from the TLC plates was linear from 10 to 1000 pg. Aflatoxin B1 is converted to the more highly fluorescent B2A derivative by treatment with 1N HCl. Experiments with aflatoxin B1 standard establish a constant conversion to B2A over approximately 3 orders of magnitude in B1 concentration. An extract of the B2A aflatoxin derivative is injected onto a reverse phase HPLC column. A flowing droplet of eluant is irradiated by an amplitude-modulated 325 nm He-Cd ion laser beam, and fluorescence from the droplet is detected by a lock-in amplifier in phase with the laser modulation. Several chromatograms are presented that demonstrate the capability of this procedure for removing interfering components in the corn extract.     

Boundary layer profiles in plasma chemical vapor deposition

A nonlinear optical spectroscopy based on degenerate four-wave mixing has made possible direct measurements of species temperature and concentration profiles through the boundary layer of a reactive plasma at atmospheric pressure. Spectra were obtained for CH and C(2) radicals over a range of conditions including those for the plasma chemical vapor deposition of diamond films. Numerical simulations based on a one-dimensional stagnation-point flow model are in good agreement with the measurements. The CH mole fraction is shown to rise and fall as a function of distance from the substrate, which is compelling experimental evidence for the complex chemistry that is occurring in the plasma boundary layer.     

Spatially resolved organic analysis of the allende meteorite

The distribution of polycyclic aromatic hydrocarbons(PAHs) in the Allende meteorite has been probed with two-step laser desorption/laser multiphoton ionization mass spectrometry. This method allows direct in situ analysis with a spatial resolution of 1 square millimeter or better of selected organic molecules. Spectra from freshly fractured interior surfaces of the meteorite show that PAH concentrations are locally high compared to the average concentrations found by wet chemical analysis of pulverized samples. The data suggest that the PAHs are primarily associated with the fine-grained matrix, where the organic polymer occurs. In addition, highly substituted PAH skeletons were observed. Interiors of individual chondrules were devoid of PAHs at our detection limit(about 0.05 parts per million).     

Chemical transformations in individual ultrasmall biomimetic containers

Individual phospholipid vesicles, 1 to 5 micrometers in diameter, containing a single reagent or a complete reaction system, were immobilized with an infrared laser optical trap or by adhesion to modified borosilicate glass surfaces. Chemical transformations were initiated either by electroporation or by electrofusion, in each case through application of a short (10-microsecond), intense (20 to 50 kilovolts per centimeter) electric pulse delivered across ultramicroelectrodes. Product formation was monitored by far-field laser fluorescence microscopy. The ultrasmall characteristic of this reaction volume led to rapid diffusional mixing that permits the study of fast chemical kinetics. This technique is also well suited for the study of reaction dynamics of biological molecules within lipid-enclosed nanoenvironments that mimic cell membranes.     

Counting low-copy number proteins in a single cell

We have designed a microfluidic device in which we can manipulate, lyse, label, separate, and quantify the protein contents of a single cell using single-molecule fluorescence counting. Generic labeling of proteins is achieved through fluorescent-antibody binding. The use of cylindrical optics enables high-efficiency (approximately 60%) counting of molecules in micrometer-sized channels. We used this microfluidic device to quantify beta2 adrenergic receptors expressed in insect cells (SF9). We also analyzed phycobiliprotein contents in individual cyanobacterial cells (Synechococcus sp. PCC 7942) and observed marked differences in the levels of specific complexes in cell populations that were grown under nitrogen-depleted conditions.     

Comment on "Organics captured from comet 81P/Wild 2 by the Stardust spacecraft"

Sandford et al. (Reports, 15 December 2006, p. 1720) reported on organic compounds captured from Comet 81P/Wild 2 by the Stardust spacecraft. We emphasize the difficulty in assigning the origin of compounds detected diffusely along particle impact tracks and show that rapid heating of aerogel that has never been exposed to cometary particle capture can generate complex aromatic molecules from low-mass carbon impurities present in the aerogel.     

Seemingly anomalous angular distributions in H + D₂ reactive scattering

When a hydrogen (H) atom approaches a deuterium (D(2)) molecule, the minimum-energy path is for the three nuclei to line up. Consequently, nearly collinear collisions cause HD reaction products to be backscattered with low rotational excitation, whereas more glancing collisions yield sideways-scattered HD products with higher rotational excitation. Here we report that measured cross sections for the H + D(2) → HD(v' = 4, j') + D reaction at a collision energy of 1.97 electron volts contradict this behavior. The anomalous angular distributions match closely fully quantum mechanical calculations, and for the most part quasiclassical trajectory calculations. As the energy available in product recoil is reduced, a rotational barrier to reaction cuts off contributions from glancing collisions, causing high-j' HD products to become backward scattered.     

Effect of various parameters on the chemical grafting of amide monomers to poly(lactic acid)

Radical melt graft copolymerizations of poly (lactic acid) (PLA) with amide monomers using benzoyl peroxide as an initiator during reactive extrusion is studied. The effects of two monomer types at various concentrations, reaction temperatures and initiator concentrations on the grafting yield are investigated. The results showed that percentage of grafting was significantly enhanced by increasing benzoyl peroxide concentrations up to 12 mpm and then decreased by an increase in the initiator concentration. Furthermore, increasing each monomer concentration up to 450 mpm, improved the grafting yield significantly. Further increase brings about a marked fall in the grafting yield. Fourier Transform Infrared Spectroscopy (FTIR), back titration and nitrogen analyses confirmed that monomers of acrylamide and methacrylamide were successfully grafted onto PLA. The Gel Permeation Chromatography (GPC) data showed that the molecular weight of the grafted PLA samples under optimum conditions does not show any dramatic drop of PLA molecular weight by thermal degradation or hydrolysis of polyester chains, while the polydispersity index is poorly affected by the chemical modification of PLA. Also, the monomer structures affected the grafting yield as well as polymer chain combination. In addition under the same conditions, the grafting yield of acrylamide was more than that of methacrylamide. Thermal properties, molecular weight, density, moisture regain and tensile properties of the samples were also measured.