3D deconvolution of spherically aberrated images using commercial software.

Refractive index mismatch between the specimen and the objective immersion oil results in spherical aberration, which causes distortion and spreading of the point spread function, as well as incorrect readings of the axial coordinates. These effects have to be taken into account when performing three-dimensional restoration of wide-field fluorescence images. By using objects with well-defined geometry (fluorescently stained Escherichia coli or actin filaments) separated from a cover slip by a layer of oil with known refractive index, we investigated the accuracy of three-dimensional shape restoration by the commercial programs Huygens and Autoquant. Aberration correction available in the software dramatically reduced the axial blur compared to deconvolution that ignored the refractive index mismatch. At the same time, it failed to completely recover the cylindrical symmetry of bacteria or of actin fibres, which showed up to a three to five times larger width along the optical axis compared to the lateral plane. The quality of restoration was only moderately sensitive to the exact values of the specimen refractive index but in some cases improved significantly by assuming a reduced NA of the objective. Because image restoration depends on the knowledge of the vertical scale, we also performed detailed measurements of the axial scaling factor and concluded (in agreement with some previous authors) that scaling is adequately described by the simple paraxial formula, even when high-NA oil-immersion objectives are used.

Ambient odour testing of concentrated animal feeding operations using field and laboratory olfactometers.

The Missouri Air Conservation Commission regulations include regulations that limit the amount of acceptable odor from confined animal feeding operations (CAFOs). The regulations concerning odor designate the use of a scentometer as a screening tool. The rules dictate that if an odor is detectable by an investigator at a dilution ratio of 5.4 using a scentometer then an air sample should be collected and sent to an olfactometry laboratory for an odor panel to determine the detection threshold and the intensity of the odor sample. The detection thresholds are determined following ASTM E679-91 and EN13725. The intensity is determined following ASTM E544-99. If the olfactometry laboratory determined the detection threshold of the sample to be above seven, then the CAFO would be in violation. If the olfactometry laboratory determined the intensity level to be above a level equivalent to 225 ppm of n-butanol, then the source of odor would be in violation. The CAFO odor rules came under scrutiny by representatives of the largest hog producer in the State of Missouri. Specifically, they argued that the detection threshold limit of seven in the CAFO portion of the rule was too low for the rule to realistically identify a violation. This paper presents the results of a study to find the appropriate regulatory level of odor as determined by laboratory olfactometry. The study took place from November 2001 to October 2002. Samples were collected from field locations that exhibited odor produced by confined animal feeding operations and from areas exhibiting no apparent odor. The odors were categorized based upon the scentometer level at which the odors were detectable, and then samples were sent to an odor evaluation laboratory for analysis by olfactometry.

Phase-morphology map of polymer-blend thin films confined to narrow strips.

Upon lateral confinement, a critical polymer-blend film at 200 degrees C has been directed to form tube, capsule, confined domain, and multiple domain configurations. A phase-morphology map is produced by varying the confinement width ( W) and film thickness ( h(0)), and interpreted using a single pore model. Using the known correlation length, capsule length, and W, the boundary, in terms of W/h(0), between configurations is predicted and found to be in good agreement with experiment. This morphology map has potential applications for microencapsulating drugs and self-assembled conducting wires.

Conversion from Sandimmune to Neoral in organ transplant recipients.

The pharmacokinetic profiles of Sandimmune and Neoral vary considerably among transplant recipients. Cyclosporine exposure is far more consistent with Neoral than it is with Sandimmune. Because intrapatient variability of drug exposure has been demonstrated to be a risk factor for chronic rejection, this difference becomes important. Neoral also has a linear dose response and a stronger correlation between trough level and drug exposure. Dose linearity greatly facilitates accurate dose titration. Results of controlled studies in which kidney, liver, and heart transplant recipients were converted from Sandimmune to Neoral have shown that conversion on a 1:1 mg basis results in more predictable bioavailability and often in reductions in cyclosporine dose. Carefully monitored conversion has not been associated with increased side effects, and any side effects that do emerge can usually be managed by taking Neoral with food, changing the dose from every 12 hours to every 8 hours, or through dose reduction.

Macroscopic evidence of the effect of interfacial slippage on adhesion.

The adhesion strengths of a viscoelastic adhesive were measured on various substrates that were prepared by grafting silanes bearing organic functional groups to silicon wafers. Conventional theories predict that adhesion should be proportional to the surface free energy of the substrate; but adhesion on a fluorocarbon surface was significantly greater than on some of the hydrocarbon surfaces, although the fluorocarbon surface has the lowest surface free energy. This result could be explained by invoking a model of adhesion based on the slippage of the adhesive at the interface.