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J W Hofstraat

Publications and source records attributed to J W Hofstraat.

3 recordsLinked to original sources

Image calibration in fluorescence microscopy.

A fluorescence image calibration method is presented based on the use of standardized uniformly fluorescing reference layers. It is demonstrated to be effective for the correction of non-uniform imaging characteristics across the image (shading correction) as well as for relating fluorescence intensities between images taken with different microscopes or imaging conditions. The variation of the illumination intensity over the image can be determined on the basis of the uniform bleaching characteristics of the layers. This permits correction for the latter and makes bleach-rate-related imaging practical. The significant potential of these layers for calibration in quantitative fluorescence microscopy is illustrated with a series of applications. As the illumination and imaging properties of a microscope can be evaluated separately, the methods presented are also valuable for general microscope testing and characterization.

Animals↗

Electroluminescent device with reversible switching between red and green emission.

Research on new materials for organic electroluminescence has recently focused strongly on phosphorescent emitters, with the aim of increasing the emission efficiency and stability. Here we report the fabrication of a simple electroluminescent device, based on a semiconducting polymer combined with a phosphorescent complex, that shows fully reversible voltage-dependent switching between green and red light emission. The active material is made of a polyphenylenevinylene (PPV) derivative molecularly doped with a homogeneously dispersed dinuclear ruthenium complex, which fulfils the dual roles of triplet emitter and electron transfer mediator. At forward bias (+4 V), the excited state of the ruthenium compound is populated, and the characteristic red emission of the complex is observed. On reversing the bias (-4 V), the lowest excited singlet state of the polymer host is populated, with subsequent emission of green light. The mechanism for the formation of the excited state of the PPV derivative involves the ruthenium dinuclear complex in a stepwise electron transfer process that finally leads to efficient charge recombination reaction on the polymer.

Journal Article↗

Trace analysis of 3-hydroxy benzo[a]pyrene in urine for the biomonitoring of human exposure to polycyclic aromatic hydrocarbons.

Determination of benzo[a]pyrene (BaP) metabolites in urine can provide direct insight into recent exposure to BaP integrated from all uptake routes. In order to detect 3-OH BaP in human urine after exposure to BaP at the workplace, extremely sensitive methods need to be developed. In this paper, a new extraction method is presented, and two laser-based fluorescence techniques are evaluated. Using HPLC with laser-induced fluorescence detection, a detection limit of 8 ng/L was obtained. With laser-excited Shpol'skii spectrometry after chemical derivatization, 3-OH BaP could be detected at even a 0.5-ng/L concentration. In a pilot study, urine samples from coke-oven workers and from occupationally nonexposed control persons were analyzed. In the control samples, the average 3-OH BaP concentration was 8.3 ng/L; the 3-OH BaP concentrations were found to be highly correlated (r2 = 0.89) with urinary 1-OH pyrene, a widely used biomarker for polycyclic aromatic hydrocarbon (PAH) exposure. Significantly elevated 1-OH pyrene concentrations were measured in urine samples from coke-oven workers, but in most samples a corresponding increase of 3-OH BaP was not observed. Possible explanations for this discrepancy are discussed.

Benzopyrenes↗