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As you may have already noted, this year introduces a new set of authors for this fundamental review. As new authors, they hope that they can do as accurate a job as did their predecessor, Professor Earl Wehry, of the University of Tennessee. The format for this review follows the basic outline used by Professor Wehry, with some modifications. They have condensed several sections and eliminated the section on gas-phase chemiluminescence. The primary areas of emphasis including advances in experimental techniques, developments in instrumentation, and applications for chemical analysis, remain the same. To keep the review at a reasonable length, they have not included articles that are only peripherally related to analytical chemistry or those that represent straightforward extensions or demonstrations of previously published research. In this first issue, it is likely that they have made some errors of omission, and they request your assistance in identifying any obvious errors. They have tried to be conscientious in surveying the literature and have also surveyed individual researchers in the field. This review covers literature indexed by Chemical Abstracts from January, 1985, Vol. 102, issue 1, through October 1987, Vol. 107, issue 16. Accordingly, there will be some overlap between this reviewmore » and Professor Wehry's last review.« less

We describe a protocol to create tissue phantoms with hydrophobic nanoporous particles. The nanopores of the particles are loaded with biological molecules at the desired compositions. Tissue phantoms are prepared by immersing dried particles into aqueous biological matrixes. The hydrophobicity of the pore surface prevents the solution from penetrating into the nanopores, thus preserving the designed molecular composition inside the particles. This protocol provides a unique approach to preparing biological systems in small domains, at micrometer and nanometer dimensions, with well-defined boundaries and tailored biological and optical properties. The nanoporous particle approach is easy when compared to the common preparation methods such as with polymers and vesicles as it involves direct loading of the biological molecules into the pores and does not require complex synthetic steps. The method is adaptable, with tunable pore and particle sizes, and robust, with a rigid boundary to protect the designed biological domain. In addition to tissue phantom preparation, this approach is applicable in systems where a well-defined biological domain is desired.

Simultaneous extraction, separation and quantitation of reduced nicotinamide adenine dinucleotide (NADH), reduced nicotinamide adenine dinucleotide phosphate (NADPH), flavin adenine dinucleotide (FAD) and flavin mononucleotide (FMN) in Chinese Hamster Ovary (CHO) cells were investigated. The separation of flavins and nicotinamide cofactors was performed by capillary electrophoresis with laser-induced fluorescence detection at the excitation wavelength of 325 nm. The separation protocol was established by investigating the excitation wavelength, high voltage and effects of buffer nature, pH and concentration. All endogenous fluorophores riboflavin, FAD, FMN, NADH and NADPH show wide linear range of quantitation. The limits of detection for the five compounds ranged from 4.5 to 23 nm. Extraction conditions were optimized for high-efficiency recovery of all endogenous fluorophores from CHO cells. To account for the complex matrix of cell extracts, a standard addition method was used to quantify FAD, FMN, NADH and NADPH in CHO cells. The quantitative results should be useful to reveal the metabolic status of cells. The protocols for extraction, separation and quantitation are readily adaptable to normal and cancer cell lines for the analysis of endogenous fluorophores. Copyright © 2008 John Wiley & Sons, Ltd.