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Detection of alpha-l-fucosidase has been shown to have relevance in diagnosing hepatocellular carcinoma. Few assays have been developed to measure this enzyme, with most relying on colorimetric techniques involving the enzyme's kinetics. While these assays are facile and quick, the sensitivity is not always sufficient for early tumor detection. To improve upon previous assays for alpha-l-fucosidase, a fluorescence based immunoassay was produced implementing an alpha-l-fucosidase specific antibody (FUCA2). The immobilization of the alpha-l-fucosidase-specific antibody onto a quartz slide was investigated with several bioconjugation approaches and an immunoassay for detection of alpha-l-fucosidase was produced. The immunoassay was utilized to produce calibration curves for quantifying alpha-l-fucosidase concentrations in both PBS and human blood serum. A detection limit of 10 nM was found using human blood serum, which is well below the diagnostic cutoff point of 80 nM. [ABSTRACT FROM AUTHOR]

Alpha-l-fucosidase is a known biomarker for hepatocellular carcinoma that has shown great potential in diagnostics. Most of the focus for this enzyme has been on the free form found in serum; however, little is known of the properties of the minor portion of membrane-bound alpha-l-fucosidase. To better understand the properties of membrane-bound alpha-l-fucosidase, this enzyme was surveyed at the air-water interface. Alpha-l-fucosidase is able to form a stable Langmuir monolayer, which was confirmed through surface-pressure and surface-potential area isotherms, as well as infrared reflection-absorption spectroscopy (IRRAS). Furthermore, an interaction between the alpha-l-fucosidase Langmuir monolayer and a specific antibody for this enzyme, FUCA2, was observed. [ABSTRACT FROM AUTHOR]

Hepatocellular carcinoma (HCC) is one of the most recurrent and lethal cancers worldwide. The low survival rate of this particular strain of carcinoma is largely due to the late stages at which it is diagnosed. Tumorigenesis of hepatocellular carcinoma is most frequently detected through ultrasonography, magnetic resonance imaging and computerized tomography scans, however, these methods are poor for detection of early tumor development. This review presents alternative hepatocellular carcinoma detection techniques through the use of protein and enzyme/isozyme biomarkers. The detection methods used to determine the serum levels of α-fetoprotein (AFP), glypican-3 (GPC3), Golgi protein 73 (GP73), α-l-fucosidase (AFU), des-γ-carboxyprothrombin (DCP), γ-glutamyl transferase (GGT) and squamous cell carcinoma antigen (SCCA) are presented and each marker's respective validity in the diagnosis of hepatocellular carcinoma is evaluated. [ABSTRACT FROM AUTHOR]

Carbon dots have received great attention as a result of the favorable optical properties these nanoparticles possess. While much work has been done toward enhancing the optical properties, little investigation has been done on the materialistic properties of these nontoxic nanoparticles. Herein, a simple one-pot procedure for producing a highly viscous, thixotropic carbon dot gel material is presented. The carbon dots possess tunable emissions that are excitation-wavelength dependent and are an ideally viscous material. [ABSTRACT FROM AUTHOR]

The host-guest properties of acetylated aryl pyrogallol[4]arene (AcPy) were studied as a Langmuir monolayer at the air-water interface. The self-assembled Langmuir monolayer properties and interactions with monovalent and divalent metal cations were investigated using surface pressure- and surface potential-area isotherms, compression-decompression cycles, stability, and infrared reflection-absorption spectroscopy (IRRAS). A favorable interaction is observed for complexation between acetylated aryl pyrogallol[4]arene with divalent calcium and cadmium cations, while no interaction is observed for monovalent sodium and potassium cations. Spectroscopic techniques allow for discrimination between cadmium and calcium complexation.