Hepatocellular carcinoma (HCC)

Background: Protein used in medicine, e.g. interferon, are immunogenic and quickly broken down by the body. Pegylation is a recognized way of preserving their integrity and reducing immune reactions, and works well with enzymes used to degrade amino acids, a recent focus of attention in controlling cancer growth. Of the two arginine-degrading enzymes being explored clinically, arginine deiminase is a decidedly foreign mycoplasm-derived enzyme, whereas human arginase 1 is a native liver enzyme. Both have been pegylated, the former with adjuncts of 20 kD, the latter with 5 kD PEG. Pegylation is done by several different methods, not all of which are satisfactory or desirable.

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The decolorisation of reactive dyeing wastewater with ultraviolet radiation and ultrasonic vibration in the presence of hydrogen peroxide was investigated by a batch operation system. Kinetic studies of the reactive dye were conducted on the effects of pH and peroxide dosage, and the performance of ultrasonic vibration on the oxidation process was also investigated. It was found that the degradation of the reactive dye followed a pseudo‐first‐order kinetic model at different pH and peroxide dosages. The relationships between the rate constants and pH, as well as peroxide concentration, were established.

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