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H Flowers

Publications and source records attributed to H Flowers.

5 recordsLinked to original sources

Ion chromatographic determination of the decomposition products of tecnazene solution irradiated by ultraviolet light: inorganic and organic anions.

Ion chromatographic (IC) methods using sodium hydroxide and methanol gradients were used for the determination of small inorganic and organic anions as decomposition products of a tecnazene solution in water irradiated by UV light. After 60 min of UV irradiation, >99% of the tecnazene was decomposed, and 11 organic and 3 inorganic anions were identified and quantified. A fourth inorganic anion, carbonate, was not quantified due to likely losses as carbon dioxide. The final content of chloride, total nitrogen, and total carbon released from the saturated tecnazene solution after 60 min of UV irradiation were 108, 85, and 38%, respectively. These results suggest that other products rich in carbon and/or nitrogen (such as phenolic compounds and nitrobenzenes) were formed during the UV irradiation of the tecnazene solution. The results obtained indicate several decomposition pathways of tecnazene in water solutions, for example, ring opening reactions, dechlorination, and replacement of the ring nitro group. The determination of nonionic decomposition products from the latter two possibilities is the subject of further study.

Anions↗

A method to detect polysialic acid in polymers of 10 or more sialyl residues synthesized in vivo and in vitro.

An immunoaffinity column has been used to detect polysialic acid containing 10 or more sialyl residues. Antibodies specific for colominic acid were purified from horse serum by immobilized colominic acid and were bound to CH-Sepharose-4B. The immunoaffinity column was used to assay the activity of CMP-NeuNAc: poly alpha 2-->8-sialosylsialyltransferase by detecting the products which were synthesized in vitro by an extract from rat brain and CMP-[14C]NeuNAc. In addition, polysialic acid was demonstrated in a fraction of glycoproteins from human neuroblastoma cells, labeled metabolically with [3H]GlcN. The column was further characterized by binding of 3H-colominic acid and by treatment of the bound polymers with endoneuraminidase, specific for the degradation of polysialic acid. The method can be used for rapid detection of polysialic acid synthesized in vivo and in vitro.

Animals↗