Biomedical subjects

S Chongchirasiri

Publications and source records attributed to S Chongchirasiri.

2 recordsLinked to original sources

PubMed2001

Application of quantitative salt iodine analysis compared with the standard method.

Laboratory investigation of 50 iodated salt samples (from producers, households, markets etc) were studied at the Research Nuclear Medicine Building, Siriraj Hospital. Two methods for the determination of iodine in salt are herein described. The standard method as recommended by The Programme Against Micronutrient Malnutrition (PAMM) / The Micronutrient Initiative (MI)/ The International Council for Control of Iodine Deficiency Disorders (ICCIDD) was the iodometric titration method. The starch-KI salt iodine quantitative method was developed in our laboratory for validation purposes. This method is high in precision, accuracy, sensitivity as well as specificity. The coefficient of variation (%CV) for intra and inter assay was below 10. Iodine contents as low as 10 ppm, could be detected. The proposed starch-KI method offered some advantages: e.g. not complicated, easier to learn and easier to perform competently, could be applied for spot qualitative test and readily performed outside the laboratory. The results obtained by the starch-KI method correlated well with the standard method (y = 0.98x - 3.22, r = 0.99).

Iodine↗

PubMed1983

Mechanism of enhanced fusion capacity of mouse red cells infected with Plasmodium berghei.

Plasmodium berghei-infected mouse red cells have enhanced fusion capacity as triggered by addition of poly(ethylene glycol) in the presence of Ca2+. The uptake of Ca2+ in P. berghei-infected cells is greater than in normal cells, and the difference in Ca2+ uptake was found to be enhanced in the presence of poly(ethylene glycol). Fusion of normal and P. berghei-infected red cells by poly(ethylene glycol) was significantly inhibited by N-tosyl-L-lysylchloromethyl ketone and phenylmethylsulphonyl fluoride. In addition, ethyleneglycolbis(aminoethylether)tetra-acetate, N-ethylmaleimide, iodoacetamide, cystamine and tetrathionate also prevented fusion in both systems. In contrast, N-tosyl-L-phenylalanylchloromethyl ketone and N-tosyl-L-arginine methyl ester did not inhibit cell fusion. The latter enhanced fusion of infected cells but was without effect on normal cells. These results indicate that a Ca2+-activated thiol proteinase may be involved in membrane fusion in malaria-infected as well as in normal red cells. However, differences in the effect of proteinase inhibitors and substrate on fusion and Ca2+ entry show that the processes leading to fusion may not be identical.

Animals↗