Rapid and highly sensitive quantitative analysis of 3-carboxy-4-methyl-5-propyl-2-furanpropionate and indole-3-acetic acid in uremic serum of patients with chronic kidney disease.
Uptake and movement of various herbicides and auxins by bean (Phaseolus vulgarisL.) petiole sections were studied. Isopropylm-chlorocarbanilate (chlorpropham) was the most mobile of the compunds studied, followed in order of decreasing mobility by: indole-3-acetic acid (IAA), 3-amino-s-triazole (amitrole), (2,4-dichlorophenoxy)acetic acid (2,4-D), 3-(3,4-dichlorophenyl)-1-methoxy-1-methylurea (linuron), and 3-amino-2,5-dichlorobenzoic acid (amiben). Amiben immobilization may have been due to glucoside formation in the tissues. IAA was rapidly transported through basipetally but not acropetally oriented tissue. Tissue orientation had little effect on the movement of the other compounds. Mobility of the compounds studied, in general, appears to be a function of the amount of uncomplexed parent chemical. Retention is likely the result of conjugation with products in the cells or of physical binding in the cells.
The relative stabilities of IAA and IBA under various tissue culture procedures were determined. IBA was significantly more stable than IAA to autoclaving. IBA was also found to be more stable than IAA in liquid Murashige and Skoog medium (MS) under growth chamber conditions. The stabilities of IBA and IAA were similar in agar-solidified MS. Light provided by cool-white fluorescent bulbs promoted degradation of IAA and IBA in both liquid and agar media. Activated charcoal in concentrations as high as 5% was found to adsorb more than 97% of IAA and IBA in liquid MS. These results have important implications for the preparation, storage, and handling of IBA and IAA in plant tissue culture. Chemical names used: indole-3-acetic acid (IAA); indole-3-butyric acid (IBA).
A surface-enhanced Raman scattering-based approach for rapid and highly sensitive quantitative analysis of 3-carboxy-4-methyl-5-propyl-2-furanpropionate and indole-3-acetic acid in saline, human serum and uremic serum of patients with chronic kidney disease