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Biomedical subjects

H K Lim

Publications and source records attributed to H K Lim.

At least 91 records · Page 5Linked to original sources

Dimethyl sulfoxide affects water flow through a nonosmolar action.

Dimethyl sulfoxide (DMSO) is a dipolar organic compound commonly used as a solvent in studies of membrane transport. DMSO also has many effects on cell function and, although the precise mechanism of action is not known completely, it has been stated to exert its effect on transport solely through osmolality. The present study was designed to examine the effects of serosal DMSO at three osmolar concentrations on Basal Water Flow and vasopressin (AVP)- and cyclic AMP-stimulated water flow (Maximal Water Flow) in the toad bladder. The results obtained were compared to equi-osmolar concentrations of mannitol and NaCl. All three agents significantly enhanced Basal Water Flow after 60 min. The results obtained on Maximal Water Flow were different depending on the final osmolality. At 300 mOsm final concentration, all three agents increased AVP-stimulated water flow. When the serosal osmolality was 600 or 900 mOsm DMSO increased Maximal Water Flow, whereas mannitol and NaCl decreased it. When 300 mOsm DMSO plus 300 mOsm mannitol (600 mOsm total)-treated hemibladders were challenged with AVP, the water flow response was similar to that of 600 mOsm DMSO alone. In the presence of verapamil, AVP-stimulated water flow was decreased markedly; when DMSO was added to verapamil-pretreated hemibladders, and they were then challenged with AVP, water flow increased significantly. In similar experiments with mannitol, water flow remained inhibited. Dimethylsulfone did not enhance AVP-stimulated water flow as compared to the same concentration of DMSO. These results demonstrate that the effects of DMSO on water transport are not mediated solely by its osmolar action.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

Evaluation of an objective method for the in vivo measurement of changes in light transmittance of the human crystalline lens.

Because the results of various vision tests and diagnostic methods are influenced by the amount of light transmitted by the lens, it would be useful to quantify changes in transmittance. We have developed a new method capable of following these changes objectively and quantitatively. The method is based on an increasing loss of fluorescence emitted by the lens substance as the probing volume is located more posteriorly along the lens axis. The loss of fluorescence is quantified by a parameter called the fluorescence reading ratio (FRR). In the present study, performed on postmortem human lenses, we evaluated the validity of our proposed in vivo method by comparing it with measurements of lens transmittance by spectrophotometry. The correlation of FRR with the transmittance between 420- and 500 nm (r greater than 0.7, P less than 0.015) indicates that the measurement of FRR can provide information on the transmittance at these wavelengths. In addition, a correlation was found between age and transmittance at 440 nm (r = 0.93, P less than 0.001) and FRR (r = 0.88, P less than 0.001).

Adult↗

Development of enantioselective gas chromatographic quantitation assay for dl-threo-methylphenidate in biological fluids.

An enantioselective gas chromatographic quantitation assay was developed for the enantiomers of dl-threo-methylphenidate in plasma and urine. dl-threo-Methylphenidate and the internal standard were acylated with N-heptafluorobutyryl-1-prolylchloride under Schotten-Baumann conditions prior to gas chromatographic separation on achiral mixed stationary phases. The derivatives were detected by means of a nitrogen-phosphorus detector. Linear and reproducible calibration curves were obtained over the concentration ranges 0.43-43.25 and 2.16-216.25 ng/ml enantiomer in plasma or urine, respectively. This enantioselective gas chromatographic quantitation assay was applied in a single oral dose disposition study of dl-threo-methylphenidate in a healthy adult volunteer. Stereoselective differences were observed in the plasma concentration-time profiles and cumulative urinary excretion profiles following oral doses of 20 and 40 mg of dl-threo-methylphenidate hydrochloride. Only d-threo-methylphenidate was detectable in plasma after 4 h.

Adult↗

Chiral pharmacology and its consequences for therapeutic monitoring.

The individual enantiomers of chiral drugs may have profound differences in their pharmacologic and toxicologic properties. Their metabolism and pharmacokinetics may also differ markedly, and the presence of one enantiomer may inhibit the metabolism of the other. Stereospecificity is required in analytical methods, whether these be chromatography or radioimmunoassay.

Chromatography↗