In the method for lithium (Li) analysis, flame emission photometry and atomic absorption spectrophotometry (AAS) have been used most frequently. In addition, lithium can be analyzed by ion-selective electrode (ISE) or fluorscence polarization immunoassay. We evaluated the comparison between AAS method based on the principle of absorption of light at 670.8 nm by Li and ISE method based on the principle of voliage difference generated by Li in contact with lithium ionophore. We compared with those obtained by AAS (AA/AE Spectrophotometer 551, Instrumentation Laboratory Co.) and ISE (SYNCHRON EL-ISE, Beckman Co.) in the serum and urine of 6 pati,,:nts- and evaluated time-related changes of serum lithium concentration after dosing in both methods. The results are summarized-as follows: 1. In within-run precision study for lithium concentration, coefficient variations (CVs, %) ranged from 1.34 to 2.17 for AAS and from 0.34 to 0.85 for ISE method. In between-run precision study for lithium concentration, CVs ranged from 1.23 to 1.72 for AAS and from 0.61 to 1.38 for ISE method. 2. The correlation study between AAS and ISE method resulted in Y= 0.946X+ 0.137 (N = 32, r= 0. 933, X= AAS, Y= ISE) for serum lithium and Y= 1. 092X+ 0. 977 (N= 28, r= 0.943, X= AAS, Y= ISE) for urine lithium. 3. Time-related changes of serum lithium concentration in both AAS and ISE method resulted in peak serum levels about 2 hours after dosing and then rapidly decreased after the peak serum level and finally arrived at nearly initial levels about 9 hours after dosing. 4. The reference range of serum lithium was found as undetectable level for both AAS and ISE method and the reference range of urine lithium to the urine creatinine was 0 0.00014 mmol/mg(mean 0.00002 mmol/mg) for AAS method.
Absorption ; Creatinine ; Immunoassay ; Ion-Selective Electrodes ; Lithium* ; Photometry ; Reference Values ; Spectrophotometry, Atomic ; Statistics as Topic

Watermelon is a popular fruit in the world with soluble solids content (SSC) being one of the major characteristics used for assessing its quality. This study was aimed at obtaining a method for nondestructive SSC detection of watermelons by means of visible/near infrared (Vis/NIR) diffuse transmittance technique. Vis/NIR transmittance spectra of intact watermelons were acquired using a low-cost commercially available spectrometer operating over the range 350~1000 nm. Spectra data were analyzed by two multivariate calibration techniques: partial least squares (PLS) and principal component regression (PCR) methods. Two experiments were designed for two varieties of watermelons [Qilin (QL), Zaochunhongyu (ZC)], which have different skin thickness range and shape dimensions. The influences of different data preprocessing and spectra treatments were also investigated. Performance of different models was assessed in terms of root mean square errors of calibration (RMSEC), root mean square errors of prediction (RMSEP) and correlation coefficient (r) between the predicted and measured parameter values. Results showed that spectra data preprocessing influenced the performance of the calibration models. The first derivative spectra showed the best results with high correlation coefficient of determination [r=0.918 (QL); r=0.954 (ZC)], low RMSEP [0.65 degrees Brix (QL); 0.58 degrees Brix (ZC)], low RMSEC [0.48 degrees Brix (QL); 0.34 degrees Brix (ZC)] and small difference between the RMSEP and the RMSEC by PLS method. The nondestructive Vis/NIR measurements provided good estimates of SSC index of watermelon, and the predicted values were highly correlated with destructively measured values for SSC. The models based on smoothing spectra (Savitzky-Golay filter smoothing method) did not enhance the performance of calibration models obviously. The results indicated the feasibility of Vis/NIR diffuse transmittance spectral analysis for predicting watermelon SSC in a nondestructive way.
Algorithms ; Citrullus ; chemistry ; Food Analysis ; methods ; Fruit ; chemistry ; Photometry ; methods ; Plant Extracts ; analysis ; Reproducibility of Results ; Sensitivity and Specificity ; Solubility ; Spectrophotometry, Infrared ; methods

No abstract available.
Cyclosporine* ; Fluorescence Polarization Immunoassay* ; Fluorescence Polarization* ; Fluorescence*

BACKGROUND: The Cobas(R) Integra is a new automated chemistry analyzer with continuous and random-access features for routine chemistries, specific proteins, electrolytes, therapeutic drugs and drugs of abuse. The system maintains 68 test-specific reagent cassettes on board and have test principles of absorbance photometry, immunoturbidometry, fluorescence polarization and ISE measurements. We evaluated the usefulness of Cobas(R) Integra in the aspect of accuracy, precision, linearity, comparison study, test speed and general performance. METHODS: We evaluated the analytical performance of the Cobas(R) Integra for T. bilirubin, CRP, BUN, creatinine, sodium, potassium, chloride, valproic acid, phenytoin and carbamazepine according to NCCLS guidelines (EP5-T2, EP6-P, EP9-T and GP10-T). RESULTS: In accuracy study, error ranges(%) of most test items, except sodium and chloride, were within analytic goals. In within-run and between-run precision study, Coefficient of variation (CV, %) of most items, except sodium, were lower than limits suggested by College of American Pathologists Survey 1991. The linearities were maintained well in the range of medically significant levels and were statistically acceptable (p<0.001). The comparison study for most items, except sodium and chloride, indicated good correlation with Hitachi 747 and TDx FLx(TM) and correlation coefficients (r) were above 0.98. Throughput was about 450 tests/hr. CONCLUSIONS: Cobas(R) Integra showed satisfactory accuracy, precision, linearity, good correlation with other analyzers and high throughput. So, we concluded that Cobas(R) integra is highly suitable for not only routine use but also emergency tests in medium to large-sized hospitals because of its high productivity and reliability.
Bilirubin ; Carbamazepine ; Chemistry* ; Creatinine ; Efficiency ; Electrolytes ; Emergencies ; Fluorescence Polarization ; Phenytoin ; Photometry ; Potassium ; Sodium ; Street Drugs ; Valproic Acid

BACKGROUND: The Cobas(R) Integra is a new automated chemistry analyzer with continuous and random-access features for routine chemistries, specific proteins, electrolytes, therapeutic drugs and drugs of abuse. The system maintains 68 test-specific reagent cassettes on board and have test principles of absorbance photometry, immunoturbidometry, fluorescence polarization and ISE measurements. We evaluated the usefulness of Cobas(R) Integra in the aspect of accuracy, precision, linearity, comparison study, test speed and general performance. METHODS: We evaluated the analytical performance of the Cobas(R) Integra for T. bilirubin, CRP, BUN, creatinine, sodium, potassium, chloride, valproic acid, phenytoin and carbamazepine according to NCCLS guidelines (EP5-T2, EP6-P, EP9-T and GP10-T). RESULTS: In accuracy study, error ranges(%) of most test items, except sodium and chloride, were within analytic goals. In within-run and between-run precision study, Coefficient of variation (CV, %) of most items, except sodium, were lower than limits suggested by College of American Pathologists Survey 1991. The linearities were maintained well in the range of medically significant levels and were statistically acceptable (p<0.001). The comparison study for most items, except sodium and chloride, indicated good correlation with Hitachi 747 and TDx FLx(TM) and correlation coefficients (r) were above 0.98. Throughput was about 450 tests/hr. CONCLUSIONS: Cobas(R) Integra showed satisfactory accuracy, precision, linearity, good correlation with other analyzers and high throughput. So, we concluded that Cobas(R) integra is highly suitable for not only routine use but also emergency tests in medium to large-sized hospitals because of its high productivity and reliability.
Bilirubin ; Carbamazepine ; Chemistry* ; Creatinine ; Efficiency ; Electrolytes ; Emergencies ; Fluorescence Polarization ; Phenytoin ; Photometry ; Potassium ; Sodium ; Street Drugs ; Valproic Acid

A fluorescence polarization immunoassay (FPIA) was developed for the analysis ofaflatoxins (AFs) using an anti-aflatoxin B1 (AFB1) monoclonal antibody and a novel fluorescein-labeled AFB1 tracer. The FPIA showed an IC50 value of 23.33 ng/mL with a limit of detection of 13.12 ng/mL for AFB1. The cross-reactivities of AFB1, AFB2, AFG1, AFG2, AFM1, and AFM2 with the antibody were 100%, 65.7%, 143%, 23.5%, 111.4%, and 2%, respectively. The group-specificity of anti-AFB1mAb indicated that the FPIA could potentially be used in a screening method for the detection of total AFs, albeit not AFG2 and AFM2. The total time required for analyzing 96 samples in one microplate was less than 5 min. This study demonstrates the potential usefulness of the FPIA as a rapid and simple technique for monitoring AFs.
Aflatoxins ; analysis ; Fluorescence Polarization Immunoassay

An apigenin molecularly imprinted polymer was prepared by bulk polymerization using apigenin as template, acrylamide (AA) as a functional monomer, ethylene glycol dimethacrylate (EDMA) as a crosslinking agent, acetonitrile and N, N-dimethylformamide as porogenic solvents, and 2, 2'-azobisisobutyronitrile (AIBN) as an initiator. The interaction between template and functional monomer was proved by ultraviolet visible (UV) spectrophotometry and based on the results, appropriate reaction solvent was selected and the synthesizing process was estimated. The molecularly imprinted polymer structure was analyzed by Fourier Transform Infrared (FT-IR) spectrophotometry. The molecularly imprinted polymer was investigated in equilibrium binding experiment to evaluate its adsorption property, the results showed that the adsorption of apigenin on molecularly imprinted polymer is higher than that on blank polymer in the studied concentration range (0.1-2.5 mmol x L(-1)). Scatchard analysis showed that two classes of binding sites existed in the apigenin imprinted polymers, with their KD and Qmax estimated to be 2.52 x 10(-4), 0.54 x 10(-3) mmol x L(-1) and 2.65, 18.89 micromol x g(-1), respectively. Molecularly imprinted polymer showed higher affinity than blank polymer.
Apigenin ; chemical synthesis ; chemistry ; Molecular Imprinting ; Molecular Structure ; Polymers ; chemical synthesis ; chemistry ; Spectrophotometry, Infrared ; Spectrophotometry, Ultraviolet

The chrome content of 8 Korean cements and 11 Korean bleaching detrgents was analyzed by the qualitative DPC method and the quantitative atomic absorption spectrophotometry and UV-visible spectrophotometry. In cements, there was no detectable chrome in 1 sample and the range of chrome content in other 7 samples was 1.32 5.29ppm. The qualitative result was welJ. correlated with the quantitative result. In bleaching detergents, there was no detectable chrome in 4 samples and the range of chrome content in other 7 samples was 0.0329 0.362ppm. However, the qualitative result was not correlated with the quantitative result.
Detergents* ; Spectrophotometry ; Spectrophotometry, Atomic

Author had already reported that urinary excretions of several electrolytes of rural Korean measured in late 1970`s were different with that of the 1960`s. This study was carried out to evaluate the difference of daily urine volume, urinary excretions of sodium and potassium between urban and rural residents in Korea. 20 urban and 28 rural residents were selected arbitrarily and the surface areas of both group didn`t show any difference. 24 hour urines were collected and sodium and potassium concentrations were analyzed by means of flame photometry. Followings were the results. 1. Daily urine volume urban residents: 1578.75 461.92 ml/day, rural residents: 1582.14 417.91 ml/day 2. Daily urinary sodium excretion urban residents: 223.95 109.61 mEq/day, rural residents: 219.68 65.60 mEq/day 3. Daily urinary potassium excretion urban residents: 75.44 28.00 mEq/day, rural residents: 49.52 14.95 mEq/day Above results reveal that daily urine volume and urinary excretion of sodium of urban residents are within the range of rural residents, while daily urinary potassium excretion of urban are much higher than that of rural one. In addition, the ratio of K/Na of urban residents is also much higher than that of rural residents and than that of 1960`s, although the ratio was still lower than those of Westerns.
Diet ; Electrolytes ; Korea ; Photometry ; Potassium* ; Sodium*

Author had already reported that urinary excretions of several electrolytes of rural Korean measured in late 1970`s were different with that of the 1960`s. This study was carried out to evaluate the difference of daily urine volume, urinary excretions of sodium and potassium between urban and rural residents in Korea. 20 urban and 28 rural residents were selected arbitrarily and the surface areas of both group didn`t show any difference. 24 hour urines were collected and sodium and potassium concentrations were analyzed by means of flame photometry. Followings were the results. 1. Daily urine volume urban residents: 1578.75 461.92 ml/day, rural residents: 1582.14 417.91 ml/day 2. Daily urinary sodium excretion urban residents: 223.95 109.61 mEq/day, rural residents: 219.68 65.60 mEq/day 3. Daily urinary potassium excretion urban residents: 75.44 28.00 mEq/day, rural residents: 49.52 14.95 mEq/day Above results reveal that daily urine volume and urinary excretion of sodium of urban residents are within the range of rural residents, while daily urinary potassium excretion of urban are much higher than that of rural one. In addition, the ratio of K/Na of urban residents is also much higher than that of rural residents and than that of 1960`s, although the ratio was still lower than those of Westerns.
Diet ; Electrolytes ; Korea ; Photometry ; Potassium* ; Sodium*