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Biomedical subjects

L H Nie

Publications and source records attributed to L H Nie.

At least 19 recordsLinked to original sources
PubMed2001

Ion chromatographic determination of calcium and magnesium cations in human saliva and urine with a piezoelectric detector.

In this present paper, simultaneous determination of Ca(2+) and Mg(2+) cations in saliva, urine was achieved using an ion chromatography method, in which a piezoelectric quartz crystal (PQC) sensor was used as a detector, and a solution containing tartaric acid (4 mmol 1(-1)) and ethylenediamine (2 mmol 1(-1)) as a mobile phase. Good linearities were obtained over the ranges of 0.8-500 mg 1(-1) Ca(2+) and 1.0-500 mg 1(-1) Mg(2+). The detection limits were 0.4 mg 1(-1) for Ca and 0.2 mg 1(-1) for Mg, respectively.

Calcium↗
PubMed2001

Simultaneous determination of nitrate and nitrite in saliva and foodstuffs by non-suppressed ion chromatography with bulk acoustic wave detector.

In the present paper, nitrate and nitrite in foodstuffs and saliva were simultaneously determined using a non-suppressed ion chromatography (IC) method with a bulk acoustic wave sensor (BAW) as detector, and 1.5 mmol/L potassium hydrogenphthalate (KHP) as mobile phase. The IC-BAW method is simple, rapid and accurate. The determination limits for nitrite and nitrate are 0.20 and 0.30 mg/L, respectively. The IC-BAW is comparable and agrees with the conventional spectrophotometric method for nitrite and nitrate determination.

Chromatography, Ion Exchange↗
PubMed2000

Determination of the binding parameters of drug to protein by equilibrium dialysis/piezoelectric quartz crystal sensor.

A novel method, equilibrium dialysis/piezoelectric quartz crystal sensor, applied to determine the binding parameters of diethyldithiocarbamate to human plasma protein is proposed. Based on the investigation of the equilibrium reaction for the binding of drug to protein, the related theoretical equations for this binding were derived. By monitoring the frequency responses of a copper-plated piezoelectric quartz crystal sensor to drug in and out of a dialysis membrane after equilibrium, the binding parameters were determined, i.e., 0.375 micromol g(-1) for beta(p), 6.496 microM for K(dp), 141.99 L mmol(-1) for K(p), and 0.043 for N. These values were in good agreement with reference values. It was found that this method may have application for studying the characteristics of the interaction between other drugs and proteins.

Biosensing Techniques↗
PubMed1998

Flow-injection determination of total ammonia and total carbon dioxide in blood based on gas-diffusion separation and with a bulk acoustic wave impedance sensor.

A novel flow-injection (FIA) system, for the rapid and direct determination of both total ammonia (T[NH3]) and total carbon dioxide (T[CO2]) in clinical blood samples, has been developed. Samples were injected into a carrier stream of H2O, then emerged with a reagent stream, where the analyte was converted into a gaseous species and diffused across a PTFE gas-permeable membrane into an acceptor stream. The trapped NH3/CO2 in the acceptor was determined on line by a bulk acoustic wave (BAW) impedance sensor. At a through-put of 20 and 65 h(-1), the proposed system exhibited a linear frequency response up to 200 micromol l(-1) ammonium and 20 mmol l(-1) bicarbonate with a detection limit of 1.0 and 10 micromol l(-1), respectively. Results obtained for T(NH3) in serum and T(CO2) in plasma were in agreement with those obtained by the conventional glutamate dehydrogenase (GDH) method and gas-sensing electrode method, respectively. The effects of composition of acceptor stream, cell constant of conductivity electrode, sample volume, flow rate and potential interferents on the FIA signals were also discussed.

Acoustics↗
PubMed1997

Ion chromatographic study of sodium, potassium and ammonium in human body fluids with bulk acoustic wave detection.

In the present paper, determination of Na+, K+ and NH4+ in saliva and serum was carried out using an ion chromatography (IC) method with a bulk acoustic wave (BAW) sensor as detector and 2.0 mmol/l nitric acid as mobile phase. The IC-BAW method is simple, rapid and accurate. Comparison between the BAW detector and the conventional conductivity detector (CDD) was discussed. The IC-BAW showed agreement with the commonly used flame photometric method for Na+ and K+ and enzymatic method for NH4+, as well as IC-CDD for those three cations.

Body Fluids↗
PubMed1996

Bulk acoustic wave sensor for investigating hemorheological characteristics of plasma and its coagulation.

A method of using a bulk acoustic wave (BAW) device to study the hemorheological phenomena is proposed. By measuring the resonant resistance of a BAW device, the dependence of the plasma viscosity on its composition is investigated. It has been found that during the process of the plasma coagulation, the frequency response of a BAW device is dominated by the change in plasma viscoelasticity, and useful information such as the coagulation time and the viscoelasticity of coagulated plasma can be obtained from the curve of frequency response. Based on the BAW quartz detection system, effects of fibrinogen, thrombin and some drugs on the plasma coagulation are investigated. The results show that the BAW device based on the oscillator method possesses some advantages, such as high sensitivity, simplicity of use, cost effectiveness and small sample volume for clinical hemorheological study.

Acoustics↗
PubMed1996

Determination of dipyridamole by modified extraction-gravimetry with a surface acoustic wave resonator sensor.

A simple and sensitive extraction-gravimetric method for the determination of dipyridamole is presented. The method is based on the extraction of free dipyridamole with chloroform, after neutralization with a basic agent, followed by measurement of the frequency shift response of the specially designed surface acoustic wave resonator sensor after evaporation of the extractant from the surface of the resonator. The frequency shift response was proportional to the amount of dipyridamole in the range 0.065-1.12 micrograms. Experimental parameters and the effect of interfering substances on the assay of dipyridamole were also examined in this study. The method was applied to the determination of dipyridamole in tablets.

Chloroform↗
PubMed1995

Determination of lactic acid and pyruvic acid in serum and cerebrospinal fluid by ion-exclusion chromatography with a bulk acoustic wave detector.

A chromatographic method base don a combination of ion-exclusion chromatography separation and bulk acoustic wave series piezoelectric quartz crystal detector quantification for the determination of pyruvic acid and lactic acid in serum and cerebrospinal fluid (CSF) was developed. The separation was carried out using a Shim-pak SCR-102H ion-exclusion column with phosphoric acid solution as eluent. The method shows an acceptable detection limit and anti-interference ability. Serum and CSF from healthy individuals and patient were analysed successfully.

Acoustics↗
PubMed1995

Application of a series piezoelectric sensor as a detector in ion chromatography.

The application of a series piezoelectric sensor as a detector for ion chromatography (IC) is investigated. The device is used with sensitive response between the series piezoelectric quartz crystal oscillation frequency and specific conductivity of liquids for ion chromatographic detection. Two platinum wires are used as conductivity electrodes and inserted oppositely in the detection cell. The dead-volume of the detection is 15 microL, the noise is less than or equal to 1 Hz, the baseline drift is 5 Hz/h, and the detection limits of F- and Na+ are 5 and 25 ng, respectively. The effects of temperature, background conductivity, cell constant of the conductivity electrode, and dead volume on the sensitivity of the detector are discussed. The detector temperature should equal that of the column. An optimum sensitivity is obtained when the cell constant is approximately 3.5 cm. The optimum range of the background conductivity of the mobile phase is 150 to 1200 microseconds. When the solution conductivity is greater than 3000 microseconds, the detector does not work satisfactorily. The proposed IC cerebrospinal fluid detection method is applied to the determination of vitamin C in apple and Zn2+, Ca2+, Mg2+, and Cu2+ in human cerebrospinal fluid.

Ascorbic Acid↗
PubMed1993

Reaction-frequencymetric method: a new analytical technique for determination of submicromolar concentration levels of vitamin C.

A new analytical technique for the assay of pharmaceutical substances at low concentration levels has been proposed and applied to the determination of vitamin C as an example of its application. It is based on the chemical reaction of vitamin C with iodine in a sodium citrate-hydrochloric acid medium, followed by measurement of the frequency change of a silver-plated piezoelectric quartz crystal. The frequency change is proportional to the vitamin C concentration from 2 x 10(-7) to 4 x 10(-6) M. The method was applied to the assay of vitamin C in pharmaceutical preparations.

Ascorbic Acid↗
PubMed1993

[Simultaneous determination of vitamin B1 and vitamin C in aqueous solution with piezoelectric crystal quartz sensors].

According to the response properties of piezoelectric crystal quartz sensors to the solution conductivity the frequency shift response was derived to show a linear dependence on the concentrations of vitamin B1 (VB1) and vitamin C (VC). This was experimentally verified and a calibration model for simultaneous determinations of the two vitamins was established. The usefulness of the technique was evaluated by quantitation of mixtures of unknown composition using common multiple linear regression (MLR) and partial least squares (PLS). The average relative standard deviations for six samples were 4.46% for VB1 and 6.63% for VC with MLR; and 1.97% for VB1 and 2.74% for VC with PLS, respectively.

Ascorbic Acid↗
PubMed1991

Extraction-frequencymetric method. A new measurement technique for determination of micro amounts of chlorpheniramine.

A new measurement technique has been proposed and applied to the determination of chlorpheniramine as an example of its application. It is based on the extraction of free chlorpheniramine into carbon tetrachloride after neutralization with a basic agent, followed by measurement of the frequency change of the specially designed ring-coated piezoelectric sensor after evaporation of the extractant from the crystal surface. The frequency change is proportional to the chlorpheniramine amount in the range 0.025-1.2 microgram. The method has been applied to the determination of chlorpheniramine maleate in pharmaceutical preparations.

Calibration↗
PubMed1991

[Use of extraction-frequency metric method for the determination of microquantities of ephedrine and its application in pharmaceutical analysis].

A new extraction--frequency metric method has been proposed for the determination of ephedrine, which can not be determined by the conventional extraction--weighing method due to its volatility. The method is based on extraction of the free alkaloid followed by measuring the frequency shift of a specially constructed ring--coated piezoelectric crystal at room temperature. The frequency shift is in linear relationship with the content of ephedrine hydrochloride over a range 0.05-1.2 micrograms with a correlation coefficient of 0.999 and a detection limit of 0.02 micrograms. Methods for the assay of ephedrine hydrochloride tablet and nasal solution have been proposed.

Chemistry Techniques, Analytical↗
PubMed1991

Transfer mechanism of quinine drug across the oil/water (O/W) interface.

The transfer phenomena of quinine drug at the aqueous 1,2-dichloroethane (DCE) interface have been studied by the current-scanning polarography. The relationships between the wave height and pH of aqueous phase, concentration of quinine as well as the rate of water drop are discussed. The effect of supporting electrolyte, buffer solution and the nature of organic solvent on the polarographic wave is studied. The transfer characteristics of quinine in aqueous phase and in organic phase are compared. The mono-protonated and diprotonated quinines can both transfer at the interface so as to produce two polarographic waves. The transfer process of quinine at the interface is simultaneously controlled by diffusion and reestablishment of the disturbed protonated equilibrium of quinine. A further investigation is made by chronopotentiometry. On the basis of the theoretical analysis, the formulae of the limiting current are derived and discussed. The theoretical results are in agreement with the experimental ones. The transfer mechanism of quinine is put forward.

Mathematics↗
PubMed1990

[Determination of microgram-amount pentoxyverine citrate using a piezoelectric detector and neutralization-extraction technique].

A new method for the rapid determination of microgram and submicrogram amounts of pentoxyverine citrate has been suggested using a ring-coated piezoelectric quartz crystal in combination with the neutralization extraction technique. The detection limit is 0.02 microgram. Frequency shift is directly proportional to the pentoxyverine citrate concentration in the range of 0.05-1.6 micrograms, with a correlation coefficient of 0.999 and a coefficient of variation of 2.3%. The new method suggests a number of advantages over the classical neutralization-extraction method.

Cyclopentanes↗