Chemiluminescence flow sensor for folic acid with immobilized reagents.

A novel chemiluminescence (CL) sensor for folic acid combined flow-injection (FI) technology was presented in this paper. The analytical reagents involved in the CL reaction, including luminol and hexacyanoferrate(III), were both immobilized on an anion-exchange column in FI system. The CL signal produced by the reaction between luminol and hexacyanoferrate(III), which were eluted from the column through sodium phosphate injection, was decreased in the presence of folic acid. The CL emission was correlated with the folic acid concentration in the range from 0.01 to 15 microg ml(-1), and the detection limit was 3.5 ng ml(-1) folic acid (3sigma). At a flow rate of 2.0 ml min(-1), including sampling and washing, could be performed in 2 min with a relative standard deviation of < 2.5%. The flow sensor could be reused more than 300 times and has been applied to the analysis of folic acid in pharmaceutical preparations. and the recovery was from 97.4% to 100.4%.     

Chemiluminescence sensor for isoniazid with controlled-reagent-release technology

A novel chemiluminescence (CL) sensor for isoniazid combined with flow-injection technology is presented in this paper. The analytical reagents, luminol and ferricyanide, were both immobilized on an anion-exchange column. The CL signal produced by the reaction between luminol and ferricyanide, which were eluted from the column through sodium phosphate injection, was decreased in the presence of isoniazid. The decreased CL intensity was linear with isoniazid concentration in the range 0.001–1.0 μg·ml⁻¹; and the detection limit was 0.35 ng·ml⁻¹ (3s). The whole process, including sampling and washing, could be completed in 2 min with a relative standard deviation of less than 4.1%. The sensor could be reused more than 400 times and has been applied for the determination of isoniazid in pharmaceutical preparations.     

Evaluation of luminol-H(2)O(2)-KIO(4) chemiluminescence system and its application to hydrogen peroxide, glucose and ascorbic acid assays

A novel chemiluminescence (CL) system was evaluated for the determination of hydrogen peroxide, glucose and ascorbic acid based on hydrogen peroxide, which has a catalytic-cooxidative effect on the oxidation of luminol by KIO(4). Hydrogen peroxide can be directly determined by luminol-KIO(4)-H(2)O(2) CL system. The detection limit was 3.0x10(-8) mol l(-1) and the calibration graph was linear over the range of 2.0x10(-7)-6.0x10(-4) mol l(-1). The relative standard deviation of H(2)O(2) was 1.1% for 2.0x10(-6) mol l(-1) (N=11). Glucose was indirectly determined through measuring the H(2)O(2) generated by the oxidation of glucose in the presence of glucose oxidase at pH 7.6. The present method provides a source for H(2)O(2), which, in turn, coupled with the luminol-KIO(4)-H(2)O(2) CL reaction system. The CL was linearly correlated with glucose concentration of 0.6-110 mug ml(-1). The relative standard deviation was 2.1% for 10 mug ml(-1) (N=11). Detection limit of glucose was 0.08 mug ml(-1). Ascorbic acid was also indirectly determined by the suppression of luminol-KIO(4)-H(2)O(2) CL system. The calibration curve was linear over the range of 1.0x10(-7)-1.0x10(-5) mol l(-1) of ascorbic acid. The relative standard deviation was 1.0% for 8.0x10(-7) mol l(-1) (N=11). Detection limit of ascorbic acid was 6.0x10(-8) mol l(-1). These proposed methods have been applied to determine glucose, ascorbic acid in tablets and injection.     

Chemiluminescence assay for uric acid in human serum and urine using flow-injection with immobilized reagents technology

A novel chemiluminescence (CL) flow sensor for the determination of uric acid in human urine and serum has been developed by using controlled-reagent-release technology. The reagents involved in the chemiluminescence (CL) reaction, luminol and periodate, are immobilized on anion-exchange resin packed in a column. After injection of water, chemiluminescence generated by released luminol and periodate in alkaline media is inhibited in presence of uric acid. By measuring the decreased chemiluminescence (CL) intensity the uric acid is sensed. The decreased response is linear in the 5.0-500.0 ng mL(-1) range, with a detection limit of 1.8 ng mL(-1). The flow sensor showed remarkable operational stability and could be easily reused for over 80 h with sampling frequency of 100 h(-1). The proposed sensor was applied to the determination of uric acid in human urine and serum, and monitoring metabolic uric acid in human urine with RSD less than 3.0%.     

Reagentless chemiluminescence flow sensor for the determination of riboflavin in pharmaceutical preparations and human urine

A novel continuous-flow sensor based on chemiluminescence (CL) detection was developed for the determination of riboflavin at pg ml(-1) levels by the immobilization of the reagents. It was found that the CL intensity from the oxidation between luminol and periodate could be enhanced in the presence of riboflavin. The increase of CL emission was correlated with the riboflavin concentration in the range from 0.04 to 200 ng ml(-1), and the detection limit was 0.02 ng ml(-1) (3s). Considering the effective reaction ions, luminol and IO4- was immobilized on anion-exchange resin. The system could produce an evident CL signal by water as eluant and it was also shown that the flow sensor could greatly improve the selectivity and sensitivity for determination of riboflavin with a high signal-to-noise ratio. A complete analysis, including sampling and washing, could be performed in 0.5 min with a relative standard deviation of less than 3.0%. The flow sensor was applied successfully to the determination of riboflavin in pharmaceutical preparations and human urine samples.     

Chemiluminescence flow-through sensor for ofloxacin using solid-phase PbO(2) as an oxidant

A novel chemiluminscence (CL) flow-through sensor for ofloxacin is described. It was based on the sensitizing effect of ofloxacin on the CL oxidation of sulfite by PbO(2) in H(2)SO(4) media. By a very simply means, the solid-phase PbO(2) was immobilized inside of the CL flow cell as CL oxidant. The column of solid PbO(2) could be reused about 400 times during a period of 50 h. The calibration graph is linear in the range 0.2-10 mug ml(-1) with a detection limit of 7.8x10(-8) g ml(-1) (S/N=3). This method has been successfully applied to determine ofloxacin in pharmaceutical preparation.     

Flow injection chemiluminescence determination of thiamine based on its enhancing effect on the luminol-hydrogen peroxide system

A new flow injection chemiluminescence (CL) method is proposed for the determination of thiamine, based upon its enhancing effect on the CL reaction of luminol with hydrogen peroxide in alkaline solution. The method allows the determination of thiamine within 0.05-8 mug ml(-1) range with a detection limit (3sigma) of 0.01 mug ml(-1). The relative standard deviation is 1.4% (n=11, 0.5 mug ml(-1) thiamine) and the sample throughput is about 90 samples h(-1). The method was successfully applied to the determination of thiamine in pharmaceutical preparations.     

A new analytical procedure for assay of lysozyme in human tear and saliva with immobilized reagents in flow injection chemiluminescence system.

A novel analytical procedure based on chemiluminescence (CL) detection was described for the determination of lysozyme at ng ml(-1) level by using controlled-reagent-release technology in a flow injection system. The analytical reagents involved in the CL reaction, including luminol and periodate, were both immobilized on the anion-exchange resins in the flow injection system. Through water injection, luminol and periodate were eluted from the anion-exchange column to generate the chemiluminescence, which was inhibited in the presence of lysozyme. By measuring the decrease of CL intensity, one could analyze the lysozyme quantitatively. The decrement of CL emission was linear over the logarithm of lysozyme concentration in the range of 30-1000 ng ml(-1). A typical analytical procedure, including sampling and washing, could be performed in 0.5 min at a flow rate of 2.0 ml min(-1), giving a throughput of 120 h(-1), with a relative standard deviation of less than 3.0%. The proposed method was applied successfully to the determination of lysozyme in human tear and saliva samples, and the recovery was from 92.0% to 105.7%.     

Simultaneous anodic stripping voltammetric determination of lead and cadmium with a carbon paste electrode modified by tributyl phosphate

A novel chemiluminescence (CL) flow sensor has been developed for the monitoring of iron(III). The analytical reagents involved in the CL reaction, including luminol and hexacyanoferrate(II) were both immobilized on an anion-exchange resin column. When sodium sulfate solution was passed through the column, these two reagents were eluted from the resins and then mixed with an iron(III) stream. By the fast reaction between iron(III) and hexacyanoferrate(II), the complex Prussian Blue was generated, which could catalyse the luminol oxidation by dissolved oxygen in alkaline aqueous solution to produce CL. The CL emission intensity was correlated with the standard iron(III) concentration in the range 0.01-Smgl^–1, and the detection limit was 7 × 10^–3mgl^–1 iron(III). A complete analysis, including sampling and washing, could be performed in l min with a relative standard deviation of less than 5%. The sensor was stable for over 200 times and has been applied successfully to the determination of iron in blood samples.     

Highly sensitive chemiluminescence flow sensor for ascorbic acid

A highly sensitive chemiluminescence(CL) flow sensor is proposed for the determination of ascorbic acid. The analytical reagents luminol and iron(II) are immobilized on anion-exchange and cation-exchange resins, respectively, and can be eluted by sodium sulphate. The calibration graphs are linear in the range 1 × 10^–9 to 1 × 10^–6 g mL^–1 and the detection limit is 4.0 × 10^–10 g mL^–1. The sensor has been applied successfully to the determination of ascorbic acid in vegetables.     

纳米银增敏化学发光体系测定间苯二酚

采用柠檬酸钠包覆化学还原法制备纳米银粒子,将该纳米银粒子加入到碱性鲁米诺-铁氰化钾化学发光体系,体系的化学发光强度明显增强,而间苯二酚的加入能抑制该体系的化学发光,据此建立了流动注射化学发光法定量分析痕量间苯二酚的新方法.考察了鲁米诺、铁氰化钾、氢氧化钠以及纳米银浓度对化学发光体系的影响.在优化的实验条件下,该方法测定...     

On-Line Monitoring of Formaldehyde In Water and Air Using Chemiluminescence Detection

A rapid and sensitive chemiluminescence flow sensor for the determination of formaldehyde was proposed in this article. The analytical reagents involved in chemiluminescence (CL) reaction, luminol and KIO₄, were both immobilized on an anion-exchange column. The CL signal produced by the reaction between luminol and KIO₄, which were eluted from the column through water injection, was decreased in the presence of formaldehyde. Formaldehyde was sensed by measuring the decrement of CL intensity, which was observed linear over the logarithm of formaldehyde concentration range of 5.0-1000.0 ng mL^?1, and the limit of detection is 1.8 ng mL^?1 (3σ). At a flow rate of 2.0 mL min^?1, including sampling and washing, could be performed in 0.5 min with a relative standard deviation of less than 3.0%. The flow sensor offered reagentless procedures and remarkable stability in determination of formaldehyde, and could be easily re-used over 80 h. The proposed flow microsensor was applied successfully in the determination of formaldehyde in artificial water samples and air.     

Pork Heart Tissue‐Based Chemiluminescence Biosensor for Pyruvic Acid

Abstract

A novel chemiluminescence (CL) animal tissue‐based sensor for pyruvic acid is presented in this paper. Pork heart tissue was chopped into small pieces and packed into a mini‐glass column as the recognition element. When pyruvic acid passed through the column, hydrogen peroxide was produced under the catalytic oxidation of oxygen by pyruvic acid oxidase present in the pork heart tissue. This produced hydrogen peroxide could react with luminol in alkaline solution to produce chemiluminescence in the presence of potassium hexacyanoferrate(III). The developed sensor system promises simplicity, fastness, stability, and sensitivity. Under the optimum conditions, CL intensities are proportional to the concentration of pyruvic acid in the range of 0.02–12 µmol/L, with a detection limit of 0.004 µmol/L (3σ). RSD is 2.3% for 0.5 µmol/L pyruvic acid (n=11). The sensor could be stable for 150 min by more than 100 times determination. The proposed method has been applied successfully to the analysis of pyruvic acid in biological samples. The results obtained by the proposed method are consistent with those obtained by spectrophotometry.     

Chemiluminescence Sensor for the Determination of Hydroxylamine by Electrostatically Immobilizing Luminol and Periodate

IntroductionAnalytical methods based on chemilumi-nescence( CL ) reactions have received considerableattention for theirapplication in various fields,ow-ing to their extremely high sensitivity along withother advantages such as wide linear dynamicrange,simple instrumentation,easy miniaturiza-tion and coupling to various separation tech-niques[1— 6] .CL sensors have been developed for be-ing used as the continuous and real- time monitorsof inorganic,organic,biological and pharmaceuti-cal comp…     

Sensitive determination of sub-nanogram amounts of rutin by its inhibition on chemiluminescence with immobilized reagents

An interesting inhibitory effect of rutin on the chemiluminescence (CL) reaction between luminol and periodate was reported, and this effect was used for the determination of rutin in medicine and human urine. The CL reagents, luminol and periodate, were both immobilized on an anion-exchange column. The CL signal produced by the reaction between luminol and periodate, which were eluted from the column through water injection, was decreased in the presence of rutin. Rutin was sensed by measuring the decrement of CL intensity, and which was observed to be linear over the logarithm of 0.1-30 ngml(-1) rutin concentration range, and the limit of detection was 0.03 ngml(-1) (3sigma). At a flow rate of 2.0 mlmin(-1), both sampling and washing could be performed in 0.5 min with a relative standard deviation of less than 3.0%. The method proposed offered reagent-less procedures and remarkable stability in the determination of rutin, and could be easily reused over 80 h. The method proposed was applied successfully in the determination of rutin in pharmaceutical preparations and monitoring the excretion of rutin in human urine.     

Flow—injection Chemiluminescence Sensor for the Determination of Gallic Acid by Immobilizing Luminol and Periodate on Anionexchange Resin

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Determination of thiamine by continuous flow chemiluminescence measurement

The chemiluminescence produced by oxidation of thiamine by ferricyanide in alkaline medium has been investigated by using a simple continuous flow analyser and a procedure developed for the determination of thiamine hydrochloride or nitrate in the range 2.00 x 10(-5)-5.00 x 10(-4)M (equivalent to 6.75-169 mug/ml thiamine hydrochloride) with coefficients of variation <2%. A measurement rate of 112/hr can be obtained. When applied to pharmaceutical formulations, the only interferent among common excipients and coexisting drugs is ascorbic acid. The results obtained for the assay of dosage forms compared well with those obtained by an official method and demonstrated an error <4%.     

Chemiluminescence determination of some fluoroquinolone derivatives in pharmaceutical formulations and biological fluids using [Ru(bipy)(3)(2+)]-Ce(IV) system

A new chemiluminescence (CL) method using flow injection has been described for the rapid and sensitive determination of three fluoroquinolone derivatives, namely ofloxacin, norfloxacin and ciprofloxacin hydrochloride. The method is based on the CL reaction of the studied fluoroquinolones with tris(2,2'-bipyridyl)ruthenium(II) [Ru(bipy)(3)(2+)] and Ce(IV) in sulfuric acid medium. Under the optimum conditions, the CL intensity is proportional to the concentration of the drugs in solution over the range 0.05-7.0 mug ml(-1) for norfloxacin, 0.05-6.0 mug ml(-1) for ciprofloxacin hydrochloride and 0.003-0.7 mug ml(-1) for ofloxacin. The limits of detection (s/n=3) were 3.1x10(-8) M norfloxacin, 2.6x10(-8) M ciprofloxacin hydrochloride and 5.5x10(-9) M ofloxacin. The method was applied successfully to the determination of these compounds in dosage forms and biological fluids.     

Chemiluminescence flow system for the determination of sulfite

A novel chemiluminescence(CL) flow system for sulfite is described based on electrostatically immobilized luminol on an anion exchange column. Sulfite is detected by the CL reaction with luminol bleeding from the column by hydrolysis. The calibration graph is linear in the range 3 × 10^–7 to 1 × 10^–5 mol/L, and the detection limit is 1 × 10^–7 mol/L. Interfering metal ions co-existing in sample solutions could be effectively eliminated on-line by an upstream cation exchanger. A complete analysis could be performed in 1 min with a relative standard deviation of less than 5%. The system could be reused for over 50 h and has been applied successfully to the determination of sulfur dioxide in air.     

地塞米松磷酸钠的流动注射-化学发光分析法的研究

实验了地塞米松磷酸钠在K3Fe（CN）6-鲁米诺、KMnO4-鲁米诺、KIO4-鲁米诺、H2O2-鲁米诺体系中的化学发光现象。结果表明,地塞米松磷酸钠能够显著增强K3Fe（CN）6-鲁米诺体系和KMnO4-鲁米诺体系的化学发光强度,而在另外两个体系中没有增强作用。结合流动注射技术,分别在K3Fe（CN）6-鲁米诺体系和KMnO4-鲁米诺体系中建立了测定地塞米松的新方法。方法的线性范围分别为1.0&#215;10^-7-1.0&#215;10^-5g/mL和6.0&#215;10^-8-1.0&#215;10^-5g/mL,检出限分别为3.0&#215;10^-8g/mL和2.0&#215;10^-8g/mL,相对标准偏差分别为1.6%和1.9%（1.0&#215;10^-6g/mL地塞米松,n=11）。此法已用于针剂和片剂样品的测定,结果与药典方法没有显著性差异。