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Cannabis is a plant that is harmful and beneficial because it contains more than 400 bioactive compounds, and the main compounds are Δ 9 tetrahydrocannabinol (THC) and cannabidiol (CBD). Currently, cannabis extracts are used in medicine, but the amount of THC as a main psychoactive component is strictly regulated. Therefore, the ability to rapidly and accurately detect THC is important. Herein, we developed a sensitive electrochemical method combining a rapid lateral flow assay (LFA) to detect THC rapidly. An electrochemical LFA device was constructed by attaching a screen-printed electrode inside a lateral-flow device to exploit the remarkable binding of THC to the cannabinoid type 2 (CB2) receptor in the test zone. The ferrocene carboxylic acid attached to the monoclonal THC antibody acts as an electroactive species when it binds to the THC in the sample before it flows continuously to the CB2 receptor region on the electrode. Under optimal conditions, the detection time is within 6 min and the devise shows excellent performance with a detection limit of 1.30 ng/mL. Additionally, the device could be applied to detect THC in hemp extract samples. The results obtained from this sensor are similar to the standard method (HPLC) for detecting THC. Therefore, this proposed device is useful as an alternative device for the on-site determination of THC because it is inexpensive, portable, and exhibits high sensitivity., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 Elsevier B.V. All rights reserved.)

We developed a novel, sensitive, and selective platform for the specific determination of aflatoxin B1 (AFB1). Single-walled carbon nanohorns decorated by a cobalt oxide composite and gold nanoparticles were created to provide facile electron transfer and improve the sensor's sensitivity. In addition, we attributed the selectivity of the proposed sensor to the specific binding property of the anti-aflatoxin B1 antibody. We clarified the specific interaction of the proposed immunosensor to AFB1 using homology modeling combined with molecular docking. In the presence of AFB1, the current signal of the modified electrode reduced; this involved specific antibody-antigen binding, including hydrophobic hydrogen bonding and pi-pi stack interactions. The new AFB1 sensor platform showed two linearity ranges of 0.01-1 ng mL -1 and 1-100 ng mL -1 , with the limit of detection at 0.0019 ng mL -1 . We investigated the proposed immunosensor in real samples, including peanuts, certified reference material of a peanut sample (labeled 206 μg kg -1 AFB1), corn, and chicken feed. The sensor's accuracy was 86.1-104.4% recovery, which agrees with the reference HPLC technique using paired t-test analysis. The present work shows excellent performance for AFB1 detection and could be applied for food quality control or modified to detect other mycotoxins., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023. Published by Elsevier B.V.)

Mercury ion (Hg 2+ ) is considered to be one of the most toxic heavy metal ions and can cause adverse effects on kidney function, the central nervous system, and the immune system. Therefore, it is important to develop a fast and simple method for sensitive and selective detection of Hg 2+ in the environment. This research proposes a portable electrochemical sensor for rapid and selective detection of Hg 2+ . The sensor platform is designed based on thymine acetic acid anchored with cysteamine-conjugated core shell Fe 3 O 4 @Au nanoparticles (Fe 3 O 4 @Au/CA/T-COOH) immobilized on a sensing area of a screen-printed carbon electrode (SPCE) with the aid of an external magnetic field embedded in a homemade electrode holder for ease of handling. In the presence of Hg 2+ , the immobilized thymine combines specifically with Hg 2+ and forms a thymine-Hg 2+ -thymine mismatch (T-Hg 2+ -T). The resulting amount of Hg 2+ was determined by differential pulse anodic stripping voltammetry (DPASV). Under optimal conditions, the sensor exhibited two wide linearities in a range from 1 to 200 μg L -1 and 200-2200 μg L -1 with the reliability coefficient of determination of 0.997 and 0.999, respectively. The detection limit (LOD) and the quantification limit (LOQ) were also determined to be 0.5 μg L -1 and 1.0 μg L -1 , respectively. The sensor was further applied for determination of Hg 2+ in water samples, a certified reference material and fish samples. The results were compared with flow injection atomic spectroscopy-inductively coupled plasma-optical emission spectroscopy (FIAS-ICP-OES) systems as a reference method. Results obtained with the proposed sensor were relatively satisfactory, and they showed no significant differences at a 95% confidence level by t-test from the standard method. Therefore, considering its fast and simple advantages, this novel strategy provides a potential platform for construction of a Hg 2+ electrochemical sensor., (Copyright © 2020 Elsevier B.V. All rights reserved.)

A novel electrochemical immunosensor was developed for label-free detection of carcinoembryonic antigen (CEA) as a cancer biomarker. The designed immunosensor was based on CEA antibody (anti-CEA) anchored with core shell Fe 3 O 4 @Au nanoparticles which were immobilized on a screen-printed carbon electrode modified with manganese dioxide decorating on graphene nanoplatelets (SPCE/GNP-MnO 2 /Fe 3 O 4 @Au-antiCEA). The SPCE was placed onto a home-made electrode holder for easy handling. The approach was based on direct binding of CEA to a fixed amount of anti-CEA on the modified electrode for the specific detection using linear sweep voltammetry (LSV) and electrochemical impedance spectroscopy (EIS) monitored in a solution containing 5 mM [Fe(CN) 6 3-/4- ] prepared in 0.1 M phosphate buffer at pH 7.4. The difference in signal response owing to the redox reaction of [Fe(CN) 6 ] 3-/4- before and after interaction with CEA was regarded as the immunosensor response corresponding directly to the CEA concentration. Under optimized conditions, the linear range of 0.001-100 ng/mL, and the detection limits of 0.10 pg/mL (LSV) and 0.30 pg/mL (EIS) were evaluated. The applicability of the immunosensor was verified by well-corresponding determination of CEA in diluted human serum samples by electrochemiluminescence (ECL) immunoassay. Therefore, the proposed immunosensor could be suitable enough for a real sample analysis of CEA., Competing Interests: Declaration of Competing Interest The authors declare no conflict of interest., (Copyright © 2020 Elsevier B.V. All rights reserved.)

In this work the development of an electrochemical sensor for the determination of polyunsaturated fatty acids (PUFAs), in particular linoleic acid, in commercially available safflower oil as complex matrix is described. The sensor consists of a carbon paste electrode with cobalt(II) phthalocyanine, Co(II)Pc, as mediator and multiwalled carbon-nanotubes (MWCNT) as nanomaterial. As carrier medium a sodium borate buffer (0.1 M, pH 9) was used. PUFAs were detected at a working voltage of 0.35-0.45 V (vs. Ag/AgCl). The sensor development was carried out in a batch system with differential pulse voltammetry (DPV) and cyclic voltammetry (CV). Sensor specification was tested by using various fatty acids (stearic acid, oleic acid, linoleic acid, linolenic acid and arachidonic acid) as well as esterified fatty acids, resulting in a specific applicability towards PUFAs, especially linoleic acid (LAH). The optimized sensor was applied in a flow injection analysis system (FIA) for the analysis of PUFAs in complex matrix. Linoleic acid was used as standard substrate to determine the analytical parameters. The linearity ranges between 7.5 and 200 μg mL -1 LAH, while the limit of detection was determined to be 2.5 μg mL -1 and the limit of quantification is approximately 7.5 μg mL -1 LAH. The LAH content was successfully detected in commercially available safflower oil via standard addition method and the results could be confirmed by a reference method. The PUFA content was calculated as LAH-equivalent., (Copyright © 2018 Elsevier B.V. All rights reserved.)

New insight into the preparation of sensitive carbon-based electrochemical electrode is provided by examining the properties of thermally reduced graphene oxide (TRGO). In this paper, TRGO was prepared by thermal reduction of graphene oxide (GO) in argon atmosphere, and characterized by Fourier transform infrared (FTIR) spectroscopy, transmission electron microscopy (TEM), selected area electron diffraction (SAED), and atomic force microscopy (AFM). Results showed that thermal reduction in argon was effective to remove oxygen-containing functional groups in GO, and graphene sheets were obtained. Furthermore, TRGO was used to prepare thermally reduced graphene oxide paste electrode (TRGOPE) which showed excellent conductivity and fast electron transfer kinetics confirmed by electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). The electrode was applied to determination of the pesticide naptalam (Nap) in square-wave voltammetric (SWV) mode. The corresponding current at approx. +1.0 V increased linearly with the Nap concentration within two linear dynamic ranges (LDR) of 0.1-1.0 μmol L -1 (LDR 1 ) and 1.0-10.0 μmol L -1 (LDR 2 ). The limits of detection (LOD) and quantification (LOQ) for Nap were calculated as 0.015 μmol L -1 and 0.051 μmol L -1 , respectively. In comparison to the carbon paste electrode (CPE) the results showed that the TRGOPE possesses advantages in terms of linearity, sensitivity and detectability., (Copyright © 2018 Elsevier B.V. All rights reserved.)

A novel human monoamine oxidase B (hMAO B) based biosensor for inhibitory measurements was developed. It allows both the characterisation of the type of enzyme inhibition and the sensitive and simple determination of inhibitors like selegiline hydrochloride. The sensor consists of a screen printed carbon working electrode modified with 20% manganese dioxide (MnO 2 ) and the enzyme hMAO B, which was immobilised on the electrode via a dialysis membrane (regenerated cellulose, molecular weight cut-off 14000). Inhibition of hMAO B is evaluated by adding different concentrations of the inhibitor selegiline hydrochloride to the enzyme and applying a defined amount of the hMAO B substrate phenylethylamine (PEA). The enzymatically formed H 2 O 2 is amperometrically detected at 0.4V vs. Ag/AgCl in a flow injection analysis (FIA) system. With 100µM PEA the sensor showed a linear correlation between peak height and inhibitor concentration in a range of 0.51-3.25µg/mL selegiline hydrochloride. LOD and LOQ were determined to be 0.15 and 0.51µg/mL, respectively. The sensor showed a repeatability of 3.7% and an intermediate precision of 8.1%. The inhibition-based biosensor was successfully employed to quantify selegiline hydrochloride in pharmaceutical samples. Kinetic studies via Lineweaver-Burk plot and enzyme quantity vs. current plot revealed that the inhibition is irreversible., (Copyright © 2017 Elsevier B.V. All rights reserved.)

This work presents the simultaneous determination of catechol (CC) and hydroquinone (HQ), employing a modified carbon paste electrode (CPE) with ferrite nanomaterial. Ferrite nanomaterial was doped with different amount of cobalt and this was investigated toward simultaneous oxidation of CC and HQ. It was shown that this modification strongly increases electrochemical characteristics of the CPE. Also, electrocatalytic activity of such materials strongly depends on the level of substituted Co in the ferrite nanoparticles. The modified electrodes, labeled as CoFerrite/CPE, showed two pairs of well-defined redox peaks for the electrochemical processes of catechol and hydroquinone. Involving of ferrite material in the structure of CPE, cause increase in the potentials differences between redox couples of the investigated compounds, accompanied with increases in peaks currents. Several important parameters were optimized and calibration curves, with limits of detection (LOD) of 0.15 and 0.3µM for catechol and hydroquinone, respectively, were constructed by employing amperometric detection. Effect of possible interfering compounds was also studied, and proposed method was successfully applied for CC and HQ quantification in real samples., (Copyright © 2016 Elsevier B.V. All rights reserved.)

In this work new designed, highly sensitive electrochemical method is developed for the determination of nitrites in tap water using glassy carbon electrode modified with graphene nanoribbons (GNs/GCE). Graphene nanoribbons (GNs) have been newly synthetized and aligned to the surface of glassy carbon electrode (GCE) and exhibited excellent electrocatalytic activity for nitrite oxidation with a very high peak currents. Studies about electrochemical behavior and optimization of the most important experimental conditions were done using cyclic voltammetry (CV), while quantitative studies were done with amperometric detection. Nitrite provides a well-defined, oxidation peak at +0.9V (vs. Ag/AgCl, 3.0M KCl) in Britton-Robinson buffer solution (BRBS) at pH 3. The influence of most possible interferent ions has been examined and was found to be negligible. Under optimized experimental conditions in BRBS at pH 3 linear calibration curves were obtained in the range from 0.5 to 105µM with the detection limit of 0.22µM. Reproducibility of ten replicate measurements of 1µM of nitrite was estimated to be 1.9%. Proposed method and constructed sensor is successfully applied for the determination of nitrite present in tap water samples without any pretreatment. This developed method represents inexpensive analytical alternative approach compared to other analytical methods., (Copyright © 2016 Elsevier B.V. All rights reserved.)

A simple, low cost, and highly sensitive electrochemical sensor, based on a Nafion/ionic liquid/graphene composite modified screen-printed carbon electrode (N/IL/G/SPCE) was developed to determine zinc (Zn(II)), cadmium (Cd(II)), and lead (Pb(II)) simultaneously. This disposable electrode shows excellent conductivity and fast electron transfer kinetics. By in situ plating with a bismuth film (BiF), the developed electrode exhibited well-defined and separate peaks for Zn(II), Cd(II), and Pb(II) by square wave anodic stripping voltammetry (SWASV). Analytical characteristics of the BiF/N/IL/G/SPCE were explored with calibration curves which were found to be linear for Zn(II), Cd(II), and Pb(II) concentrations over the range from 0.1 to 100.0 ng L(-1). With an accumulation period of 120 s detection limits of 0.09 ng mL(-1), 0.06 ng L(-1) and 0.08 ng L(-1) were obtained for Zn(II), Cd(II) and Pb(II), respectively using the BiF/N/IL/G/SPCE sensor, calculated as 3σ value of the blank. In addition, the developed electrode displayed a good repeatability and reproducibility. The interference from other common ions associated with Zn(II), Cd(II) and Pb(II) detection could be effectively avoided. Finally, the proposed analytical procedure was applied to detect the trace metal ions in drinking water samples with satisfactory results which demonstrates the suitability of the BiF/N/IL/G/SPCE to detect heavy metals in water samples and the results agreed well with those obtained by inductively coupled plasma mass spectrometry., (Copyright © 2016 Elsevier B.V. All rights reserved.)

An amperometric biosensor based on chemisorption of glucose oxidase (GOx) on Au seeds decorated on magnetic core Fe3O4 nanoparticles (Fe3O4@Au) and their immobilization on screen-printed carbon electrode bulk-modified with manganese oxide (SPCE{MnO2}) was designed for the determination of glucose. The Fe3O4@Au/GOx modified SPCE{MnO2} was used in a flow-injection analysis (FIA) arrangement. The experimental conditions were investigated in amperometric mode with the following optimized parameters: flow rate 1.7 mL min(-1), applied potential +0.38 V, phosphate buffer solution (PBS; 0.1 mol L(-1), pH 7.0) as carrier and 3.89 unit mm(-2) enzyme glucose oxidase loading on the active surface of the SPCE. The designed biosensor in FIA arrangement yielded a linear dynamic range for glucose from 0.2 to 9.0 mmol L(-1) with a sensitivity of 2.52 µA mM(-1) cm(-2), a detection limit of 0.1 mmol L(-1) and a quantification limit of 0.3 mmol L(-1). Moreover, a good repeatability of 2.8% (number of measurements n=10) and a sufficient reproducibility of 4.0% (number of sensors n=3) were achieved. It was found that the studied system Fe3O4@Au facilitated not only a simpler enzyme immobilization but also provided wider linear range. The practical application of the proposed biosensor for FIA quantification of glucose was tested in glucose sirup samples, honeys and energy drinks with the results in good accordance with those obtained by an optical glucose meter and with the contents declared by the producers., (Copyright © 2015. Published by Elsevier B.V.)

A simple hydrodynamic chronoamperometric method based on the application of an unmodified carbon paste electrode (CPE) and bulk-modified with different contents of MnO2 was investigated for the determination of H2O2. The optimized method involving the CPE with 5% of MnO2 was applied for the determination of the H2O2 consumption in samples of groundwater from the Central Banat region (Province of Vojvodina, Serbia) treated by the Fenton (Fe(2+) and H2O2) and Fenton-like (Fe(3+) and H2O2) reagents to remove natural organic matter at different initial concentrations of iron species, and of their ratios to the initial concentration of H2O2. Under optimized conditions, with a working potential of 0.40V vs. the saturated calomel electrode and a phosphate buffer solution (pH 7.5) as supporting electrolyte, the method enabled the quantitation of H2O2 in the concentration interval from 1.4 to 65 μg mL(-1) with a relative standard deviation of less than 10%. The results obtained for the H2O2 consumption are in good agreement with those obtained by parallel measurements related to the efficiency of organic matter removal., (Copyright © 2014 Elsevier B.V. All rights reserved.)

Background: Although traumatic lacerations of the olecranon (OB) and praepatellar bursae (PB) are common entities often associated with complications, no study could be found on this injury. The aim of this study was to survey the current treatment concepts for acute traumatic laceration of the OB and PB in Germany, Austria and Switzerland., Materials and Methods: An international online survey was conducted among orthopaedic and trauma surgeons in Germany (TraumaNetwork DGU), Austria (Austrian Society of Trauma (ÖGU) and Orthopaedic (ÖGO) Surgeons) and Switzerland (Swiss Orthopaedic Surgeons and Swiss Society of Infectious Disease (CH)) (n=1967). The survey comprised of five demographical questions, the current treatment concepts were evaluated using a case study., Results: The overall-response-rate was 16% (12-46%). 88% of the responding physicians were male, aged 47.5 ± 10.2 years with a mean working experience of 20.1 ± 10.6 years. 54% of the surveyed physicians were either senior or chief physicians. Treatment concepts varied significantly between DGU and ÖGO/CH (p=0.02/p=0.006), no significant differences could be found between DGU and ÖGU. Generally, German and Austrian trauma surgeons favoured bursectomy (86.7%/90.9%) and immobilisation (68.3%/77.3%). Austrian orthopaedic surgeons performed fewer bursectomies (69.3%) but had the highest proportion for administering antibiotics (73.9%). Less than 50% of Swiss physicians indicated bursectomy as a treatment option., Conclusion: Overall, this survey revealed a significant heterogeneity in treatment approaches in Central Europe. Further evidence is needed to identify the best treatment concepts for traumatic lacerations of the OB and PB., (Copyright © 2012 Elsevier Ltd. All rights reserved.)

Hydrogen peroxide and nicotinamide adenine dinucleotide (NADH) may be determined amperometrically using screen-printed electrodes chemically modified with iron(III) hexacyanoosmate(II) (Osmium purple) in flow injection analysis (FIA). The determination is based on the exploitation of catalytic currents resulting from the oxidation/reduction of the modifier. The performance of the sensor was characterized and optimized by controlling several operational parameters (applied potential, pH and flow rate of the phosphate buffer). Comparison has been made with analogous complexes of ruthenium (Ruthenium purple) and iron (Prussian blue). Taking into account the sensitivity and stability of corresponding sensors, the best results were obtained with the use of Osmium purple. The sensor exhibited a linear increase of the amperometric signal with the concentration of hydrogen peroxide in the range of 0.1-100 mg L(-1) with a detection limit (evaluated as 3sigma) of 0.024 mg L(-1) with a R.S.D. 1.5% for 10 mg L(-1) H2O2 under optimized flow rate of 0.4 mL min(-1) in 0.1M phosphate buffer carrier (pH 6) and a working potential of +0.15 V versus Ag/AgCl. Afterwards, a biological recognition element--either glucose oxidase or ethanol dehydrogenase--was incorporated to achieve a sensor facilitating the determination of glucose or ethanol, respectively. The glucose sensor gave linearity between current and concentration in the range from 1 to 250 mg L(-1) with a R.S.D. 2.4% for 100 mg L(-1) glucose, detection limit 0.02 mg L(-1) (3sigma) and retained its original activity after 3 weeks when stored at 6 degrees C. Optimal parameters in the determination of ethanol were selected as: applied potential +0.45 V versus Ag/AgCl, flow rate 0.2 mL min(-1) in 0.1 M phosphate buffer carrier (pH 7). Different structural designs of the ethanol sensor were tested and linearity obtained was up to 1000 mg L(-1) with a maximum R.S.D. of 5.1%. Applications in food analysis were also examined.

A chemiluminescence one-shot sensor for hydrogen peroxide is described. It is prepared by immobilization of cobalt chloride and sodium lauryl sulphate in hydroxyethyl cellulose matrix cast on a microscope cover glass. Luminol, sodium phosphate and the sample are mixed before use and applied on the membrane by a micropipette. The calibration graph is linear in the range 20-1600mug/L, and the detection limit of the method (3sigma) is 9mug/L. A relative standard deviation of 4.5% was obtained for 100mug/L H(2)O(2) (n=11). The sensor has been applied successfully to the determination of hydrogen peroxide in rainwater.

A screen-printed amperometric biosensor based on carbon ink double bulk-modified with MnO(2) as a mediator and glucose oxidase as a biocomponent was investigated for its ability to serve as a detector for bonded glucose in different compounds, such as cellobiose, saccharose, (-)-4-nitrophenyl-beta-d-glucopyranoside, as well as in beer samples by flow-injection analysis (FIA). The biosensor could be operated under physiological conditions (0.1M phosphate buffer, pH 7.5) and exhibited good reproducibility and stability. Bonded glucose was released with glucosidase in solution, and the free glucose was detected with the modified screen-printed electrode (SPE). The release of glucose by the aid of glucosidase from cellobiose, saccharose and (-)-4-nitrophenyl-beta-d-glucopyranoside in solution showed that stoichiometric quantities of free glucose could be monitored in all three cases. The linear range of the amperometric response of the biosensor in the FIA-mode flow rate 0.2mLmin(-1), injection volume 0.25mL, operation potential 0.48V versus Ag/AgCl) extends from 11 to 13,900mumolL(-1) glucose in free form. The limit of detection (3sigma) is 1mumolL(-1) glucose. A concentration of 100mumolL(-1) yields a relative standard deviation of approximately 7% with five injections. These values correspond to the same concentrations of bonded glucose supposed that it is liberated quantitatively (incubation for 2h with glucosidase). Bonded glucose could be determined in beer samples using the same assay. The results corresponded very well with the reference procedure.

An overview is presented which summarizes our accomplishment in the development of sensors and biosensors based on heterogenous carbon electrodes modified with manganese dioxide. Brief account of each sensor and biosensor has been given and example of real sample applications provided where appropriate.

A new stripping method for the determination of arsenic in water samples with a gold film-plated carbon paste electrode has been developed for the use in constant current stripping analysis (CCSA). In the novelized procedure, differentiation between As(III) and chemically pre-reduced As(V), the effect of Cu(II) on the response of arsenic, and the stability of sample solutions were studied in detail. Compared to the voltammetric approach, the method utilizing CCSA offers a more rapid procedure with improved analytical characteristics such as reproducibility, selectivity over the Cu(II) ions, or lower detection limit (3 ppb for As(III) and 0.5 ppb for As(V), respectively). The possibilities of the optimized method are demonstrated by determinations of As(III), As(V), and total arsenic in samples of polluted river water.

A method is described for the voltammetric determination of titanium(IV) using a carbon paste electrode modified in situ with cetyltrimethylammonium bromide. The cationic micellar surfactant adsorbs onto the electrode particularly at negative potentials, simultaneously preconcentrating titanium(IV) as the oxalate complex with reduction to titanium(III). Anodic stripping voltammetry exploiting reoxidation can be used for the determination of trace levels of titanium(IV). Linearity between current and concentration exists between 5 and 160 mug l(-1) Ti(IV) (preconcentration time 2 min). The limit of detection (calculated as 3sigma) is 0.1 mug l(-1), with a preconcentration time of 10 min.

Strip-type, preconcentrating/voltammetric sensors, prepared by incorporating a cation-exchange resin within screen-printed carbon inks, are described. Such single-use strips combine the efficient electrostatic accumulation of heavy metals with the use of "mercury-free" surfaces. The uptake of copper(II) from dilute solutions (under open circuit conditions) is followed by voltammetric measurements in a separate blank solution. Various experimental variables have been optimized to yield low detection limits (e.g. 0.5 mug 1(-1) with 10 min accumulation) and good reproducibility (relative standard deviation, 2%). The applicability to assays of drinking water is demonstrated.

Carbon paste electrodes, preanodized in alkaline medium at 1.4 V vs SCE for a short period of time, exhibit a great shift of the oxidation potential of uric acid in cathodic direction and a marked enhancement of its current response, compared to unpretreated electrodes. These effects are dependent on the preanodization potential and the time imposed on the electrodes as well as on the alkalinity of the supporting electrolyte. The enhanced voltammetric response can be used to determine uric acid in the concentration range of 5.0-4.0 x 10(4) mug/1 (3.0 x 10(-8)-2.4 x 10(-4)M) with a detection limit (3sigma) of 2.0 mug/1 (1.2 x 10(-8)M). Ascorbic acid in less than 30-fold excess does not interfere. For multiple determinations (5 runs), the relative standard deviation is 2.1% at a concentration of 1 mg/1 uric acid. The proposed procedure can be used to determine uric acid in human urine and serum without any preliminary treatment of the samples in an accurate, rapid and simple way.

Cadmium and lead were determined in the parts of a filter cigarette after fractional smoking. The partitioning of these elements into the main smoke stream, consisting of particulates and gases, also into the side stream, the ash and the butt was determined. Approximately 70% of the lead mobilized by the smoking process was found in the ash; about 50% of the cadmium was transferred into the side stream. The overall trend shows an increase in the amount of the metals in the main stream as the number of puffs is increased. A model for the behavior of the main stream components within the cigarette was developed and showed a high analogy with the Lambert-Beer law describing the absorption of light.

A voltammetric method is presented for the determination of nitrite by use of a carbon-paste electrode chemically modified with an anion-exchanger. Because it is possible to accumulate nitrite on the electrode surface, trace nitrite concentrations down to 1 ng/ml can be determined.