共查询到20条相似文献,搜索用时 46 毫秒
1.
Liang Wang Jun Yue Bai Peng Fei Huang Hong Jing Wang Xiao Wei Wu Yu Qing Zhao 《Mikrochimica acta》2007,158(1-2):73-78
The electrochemical behaviors of uric acid (UA) at the penicillamine (Pen) self-assembled monolayers modified gold electrode
(Pen/Au) have been studied. The Pen/Au electrode is demonstrated to promote the electrochemical response of UA by cyclic voltammetry
(CV). The diffusion coefficient D of UA is 6.97 × 10−6 cm2 s−1. In differential pulse voltammetric (DPV) measurements, the Pen/Au electrode can separate the UA and ascorbic acid (AA) oxidation
potentials by about 120 mV and can be used for the selective determination of UA in the presence of AA. The detection limit
was 1 × 10−6 mol L−1. The modified electrode shows excellent sensitivity, good selectivity and antifouling properties. 相似文献
2.
Jahan Bakhsh Raoof Abolfazl Kiani Reza Ojani Roudabeh Valiollahi Sahar Rashid-Nadimi 《Journal of Solid State Electrochemistry》2010,14(7):1171-1176
Gold nanoparticles (GNs) could be efficiently immobilized on binary mixed self-assembled monolayers (SAMs) on a gold surface
composed of 1,6-hexanedithiol and 1-octanethiol (nano-Au/SAMs gold electrode). This GN chemically modified electrode was used
for electrochemical determination of ascorbic acid (AA) and dopamine (DA) in aqueous media. The result showed that the GN-modified
electrode could clearly resolve the oxidation peaks of AA and DA, with a peak-to-peak separation (∆E
p) of 110 mV enabling determination of AA and DA in the presence of each other. The linear analytical curves were obtained
in the ranges of 0.3–1.4 mM for AA and 0.2–1.2 mM for DA concentrations using differential pulse voltammetry. The detection
limits (3σ) were 9.0 × 10−5 M for AA and 9.0 × 10−5 M for DA. 相似文献
3.
In this paper, the silver doped poly (L-glutamic acid) modified glassy carbon electrode (PLG-Ag/GCE) was fabricated through
an electrochemical immobilization. The modified electrode was used for simultaneous determination of uric acid (UA) and ascorbic acid (AA) in 0.1 M phosphate buffer solutions (PBS). The cyclic voltammetric signals of UA and AA were well separated with a potential
difference of 396 mV in pH 3.0 phosphate buffer solution. The linear calibration curves were obtained in the concentration
range 5.00 × 10−7–1.00 × 10−4 M for UA and 8.00 × 10-6–5.00 × 10−3 M for AA with the detection limits of 3 × 10−7 M and 4 × 10−6 M, respectively. The relative standard deviations were 1.3 and 1.0% for the determinations of UA and AA for 20 continuous
measurements. The signal was highly stable and reproducible. This method was successfully applied to the determination of
UA in human urine samples. 相似文献
4.
A poly(caffeic acid) thin film was deposited on the surface of a glassy carbon electrode by potentiostatic technique in an
aqueous solution containing caffeic acid. The poly(caffeic acid)-modified electrode was used for the determination of ascorbic
acid (AA), dopamine (DA), and their mixture by cyclic voltammetry. This modified electrode exhibited a potent and persistent
electron-mediating behavior followed by well-separated oxidation peaks toward AA and DA at a scan rate of 10 mV s−1 with a potential difference of 135 mV, which was large enough to determine AA and DA individually and simultaneously. The
catalytic peak current obtained was linearly dependent on the AA and DA concentrations in the range of 2.0 × 10−5−1.2 × 10−3 and 1.0 × 10−6−4.0 × 10−5 mol L−1 in 0.15 mol L−1 phosphate buffer (pH 6.64). The detection limits for AA and DA were 9.0 × 10−6 and 4.0 × 10−7 mol L−1, respectively. The modified electrode shows good sensitivity, selectivity, and stability and has been applied to the determination
of DA and AA in real samples with satisfactory results. 相似文献
5.
Submerged fermentation experiments were carried out to study the stimulating effects of the surfactant Span 20 on the growth
of Aspergillus niger XP mutant and oxalic acid production from the post-refining fatty acids. Span 20 concentration of 0.75 g dm−3 was found to be the most suitable for oxalic acid production from fatty acids. Using this dose and a fermentation medium
containing 30 g dm−3 of post-refining fatty acids, the oxalic acid production, oxalate yield, and overall oxalate productivity were the highest.
Presented at the 33rd International Conference of the Slovak Society of Chemical Engineering, Tatranské Matliare, 22–26 May
2006. 相似文献
6.
Lei Zhang 《Mikrochimica acta》2008,161(1-2):191-200
A covalently modified glassy carbon electrode with cysteine has been fabricated via an electrochemical oxidation procedure
and was applied to induce the electrochemical differentiation between dopamine (DA) and ascorbic acid (AA). Based on the electrostatic
interactions between the negatively charged groups on the electrode surface and DA and AA, the modified electrode enhanced
the oxidation of DA, reducing the overpotential by 180 mV, and hindered the oxidation of AA, shifting the oxidation potential
positively by 170 mV. The peak current for DA at the modified electrode was greatly enhanced and that for AA was significantly
decreased, which allows the determination of DA in the presence of AA. The differential pulse peak current was linearly dependent
on DA concentration over the range of 5 × 10−6–2 × 10−4 mol L−1. The detection limit was 1.8 × 10−6 mol L−1. The selectivity and sensitivity for dopamine is due to charge discrimination and analyte accumulation. The modified electrode
has been applied to the determination of DA in the presence of AA.
Correspondence: L. Zhang, Department of Chemistry, College of Life and Environmental Science, Shanghai Normal University,
Guilin Rd 100, Shanghai 200234, P.R. China 相似文献
7.
A method for the simultaneous quantification of eicosapentaenoic acid (EPA), docosahexaenoic acid (DHA) and arachidonic acid (AA) in human plasma by HPLC–tandem mass spectrometry (HPLC‐MS/MS) was developed and validated. Free and esterified forms of fatty acids were hydrolysed from plasma samples in the presence of an internal standard and subjected to liquid–liquid extraction. The chromatographic run time was 3.5 min per sample. The assay was linear from 0.5 to 300 mg/L (r2 > 0.997, n = 18). Based on matrix addition, accuracy deviation was <15%, except for AA at 10 mg/L (30–90%), whereas precision was <8% for all fatty acids studied. The method was applied to the measurement of these omega‐3 fatty acids in a fish oil supplement study with healthy volunteers. Healthy males (n = 4) were administered a supplement containing 465 mg EPA and 375 mg DHA per capsule (Omacor®). A dose of two capsules was given daily over a 4 week period. Pre‐treatment concentrations varied between subjects for EPA (17–68 mg/L), DHA (36–63 mg/L) and AA (121–248 mg/L). During the dosing period EPA increased 460–480% from the baseline concentration, while DHA increased 150–160%. The EPA–AA ratio increased from 0.07–0.56 to 0.3–3.1 after 4 weeks of dosing. In conclusion, the method described could be suitable for monitoring EPA, DHA and AA in clinical studies that may aid in achieving optimal concentrations of these fatty acids in patients who could be at risk of sudden cardiac death. Copyright © 2010 John Wiley & Sons, Ltd. 相似文献
8.
A glassy carbon electrode was modified with electropolymerized film of diphenylamine sulfonic acid (DPASA). Electropolymerization was performed by cyclic voltammetry in 0.1 M KCl solution. The modified electrode showed an excellent
electrocatalytic effect towards oxidation of dopamine (DA) and ascorbic acid (AA). Electrostatic interaction between the negatively charged poly(DPASA) film and either cationic DA species or anionic AA
species favorably contributed to the redox response of DA and AA. Anodic peaks of DA and AA in their mixture were well separated
by ca 168 and −11.8 mV. The proposed modified electrode was utilized for selective determination of dopamine in the concentration
range of 5.0 × 10t7–2.0 × 10−5 M in the presence of high concentration of ascorbic acid. Detection limit was 6.5 × 10−9 M. 相似文献
9.
Simultaneous determination of arbutin (ART) and l-ascorbic acid (AA) by HPLC with chemiluminescence detection is proposed for the first time. This method is based on the CL
reaction of acidic potassium permanganate with ART and AA in the presence of formaldehyde as enhancer. The separation was
performed on a C18 column with a 90:10 (v/v) mixture of 0.02 M phosphate buffer and methanol as mobile phase. The effects of several conditions on HPLC resolution and
CL emission were studied systematically. The linear ranges were 0.5–50 and 1–200 μg mL−1 for ART and AA, respectively. The detection limits were 0.2 and 0.3 μg mL−1, respectively. The method was successfully applied to the determination of ART and AA in whitening cosmetics. 相似文献
10.
Hadi Beitollahi Mohammad Mazloum Ardakani Hossein Naeimi Bahram Ganjipour 《Journal of Solid State Electrochemistry》2009,13(3):353-363
The preparation and electrochemical characterization of a carbon nanotube paste electrode modified with 2,2′-[1,2-ethanediylbis
(nitriloethylidyne)]-bis-hydroquinone, referred to as EBNBH, was investigated. The EBNBH carbon nanotube paste electrode (EBNBHCNPE)
displayed one pair of reversible peaks at E
pa = 0.18 V and E
pc = 0.115 V vs Ag/AgCl. Half wave potential (E
1/2) and ΔE
p were 0.148 and 0.065 V vs Ag/AgCl, respectively. The electrocatalytic oxidation of ascorbic acid (AA) has been studied on
EBNBHCNPE, using cyclic voltammetry, differential pulse voltammetry and chronoamperometry techniques. It has been shown that
the oxidation of AA occurs at a potential where oxidation is not observed at the unmodified carbon paste electrode. The heterogeneous
rate constant for oxidation of AA at the EBNBHCNPE was also determined and found to be about 1.07 × 10−3 cm s−1. The diffusion coefficient of AA was also estimated as 5.66 × 10−6 cm2 s−1 for the experimental conditions, using chronoamperometry. Also, this modified electrode presented the property of electrocatalysing
the oxidation of AA and uric acid (UA) at 0.18 and 0.35 V vs Ag/AgCl, respectively. The separations of anodic peak potentials
of AA and UA reached 0.17 V. Using differential pulse voltammetry, the calibration curves for AA and UA were obtained over
the range of 0.1–800 μM and 20–700 μM, respectively. With good selectivity and sensitivity, the present method provides a
simple method for selective detection of AA and UA in biological samples. 相似文献
11.
Saeed Shahrokhian Hamid Reza Zare-Mehrjardi Habibollah Khajehsharifi 《Journal of Solid State Electrochemistry》2009,13(10):1567-1575
A chemically modified carbon-paste electrode (CPE) is prepared by incorporating congo red (CR) immobilized on multi-walled
carbon nanotube (MWCNT). The results show that CR is effectively immobilized on the surface of MWCNT under the ultrasonic
agitation in aqueous solution and further incorporating the nafion. The prepared electrode, due to the electrostatic repulsions
between the CR and ascorbate anion, is capable to mask the response of the ascorbic acid (AA) completely and provide an effective
method for the detection of minor amounts of uric acid (UA) in the presence of high concentrations of AA. On the other hand,
an increase in the microscopic area of the electrode by addition of MWCNT together with the electrocatalytic activity caused
to a significant enhancement in the voltammetric response to UA. Optimization of the amounts of composite modifier in the
matrix of CPE is performed by cyclic and differential pulse voltammetric measurements. The modified electrode shows a linear
response to UA in the range of 1.0 × 10−7–1.0 × 10−4 M with a detection limit of 1.0 × 10−8 M. The electrode exhibits excellent accuracies for the determination of UA in the presence of high concentrations of AA (a
recovery of 97.6%). The response of the electrode toward sulfhydryl compounds such as cysteine, penicillamine, and glutathione
is not considerable. This reveals a good selectivity for the voltammetric response toward UA. The effective electrocatalytic
property, ability for masking the voltammetric responses of the other biologically reducing agents, ease of preparation, and
surface regeneration by simple polishing together with high reproducibility and stability of the responses make the modified
electrode suitable for the selective and sensitive voltammetric detection of sub-micromolar amounts of UA in clinical and
pharmaceutical preparations. 相似文献
12.
Xiaomei Cao Yanhong Xu Liqiang Luo Yaping Ding Ying Zhang 《Journal of Solid State Electrochemistry》2010,14(5):829-834
A glassy carbon electrode (GCE) modified with the film composed of chitosan incorporating cetylpyridine bromide is constructed
and used to determine uric acid (UA) and ascorbic acid (AA) by differential pulse voltammetry (DPV). This modified electrode
shows efficient electrocatalytic activity and fairly selective separation for oxidation of AA and UA in mixture solution.
UA is catalyzed by this modified electrode in phosphate buffer solution (pH 4.0) with a decrease of 80 mV, while AA is catalyzed
with a decrease of 200 mV in overpotential compared to GCE, and the peak separation of oxidation between AA and UA is 260
mV, which is large enough to allow the determination of one in presence of the other. Under the optimum conditions, the anodic
peak currents (I
pa) of DPV are proportional to the concentration of UA in the range of 2.0 × 10−6 to 6.0 × 10−4 M, with the detection limit of 5.0 × 10−7 M at a signal-to-noise ratio of 3 (S/N = 3) and to that of AA in the range of 4.0 × 10−6 to 1.0 × 10−3 M, with the detection limit of 8.0 × 10−7 M (S/N = 3). 相似文献
13.
Nanostructured platinum-gold (Pt–Au) hybrid film modified glassy carbon electrode (GCE) was fabricated by electro-deposition
method in the presence of 2 × 10−4 mol l−1
l-cysteine. To examine the surface morphological analysis, the (Pt–Au) hybrid film were electrochemically deposited on transparent
semiconductor indium tin oxide (ITO) electrodes for scanning electron microscopy (SEM) and energy dispersive spectroscopy
(EDS) studies. From the SEM analysis, it was observed that the deposited nanoplatinum (250–400 nm) was formed as a cauliflower-shaped
structure with the gold nanoparticles (30–90 nm). The concentration variation of additive l-cysteine results in the formation of cauliflower-shaped platinum nanoparticles. Further, the Pt–Au hybrid film modified GCE
could be used for the detection of catecholamine neurotransmitters epinephrine (EP), norepinephrine (NEP) individually and
in the presence of ascorbic acid (AA) in pH 7 phosphate-buffered solutions (PBS). Furthermore, the proposed Pt–Au hybrid film
could be applied for the detection of epinephrine in injection solution and ascorbic acid from commercially available vitamin
C tablets. 相似文献
14.
I. I. Tverdokhlebova I. A. Ronova V. M. Men'shov N. V. Pertsova 《Russian Chemical Bulletin》1998,47(12):2348-2351
Molecular-weight parameters of new silane homo- and copolymers were analyzed. For all polymers, theM
w values are close ((6.0–8.6)·104), the curves of molecular weight distribution are unimodal, andM
w/M
n=2−2.5. Cyclic fragments or those containing the −C=C− groups make the major contribution to the polysilane chain rigidity.
Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 12, pp. 2430–2433, December, 1998. 相似文献
15.
Reza Ojani Jahan-Bakhsh Raoof Ebrahim Zarei Seyed Naser Azizi Maryam Abrishamkar 《Monatshefte für Chemie / Chemical Monthly》2012,40(8):7-12
Abstract
This paper describes microwave-assisted synthesis of a new MFI-type zeolite, Zeolite Secony Mobile (ZSM-5), its characterization by X-ray diffractometry (XRD), Fourier transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM), and its application for fabrication of a modified carbon paste electrode. This novel electrode was employed for sensitive and simultaneous determination of dopamine and uric acid at biological pH (pH 7.0). The results show that this zeolite-modified carbon paste electrode significantly improves the electron transfer rate and reduces the overpotential of dopamine and uric acid oxidation without any fouling effect due to deposition of their oxidized products. The linear analytical curves were obtained in the ranges of 9.0 × 10−6–4.9 × 10−4 and 8.0 × 10−6–9.0 × 10−4 M for dopamine and uric acid, respectively, by using differential pulse voltammetry based on oxidation of these biomolecules. The detection limits (2σ) were determined for dopamine and uric acid as 7.9 × 10−6 and 7.1 × 10−6 M, respectively. This method has been successfully employed for quantification of dopamine and uric acid in real samples. 相似文献16.
Effect of pH and ionic strength on the interaction of humic acid with aluminium oxide 总被引:4,自引:0,他引:4
E. Tombácz Á. Dobos M. Szekeres H. D. Narres E. Klumpp I. Dékány 《Colloid and polymer science》2000,278(4):337-345
The effect of pH and neutral electrolyte on the interaction between humic acid/humate and γ-AlOOH (boehmite) was investigated.
The quantitative characterization of surface charging for both partners was performed by means of potentiometric acid–base
titration. The intrinsic equilibrium constants for surface charge formation were logK
a,1
int=6.7±0.2 and logK
a,2
int = 10.6±0.2 and the point of zero charge was 8.7±0.1 for aluminium oxide. The pH-dependent solubility and the speciation of
dissolved aluminium was calculated (MINTEQA2). The fitted (FITEQL) pK values for dissociation of acidic groups of humic acid were pK
1 = 3.7±0.1 and pK
2 = 6.6±0.1 and the total acidity was 4.56 mmol g−1. The pH range for the adsorption study was limited to between pH 5 and 10, where the amount of the aluminium species in the
aqueous phase is negligible (less than 10−5 mol dm−3) and the complicating side equilibria can be neglected. Adsorption isotherms were determined at pH ∼ 5.5, ∼8.5 and ∼9.5,
where the surface of adsorbent is positive, neutral and negative, respectively, and at 0.001, 0.1, 0.25 and 0.50 mol dm−3 NaNO3. The isotherms are of the Langmuir type, except that measured at pH ∼ 5.5 in the presence of 0.25 and 0.5 mol dm−3 salt. The interaction between humic acid/humate and aluminium oxide is mainly a ligand-exchange reaction with humic macroions
with changing conformation under the influence of the charged interface. With increasing ionic strength the surface complexation
takes place with more and more compressed humic macroions. The contribution of Coulombic interaction of oppositely charged
partners is significant at acidic pH. We suppose heterocoagulation of humic acid and aluminium oxide particles at pH ∼ 5.5
and higher salt content to explain the unusual increase in the apparent amount of humic acid adsorbed.
Received: 20 July 1999 /Accepted in revised form: 20 October 1999 相似文献
17.
Jun Yue Bai Liang Wang Hong Jing Wang Peng Fei Huang Yu Qing Zhao Sheng Di Fan 《Mikrochimica acta》2006,156(3-4):321-326
The electrochemical behavior of epinephrine (EP) at a mercaptoacetic acid (MAA) self-assembled monolayer modified gold electrode
was studied. The MAA/Au electrode is demonstrated to promote the electrochemical response of epinephrine by cyclic voltammetry.
The possible reaction mechanism is also discussed. The diffusion coefficient D of EP is 6.85 × 10−6 cm2 s−1. In 0.1 mol L−1 phosphate buffer (pH 7.20), a sensitive oxidation peak was observed at 0.177 V, and the peak current is proportional to the
concentration of EP in the range of 1.0 × 10−5–2.0 × 10−4 mol L−1 and 1.0 × 10−7–1.0 × 10−6 mol L−1. The detection limit is 5 × 10−8 mol L−1. The modified electrode is highly stable and can be applied to the determination of EP in practical injection samples. The
method is simple, quick, sensitive and accurate. 相似文献
18.
Eyup Bagci 《Chemistry of Natural Compounds》2006,42(6):645-648
In this study, the fatty acid contents of some Astragalus L. (Fabaceae) species from Turkey were determined by GC and GC-MS techniques. The seed oils of Astragalus sp. (A. echinops Aucher ex. Boiss., A. subrobustos Boriss., A. jodostachys, Boiss. & Buhse., A. falcatus Lam., A. fraxinifolius DC.) contained linolenic (between 23–41.%), linoleic (23–37%), and oleic acids (8–19%) as the major components. Fatty acid
composition of the studied Astragalus taxa showed uniform fatty acid patterns. Palmitic and stearic acids were the major saturated fatty acids in the seed oils.
The amounts of unsaturated fatty acids were higher than saturated fatty acids.
Published in Khimiya Prirodnykh Soedinenii, No. 6, pp. 526–528, November–December, 2006. 相似文献
19.
Gourisankar Panda Md. Selim Rupali Pal Kalyan K. Mukherjea 《Monatshefte für Chemie / Chemical Monthly》2009,33(2):281-286
Abstract
The interaction of cobalt(II)-glutathione (CoGSH) with deoxyribonucleic acid (DNA) has been studied by UV–vis, fluorescence, circular dichroism (CD), thin-film infrared (IR), and viscometric techniques. From the UV-spectroscopic method, binding constant (K b) was determined and was found to be 2.3 × 106 M−1. In fluorimetric analysis, the quenching of fluorescence intensity of DNA bound to ethidium bromide (EB) was investigated. The Stern–Volmer quenching constant (K sv) was also estimated from this study and was found to be 2.8 × 106 M−1at 37 °C. The solution CD spectra of DNA and DNA–CoGSH indicate that in each case, DNA exists in the ‘B’ conformation and suggested an intercalative binding mode. Thin-film IR data also reveal that DNA attains the ‘B’ family of conformations after interaction with CoGSH complex. The increase in DNA viscosity in the presence of CoGSH complexes is attributed to the lengthening of DNA helix due to intercalation. 相似文献20.
Zhao J Li G Wang BM Liu W Nan TG Zhai ZX Li ZH Li QX 《Analytical and bioanalytical chemistry》2006,386(6):1735-1740
Glycyrrhizic acid (GL) is a major active compound of licorice. The specific monoclonal antibody (MAb) (designated as 8F8A8H42H7) against GL was produced with the immunogen GL–BSA conjugate. The dissociation constant (K
d) value of the MAb was approximately 9.96×10−10 M. The cross reactivity of the MAb with glycyrrhetic acid was approximately 2.6%. The conventional indirect competitive enzyme-linked
immunosorbent assay (icELISA) and simplified icELISA adapted with a modified procedure were established using the MAb. The
IC50 value and the detect range by the conventional icELISA were 1.1 ng mL−1 and 0.2–5.1 ng mL−1, respectively. The IC50 value and the detect range by the simplified icELISA were 5.3 ng mL−1 and 1.2–23.8 ng mL−1, respectively. The two icELISA formats were used to analyze GL contents in the roots of wild licorice and different parts
of cultivated licorice (Glycyrrhiza uralensis Fisch). The results obtained with the two icELISAs agreed well with those of the HPLC analysis. The correlation coefficient
was more than 0.98 between HPLC and the two icELISAs. The two icELISAs were shown to be appropriate, simple, and effective
for the quality control of raw licorice root materials. 相似文献