ライフサイエンスコーパス: voltammetric

1 CO2 to methanol and formate, based on cyclic voltammetric, (13)C NMR, IR, and GC analyses.

2 Spectroscopic and voltammetric analyses performed within this work suggest

3 Voltammetric analyses showed that Hb(A1c) binding decrea

4 examined by UV-vis spectroscopic and cyclic voltammetric analyses, while the supramolecular interact

5 dex, DPPH, FRAP), HPLC (phloroglucinolysis), voltammetric analysis (Linear Sweep Voltammetry, LSV).

6 ive to traditional E-AB sensors that rely on voltammetric analysis and a potentiostat, opening up the

7 e did not show oxygen interference in cyclic voltammetric analysis and distinct catalytic current wit

8 ents using the flow system platform includes voltammetric analysis of organometallic compounds and qu

9 The dielectric voltammetric analysis was carried out from 0 V to 2 V.

10 Using differential pulse voltammetric analysis, a detection limit of 100 pM with

11 ificant advances in experiment and theory of voltammetric analysis, reliable recovery of the paramete

12 l response of the AQ label using square-wave voltammetric analysis.

13 and acetone has shown to be appropriate for voltammetric analysis.

14 resh samples were analysed with conventional voltammetric analyzer, after dissolution of the samples

15 Voltammetric and amperometric studies showed that: (i) A

16 troreduction of H2O2 was described by cyclic voltammetric and amperometric techniques.

17 Voltammetric and confocal microscopy studies showed the

18 Voltammetric and ECL analyses evidenced that the rutheni

19 performance of this device was evaluated by voltammetric and flow injection analyses of oxygen which

20 In this sense, voltammetric and photoluminescence measurements were con

21 Voltammetric and pulse techniques confirmed the redox be

22 Both voltammetric and SECM responses of the prepared nanoelec

23 Complementary voltammetric and spectroscopic experiments show that the

24 Combined cyclic voltammetric and surface enhanced spectroscopic investig

25 Experimentally, both voltammetric and thermodynamic selectivity coefficients

26 In this work, we report on a novel voltammetric approach based on a thin polymeric membrane

27 Finally, it seems that the present voltammetric approach could find its application in food

28 In this work, a simple and label-free voltammetric aptasensor for the detection of OPN, using

29 The resulting voltammetric aptasensor was used to detect OPN in standa

30 is specific signature further applied in the voltammetric assay of CFX in pharmaceutical formulation

31 etric cell for simultaneous anodic stripping voltammetric (ASV) determination of Pb(II) and Cd(II) at

32 hly hydrogenated to ensure that a reversible voltammetric behavior is obtained for Fe(CN)6](3-/4-); a

33 In this Article, the voltammetric behavior of 25B NBOMe and 25I NBOMe were in

34 The cathodic voltammetric behavior of all the macrocyclic compounds c

35 E provided a synergistic augmentation on the voltammetric behavior of electrochemical oxidation of ad

36 The cathodic voltammetric behavior of pillar[5]quinone was investigat

37 Furthermore, the cyclic voltammetric behavior of Ses and the effects of scan rat

38 To address the lack of knowledge of the voltammetric behavior of the cephalosporin antibiotics,

39 The electrochemical cyclic voltammetric behavior was characteristic of bulk Pt in b

40 6](3-/4-) redox system presents a reversible voltammetric behavior, whereas the oxidation overpotenti

41 The present paper describes the voltammetric behaviour and the quantitative determinatio

42 sensitive acetylcholinesterase (AChE) cyclic voltammetric biosensor based on zinc oxide (ZnO) nanocub

43 The aptamer was then integrated in a voltammetric biosensor utilizing graphene-modified scree

44 potentiometric, impedimetric, amperometric, voltammetric biosensors for the detection of different b

45 The development of a voltammetric boron doped diamond (BDD) pH sensor is desc

46 er, and they are brought in contact with the voltammetric cell for simultaneous anodic stripping volt

47 trically on either side of a three-electrode voltammetric cell with a bismuth citrate-loaded graphite

48 approaches the reversible limit, because the voltammetric characteristics become insensitive to elect

49 er coefficient, alpha) are irrelevant in the voltammetric characterization of a reversible reaction,

50 d pH > 13 strongly enhanced the precatalytic voltammetric charge of the Ni-Fe oxyhydroxide redox peak

51 The first voltammetric charging-discharging cycle has an electrode

52 and pulse, differential forward and backward voltammetric components can be composed, which is a uniq

53 ntified by monitoring the differential pulse voltammetric current as a function of the adsorbed DNA.

54 E films displayed redox activity depicted by voltammetric current peaks near -0.4 V.

55 The observed voltammetric current plateau, even for a single atom, wh

56 The stripping voltammetric current response to the divalent ion is enh

57 underlying electrode surface, resulting in a voltammetric current response with less than <1.5% RSD v

58 fined (but kinetically limited) steady-state voltammetric current responses for the cysteine-cystine

59 y was achieved by monitoring the decrease in voltammetric current signals of a redox probe taken in t

60 t electrode is indicated by a sudden drop in voltammetric current, a consequence of restricted mass t

61 The voltammetric curves of the prepared fullerenylstyrenes w

62 Cyclic voltammetric (CV) analysis indicated that modification p

63 detectable in 10 s by multicomponent cyclic voltammetric (CV) analysis on unmodified glassy carbon u

64 initially subjected to long-term consecutive voltammetric cycling, was also investigated by cyclic vo

65 er kinetic and thermodynamic parameters from voltammetric data and were able to show that the techniq

66 e, is an invaluable tool for the analysis of voltammetric data collected in vivo with acutely implant

67 nitiator phenyliodine(III) diacetate (PIDA), voltammetric data demonstrate that the enhanced reactivi

68 An examination of the voltammetric data for water oxidation in borate buffered

69 This study addresses these approaches using voltammetric data from three different experiments in fr

70 N) used in the BioET system to interpret the voltammetric data was able to provide a correct predicti

71 Cyclic voltammetric data, and ultraviolet photoelectron spectro

72 le subtraction of the drift component to the voltammetric data.

73 Cyclic voltammetric deposition of o-phenylenediamine (o-PD) fil

74 ne for magnetic collection and the other for voltammetric detection - and their incorporation onto a

75 The implementation of conductive MOFs in voltammetric detection holds promise for further develop

76 The voltammetric detection of less than 1 ppm of ammonia gas

77 that offers rapid and selective square-wave voltammetric detection of OP vapor threats and wireless

78 rticular, the electrode was employed for the voltammetric detection of pH and hypochlorite (OCl(-)) i

79 The square-wave voltammetric detection of phosphomolybdate was performed

80 drop-casted film electrodes that facilitate voltammetric detection of redox active neurochemicals in

81 In this work, the ion-transfer voltammetric detection of the protonated beta-blocker pr

82 dies of contaminated soils with miniaturized voltammetric detection, (iii) online phospholipid remova

83 functionality and stability evaluation using voltammetric detection.

84 phite paste electrode (GPE) for simultaneous voltammetric determination of 4-Amino Phenol (AP), Pheno

85 ial design, the biosensor was applied to the voltammetric determination of chlorogenic acid (CGA) mea

86 crofabricated for the in situ ultrasensitive voltammetric determination of DNA mutation in a microwel

87 thin a carbon paste electrode for the cyclic voltammetric determination of famciclovir (FCV).

88 The successful voltammetric determination of hemoglobin is achieved in

89 d method has been successfully tested in the voltammetric determination of hydroquinone and catechol

90 rous silica/multiwalled carbon nanotubes for voltammetric determination of the fungicide carbendazim

91 ctively) were successfully used to fabricate voltammetric diagnostic assay via immobilization onto ch

92 with differential pulse adsorptive stripping voltammetric (DPAdSV) techniques for preconcentration an

93 has been studied by both differential pulse voltammetric (DPV) as well as impedimetric techniques.

94 ough measuring changes in differential pulse voltammetric (DPV) peak current of [Fe(CN)6](3-/4-) redo

95 relationship between the differential pulse voltammetric (DPV) stripping signal of silver and the lo

96 The RuNPs/GC based differential pulse voltammetric (DPV) technique can determine the concentra

97 Differential pulse voltammetric (DPV) technique, was used for rapid and sen

98 d electrochemically using Differential Pulse Voltammetric (DPV) technique.

99 ion of the code to support the processing of voltammetric (e.g., square-wave and cyclic) and chronoam

100 heavy metal catalysis, giving rise to useful voltammetric electroanalytical signatures in model aqueo

101 e classified and characterized by applying a voltammetric electronic tongue (VE-tongue) coupled to an

102 Fast, simple in use and highly effective voltammetric enantiosensor dedicated for determination o

103 The demonstrated voltammetric enantiosensors are characterized by the low

104 havior and were successfully applied for the voltammetric evaluation of the nanochannels (20 nm pore

105 mprehensive response mechanisms based on the voltammetric exchange and transfer of millimolar multiio

106 By contrast, the voltammetric exchange of calcium ion (nI = 3) with lithi

107 oxidative scan on the time scale of a cyclic voltammetric experiment.

108 f the parameters analyzed using as input the voltammetric experimental data (i.e. r>0.9).

109 discuss the implications of our findings for voltammetric experiments more generally.

110 e been fitted to an extensive series of a.c. voltammetric experiments undertaken at macrodisk glassy

111 Voltammetric experiments were carried out from 0.0 to -1

112 Voltammetric experiments were carried out to measure the

113 tal noise and inherent system variability in voltammetric experiments.

114 In comparison to adsorption, voltammetric extraction of protamine requires approximat

115 The voltammetric features of electrochemical drift are varie

116 Principal component analysis of the voltammetric fingerprint of brewed coffees revealed that

117 gnal isolation from in vivo fast-scan cyclic voltammetric (FSCV) data due to its superior noise remov

118 bin in the blood samples determined by using voltammetric/gravimetric detection is in perfect agreeme

119 our knowledge, this is the first report of a voltammetric immunosensor capable of both diagnosing and

120 Herein we report the first serum insulin voltammetric immunosensor for diagnosis of type 1 and ty

121 Here, we developed a voltammetric immunosensor for the sensitive detection of

122 t have been used for this purpose, including voltammetric, impedimetric, capacititive, and potentiome

123 thus causing a change in redox current upon voltammetric interrogation.

124 The voltammetric investigations were performed with three-el

125 excess amount of a target ion to facilitate voltammetric ion transfer across the membrane/water inte

126 With a new voltammetric ion-exchange mechanism, the primary ion is

127 The voltammetric label is a hollow polyelectrolyte shell con

128 demonstrated on several examples, including voltammetric mapping of electrocatalytic reactions on el

129 spot boron doped diamond (BDD) electrode for voltammetric measurement of both pH and analyte concentr

130 ng electrochemical microscopy (SECM) enables voltammetric measurement of ultrafast electron-transfer

131 result, the method enables interference free voltammetric measurements of the electro reduction of th

132 Cyclic voltammetric measurements showed that TCNQ and GO trigge

133 Dopamine was detected by voltammetric measurements, displaying a 3.5 x 10(-5) mol

134 In this work, a square-wave voltammetric method based on sulphite electrochemical re

135 presents a sensitive, selective and low-cost voltammetric method for the determination of caffeine us

136 We propose here a novel voltammetric method for the determination of platinum at

137 d large-amplitude alternating current (FTAC) voltammetric method that is made up of two sine waves ha

138 A simple and sensitive voltammetric method using edge plane pyrolytic graphite

139 uM and 1.0muM respectively using square wave voltammetric method.

140 hemistry of bisphenol A (BPA) was studied by voltammetric methods at a surface of carbon paste electr

141 cales, using complementary microdialysis and voltammetric methods during adaptive decision-making.

142 Cost effective, simple and accurate two voltammetric methods for determination of boron in hazel

143 interrogation of these sensors has relied on voltammetric methods, such as square-wave voltammetry, w

144 spectroscopy (EIS), UV-vis spectroscopy, and voltammetric methods.

145 We performed high-resolution voltammetric microsensor measurements and demonstrated l

146 phases toward mixing processes, we performed voltammetric microsensor measurements, sequential Fe ext

147 th were observed as well as the shift of the voltammetric midpeak potential.

148 formed in controlled-potential (amperometric/voltammetric) modes.

149 Voltammetric modulation of the hybrid technique consists

150 hemodynamic responses (using a novel in vivo voltammetric monitoring method, analogous to blood oxyge

151 eds of nanometer thickness) for simultaneous voltammetric multianalyte ion activity detection trigger

152 Remarkably, voltammetric Na(+) and Li(+) selectivity against calcium

153 ter interface, thereby kinetically improving voltammetric Na(+) selectivity against calcium, strontiu

154 Here, we present a voltammetric nanosensor for reliable pH assessment betwe

155 a 1:2 complex thermodynamically hampers the voltammetric observation of a 1:1 complex.

156 cal UV-vis traces consistently confirmed our voltammetric observations, evidencing both a more cathod

157 MWCNTs (CA@MWCNT) through continuous cyclic voltammetric on the surface of pencil graphite electrode

158 ot BDD electrode was found active toward the voltammetric oxidation of OCl(-), with OCl(-) showing a

159 ent linear correlation between the monitored voltammetric peak current and the ETTA concentration in

160 n an analytically useful signal allowing the voltammetric peak height to be successfully correlated w

161 The height of the voltammetric peak increased in the presence of cerulopla

162 The occurrence of the voltammetric peak is the consequence of a strong associa

163 e non-Nernstian pH shift of the step-related voltammetric peak of the Pt(553) electrode is investigat

164 and INH with an enhanced analytical signal (voltammetric peak) over that achievable at unmodified (b

165 At a potential corresponding to the first voltammetric peak, bulk electrolysis of 1-5 affords the

166 ut at the reduction potential of their first voltammetric peak, conducted to electrogenerated phenacy

167 titative analysis of concentration-dependent voltammetric peak-current enhancement revealed significa

168 of well-defined and nearly reversible cyclic voltammetric peaks at -0.34 and -0.45 vs. Ag/AgCl.

169 trochemical measurements showed two pairs of voltammetric peaks owing to intervalence charge transfer

170 The voltammetric peaks were due to the redox of enzyme cofac

171 The Au-SH-OC-DPCs showed a good voltammetric performance in the electrochemical detectio

172 Extremely suitable voltammetric performance was demonstrated for the electr

173 With a view to producing a quinone-based voltammetric pH electrode that can function universally

174 In this work, we describe a voltammetric pH sensor that uses a three-dimensional (3D

175 The voltammetric pH sensor utilizes GSPEs which are chemical

176 BDD electrode that were responsible for the voltammetric pH signal.

177 selectivity toward D- and L-Trp as shown in voltammetric, photoluminescence and molecular docking re

178 A voltammetric platform based on modifying glassy carbon e

179 The voltammetric platform has successfully been applied for

180 The proposed voltammetric platform offers advantages such as high sen

181 The proposed voltammetric platform, RuNPs/CNTs/GCE, highly improved t

182 rimental correlation is observed between the voltammetric potential and pH over the entire pH range o

183 This signal can be voltammetric, potentiometric, conductometric or impedime

184 The voltammetric procedure was evaluated by prescreening of

185 and validated using an adsorptive stripping voltammetric procedure.

186 latform, RuNPs/CNTs/GCE, highly improved the voltammetric process of capsaicin in comparison to the C

187 The voltammetric profile (cyclic, differential and square wa

188 The voltammetric profile of all coffee samples was quite sim

189 reversible shift of a capacitive peak in the voltammetric profile of the electrode is assigned to an

190 ctrochemical behavior (current intensity and voltammetric profile) was obtained for model analytes, s

191 pattern recognition methods, the determined voltammetric profiles were able to discriminate between

192 Here, we report the voltammetric quantification of electrostatic ion enrichm

193 with cocaine self-administration and ex vivo voltammetric recording of dopamine signaling in the core

194 d an appetitive Pavlovian discrimination and voltammetric recordings of real-time DA release were tak

195 is suitable for performing amperometric and voltammetric recordings with high sensitivity and tempor

196 The voltammetric response for nano- to micrometer-sized elec

197 By observing a cyclic voltammetric response from the ss-HSDNA/rGOae electrode

198 ntial window" within which the target drug's voltammetric response is dominant and interference is el

199 The voltammetric response of a UTLC was found to be largely

200 It is shown that analysis of the voltammetric response of an outer sphere redox couple ca

201 It is based on the record of the voltammetric response of antioxidant compounds when glas

202 study the effects of pH and scan rate on the voltammetric response of caffeine and paracetamol.

203 ement simulations quantitatively capture the voltammetric response of coupled electron and phase tran

204 intermediate (confirmed by investigating the voltammetric response of ICl and I2 under these conditio

205 time, accumulation potential and time on the voltammetric response of MFA were investigated.

206 ct of various experimental parameters on the voltammetric response of nitrite was investigated.

207 Nernstian pathway over a wide pH range, the voltammetric response of strongly electronically coupled

208 The voltammetric response of the electrode is not compromise

209 The voltammetric response of these systems shows peculiar de

210 The bipolar nature of the voltammetric response offers an effective way of mass tr

211 . 1 nM concentrations, and the unprecedented voltammetric response to 100 pM dopamine was obtained wi

212 heights while bare and Pc/GCE had almost no voltammetric response to 2 muM physostigmine in PBS at a

213 The effect of foreign species on the voltammetric response was also evaluated.

214 The anodic voltammetric response, corresponding to the catalytic AT

215 resulting in electrode arrays with a tunable voltammetric response.

216 nfluence of coupled chemical kinetics on the voltammetric response.

217 oducibility (4.8%) displayed by the relevant voltammetric responses confirmed that this strategy can

218 Ferricyanide voltammetric responses correlate with the increased perm

219 cess is succeeded by proton transfer and the voltammetric responses depend on two dimensionless param

220 idization with its complementary strand, the voltammetric responses enable corroborating the linear r

221 tuted dihomooxacalix[4]arene bidentate urea, voltammetric responses evolve from diffusion-controlled

222 ects and distorted/buried by the interfering voltammetric responses of endogenous electroactive speci

223 e was achieved by monitoring the decrease of voltammetric responses of H2O2 peak current.

224 The cyclic voltammetric responses of individual palladium-coated ca

225 Voltammetric responses of the array of sensors demonstra

226 Characteristic voltammetric responses recorded for such compounds, incl

227 It is found that SCs exhibit voltammetric responses that can be used for their detect

228 Under the optimized circumstance best voltammetric responses were produced by A-MWCNT/Hyalu/l-

229 model the effects of different parameters on voltammetric responses.

230 cycle can be elucidated on the basis of the voltammetric responses.

231 The obtained voltammetric results confirmed the good electrochemical

232 onal, important deviations are found between voltammetric results from wines.

233 Additionally, voltammetric results were complemented with electrochemi

234 y and scanning electron microscopy while the voltammetric results were confirmed by surface plasmon r

235 ber of experimental variables, including the voltammetric scan rate and concentration of redox specie

236 n solvent viscosity, electrode geometry, and voltammetric scan rate.

237 At slow cyclic voltammetric scan rates (<1000 mV s(-1)) oxidation of th

238 electrochemical drift to the subsequent full voltammetric scan using partial-least-squares regression

239 les at the same location and within a single voltammetric scan.

240 triangular sweep followed by a conventional voltammetric scan.

241 Voltammetric scanning electrochemical cell microscopy (S

242 nection to enzymatic flow detector and rapid voltammetric scanning, respectively.

243 films-synthesized by traditional sequential voltammetric scanning-by using spectroelectrochemistry,

244 or as well as its stability against repeated voltammetric scans and against deployment in and reuse f

245 Square-wave voltammetric scans of 94 different clinical P. aeruginos

246 Field-deployable voltammetric screening coupled with complementary labora

247 The results highlight the flexibility of voltammetric SECCM for electrochemical imaging and prese

248 luated quantitatively by newly introducing a voltammetric selectivity coefficient in addition to a th

249 The kinetic improvement of voltammetric selectivity is evaluated quantitatively by

250 Here, we report that the voltammetric selectivity of thin ionophore-based polymer

251 The utility of 2D MOFs in voltammetric sensing is measured by the detection of asc

252 piperine in black pepper is reported using a voltammetric sensor based on a glassy carbon (GC) electr

253 Here, we devise a wearable voltammetric sensor development strategy-centering on en

254 nine and dasatinib is facilitated as a novel voltammetric sensor.

255 ained electrode (G/My-SWCNT/Nafion) showed a voltammetric signal due to a one-step redox reaction of

256 ested with the reduced 7ESTAC01, showing the voltammetric signal of guanine and adenine, increase in

257 rane exhibited a significant sodium transfer voltammetric signal whereas a thicker film (180 nm) did

258 with GSR shows the significant variations in voltammetric signals and the presence or absence of GSR-

259 s in the array show highly consistent cyclic voltammetric signals in Au surface cleaning experiments

260 with aqueous acetate buffer, characteristic voltammetric signals mainly associated to the oxidation

261 By monitoring the differential voltammetric signals, the sensors enable accurate predic

262 brands of cider and ageing degrees, based on voltammetric signals, utilizing dedicated data preproces

263 A typical NKA voltammetric signature was monitored via the anodic reac

264 The voltammetric SMN carbon nanofiber-based immunosensor sho

265 Differential pulse voltammetric studies of Anti-Tnf-alpha/FNAB/PC-Au for pr

266 Cyclic voltammetric studies of catechol on the enzyme modified

267 Differential pulse voltammetric studies revealed that the fabricated electr

268 Cyclic voltammetric studies showed that the GO-PcCo/glassy carb

269 rminations of D and k(0) in glyceline DES by voltammetric studies using the Nicholson approach is pro

270 Voltammetric studies with dissolved and surface-confined

271 ized by NMR, ESI-MS, UV-vis, ITC, and cyclic voltammetric studies.

272 ters of interest in dynamic electrochemical (voltammetric) studies is usually undertaken via heuristi

273 proposed method for Mb detection is based on voltammetric suppression of the Br-Py signal when the im

274 subtracted from the observed current to the voltammetric sweep, removing artifacts associated with e

275 dict the nonfaradaic current response to the voltammetric sweep, the step current response is differe

276 detection of different cephalosporins in one voltammetric sweep.

277 (CP) microneedle electrodes for square wave voltammetric (SWV) detection of the fentanyl and nerve a

278 ion of Py and PLP by a square wave stripping voltammetric technique (SWSV).

279 e for quantitative characterization with any voltammetric technique and with the most common electrod

280 A new voltammetric technique designed as a hybrid between diff

281 A square wave voltammetric technique was used for the detection.

282 p and optimized Square-Wave Anodic Stripping Voltammetric technique was used.

283 Using a differential pulse voltammetric technique, arsenite is oxidized to arsenate

284 By moving to a pulsed voltammetric technique, where for each potential step pr

285 y of their redox behavior by means of pulsed voltammetric techniques and small-scale electrolysis com

286 The application of voltammetric techniques to the study of chemical speciat

287 eady considered as one of the most sensitive voltammetric techniques, and a high frequency alternatin

288 s alternative to more common thin-film-based voltammetric techniques, potentiometric titration offers

289 idation potential of polyphenolic compounds, voltammetric techniques, such as cyclic voltammetry (CV)

290 square wave and differential pulse stripping voltammetric techniques.

291 ly characterized by common spectroscopic and voltammetric techniques.

292 Cyclic voltammetric tests were performed in order to evaluate t

293 s the credibility of transient d.c. and a.c. voltammetric theory-experiment comparisons for recovery

294 Voltammetric thin layer ( approximately 200 nm) ionophor

295 tions which may not be at equilibrium on the voltammetric time scale.

296 s also found to be important and affects the voltammetric tip response in a nanogap geometry.

297 tions of differential pulse anodic stripping voltammetric transduction, a linear relationship between

298 We characterize the "Jackson" voltammetric waveform for FSCAV and show highly stable,

299 First, we have implemented voltammetric waveforms in pairs that consist of a smalle

300 g distinct Gaussian peak shaped ion transfer voltammetric waves that are analyzed in terms of their p