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 Voltammetric analyses showed that Hb(A1c) binding decrea

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

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

5 Zn(+2) in water is carried out by stripping voltammetric analysis using RGO/Bi nanocomposite as an e

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

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

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

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

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

11 Voltammetric and confocal microscopy studies showed the

12 Voltammetric and ECL analyses evidenced that the rutheni

13 livery of drugs with minimum consumption for voltammetric and electrophysiological studies of a varie

14 In this sense, voltammetric and photoluminescence measurements were con

15 Experimentally, both voltammetric and thermodynamic selectivity coefficients

16 coverage up to 8 x 10(13) molecules/cm(2) by voltammetric and XPS analyses.

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

18 Importantly, this stripping voltammetric approach enables the absolute determination

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

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

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

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

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

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

25 Finally, we find that our model predicts the voltammetric behavior of a redox-active methylene blue t

26 The cathodic voltammetric behavior of all the macrocyclic compounds c

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

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

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

30 6](3-/4-) redox system presents a reversible voltammetric behavior, whereas the oxidation overpotenti

31 *-/2-(0) differences or other aspects of the voltammetric behavior.

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

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

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

35 multisensor system formed by nanostructured voltammetric biosensors based on phenol oxidases (tyrosi

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

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

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

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

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

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

42 The voltammetric characterization of each electrode shows cu

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

44 The first voltammetric charging-discharging cycle has an electrode

45 e "reversible" (infinitely fast) limit under voltammetric conditions have been inappropriately analyz

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

47 ed as a decrease in the amperommetric and/or voltammetric current from the solution redox species fer

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

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

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

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

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

53 enhanced differential pulse anodic stripping voltammetric current vis-a-vis the corresponding imprint

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

55 x probe and it relays on measuring catalytic voltammetric currents.

56 e size determination and the construction of voltammetric curves for individual NPs.

57 Cyclic and differential pulse voltammetric (CV and DPV) measurements and spectroelectr

58 Cyclic voltammetric (CV) analysis indicated that modification p

59 Cyclic voltammetric (CV) and Electrochemical Impedance Spectros

60 u electrodes were characterized using cyclic voltammetric (CV) and fluorescence techniques, respectiv

61 s were characterized and tested using Cyclic Voltammetric (CV) and Square Wave Voltammetry (SQW) meas

62 rochemical impedance technique (EIS), cyclic voltammetric (CV) technique and atomic force microscopic

63 ttle indication of passivation with repeated voltammetric cycling but a relatively high background si

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

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

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

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

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

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

70 Voltammetric data were parsed into slow and phasic compo

71 Cyclic voltammetric data, and ultraviolet photoelectron spectro

72 correct the detected potential shift in 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 uorooctanesulfonate allows for its stripping voltammetric detection at 50 pM in the presence of 1 mM

76 been examined as media for room temperature voltammetric detection of highly basic stilbene dianions

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

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

79 sing multiple scan rates is adaptable to the voltammetric detection of other tyrosine-containing neur

80 In comparison, the voltammetric detection of perfluoroalkanecarboxylates is

81 The square-wave voltammetric detection of phosphomolybdate was performed

82 acidic dissolution of the QDs and stripping voltammetric detection of the Cd(II) released.

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

84 functionality and stability evaluation using voltammetric detection.

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

86 NTs nanocomposite was used for the sensitive voltammetric determination of cysteamine (CA), nicotinam

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

88 rnating least-squares (MCR-ALS) was used for voltammetric determination of dopamine (DA) in the prese

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

90 The successful voltammetric determination of hemoglobin is achieved in

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

92 We report the first direct cyclic voltammetric determination of the valence and conduction

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

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

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

96 aptamer produces a strong differential pulse voltammetric (DPV) signal.

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

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

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

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

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

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

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

104 for 1b, 0.92 V for 1c), providing the first voltammetric evidence for the radical cation [Ar2S2](+).

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 ion, that is, at a constant scan rate of the voltammetric experiment.

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

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

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

111 proaches have been applied to a series of AC voltammetric experiments undertaken on the [Fe(CN)6](3-/

112 Voltammetric experiments were carried out from 0.0 to -1

113 Voltammetric experiments were carried out to measure the

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

115 ce-formed FeS has a significant influence on voltammetric Fe(II) determination, since reduction of Fe

116 Easy-to-use analytical expressions for the voltammetric features are derived for the particular cas

117 surface concentration dependence of the main voltammetric features.

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

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

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

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

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

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

124 A detailed cyclic voltammetric investigation of the reduction of moderatel

125 proposed mechanism was further supported by voltammetric investigations with an authentic sample of

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

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

128 tylthiophene)-modified gold electrode during voltammetric ion-to-electron transduction.

129 The voltammetric label is a hollow polyelectrolyte shell con

130 ine diffusion coefficients from steady-state voltammetric limiting current values, derived from micro

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

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

133 Voltammetric measurements at individual electrodes combi

134 Cyclic voltammetric measurements showed that TCNQ and GO trigge

135 imulus can then be monitored by conventional voltammetric measurements.

136 r was assessed by longtime continuous cyclic voltammetric measurements.

137 ng the electrode from a potentiostat between voltammetric measurements.

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

139 A high sensitive voltammetric method for rapid determination of thrombin

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

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

142 The reported voltammetric method is cheap, rapid and simple, and it c

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

144 Applying the proposed voltammetric method the total antioxidant capacity of th

145 is work we report on a new, rapid and simple voltammetric method to determine the total antioxidant c

146 A simple and sensitive voltammetric method was developed to determine the amoun

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

148 uld be considered as a useful tool for other voltammetric methodologies where more accurate or faster

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

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

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

152 anning electrochemical microscopy (SECM) and voltammetric methods.

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

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

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

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

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

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

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

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

161 loratory analysis is applied to classify the voltammetric patterns, confirming the capability to diff

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

163 The protein desorption voltammetric peak exhibited a 6-fold increase in the cur

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

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

166 A characteristic voltammetric peak is evidenced for all the investigated

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

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

169 the surface coverage, midpeak potential, and voltammetric peak separation for the phendione ligand, a

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

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

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

173 Each biorecognition event yields a distinct voltammetric peak, which position and size reflects the

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

175 titative differential pulse anodic stripping voltammetric peaks on the proposed sensor.

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

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

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

179 The voltammetric pH sensor utilizes GSPEs which are chemical

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

181 A voltammetric platform based on modifying glassy carbon e

182 The voltammetric platform has successfully been applied for

183 The proposed voltammetric platform offers advantages such as high sen

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

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

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

187 The voltammetric procedure was evaluated by prescreening of

188 and validated using an adsorptive stripping voltammetric procedure.

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

190 The voltammetric profile (cyclic, differential and square wa

191 The voltammetric profile of all coffee samples was quite sim

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

193 is confirmed by the appearance of sigmoidal voltammetric profile, characteristic behavior of linear

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

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

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

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

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

199 odes caused a marked drop in the square wave voltammetric reduction signal of the [Fe(CN)6](4-/3-) re

200 approach enables one to obtain the transient voltammetric response and electrocatalytic effects of si

201 The factors controlling the voltammetric response are determined by both simulation

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

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

204 ng mode, the compound yielded a well-defined voltammetric response in phosphate buffer, pH 2.5 at +1.

205 Then, the voltammetric response of a DNA-immobilized CNTPE was inv

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

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

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

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

210 te cyclic voltammetry to discuss the overall voltammetric response of closed bipolar electrodes (BPEs

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

212 significant variation in differential pulse voltammetric response of methylene blue on the probe mod

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

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

215 ing in the direct recording of the transient voltammetric response of single NPs.

216 tether, to predict and better understand the voltammetric response of surface-confined redox molecule

217 The voltammetric response of the electrode is not compromise

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

219 The voltammetric response towards six phenolic compounds dem

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

221 The anodic voltammetric response, corresponding to the catalytic AT

222 resulting in electrode arrays with a tunable voltammetric response.

223 ly that can be manipulated to offer a simple voltammetric response.

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

225 Ferricyanide voltammetric responses correlate with the increased perm

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

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

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

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

230 The cyclic voltammetric responses of individual palladium-coated ca

231 Characteristic voltammetric responses recorded for such compounds, incl

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

233 model the effects of different parameters on voltammetric responses.

234 A non-linear correlation between cyclic voltammetric results and ABTS or Folin-Ciocalteau data w

235 Additionally, voltammetric results were complemented with electrochemi

236 ow at the same substrate to substantiate the voltammetric results.

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

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

239 We find that at sufficiently slow cyclic voltammetric scan rates the electrochemical reaction beh

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

241 Voltammetric scanning electrochemical cell microscopy (S

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

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

244 erature or by coulometric analysis of linear voltammetric scans.

245 Field-deployable voltammetric screening coupled with complementary labora

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

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

248 The kinetic improvement of voltammetric selectivity is evaluated quantitatively by

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

250 ower than a previously reported dip-and-read voltammetric sensor for oxidized DNA.

251 this paper, a highly sensitive and selective voltammetric sensor for the determination of nitrite is

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

253 sensor overcomes the limitations of existing voltammetric sensors and provides a mercury-free sensing

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

255 ed electrodes were developed with a suitable voltammetric signal on which the polyphenol oxidation is

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

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

258 asis of these features, leading to increased voltammetric signals for myoglobin, hemoglobin, and cyto

259 erpretation is given for previously recorded voltammetric signals in sulfide and iron rich environmen

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

261 This method provides well-defined voltammetric signals, characteristic of the heme-ligand

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 Cyclic voltammetric studies revealed that, on the hybrid materi

268 Square wave voltammetric studies revealed the presence of an unknown

269 Cyclic voltammetric studies showed that compounds 2-7 undergo r

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

271 Cyclic voltammetric studies showed that the NiONPs/Nafion-MWCNT

272 The voltammetric studies showed that, regardless of CHIT mat

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

274 Voltammetric studies with dissolved and surface-confined

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

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

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

278 y was essentially unchanged after 400 cyclic voltammetric sweeps, suggesting long-term viability unde

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

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

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

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

283 V using differential pulse anodic stripping voltammetric technique.

284 s, using differential pulse anodic stripping voltammetric technique.

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

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

287 square wave and differential pulse stripping voltammetric techniques.

288 metry, transmission electron microscopy, and voltammetric techniques.

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

290 Voltammetric thin layer ( approximately 200 nm) ionophor

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

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

293 ic properties of this film were evaluated by voltammetric, UV-Vis spectrophotometric and gas chromato

294 These features, a too small second cyclic voltammetric wave and extra current between the two wave

295 suggests that the protonation/deprotonation voltammetric wave involves physisorbed rather than chemi

296 The quasireversible cyclic voltammetric wave observed at -0.58 V vs SCE at a Pt ele

297 sometimes appears to be a small, broad third voltammetric wave, have previously been attributed to di

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

299 We have developed and characterized a novel voltammetric waveform for the selective quantification o

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