2011
DOI: 10.1590/s0103-50532011000900007
|View full text |Cite
|
Sign up to set email alerts
|

Determination of efavirenz in diluted alkaline electrolyte by cathodic adsorptive stripping voltammetry at the mercury film electrode

Abstract: Um método de redissolução para a determinação do agente anti-retroviral efavirenz em concentrações submicromolares e meio eletrolítico alcalino diluído é descrito. As condições experimentais ótimas encontradas são: NaOH 2,0 × 10 -3 mol L -1, potencial de acumulação −0,10 V, amplitude de pulso 50 mV e velocidade de varredura 50 mV s ). As condições mais convenientes para a medida da concentração de efavirenz na presença de ATP, DNA, diversos metais e outros antivirais foi também investigada. A utilidade do méto… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

2
14
0

Year Published

2012
2012
2023
2023

Publication Types

Select...
6
1

Relationship

1
6

Authors

Journals

citations
Cited by 9 publications
(16 citation statements)
references
References 14 publications
2
14
0
Order By: Relevance
“…Eight successive measurements (using 30 s accumulation times at -0.50 V; final potential at −1.1 V; 60 s condition times at −0.9 V; scan rate, 200 mV·s −1 and 1.0 × 10 −3 mol·L −1 of NaOH as supporting electrolyte ) yielded a mean peak current of 8453 ± 97 nA and a range of 8312 -8625 nA. Such precision compares favorably with that reported for other compounds measured by adsorptive stripping analysis [28] [29]. Figure 4 shows linear CV voltammograms for solutions of increasing hypoxanthine concentration (steps of 10 ppb), in the presence of 0.50 ppm copper (II), after 120 s of accumulation time at −0.5 V. Well-defined stripping peaks were observed over this concentration range.…”
Section: Quantitative Utilitysupporting
confidence: 73%
“…Eight successive measurements (using 30 s accumulation times at -0.50 V; final potential at −1.1 V; 60 s condition times at −0.9 V; scan rate, 200 mV·s −1 and 1.0 × 10 −3 mol·L −1 of NaOH as supporting electrolyte ) yielded a mean peak current of 8453 ± 97 nA and a range of 8312 -8625 nA. Such precision compares favorably with that reported for other compounds measured by adsorptive stripping analysis [28] [29]. Figure 4 shows linear CV voltammograms for solutions of increasing hypoxanthine concentration (steps of 10 ppb), in the presence of 0.50 ppm copper (II), after 120 s of accumulation time at −0.5 V. Well-defined stripping peaks were observed over this concentration range.…”
Section: Quantitative Utilitysupporting
confidence: 73%
“…Spectrophotometric (6)(7)(8)(9), chromatographic [10][11][12][13][14][15][16] and electrochemistry (17)(18) analytical methods have been developed for the determination of lamivudine. As a result of advancements in properties of the adsorptive stripping voltammetry, new methodologies have been developed for adenine, thymine, guanine, ATP, DNA and antiretroviral drugs determinations, employing alkaline solution with lower ionic strength as the supporting electrolyte (19)(20)(21)(22)(23)(24)(25). Using this alkaline electrolyte, the present work found a new stripping voltammetric procedure for trace detection of lamivudine based on its adsorption at the thin film mercury electrode.…”
Section: Introductionmentioning
confidence: 99%
“…The EFZ directly binds to the RT that causes a disruption of the enzyme's catalytic site, which hinders the formation of viral double‐stranded DNA from the single‐stranded viral RNA genome . EFZ is a first‐line drug and it is usually prescribed either in combination with protease inhibitor or nucleoside reverse‐transcriptase inhibitor for the management of the disease . EFZ is metabolized in human system into hydroxylated compounds by cytochrome P450 (CPY) with CYP2B6 and CYP2A4 being the major isozymes responsible for the biotransformation and excreted through the urine and feces.…”
Section: Introductionmentioning
confidence: 99%
“…Electrochemical techniques have been explored to overcome these difficulties as they are advantageous and provide high selectivity, sensitivity, convenient tool with fast response, reproducibility, and the analysis can be carried out without complicated sample pretreatment . However to the best of our knowledge, very scarce attempts have been made for the determination of EFZ by electrochemical methods . In these methods dsDNA or NiO nanoparticle modified glassy carbon electrodes were used and a very low linear dynamic range was observed.…”
Section: Introductionmentioning
confidence: 99%