Abstract:The measurement of antibiotics in environmental water systems is increasingly becoming a top priority for global environmental watchdog organisations, as the looming threat of emerging contaminants moves to centre stage. A novel chemical sensor based on polyamic acid (PAA) semiconducting polymer and cobalt nanoparticles (CoNP) was developed and used to demonstrate proof of concept evidence for measurement of norfloxacin at trace concentrations in aqueous systems. Polyamic acid and cobalt nanoparticles were bot… Show more
“…The LOD and the LOQ were identified by dividing the standard deviation (Sy) value obtained from the lowest concentrations of analyte prepared for determining the linearity range with the slope of the linearity line (S). Equations ( 4) and (5) were used for estimating LOD and LOQ parameters, respectively, for TBN and LGN [38].…”
Section: Limit Of Detection (Lod) and Limit Of Quantification (Loq)mentioning
Herein, we reported an HPLC method for the simultaneous determination of tibezonium iodide (TBN) and lignocaine hydrochloride (LGN). The method was developed according to the International Conference for Harmonization guidelines (ICH) Q2R1 using Agilent® 1260 with a mobile phase consisting of acetonitrile and phosphate buffer (pH 4.5) in a volumetric ratio of 70:30 and flowing through a C8 Agilent® column at 1 mL/min. The results revealed that TBN and LGN peaks were isolated at 4.20 and 2.33 min, respectively, with a resolution of 2.59. The accuracy of TBN and LGN was calculated to be 100.01 ± 1.72% and 99.05 ± 0.65% at 100% concentration, respectively. Similarly, the respective precision was 100.03 ± 1.61% and 99.05 ± 0.48%. The repeatability for TBN and LGN was found to be 99.05 ± 0.48% and 99.19 ± 1.72%, respectively, indicating that the method was precise. The respective regression co-efficient (r2) for TBN and LGN was found to be 0.9995 and 0.9992. Moreover, the LOD and LOQ values for TBN were 0.012 and 0.037 µg/mL, respectively, while for LGN, they were 0.115 and 0.384 µg/mL, respectively. The calculated greenness of the method for ecological safety was found to be 0.83, depicting a green contour on the AGREE scale. No interfering peaks were found when the analyte was estimated in dosage form and in volunteers’ saliva, depicting the specificity of the method. Conclusively, a robust, fast, accurate, precise and specific method was successfully validated to estimate TBN and LGN.
“…The LOD and the LOQ were identified by dividing the standard deviation (Sy) value obtained from the lowest concentrations of analyte prepared for determining the linearity range with the slope of the linearity line (S). Equations ( 4) and (5) were used for estimating LOD and LOQ parameters, respectively, for TBN and LGN [38].…”
Section: Limit Of Detection (Lod) and Limit Of Quantification (Loq)mentioning
Herein, we reported an HPLC method for the simultaneous determination of tibezonium iodide (TBN) and lignocaine hydrochloride (LGN). The method was developed according to the International Conference for Harmonization guidelines (ICH) Q2R1 using Agilent® 1260 with a mobile phase consisting of acetonitrile and phosphate buffer (pH 4.5) in a volumetric ratio of 70:30 and flowing through a C8 Agilent® column at 1 mL/min. The results revealed that TBN and LGN peaks were isolated at 4.20 and 2.33 min, respectively, with a resolution of 2.59. The accuracy of TBN and LGN was calculated to be 100.01 ± 1.72% and 99.05 ± 0.65% at 100% concentration, respectively. Similarly, the respective precision was 100.03 ± 1.61% and 99.05 ± 0.48%. The repeatability for TBN and LGN was found to be 99.05 ± 0.48% and 99.19 ± 1.72%, respectively, indicating that the method was precise. The respective regression co-efficient (r2) for TBN and LGN was found to be 0.9995 and 0.9992. Moreover, the LOD and LOQ values for TBN were 0.012 and 0.037 µg/mL, respectively, while for LGN, they were 0.115 and 0.384 µg/mL, respectively. The calculated greenness of the method for ecological safety was found to be 0.83, depicting a green contour on the AGREE scale. No interfering peaks were found when the analyte was estimated in dosage form and in volunteers’ saliva, depicting the specificity of the method. Conclusively, a robust, fast, accurate, precise and specific method was successfully validated to estimate TBN and LGN.
“…The Nyquist plane plot of GO-CS/GCE was a straight line in the low frequency region, indicating a lower resistance than the bare electrode. This trend can be a result of two issues: (i) the large surface area of GO nasnosheets that resulted in the improvement current response and (ii) the electrostatic attraction between anionic probe ([Fe(CN) 6 ] À 3/À 4 ) and the positively charged amine residues of CS backbone, leading to an enhancement of [Fe(CN) 6 ] À 3/À 4 diffusion to the modified electrode surface [14]. Considering the small value of ΔEp and larger current response at modified electrode, it seems that charge transfer is quasi-reversible and fast, indicating the ability of this nanocomposite to produce a favorable microenvironment to face facile electron-transfer reaction.…”
Section: Electrochemical Characteristics Of the Modified Electrodementioning
confidence: 99%
“…On the other hand, electroanalytical methods, in particular, have been applied for the determination of electroactive species [12]. They are powerful alternative methods for the analysis of pharmaceuticals due to their operation simplicity, rapidity, cost-effective and economical features [13][14].…”
The development of selective and simple methods for the determination of different analytes is of great interest. This is the first time to show the applicability of graphene oxide-chitosan (GO-CS) nanocomposite for designing an electrochemical nanosensor for determination of Amlodipine, Valsartan, and Hydrochlorothiazide, simultaneously. Differential pulse voltammet-rics current of AML, HCT, and VAL increased linearly in the ranges of 0.1-110, 0.1-110, and 1-230 μM with LOD of 5.5 × 10 À 2 , 3.5 × 10 À 2 and 8.6 × 10 À 2 μM, respectively. Finally, GO-CS/GCE was used for the detection of these drugs in commercial tablets and compared with the reference method (HPLC).
“…LoD, defined as the lowest quantity or concentration of a component that can be reliably detected with a given analytical method, is the key index representing the detection capability. The typical way to calculate the LoD is based on the standard deviation of the response (S y ) of the curve and the slope of the calibration curve (S) at levels approximating the LoD according to the formula: LoD = 3.3(S y /S) 125 . However, the LoD obtained from this approach is usually beyond the physical detection limit when considering the sample volume.…”
Biological research and diagnostic applications normally require analysis of trace analytes in biofluids. Although considerable advancements have been made in developing precise molecular assays, the trade-off between sensitivity and ability to resist non-specific adsorption remains a challenge. Here, we describe the implementation of a testing platform based on a molecular-electromechanical system (MolEMS) immobilized on graphene field-effect transistors. A MolEMS is a self-assembled DNA nanostructure, containing a stiff tetrahedral base and a flexible single-stranded DNA cantilever. Electromechanical actuation of the cantilever modulates sensing events close to the transistor channel, improving signal-transduction efficiency, while the stiff base prevents non-specific adsorption of background molecules present in biofluids. A MolEMS realizes unamplified detection of proteins, ions, small molecules and nucleic acids within minutes and has a limit of detection of several copies in 100 μl of testing solution, offering an assay methodology with wide-ranging applications. In this protocol, we provide step-by-step procedures for MolEMS design and assemblage, sensor manufacture and operation of a MolEMS in several applications. We also describe adaptations to construct a portable detection platform. It takes ~18 h to construct the device and ~4 min to finish the testing from sample addition to result.
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