Resonance Rayleigh Scattering for the Determination of Chlorpromazine and Promethazine

2006 ◽  
Vol 59 (12) ◽  
pp. 915 ◽  
Author(s):  
Lanxiang An ◽  
Shaopu Liu ◽  
Zhongfang Liu ◽  
Ling Kong ◽  
Xiaoli Hu

Chlorpromazine (CPZ) and promethazine (PZ) can react with potassium ferrioxalate (PF) to form 3:1 ion-association complexes, which can result in a significant enhancement of resonance Rayleigh scattering (RRS) intensity. The maximum scattering peaks are located at 368 nm for CPZ-PF and 370 nm for PZ-PF. The RRS spectroscopic characteristics, the optimum conditions of reactions, and influencing factors have been studied for CPZ-PF and PZ-PF. There is a linear relationship between the RRS intensity and the drug concentration in the range of 0.02–8.00 μg mL–1 for CPZ and 0.04–9.00 μg mL–1 for PZ, and the detection limits (3σ) are 6.6 ng mL–1 for CPZ and 10.6 ng mL–1 for PZ. The proposed method has been applied to determine CPZ in urine and serum samples with satisfactory results. Moreover, the reaction mechanism and the reasons for intensity enhancement of RRS have been discussed.

2013 ◽  
Vol 787 ◽  
pp. 400-403
Author(s):  
Jin Chao Dong ◽  
Ai Hui Liang ◽  
Zhi Liang Jiang

Hemin aptamer was used to modify gold nanoparticles (AuNPs) to obtain a stable aptamer-nanogold probe (AussDNA). In the condition of pH 8.0 Tris-HCl buffer solution containing 50mmol/L NaCl, the substrate chain of AussDNA was cracked by hemin to produce a short single-stranded DNA(ssDNA) and then further combined with hemin to form a stable hemin-ssDNA conjugate. The AuNPs released from AussDNA would be aggregated in the condition of 50mmol/L NaCl and exhibited a strong resonance Rayleigh scattering (RRS) peak at 368nm. Under the selected conditions, the increased RRS intensity (ΔI368nm) was linear to hemin concentration in the range of 5-750nmol/L, with a detection limit of 66 pmol/L. This RRS method was applied to determination of residual hemin in serum samples, with satisfactory results. The remnant AussDNA in the solution exhibited a strong catalytic activity on the gold particle reaction of HAuCl4-vitamine C (VC) that can be monitored by RRS technique at 368 nm. When the hemin concentration increased, the AussDNA decreased, the catalysis decreased, and the RRS intensity at 368nm decreased. The decreased RRS intensity ΔI368nmwas linear to the hemin concentration in the range of 1-200nmol/L, with a detection limit of 54 pmol/L. Accordingly, a sensitivity, selectivity, and simplicity new method of resonance Rayleigh scattering spectra to detect hemin using aptamer-modified nanogold as catalyst was established.


2017 ◽  
Vol 2017 ◽  
pp. 1-6 ◽  
Author(s):  
Liping Wu ◽  
Yue Liu ◽  
Rong Huang ◽  
Huawen Zhao ◽  
Weiqun Shu

A rapid, simple, and novel method for folate receptor α (FRα) determination is reported here. A probe of gold nanoparticles (Au NPs) modified with anti-FRα antibody was synthesized under the optimized conditions first. The antibody-modified Au NPs would aggregate when FRα was added to the probe for the specific interaction between antibody and antigen, resulting in the enhancement of resonance Rayleigh scattering (RRS) intensity. There is a linear relationship between the change of RRS intensity (ΔIRRS) and the concentration of FRα, with the detecting range of 0.50–37.50 ng·mL−1 and the limit of determination of 0.05 ng·mL−1. The determination of FRα in serum samples was realized with the advantages of high selectivity, high sensitivity, and easy operation.


2013 ◽  
Vol 680 ◽  
pp. 141-144 ◽  
Author(s):  
Qing Ye Liu ◽  
Gui Qing Wen ◽  
Kun Li ◽  
Ai Hui Liang

In pH 6.6 Na2HPO4- citric acid buffer solution and in the presence of KCl, the immunoreaction between hCG and nanosilver-labeled anti-hCG took place, the immunonanosilver-complex was formed and deposited, caused the resonance Rayleigh scattering (RRS) intensity at 510 nm decreased. In the optimal condition, the decreased RRS intensity responds linearly with the concentration of hCG over 0.125-1.75 µg/mL. Based on this, a new and simple RRS method has been proposed for the determination of hCG in serum samples, with satisfactory results.


2021 ◽  
Vol 8 (1) ◽  
pp. 201545
Author(s):  
Mohamed A. Abdel-Lateef ◽  
Sayed M. Derayea ◽  
Deena A. M. Nour El-Deen ◽  
Albandary Almahri ◽  
Mohamed Oraby

Terbinafine hydrochloride is a potent antifungal drug indicated for oral and topical treatment of mycoses. A resonance Rayleigh scattering (RRS) method was developed for the determination of terbinafine hydrochloride through a feasible complexation reaction with erythrosine B. In a weakly acidic medium (acetate buffer, pH 5.0), terbinafine hydrochloride can react with erythrosine B through the electrostatic attraction and virtue of hydrophobic force to form an ion-association complex. The reaction resulted in the appearance of a new RRS peak at 369 nm. The RRS peak was increased by increasing the concentration of terbinafine hydrochloride in the linear range of 0.1–1.5 µg ml −1 . All the reaction conditions (erythrosine B concentration, buffer volume, diluting solvent and pH) were optimized. The detection limit was 0.029 µg ml −1 while the quantitation limit was 0.089 µg ml −1 . The suggested method after its validation was successfully applied for the determination of terbinafine hydrochloride in different pharmaceutical formulations (tablets and cream) with sufficient recovery.


2014 ◽  
Vol 881-883 ◽  
pp. 65-69
Author(s):  
Hui Ping Xi ◽  
Xiu Wei Fang

A new method for the determination of Gemifloxacin (GMFX) by using Resonance Rayleigh scattering was put forward. In HAc-NaAc buffer solution of pH 5 - 6, terbium (III) and antibiotics GMFX could form cationic complexes, which coulf further form 1 :2 : 1 (Tb3+ : GMFX :AR) ternary ion association complexes by the reaction with Alizarin Red (AR) anion through electrostatic and hydrophobic interaction. The new Resonance Rayleigh scattering (RRS) spectra would appear, and the two scattering peaks were located at 370nm and 590 nm. At 370 nm, the scattering enhancement (ΔI) was proportional to GMFX of certain concentration and its linear range and detection limit (3σ) were 0.005 ~ 4.00 μg.mL-1and 14.5 ng.mL-1. This method is simple, fast, with good selectivity and reproducibility, and it can be used for determination of GMFX drug in various body fluids.


2018 ◽  
Vol 69 (3) ◽  
pp. 627-631 ◽  
Author(s):  
Viorica Ohriac (Popa) ◽  
Diana Cimpoesu ◽  
Adrian Florin Spac ◽  
Paul Nedelea ◽  
Voichita Lazureanu ◽  
...  

Pain is defined as a disagreeable sensory and emotional experience related to a tissue or potential lesion. Paracetamol (Acetaminophen) is the most used non-morphine analgesic. For the determination of paracetamol we developed and validated the high performance liquid chromatography (HPLC) analysis using a Dionex Ultimate 3000 liquid chromatograph equipped with a multidimensional detector. After determining the optimum conditions of analysis (80/20 water / acetonitrile mobile phase, flow rate 1.0 mL / min, detection wavelength 245 nm) we validated the method following the following parameters: linearity of response function, linearity of results, limit (LD = 0.66 mg / mL) and quantification limit (LQ = 2.00 mg / mL), and precision. The method of determining paracetamol by HPLC was applied to 30 samples of serum collected from patients who had pain and were treated with paracetamol.


2010 ◽  
Vol 20 (12) ◽  
pp. 1552-1556 ◽  
Author(s):  
Li Fan ◽  
Shao-Pu Liu ◽  
Da-Cheng Yang ◽  
Xiao-Li Hu

2013 ◽  
Vol 788 ◽  
pp. 23-26
Author(s):  
Gui Qing Wen ◽  
Ai Hui Liang

In HCl medium and in the presence of CuSO4, Na3AsO4 can be reduced by NaH2PO2 to form As nanoparticles (AsNs) which exhibited a strong resonance Rayleigh scattering (RRS) peak at 370 nm. Under the chosen conditions, the increased intensity at 370 nm was linear to As5+ concentration in the range of 0.48-38.0×10-6 mol/L, with a regression equation of ΔI370nm = 82.3 CAs + 33.9, a correlation coefficient of 0.9878 and a detection limit of 2.0×10-7 mol/L As5+. The proposed method was applied to detect As5+ concentration in waste water, with simplicity, rapidity and accuracy. Thus, a novel RRS spectral method was established to determine As5+.


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