ELECTROCHEMICAL BEHAVIOR OF XANTHENE FOOD DYE ERYTHROSINE AT GLASSY CARBON ELECTRODE AND ITS ANALYTICAL APPLICATIONS

Erythrosine is a xanthene food dye used in the food industries to enhance the appearance of the food. The electrochemical behavior of erythrosine at glassy carbon electrode was investigated by cyclic and differential pulse voltammetry. The oxidation peak of erythrosine was observed in phosphate buffer of pH 5.0. The influence of different pH, scan rate and concentration were evaluated. The probable reaction mechanism involved in the oxidation of erythrosine was also proposed. Differential pulse voltammetric method with good precision and accuracy was developed for the determination of erythrosine dye in real samples. The peak currents were found to be linearly dependent on the concentration range of 1 x 10-5 to 6 x 10-4 M. The limit of detection (LOD) and limit of quantification (LOQ) were noticed to be 1.9 x 10-7 and 6.6 x 10-7 M respectively

Electrochemical detection of chlorpheniramine maleate in the presence of an anionic surfactant and its analytical applications

Improvement of methods for the detection of an analyte at low concentration with high sensitivity has become an important point of interest. In reflection of this fact, an effort has been made to know the electrochemical behavior of chlorpheniramine maleate in the presence of an anionic surfactant. Voltammograms were obtained in the range of 6.0 - 11.2 pH and maximum peak current (Ip) was observed at pH 10.4. Various physico-chemical parameters such as, process on the surface of the electrode, which was found to be diffusion controlled, heterogeneous rate constant, number of electrons transferred and charge transfer coefficient were estimated. Square wave voltammetry of chlorpheniramine maleate at the modified electrode exhibited a linear calibration curve in the concentration range of 1.0-100 ÎźM, with a limit of detection of 28 nM. The proposed technique was successfully used for the determination of chlorpheniramine maleate in pharmaceuticals as well as in biological samples.The accepted manuscript in pdf format is listed with the files at the bottom of this page. The presentation of the authors' names and (or) special characters in the title of the manuscript may differ slightly between what is listed on this page and what is listed in the pdf file of the accepted manuscript; that in the pdf file of the accepted manuscript is what was submitted by the author

Stewart-Bluefarb acroangiodermatitis in a case of Parkes-Weber syndrome

Stewart-Bluefarb acroangiodermatitis is the occurrence of pseudo-kaposiform changes with an underlying arterio-venous malformation. Parkes-Weber syndrome is a triad of arterio-venous malformation with varicose veins with bony and soft-tissue hypertrophy involving the extremity. A 13 year-old-female presented with ulcerated growth with bleeding episodes on right leg since past four years. A reddish discoloration over right leg was noticed at four years of age which remained unchanged until nine years of age, after which it showed rapid increase in size along with disproportionate increase in length and girth of right lower limb. Examination revealed hyperpigmented soft verrucous plaque over the right lower one-third of leg, along with presence of ulcers and dilated tortuous veins in the right lower leg with thrill and bruit over the right popliteal and inguinal region. A differential diagnosis of verrucous hemangioma and arterio-venous malformation with pseudo-kaposiform change was considered. Skin biopsy showed multiple fenestrated capillaries with perivascular lymphocyte infiltrate suggestive of capillary malformations. X-ray showed osteolytic defect in right tibia. Duplex ultrasound and magnetic resonance imaging of right leg showed multiple fast flowing small and medium sized arterio-venous malformations of small to moderate size. Thus, on the basis of clinical and radiological features, we made a diagnosis of Stewart-Bluefarb type of acroangiodermatitis with Parkes-Weber syndrome. She was managed conservatively with compression stockings

Nano molar detection of acyclovir, an antiviral drug at nanoclay modified carbon paste electrode

A nano level voltammetric sensing method has been developed for determination of acyclovir (ACV) at nano clay modified carbon paste sensor by employing cyclic voltammetry (CV) and square wave voltammetry (SWV) techniques in pH5.0. The electro-oxidation current of ACV was enhanced two times greater by the modification of the sensor. The modifier nano clay was characterized by utilizing X-ray diffraction (XRD) and scanning electronic microscope (SEM). The influence of parameters like scan rate, pH, accumulation time, amount of the modifier and concentration on the peak current of the drug were studied. The effect of ACV concentration variation was studied using SWV technique and got lowest detection limit compared to the earlier reported techniques. The fabricated sensor was employed for the determination of acyclovir in pharmaceutical and biological samples. Keywords: Antiviral drug, Nano clay particles, Electro-oxidation, Square wave voltammetry, Pharmaceutical analysi