CARDIOPROTECTIVE EFFECT OF DICHLOROMETHANE VALERIAN (VALERIANA OFFICINALIS) EXTRACT ON ISCHEMIA-REPERFUSION-INDUCED CARDIAC INJURIES IN RATS.

Background: Valepotriate is an active ingredient of valerian (Valeriana officinalis) with strong antioxidant activity that is effective for numerous cardiovascular diseases. Objective: The aim of this study was to investigate the effect of an active ingredient of V. officinalis extract on ischemia-reperfusion-induced cardiac injuries in male rats. Methods: Thirty-two male rats were subjected to ischemia for 40 minutes and reperfusion for five days. The rats were divided into 4 groups of 8 each; group 1 (control) was given normal saline, and groups 2-4 were gavaged with 0.2, 0.1, 0.05 mg/kg of valepotriate extract, respectively, and received extract (0.2 mg/kg ip) two weeks before ischemia induction. Results: Dichloromethane V. officinalis (valepotriate) extract exerted a protective effect against ischemia-reperfusion-induced injuries. So that infarct size and number of ventricular arrhythmia and ventricular escape beats decreased compared to the control group. Moreover, ST segment amplitude, QTC interval, and heart rate decreased in the injured hearts and serum levels of antioxidant enzymes glutathione peroxidase, catalase, and superoxide dismutase increased. Biochemical markers malondialdehyde and lactate dehydrogenase also decreased on day 5 after the onset of reperfusion. Conclusion: V. officinalis extract may have a protective effect against myocardial ischemia-reperfusion by producing antioxidant effects.

The fabrication of a new electrochemical sensor based on electropolymerization of nanocomposite gold nanoparticle-molecularly imprinted polymer for determination of valganciclovir.

A new sensitive and selective electrochemical sensor was successfully developed for the determination of valganciclovir. It is based on one-step electropolymerization of the molecularly imprinted polymer composed from 2,2'-dithiodianiline, gold nanoparticles, and valganciclovir on a glassy carbon electrode modified with carboxyl-functionalized multiwalled carbon nanotubes via cyclic voltammetry. The gold nanoparticles were introduced into the polymer composite for the development of electrical response by facilitating charge transfer. The fabrication process of the sensor was characterized by cyclic voltammetry and electrochemical impedance spectroscopy. Under the optimized condition calibration curve of the imprinted sensor has two linear concentration ranges from 1.0 to 500.0nM and 500.0 to 2000.0nM, with the limit of detection of 0.3nM. The relative standard deviation (RSD) for seven parallel determination of 1.0µM valganciclovir at optimum conditions was found to be 2.9%. The imprinted sensor has the advantages of high porous surface structure, ease of preparation, good reproducibility, good repeatability and high selectivity and sensitivity. Furthermore, the proposed method was successfully intended for the determination of valganciclovir in real samples.

Fabrication of an electrochemical sensor based on computationally designed molecularly imprinted polymer for the determination of mesalamine in real samples.

A novel electrochemical sensor based on mesalamine molecularly imprinted polymer (MIP) film on a glassy carbon electrode was fabricated. Density functional theory (DFT) in gas and solution phases was developed to study the intermolecular interactions in the pre-polymerization mixture and to find the suitable functional monomers in MIP preparation. On the basis of computational results, o-phenylenediamine (OP), gallic acid (GA) and p-aminobenzoic acid (ABA) were selected as functional monomers. The MIP film was cast on glassy carbon electrode by electropolymerization of solution containing ternary monomers and then followed by Ag dendrites (AgDs) with nanobranch deposition. The surface feature of the modified electrode (AgDs/MIP/GCE) was characterized by scanning electron microscopy (SEM) and electrochemical impedance spectroscopy (EIS). Under the optimal experimental conditions, the peak current was proportional to the concentration of mesalamine ranging from 0.05 to 100 µM, with the detection limit of 0.015 µM. The proposed sensor was applied successfully for mesalamine determination in real samples.