Green Synthesis of Fe-Cu Bimetallic Supported on Alginate-Limestone Nanocomposite for the Removal of Drugs from Contaminated Water.

In this study Fe-Cu supported on Alginate-limestone (Fe-Cu/Alg-LS) was prepared. The increase in surface area was the main motivation for the synthesis of ternary composites. Scanning electronic microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), and transmission electron microscopy (TEM) were used to examine the surface morphology, particle size, percentage of crystallinity, and elemental content of the resultant composite. Fe-Cu/Alg-LS was used as an adsorbent for the removal of drugs such as ciprofloxacin (CIP) and levofloxacin (LEV)from contaminated medium. The adsorption parameters were computed using kinetic and isotherm models. The maximum removal efficiency of CIP (20 ppm) and LEV (10 ppm) was found to be 97.3% and 100%, respectively. The optimal conditions were pH 6 and 7 for CIP and LEV, optimum contact time 45, 40 min for CIP and LEV, and temperature of 303 K. The pseudo-second-order model, which confirmed the chemisorption properties of the process, was the most appropriate kinetic model among the ones used, and the Langmuir model, which was the most appropriate isotherm model. Moreover, the parameters of thermodynamics were also assessed. The results imply that the synthesized nanocomposites can be used to remove hazard materials from aqueous solutions.

A comparative and simultaneous analysis of indoxyl sulfate and sodium butyrate in human plasma by SPE and HPLC methods for kidney patients.

A comparison of high-performance liquid chromatography (HPLC) and solid-phase extraction (SPE) methods is carried out for the simultaneous analysis of indoxyl sulfate and sodium butyrate in plasma using Phenyl (250 × 4.6 mm; 5 µm) and SunShell (150 × 4.6 mm, 2.6 µm) columns with mobile phases ammonium acetate (20 mM)-ACN (95:5, v/v) and water-ACN (90:10), respectively. The values of the retention, separation and resolution factors for indoxyl sulfate and sodium butyrate were 3.1, 1.29 and 2.0 with phenyl and 1.0, 1.55 and 1.60 with SunShell columns. The values of the theoretical plates were in the range of 650 to 1600 while the tailing factors were 0.98 to 1.0. The limits of the detection and quantification of sodium butyrate and indoxyl sulfate were 0.1-1.9 and 0.43-9.2 µg with these columns. The hydrogen bondings and π-π interactions were responsible for the separation of these molecules. The multi-wall carbon nanotubes (MWCNTs) served as a good sorbent in SPE extraction. The developed SPE and HPLC methods were quick, robust, exact and economic for the analysis of indoxyl sulfate and sodium butyrate. The reported SPE and HPLC methods can be useful to determine the reported molecules in plasma.

HPLC enantio-separation and chiral recognition mechanism of quinolones on vancomycin CSP.

A new HPLC method was developed for the enantio-separation and chiral recognition mechanism of quinolones (lomefloxacine, ofloxacine, primaquine and quinacrine) on Vancomycin CSP. The column used was Chirabiotic V column (150 × 4.6 mm, 5.0 µm) with two mobile phases i.e. (I) MeOH:ACN:H2O:TEA (50:30:20:0.1%) and (II) MeOH:ACN: H2O:TEA (70:10:20:0.1%) at 1.0 mL/minute flow rate with various UV detection. The values of retention, separation and resolution factors in a solvent system I were ranged from 2.20 to 5.05, 1.70 to 1.96 and 1.75 to 2.20 while these values were 1.93 to 6.85, 1.62 & 2.01 and 2.30 & 2.40 in solvent system II. The limits of detection and quantification were ranged from 8.0 to 10.5 µg and 24.4 to 33.5 µg. The resolution was controlled mainly by π-π interactions along with other forces like hydrogen bonding, van der Waal's forces, steric effects, etc. The determination of the chiral recognition mechanism may be beneficial to separate other racemates successfully. The method is fast precise and efficient and may be utilized to analyze enantiomers of the reported quinolones.

Spectroscopic and In Silico DNA Binding Studies on the Interaction of Some New N-Substituted Rhodanines with Calf-thymus DNA: In Vitro Anticancer Activities.

BACKGROUND: In this era of science, cancer is a black dot on the face of humankind. Consequently, the search of promising anticancer agents continues. AIMS: Here we designed and synthesized new N-substituted rhodanines (RD1-7), evaluated their multispectroscopic interaction with calf thymus DNA, in silico and anticancer studies against MDA-MB-231cancer cell line. METHODS: By MTT assay rhodanine RD1 was found to be the most potent with IC50 value of 72.61 µM. In addition, DNA binding studies (UV-vis and fluorescence) revealed strong binding affinity of RD1-7 with DNA (Kb in the range of 1.5-7.4 × 105 M-1). Moreover, molecular docking study, experimental DNA binding and anticancer studies are all well agreed to each other. RESULTS: It was observed that H-bonding and hydrophobic attractions were responsible for stability of DNAcompound adducts. Besides, the reported rhodanines (RD1-7) were found as minor groove binders of DNA. Concisely, RD1-7 indicated promising pharmacological properties and hence, shows auspicious future for the development of novel anticancer agents. CONCLUSION: The reported rhodanines showed excellent anticancer properties. Therefore, the described rhodanines may be used as potential anticancer agents in the future.