A Novel Chronoimpedimetric Glucose Sensor in Real Blood Samples Modified by Glucose‐imprinted Pyrrole‐Aminophenylboronic Acid Modified Screen Printed Electrode

In this study, a molecularly imprinted sensor technology is engineered to detect glucose in real blood samples by chronoimpedimetrically. The imprinting process of glucose (Glc) was carried out by electrochemical polymerization of aminophenylboronic acid (APBA) and pyrrole (Py) by performing cyclic voltammetry (CV). Afterwards, glucose molecule was removed from imprinted surface by 5 % acetic acid to reveal glucose imprinted cavities. Electrochemical Impedance Spectroscopy (EIS) was used to characterize sensor modification steps and glucose removal. Glucose monitoring process was carried out chronoimpedimetrically(CI) for the first time in real blood samples. Calibration curve was prepared between 20–800 mg/dL. The standard deviations of the 18 calibration curves R² were calculated as 0.9866±0.0066 to assess reproducibility. Recovery was calculated by using 105 mg/dL Glc Serum Sample, which was monitored by auto analyzer and into this sample 50 mg/dL Glc added and our sensor response was 147.92±2.43 mg/dL, 98.6±1.62 % (n=5). Non‐imprinted (NIP) sensor gave no signal for the glucose concentration.     

Sol-gel thin films with anti-reflective and self-cleaning properties

Self-cleaning photocatalytic TiO₂ films are beneficial since they reduce the maintenance cost and enhance the efficiency of various optical systems, especially thermal and photovoltaic solar systems. However, the presence of a TiO₂ layer on glass reduces the transmission of incident light, which leads to a decrease in efficiency. This drawback can be overcome by applying a layer of anti-reflective coating beneath the TiO₂ layer. Generally, the anti-reflective layer is porous silica. The presence of the anti-reflective layer compensates for the loss of light transmittance caused by the photocatalytic TiO₂ top layer. This paper reviews some of the previous and the latest fundamental studies in the literature on anti-reflective, self-cleaning and multi-functional films.     

A novel, ultra sensible biosensor built by layer-by-layer covalent attachment of a receptor for diagnosis of tumor growth

In the presented research, a novel, ultra sensitive biosensor for the impedimetric detection of vascular endothelial growth factor (VEGF) is introduced. The human vascular endothelial growth factor receptor 1 (VEGF-R1, Flt-1) was used as a biorecognition element for the first time. The immobilization of VEGF-R1 on glassy carbon electrodes was carried out using layer-by-layer covalent attachment of VEGF-R1. The electrochemical properties of the layers constructed on the electrodes were characterized by electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). The differences in electron transfer resistance (R_et) between the working solution and the biosensor surface, recorded by the redox probe K₃[Fe(CN)₆]/K₄[Fe(CN)₆], confirmed the binding of VEGF to VEGF-R1. The new biosensor allowed a detection limit of 100 fg mL⁻¹ with a linear range of 100–600 fg mL⁻¹ to be obtained. The biosensor also exhibited good repeatability (with a correlation coefficient of 1.95%), and reproducibility.     

On the vibration of laminated nonhomogeneous orthotropic shells

In this paper, an analytical procedure is given to study the free vibration of the laminated homogeneous and non-homogeneous orthotropic conical shells with freely supported edges. The basic relations, the modified Donnell type motion and compatibility equations have been derived for laminated orthotropic truncated conical shells with variable Young’s moduli and densities in the thickness direction of the layers. By applying the Galerkin method, to the basic equations, the expressions for the dimensionless frequency parameter of the laminated homogeneous and non-homogeneous orthotropic truncated conical shells are obtained. The appropriate formulas for the single-layer and laminated complete conical and cylindrical shells made of homogeneous and non-homogeneous, orthotropic and isotropic materials are found as a special case. Finally, the influences of the non-homogeneity, the number and ordering of layers and the variations of the conical shell characteristics on the dimensionless frequency parameter are investigated. The results obtained for homogeneous cases are compared with their counterparts in the literature.     

Human Papilloma Virus-11 DNA Detection by Graphene-PAMAM Modified Impedimetric CRISPR-dCas9 Biosensor

Human Papilloma Virus-11 (HPV-11) is leads to condylomata acuminata (CA), which has commonly known as genital wards that global widespread incidence of 160 to 289 cases per year. In the first-time literature, we detect HPV-11 DNA by using dCas9 modified graphene oxide-PAMAM modified electrodes, impedimetrically. Chronoimpedimetric detection was facilitated the biosensor response time optimization of HPV-11 DNA in 5 minutes. The biosensor has ability to analyze HPV-11 DNA between 50 pM and 1000 pM with good linearity, sensitivity and selectivity. Moreover, we tested our biosensor in real samples matrix by considering recovery of the samples.     

1H and 13C NMR studies on 3-aryl-2-thioxo-4-oxazolidinones and 3-arylrhodanines

3-Aryl-2-thioxo-4-oxazolidinones and 3-arylrhodanines have been studied for magnetic non-equivalence of diastereotopically related proton and ¹³C nuclei in rotational isomers, and for steric interactions between the aryl and heterocyclic moieties of these compounds. For the majority of rotational isomers the barriers to internal rotation about the aryl C? N bond were >100 kJ mol^?1, due to the steric bulk of the thiocarbonyl group. Chemical isolation of several of the diastereomers was achieved. The enhanced steric effect and the difference in the electronic effect of the sulphur atom in relation to the oxygen atom appeared to have no influence on the small chemical shift differences of the rotational isomers, detected for some ¹H and some ¹³C nuclei.     

The Influence of Unsaturated Hydrocarbon Ligands on the Stabilization of Platinum Tetramer

In the present study, Pt₄(CH)_n (1 ≤ n ≤ 7) and Pt₄(benzene)₂ metalorganic complexes have been investigated by performing density functional theory within spin polarized local density approximation, generalized gradient approximation and hybrid exchange correlation functionals in terms of the geometric properties, stability and energetics, electronic properties and chemical reactivity indexes. Locally stable isomers are distinguished from transition states by vibrational frequency analysis. Our calculations indicate that Pt₄(CH)₄ and Pt₄benzene metal hydrocarbon complexes are the most stable structures among the studied species.     

Microwave‐assisted synthesis of 1,3′‐diaza‐flavanone/flavone and their alkyl derivatives with antimicrobial activity

A simple environmentally friendly solid‐phase microwave‐assisted method was used to synthesis of the 1,3′‐diazaflavanone ( 2 ) and 1,3′‐diazaflavone ( 3 ) from the cyclization of 2′‐amino (E)‐3″‐azachalcone ( 1 ). Ten new N‐alkyl (C_5–12,14,15)‐substituted 1,3′‐diazaflavanonium bromides ( 2a–j ) were prepared from compound 2 with corresponding alkyl halides in acetonitrile under reflux. In addition, nine new N,N′‐dialkyl (C_5–12,14)‐substituted 1,3′‐diazaflavonium bromides ( 3a–i ) were also synthesized from compound 3 with corresponding alkyl halides using basic silica in acetonitrile. The antimicrobial activities of compounds 1–3 , 2a–j , and 3a–i were tested against Gram‐positive (G+) (Bacillus subtilis, Staphylococcus epidermidis, Staphylococcus aureus, and Enterococcus faecalis) and Gram‐negative (G?) (Escherichia coli, Klebsiella pneumonia, Pseudomonas aeruginosa, Proteus vulgaris, Salmonella typhimirium, Yersinia pseudotuberculosis, and Enterobacter cloaceae) microorganisms. They showed good antimicrobial activity against the Gram‐positive bacteria tested with the minimal inhibitory concentration values less than 7.8 μg/mL in most cases. The optimum length of the alkyl chain for better and broader activity is situated in the range of 9–12 carbon atoms in the series of compounds 2a–j and five to six carbon atoms in the series of compounds 3a–i . The nonalkylated compounds 1–3 were not effective, as were the ones alkylated with five or six C alkyl groups ( 2a and 2b ) and 8–13 C alkyl groups for N,N′‐dialkyl compounds ( 3c–3i ). The antimicrobial activity increased as the length of the alkyl substitution increased from 8 to 12 carbons in compounds 2a–j . However, antimicrobial activity decreased as the length of the alkyl substitution increased from 7 to 13 carbons in compounds 3c–i . J. Heterocyclic Chem., (2012)