A novel way to production yttrium glass microspheres for medical applications

In this paper a novel method of producing yttrium aluminum silicate microspheres is reported. Yttrium aluminum silicate microspheres around 20–50 μm in size were obtained when an aqueous solution of Y(NO₃)₃ and Al(NO₃)₃ was added to tetraethyl orthosilicate (TEOS) and pumped into stirred silicone oil. The particles produced by this method are regularly shaped and very close to spherical. The amorphous structure, Y-O-Si bonds, spherical shapes, composition, and element distribution were investigated by X-ray diffraction (XRD), fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), X-ray fluorescence spectroscopy (XRF), carbon/sulfur analysis, and SEM/EDS mapping analysis. The results obtained demonstrate that the silicone oil spheroidization method is suitable for the production of yttrium aluminum silicate microspheres. This study also reveals that a high temperature is not required for the production of yttrium aluminum silicate microspheres.     

Microwave-Assisted Pretreatment of Sago Palm Bark

Three types of microwave-assisted diluted solvents were employed using 0.1 N H₂SO₄ (MSA), 0.1 N NaOH (MSH), and 0.01 N NaHCO₃ (MSB). These solvents were evaluated as possible pretreatment routes for sago palm bark (SPB) with their effects on the pretreated substrate. A variety of analyses, consisting of fiber analysis, energy dispersive X-ray spectroscopy (EDX), X-ray fluorescence spectrometer (XRF), X-ray powder diffraction (XRD), thermogravimetric analysis (TGA), scanning electron microscope (SEM), and high-performance liquid chromatography (HPLC), were performed to understand the pretreatment effects on the chemical and physical characteristics of SPB and pretreatment liquor. The thermal analysis has revealed that higher hemicellulose degradation was also found in MSA pretreatment. In the analyses of the pretreatment liquid for the extracted monomeric sugar, a higher amount of glucose was found (9 mg/g) using MSH pretreatment and the highest xylose level was found (4 mg/g) using MSA pretreatment. The analysis of the formation of inhibitors has shown that acetic acid was only found in the MSH pretreatment.     

A study on fluorescence properties of Eu3+ ions in alkali lead tellurofluoroborate glasses

Glasses with chemical composition of (in mol.%): 26 RF-20 PbO-10 TeO2-43 H3BO3-1 EuO3 (RLTB) were prepared by conventional melt quenching method. The Judd-Ofelt intensity parameters Ω2 and Ω6 were obtained from the absorption intensities of 7F0→5D2 and 7F0→5L6 transitions, respectively. In order to overcome the problem of applicability of Judd-Ofelt analysis at room temperature due to the overlapping of the transitions originating from 7F0 and 7F1 levels of Eu3+ ion, the effect of the thermalization on the population of energy levels was taken into account. The photoluminescence spectra contained five emission bands originating from the 5D0 metastable state to 7FJ (J=0, 1, 2, 3, 4) lower lying states. The decay profiles were found to be single exponential in all the three glasses. The measured lifetimes (τmes) were in good agreement with the calculated lifetimes (τcal) obtained by using the thermally corrected Judd-Ofelt intensity parameters.     

Oriented immobilized anti-LDL antibody carrying poly(hydroxyethyl methacrylate) cryogel for cholesterol removal from human plasma

Low density lipoprotein (LDL) cholesterol is a major ingredient of the plaque that collects in the coronary arteries and causes coronary heart diseases. Among the methods used for the extracorporeal elimination of LDL from intravasal volume, immunoaffinity technique using anti-LDL antibody as a ligand offers superior selectivity and specificity. Proper orientation of the immobilized antibody is the main issue in immunoaffinity techniques. In this study, anti-human β-lipoprotein antibody (anti-LDL antibody) molecules were immobilized and oriented through protein A onto poly(2-hydroxyethyl methacrylate) (PHEMA) cryogel in order to remove LDL from hypercholesterolemic human plasma. PHEMA cryogel was prepared by free radical polymerization initiated with N,N,N′,N′-tetramethylene diamine (TEMED). PHEMA cryogel with a swelling degree of 8.89 g H₂O/g and 67% macro-porosity was characterized by swelling studies, scanning electron microscope (SEM) and blood compatibility tests. All the clotting times were increased when compared with control plasma. The maximum immobilized anti-LDL antibody amount was 63.2 mg/g in the case of random antibody immobilization and 19.6 mg/g in the case of oriented antibody immobilization (protein A loading was 57.0 mg/g). Random and oriented anti-LDL antibody immobilized PHEMA cryogels adsorbed 111 and 129 mg LDL/g cryogel from hypercholesterolemic human plasma, respectively. Up to 80% of the adsorbed LDL was desorbed. The adsorption–desorption cycle was repeated 6 times using the same cryogel. There was no significant loss of LDL adsorption capacity.     

Magnetic hydrophobic affinity nanobeads for lysozyme separation

N-Methacryloyl-l-phenylalanine (MAPA) containing poly(2-hydroxyethylmethacrylate) based magnetic [mag-poly(HEMA–MAPA)] nanobeads was prepared for lysozyme purification form chicken egg white. MAPA was synthesized by reacting methacryloyl chloride with l-phenylalanine methyl ester and provided hydrophobic functionality to the nanobeads. Size of mag-poly(HEMA–MAPA) nanobeads was 386 nm and obtained by surfactant free emulsion polymerization of HEMA and MAPA having a specific surface area of 580 m²/g. Mag-poly(HEMA–MAPA) nanobeads were characterized by FTIR, AFM, TEM, ESR, and elemental analysis. Lysozyme adsorption experiments were investigated under different conditions in batch system (i.e., medium pH, protein concentration, temperature, salt type). Lysozyme adsorption capacity of mag-poly(HEMA) and mag-poly(HEMA–MAPA) nanobeads from aqueous solutions was estimated as 24 and 517 mg/g, respectively. Lysozyme molecules were desorbed with 50% ethylene glycol solution with 98% recovery. It was observed that mag-poly(HEMA–MAPA) nanobeads can be used without significant decrease in lysozyme adsorption capacity after ten adsorption–desorption cycles. Mag-poly(HEMA–MAPA) nanobeads was used for the purification of lysozyme from chicken egg white. Purity of lysozyme was estimated by SDS-PAGE.     

Sink-oriented tree based data dissemination protocol for mobile sinks wireless sensor networks

Wireless Networks - Data dissemination toward static sinks causes the nearby nodes to deplete their energy quicker than the other nodes in the field (i.e., this is referred to as the hotspot...     

Heart rate variability in low birth weight growth restricted children during sleep and wake stages

Intrauterine growth restricted (IUGR) individuals have greater predisposition to develop a metabolic syndrome in later life manifesting itself as obesity, hypertension, type 2 diabetes or cardiovascular disease. Poor fetal growth may alter the regularity mechanism of cardiac autonomic system that is involved in the development of these diseases. The malfunctioning of the cardiac autonomic system assessed by decrease in heart rate variability (HRV) is associated with negative cardiovascular outcomes. This study is aimed at investigating the risk of development of coronary heart disease in IUGR children in later life. For that purpose HRV analysis of normal and growth restricted children was performed during sleep and wake stages. The study group consisted of 9–10 years old, 32 normal, 20 low birth weight IUGR children. The standard time domain HRV metrics (mean RR, SDNN, RMSSD, NN50 and pNN50) and Poincaré indices (SD₁ and SD₂) were used to analyse and compare the RR-interval time series of these groups. The IUGR children showed lower HRV as compared with normal children during both sleep and wake stages. The significantly decreased HRV during sleep provide an evidence of autonomic derangement that may be associated with higher risk of lethal arrhythmias in the IUGR children in later life.     

Separation and purification of hyaluronic acid by glucuronic acid imprinted microbeads

The purification of hyaluronic acid (HA) is relatively significant to use in biomedical applications. The structure of HA is formed by the repetitive units of glucuronic acid and N-acetyl glucosamine. In this study, glucuronic acid-imprinted microbeads have been supplied for the purification of HA from cell culture (Streptococcus equi). Histidine-functional monomer, methacryloylamidohistidine (MAH) was chosen as the metal-complexing monomer. The glucuronic acid-imprinted poly(ethyleneglycoldimethacrylate-MAH-Copper(II)) [p(EDMA-MAH-Cu²⁺)] microbeads have been synthesized by typical suspension polymerization procedure. The template glucuronic acid has been removed by employing 5 M methanolic KOH solution. p(EDMA-MAH-Cu²⁺) microbeads have been characterized by elemental analysis, Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) images and swelling studies. Moreover, HA adsorption experiments have been performed in a batch experimental set-up. Purification of HA from cell culture supernatant has been also investigated by determining the hyaluronidase activity using purified HA as substrate. The glucuronic acid imprinted p(EDMA-MAH-Cu²⁺) particles can be used many times with no significant loss in adsorption capacities. Also, the selectivity of prepared molecular imprinted polymers (MIP) has been examined. Results have showed that MIP particles are 19 times more selective for glucuronic acid than N-acetylglucose amine.     

Multi-rule Multi-objective Simulated Annealing Algorithm for Straight and U Type Assembly Line Balancing Problems

The task of balancing of assembly lines is of considerable industrial importance. It consists of assigning operations to workstations in a production line in such a way that (1) no assembly precedence constraint is violated, (2) no workstations in the line takes longer than a predefined cycle time to perform all tasks assigned to it, and (3) as few workstations as possible are needed to perform all the tasks in the set. This paper presents a new multiple objective simulated annealing (SA) algorithm for simple (line) and U type assembly line balancing problems with the aim of maximizing “smoothness index” and maximizing the “line performance” (or minimizing the number of workstations). The proposed algorithm makes use of task assignment rules in constructing feasible solutions. The proposed algorithm is tested and compared with literature test problems. The proposed algorithm found the optimal solutions for each problem in short computational times. A detailed performance analysis of the selected task assignment rules is also given in the paper.