Development of Neuropeptide Y and Cell-Penetrating Peptide MAP Adsorbed onto Lipid Nanoparticle Surface

Functionalization of nanoparticles surfaces have been widely used to improve diagnostic and therapeutic biological outcome. Several methods can be applied to modify nanoparticle surface; however, in this article we focus toward a simple and less time-consuming method. We applied an adsorption method on already formulated nanostructured lipid carriers (NLC) to functionalize these nanoparticles with three distinct peptides sequences. We selected a cell-penetrating peptide (CPP), a lysine modified model amphipathic peptide (Lys(N₃)-MAP), CPP/drug complex, and the neuropeptide Y. The aim of this work is to evaluate the effect of several parameters such as peptide concentration, different types of NLC, different types of peptides, and incubation medium on the physicochemical proprieties of NLC and determine if adsorption occurs. The preliminary results from zeta potential analysis indicate some evidence that this method was successful in adsorbing three types of peptides onto NLC. Several non-covalent interactions appear to be involved in peptide adsorption with the possibility of three adsorption peptide hypothesis that may occur with NLC in solution. Moreover, and for the first time, in silico docking analysis demonstrated strong interaction between CPP MAP and NPY Y1 receptor with high score values when compared to standard antagonist and NPY.     

通过有光阑近轴ABCD光学系统激光束的近似解析传输公式

用傅立叶级数展开法研究光束通过有光阑限制的近轴ABCD光学系统的传输特性,导出了光阑透射率函数不同时的传输公式。硬边光阑的情况可作为其它光阑的特例得到,其它光阑也可视作硬边光阑来处理。数值计算表明了该方法快速的优点,并得到与用Collins公式直接积分一致结果。     

激光对红外系统的失效机理和破坏效应研究

根据红外光学系统的会聚特性,用光学增益方法分析了红外系统中各元件对应的光强分布,确定了位于焦面附近光学元件是激光破坏的易损部件,并提出了强激光对红外系统元件损伤,造成其探测、制导功能失效的硬破坏机理;由红外滤光片、探测器和信号处理电路与入射激光波长的光谱响应分析,提出了弱激光对红外系统干扰,导致其探测、制导功能在激光辐照一段时间内失效的软破坏机理;开展了激光辐照红外系统的失效验证实验,较好地解释了其失效的机理和效应。     

Vibrational analysis of d-PCL(530)/siloxane-based hybrid electrolytes doped with two lithium salts

The present study has been focused on environmentally friendly sol–gel-derived electrolytes based on a di-urethane cross-linked d-PCL(530)/siloxane network [where d represents di, PCL identifies the poly(ε-caprolactone) biopolymer, and 530 is the average molecular weight in grams per mole] doped with a wide range of concentration of lithium perchlorate and lithium bis(trifluoromethanesulfonyl)imide. Fourier Transform Infrared and Raman spectroscopies have been applied to evaluate the extent of ionic association. Characteristic bands of the PCL(530) segments, of the urethane cross-links, and of the anions have been examined to gain insight into the cation/biopolymer, cation/anion, and cation/cross-link interactions. In both electrolyte systems, “free” ions and contact ions have been identified. The addition of salt modifies the hydrogen-bonded array of the host matrix, causing the destruction/formation of the urethane/urethane aggregates.     

Production of metakaolin from industrial cellulose waste

Research focused on the transformation and utilization of industrial wastes into products of commercial interest plays an increasingly important role. Residual pulp can become useful in the manufacture of different materials, providing high value to this waste and reducing its environmental impact when disposed of improperly in the environment. The main constituents of this waste are kaolin and calcium carbonate (CaCO₃). Starting from kaolin, metakaolin can be produced by calcination of the residue at 630?°C for 2?h in a rotary reactor with air flow, followed by solubilization with hydrochloric acid to remove the CaCO₃. The development of technological alternatives aimed at the reuse of certain wastes can result in applications of real economic interest to the chemical industry and ceramics and glass, which is the case in this study. The raw material and metakaolin obtained were analyzed by thermogravimetric analysis and derivative thermogravimetric analysis, X-ray diffraction, and X-ray fluorescence spectroscopy with promising results. This is because metakaolin was obtained free of contamination by other materials.     

Influence of hydrogen bonds on the molecular structure and conformations of two (C30H48O2) pentacyclic triterpene isomers

The structural study of two (C₃₀H₄₈O₂) pentacyclic triterpene (PCTT) isomers is presented. These terpenes, known as 30-hydroxy-lup-20(29)-en-3-one (1) and (11α)-11-hydroxy-lup-20(29)-en-3-one (2), were isolated from Maytenus imbricata Mart. Ex Reissek (Celastraceae). The molecular structure of 1 and 2 differs in the position of the hydroxyl group. Both compounds crystallize in non-centrosymmetric space groups with two molecules in the asymmetric unit. The crystal structure of 1 shows a triclinic P1 space group (a = 9.5518(1) ?, b = 9.7083(1) ?, c = 14.4696(2) ?, α = 93.832(1)°, β = 102.833(1)°, and γ = 103.307(1)°), while compound 2 crystallizes in a monoclinic P2₁ one (a = 13.4439(16) ?, b = 14.4463(14) ?, c = 13.5224(9) ? and β = 99.703(8)°). The two molecules independent by symmetry of 1 differ slightly due to the presence of static disorder in oxygen atoms. In addition, the intermolecular geometries of 1 and 2 were analysed, and in each isomer the crystal packing is stabilized by O-H…O intermolecular hydrogen bonds and van der Waals forces.     

Studies on crude oil‐water biphasic mixtures by low‐field NMR

Low‐field ¹H NMR was used in this work for the analysis of mixtures involving crude oils and water. CPMG experiments were performed to determine the transverse relaxation time (T₂) distribution curves, which were computed by the inverse Laplace transform of the echo decay data. The instrument's ability of quantifying water and petroleum in biphasic mixtures following different methodologies was tested. For mixtures between deionized water and petroleum, one achieved excellent results, with root mean squared error of cross‐validation (RMSECV) of 0.8% for a regression between the water content (wt %) and the relative area of the water peak in the T₂ distribution curve, or a standard deviation of 0.9% for the relationship between the water content and the relative water peak area, corrected by the relative hydrogen index of the crude. In the case of biphasic mixtures of Mn²⁺‐doped water and crude oils, the best result of RMSECV = 1.6% was achieved by using the raw magnetization decay data for a partial least squares regression. Copyright © 2012 John Wiley & Sons, Ltd.     

Stress Field Evolution under Mechanically Simulated Hull Slamming Conditions

The effect of repeated loading from mechanically simulated hull slamming on foam core sandwich composites was investigated utilizing a novel technique that simultaneously measured temperature and displacement while cyclic loading occurred. Thermoelastic Stress Analysis (TSA) and Digital Image Correlation (DIC) techniques were combined using a single infrared camera for characterization of the foam core. Improved stress fields with TSA results were found through deformation compensation. Initial work approximating hull slamming conditions mechanically utilizing a custom device were performed. Mechanically loading offers several benefits over water impact investigations, including easy access to the sample during the slamming event, an unobstructed optical path, and accelerated testing. Evolving stress fields under long-duration, repeated simulated hull slamming loading were observed around a growing delamination crack between the foam core and skin.     

Synchronization and Non-Smooth Dynamical Systems

In this article we establish an interaction between non-smooth systems, geometric singular perturbation theory and synchronization phenomena. We find conditions for a non-smooth vector fields be locally synchronized. Moreover its regularization provide a singular perturbation problem with attracting critical manifold. We also state a result about the synchronization which occurs in the regularization of the fold-fold case. We restrict ourselves to the 3-dimensional systems (ℓ = 3) and consider the case known as a T-singularity.