Evaluation of Digitally Encoded Layer‐by‐layer Coated Microparticles as Cell Carriers

To obtain more biologically relevant data there is a growing interest in the use of living cells for assaying the biological activity of unknown chemical compounds. Density ‘multiplex’ cell‐based assays, where different cell types are mixed in one well and simultaneously investigated upon exposure to a certain compound are beginning to emerge. To be able to identify the cells they should be attached to microscopic carriers that are encoded. This paper investigates how digitally encoded microparticles can be loaded with cells while keeping the digital code in the microcarriers readable. It turns out that coating the surface of the encoded microcarriers with polyelectrolytes using the layer‐by‐layer (LbL) approach provides the microcarriers with a ‘highly functional’ surface. The polyelectrolyte layer allows the growth of the cells, allows the orientation of the cell loaded microcarriers in a magnetic field, and does not hamper the reading of the code. It has further been shown that the cells growing on the polyelectrolyte layer can become transduced by adenoviral particles hosted by the polyelectrolyte layer. It is concluded that the digitally encoded microparticles are promising materials for use in biomedical and pharmaceutical in‐vitro research where cells are used as tools.     

Visualisation of interlaboratory comparison results in PomPlots

In this work a novel graphical method is applied to the presentation of intercomparison results. This is demonstrated with the results of a recent intercomparison in measuring the ¹³⁷Cs, ⁴⁰K, and ⁹⁰Sr activity concentration in milk powder. The “PomPlot”, an intuitive graphical method, is used for producing a summary overview of the participants’ results of a common measurand. The “PomPlot” displays (relative) deviations of individual results from the reference value on the horizontal axis and (relative) uncertainties on the vertical axis.     

Complexation of gadolinium(III) ions on top of nanometre-sized magnetoliposomes

The complex of diethylenetriaminepentaacetate (DTPA) with the paramagnetic gadolinium ion [Gd(III)] is a well-known blood pool contrast agent for magnetic resonance imaging (MRI). To obtain MRI pictures from other anatomical structures, for instance from tissues containing cells with phagocytic activity, larger colloidal complexes have to be constructed. Therefore, in view of modifying the physiological behaviour, the DTPA chelate was first hydrophobized by covalently linking it to phosphatidylethanolamine (PE), and the resulting conjugate was then incorporated into nanometre-sized, sonicated phospholipid vesicles. Qualitative information on the affinity of the PE–DTPA derivative for Gd(III) ions was derived from competition experiments using the dye Arsenazo. Furthermore, it was found that only the membranotropic adducts residing in the outer shell of the vesicle bilayer are accessible to the lanthanide ion. The vesicular particulate was also used as a vehicle to transport PE–DTPA into the coating of so-called magnetoliposomes which consist of nanometre-sized iron oxide cores onto which a phospholipid bilayer is strongly chemisorbed. After loading the resulting structures with Gd(III), this new type of magnetoliposome may offer unique potentialities as a novel bi-label MRI contrast medium.     

An efficient numerical method for the resolution of the Kirchhoff‐Love dynamic plate equation

We solve numerically the Kirchhoff‐Love dynamic plate equation for an anisotropic heterogeneous material using a spectral method. A mixed velocity‐moment formulation is proposed for the space approximation allowing the use of classical Lagrange finite elements. The benefit of using high order elements is shown through a numerical dispersion analysis. The system resulting from this spatial discretization is solved analytically. Hence this method is particularly efficient for long duration experiments. This time evolution method is compared with explicit and implicit finite differences schemes in terms of accuracy and computation time. © 2004 Wiley Periodicals, Inc. Numer Methods Partial Differential Eq, 2005     

Identification of the impedance model of an implanted cochlear prosthesis from intracochlear potential measurements

Those suffering from a severe to profound sensorineural hearing loss can obtain substantial benefit from a cochlear implant prosthesis. An electrode array implanted in the inner ear stimulates auditory nerve fibers by direct injection of electrical current. A major limitation of today's technology is the imprecise control of intracochlear current flow, particularly the relatively wide spread of neural excitation. A better understanding of the intracochlear electrical fields is, therefore, required. This paper analyzes the structure of intracochlear potential measurements in relation to both the subject's anatomy and to the properties of the electrode array. An electrically equivalent network is proposed, composed of small lumped circuits for the interface impedance and for the cochlear tissues. The numerical methods required to estimate the model parameters from high-quality electrical potential recordings are developed. Finally, some models are presented for subjects wearing a Clarion CII device with a HiFocus electrode and discussed in terms of model reliability.     

Anion recognition by alpha-arylazo-N-confused calix[4]pyrroles

The first example of substitution reaction in the free alpha-position of N-confused calix[4]pyrroles is reported: azo-coupling with various arenediazonium salts. The obtained azocompounds were used for studies of their anion-binding properties by UV-Vis spectroscopy.     

提高FPGA-PWM计数器性能的位交换

当你需要一些模拟输出,并且系统中有一片FPGA时,你可能选择采用一个PWM模块和一个简单的低通滤波器,如图1所示.FPGA的输出通常是一种固定频率、可变占空比的波形,由一个计数器和一个数字比较器生成(表1).     

An Interference Approach to Perturbed Angular Correlation Spectroscopy

This paper recalls the formalism of H. J. Leisi, which shows an alternative way to understand Perturbed Angular Correlation Spectroscopy: as a quantum interference effect. This revised version was published online in July 2006 with corrections to the Cover Date.     

Flexible Nanosomes (SECosomes) Enable Efficient siRNA Delivery in Cultured Primary Skin Cells and in the Viable Epidermis of Ex Vivo Human Skin

The extent to which nanoscale‐engineered systems cross intact human skin and can exert pharmacological effects in viable epidermis is controversial. This research seeks to develop a new lipid‐based nanosome that enables the effective delivery of siRNA into human skin. The major finding is that an ultraflexible siRNA‐containing nanosome—prepared using DOTAP, cholesterol, sodium cholate, and 30% ethanol—penetrates into the epidermis of freshly excised intact human skin and is able to enter into the keratinocytes. The nanosomes, called surfactant‐ethanol‐cholesterol‐osomes (SECosomes), show excellent size, surface charge, morphology, deformability, transfection efficiency, stability, and skin penetration capacity after complexation with siRNA. Importantly, these nanosomes have ideal characteristics for siRNA encapsulation, in that the siRNA is stable for at least 4 weeks, they enable highly efficient transfection of in vitro cultured cells, and are shown to transport siRNA delivery through intact human skin where changes in the keratinocyte cell state are demonstrated. It is concluded that increasing flexibility in nanosomes greatly enhances their ability to cross the intact human epidermal membrane and to unload their payload into targeted epidermal cells.