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Cellular Material (cellular + material)
Selected AbstractsMicrostructure and Transport Properties of Cellular Materials: Representative Volume ElementADVANCED ENGINEERING MATERIALS, Issue 10 2009Emmanuel Brun The representative volume element (RVE) plays a central role in efforts to predict the effective thermo-physical and transport properties of heterogeneous materials. A quantitative definition of its size is proposed in this work. It is shown that RVE depends on the morphological or physical property being investigated. The methodology is applied to real samples of open-celled materials (such as metallic foam) whose structure is obtained from X-Ray microtomography. [source] Influence of Solid Phase Conductivity and Cellular Structure on the Heat Transfer Mechanisms of Cellular Materials: Diverse Case Studies,ADVANCED ENGINEERING MATERIALS, Issue 10 2009Eusebio Solórzano An analysis on the influence of solid phase thermal conductivity and cellular structure on the heat transfer mechanisms (HTMs) by means of studding diverse case studies combining theoretical and experimental data. The radiation and conduction mechanisms have been analyzed for cellular materials based on insulating and conductive matrixes using similar concepts and models for both types of materials. [source] Heat-Transfer Coefficient for Cellular Materials Modelled as an Array of Elliptic Rods,ADVANCED ENGINEERING MATERIALS, Issue 10 2009Marcelo J. S. de Lemos Convective heat-transfer coefficients in foam-like materials, modelled as an array of elliptic rods, are numerically determined. An incompressible fluid is considered, flowing through an infinite foam-like material with an arbitrary solid temperature. A repetitive cell is identified and periodic boundary conditions are applied. Turbulence is handled with both low and high Reynolds number formulations. The interfacial heat-transfer coefficient is obtained by volume integrating the distributed variables obtained within the cell. The results indicate that, for the same mass-flow rate, materials formed by elliptic rods have a lower interfacial heat-transfer coefficient compared to other media modelled as staggered arrays of square rods. [source] A new look at an old visual system: structure and development of the compound eyes and optic ganglia of the brine shrimp artemia salina linnaeus, 1758 (branchiopoda, anostraca)DEVELOPMENTAL NEUROBIOLOGY, Issue 2 2002Miriam Wildt Abstract Compared to research carried out on decapod crustaceans, the development of the visual system in representatives of the entomostracan crustaceans is poorly understood. However, the structural evolution of the arthropod visual system is an important topic in the new debate on arthropod relationships, and entomostracan crustaceans play a key role in this discussion. Hence, data on structure and ontogeny of the entomostracan visual system are likely to contribute new aspects to our understanding of arthropod phylogeny. Therefore, we explored the proliferation of neuronal stem cells (in vivo incorporation of bromodeoxyuridine) and the developmental expression of synaptic proteins (immunohistochemistry against synapsins) in the developing optic neuropils of the brine shrimp Artemia salina Linnaeus, 1758 (Crustacea, Entomostraca, Branchiopoda, Anostraca) from hatching to adulthood. The morphology of the adult visual system was examined in serial sections of plastic embedded specimens. Our results indicate that the cellular material that gives rise to the visual system (compound eyes and two optic ganglia) is contributed by the mitotic activity of neuronal stem cells that are arranged in three band-shaped proliferation zones. Synapsin-like immunoreactivity in the lamina ganglionaris and the medulla externa initiated only after the anlagen of the compound eyes had already formed, suggesting that the emergence of the two optic neuropils lags behind the proliferative action of these stem cells. Neurogenesis in A. salina is compared to similar processes in malacostracan crustaceans and possible phylogenetic implications are discussed. © 2002 Wiley Periodicals, Inc. J Neurobiol 52: 117,132, 2002 [source] Utility of the thromboplastin-plasma cell-block technique for fine-needle aspiration and serous effusionsDIAGNOSTIC CYTOPATHOLOGY, Issue 2 2009D.M.L.T., Manisha B. Kulkarni M.Sc. Abstract (I) To assess the feasibility of thromboplastin-plasma (TP) method for cell block, (II) to concentrate the minimal cellular material from effusions and needle-rinses by block preparation and improve visual details, (III) to compare conventional cytological smears with cell blocks for final assessment, and (IV) to assess utility of immunocytochemistry (ICC) for diagnostic accuracy. Seventy cell blocks were prepared by TP technique using surplus fluid from 38 serous effusions, and for 32 ultrasonography-guided fine-needle aspiration cytology (FNAC) material, rinses of syringes and needles were collected in normal saline after conventional cytological smears. Then, cell blocks were compared with conventional smears for adequacy, morphologic preservation, and ICC. Absolute concordance seen in 66 cases (94%) between the smears and cell blocks. Advantages with the blocks were cellular concentration in a limited field and better cellular preservation with architectural pattern. Quality of ICC was comparable to that of standard controls. Diagnostic discrepancy was seen in two cases where cell blocks were positive but smears were negative. Two cell blocks were nonrepresentative. Cell block serves as a useful adjunct to traditional cytological smears. TP method is simple, cost effective, and reproducible. It is easy when compared with agar-embedding technique. Ancillary techniques like ICC can be performed successfully. Diagn. Cytopathol. 2009. © 2008 Wiley-Liss, Inc. [source] Improvement of diagnostic accuracy and screening conditions with liquid-based cytologyDIAGNOSTIC CYTOPATHOLOGY, Issue 11 2006Doris Schledermann M.D. Abstract The aim of this population-based study was to compare the histological follow-up diagnoses of cervicocytological neoplasia (dysplasia, carcinoma in situ and carcinoma) in conventional Papanicolaou (CP) smear and ThinPrep® PapTestÔ samples (TP). All cytological samples from the County of Funen, Denmark, in the periods 2000 (n = 34,832) and 2002 (n = 29,995) were included in the study. In 2000 and 2002, the specimens were CP and TP, respectively. The detection rate of , mild dysplasia was 0.8% in CP and 1.4% in TP, showing a 75% increase in TP when compared with CP (p < 0.001). Histological follow-up of , moderate dysplasia revealed a neoplastic lesion in 77.1% and 87.9% in CP and TP, respectively (P < 0.001). The present study indicates that the diagnostic accuracy of cervical cytology is improved with liquid-based cytology. In addition, we focus on the optimized cellular material that shows the diagnostic details very clearly to the microscopist and leads to radically improved screening conditions. Diagn. Cytopathol. 2006;34: 780,785. © 2006 Wiley-Liss, Inc. [source] Thyroid tumor marker genomics and proteomics: Diagnostic and clinical implicationsJOURNAL OF CELLULAR PHYSIOLOGY, Issue 3 2010Angelo Carpi Two systems biology concepts, genomics and proteomics, are highlighted in this review. These techniques are implemented to optimize the use of thyroid tumor markers (TTM). Tissue microarray studies can produce genetic maps and proteomics, patterns of protein expression of TTM derived from preoperative biopsies and specimens. For instance, papillary and medullary thyroid cancers harbor RAS, RET, and BRAF genetic mutations. Follicular thyroid cancers harbor translocations and fusions of certain genes (PAX 8 and PPAR-gamma). Proteomic analysis from various tissue sources can provide useful information regarding the overall state of a thyroid cancer cell. Understanding the molecular events related to these genetic and protein alterations can potentially clarify thyroid cancer pathogenesis and guide appropriate molecular targeted therapies. However, despite the realization that these emerging technologies hold great promise, there are still significant obstacles to the routine use of TTM. These include equivocal thyroid nodule tissue morphologic interpretations, inadequate standardization of methods, and monetary costs. Interpretative shortcomings are frequently due to the relative scarcity of cellular material from fine-needle aspiration biopsy (FNAB) specimens. This can be rectified with large needle aspiration biopsy (LNAB) techniques and is exemplified by the favorable performance of galectin-3 determinations on LNAB specimens. J. Cell. Physiol. 224: 612,619, 2010. © 2010 Wiley-Liss, Inc. [source] Progress and limitations in the use of in vitro cell cultures to serve as a permeability screen for the blood-brain barrierJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 11 2001Mark Gumbleton Abstract A relatively simple, widely applicable, and robust in vitro method of predicting blood-brain barrier (BBB) permeability to central nervous system-acting drugs is an increasing need. A cell-based model offers the potential to account for transcellular and paracellular drug diffusional processes, metabolism, and active transport processes, as well as nondefined interactions between a drug and cellular material that may impact upon a membrane's overall permeability profile. Any in vitro BBB cell model to be utilized for the transendothelial BBB permeability screening of potential central nervous system drugs must display reproducible solute permeability, and a number of other general criteria including: a restrictive paracellular barrier; a physiologically realistic cell architecture; the functional expression of key transporter mechanisms; and allow ease of culture to meet the technical and time constraints of a screening program. This article reviews the range of in vitro cell-based BBB models available, including the primary/low passage bovine and porcine brain endothelial cultures as well as the spectrum of immortalized brain endothelial cell lines that have been established. The article further discusses the benefits and limitations of exploiting such systems as in vitro BBB permeability screens. © 2001 Wiley-Liss, Inc. and the American Pharmaceutical Association J Pharm Sci 90:1681,1698, 2001 [source] Aryl acrylate based high-internal-phase emulsions as precursors for reactive monolithic polymer supportsJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 2 2005Peter Krajnc Abstract Water-in-oil high-internal-phase emulsions (HIPEs), containing 4-nitrophenyl acrylate and 2,4,6-trichlorophenyl acrylate as reactive monomers, were prepared and polymerized, and highly porous monolithic materials resulted. The novel materials were studied by combustion analysis, Fourier transform infrared spectroscopy scanning electron microscopy, mercury porosimetry, and N2 adsorption/desorption analysis. With both esters, cellular macroporous monolithic polymers were obtained; the use of 4-nitrophenyl acrylate resulted in a cellular material with void diameters between 3 and 7 ,m and approximately 3-,m interconnects, whereas the use of 2,4,6-trichlorophenyl acrylate yielded a foam with void diameters between 2 and 5 ,m, most interconnects being around 1 ,m. The resulting monoliths proved to be very reactive toward nucleophiles, and possibilities of functionalizing the novel polymer supports were demonstrated via reactions with amines bearing additional functional groups and via the synthesis of an acid chloride derivative. Tris(hydroxymethyl)aminomethane and tris(2-aminoethyl)amine derivatives were obtained. The hydrolysis of 4-nitrophenylacrylate removed the nitrophenyl group, yielding a monolithic acrylic acid polymer. Furthermore, functionalization to immobilized acid chloride was performed very efficiently, with more than 95% of the acid groups reacting. The measurement of the nitrogen content in 4-nitrophenyl acrylate poly(HIPE)s after various times of hydrolysis showed the influence of the total pore volume of the monolithic polymers on the velocity of the reaction, which was faster with the more porous polymer. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 296,303, 2005 [source] Aspects of biopsy procedures prior to preimplantation genetic diagnosisPRENATAL DIAGNOSIS, Issue 9 2001Anick De Vos Abstract Today, preimplantation genetic diagnosis (PGD) is offered in over 40 centres worldwide for an expanded range of genetic defects causing disease. This very early form of prenatal diagnosis involves the detection of affected embryos by fluorescent in situ hybridization (FISH) (sex determination or chromosomal defects) or by polymerase chain reaction (PCR) (monogenic diseases) prior to implantation. Genetic analysis of the embryos involves the removal of some cellular mass from the embryos (one or two blastomeres at cleavage-stage or some extra-embryonic trophectoderm cells at the blastocyst stage) by means of an embryo biopsy procedure. Genetic analysis can also be performed preconceptionally by removal of the first polar body. However, additional information is then often gained by removal of the second polar body and/or a blastomere from the embryo. Removal of polar bodies or cellular material from embryos requires an opening in the zona pellucida, which can be created in a mechanical way (partial zona dissection) or chemical way (acidic Tyrode's solution). However, the more recent introduction of laser technology has facilitated this step enormously. Different biopsy procedures at different preimplantation stages are reviewed here, including their pros and cons and their clinical applications. The following aspects will also be discussed: safety of zona drilling by laser, use of Ca2+/Mg2+ -free medium for decompaction, and removal of one or two cells from cleavage-stage embryos. Copyright © 2001 John Wiley & Sons, Ltd. [source] Influence of Solid Phase Conductivity and Cellular Structure on the Heat Transfer Mechanisms of Cellular Materials: Diverse Case Studies,ADVANCED ENGINEERING MATERIALS, Issue 10 2009Eusebio Solórzano An analysis on the influence of solid phase thermal conductivity and cellular structure on the heat transfer mechanisms (HTMs) by means of studding diverse case studies combining theoretical and experimental data. The radiation and conduction mechanisms have been analyzed for cellular materials based on insulating and conductive matrixes using similar concepts and models for both types of materials. [source] Conducting Nanocomposite Polymer Foams from Ice-Crystal-Templated Assembly of Mixtures of ColloidsADVANCED MATERIALS, Issue 28 2009Catheline A. L. Colard Fabrication of conducting nanocomposite- reinforced soft polymer foams is demonstrated. These multicomponent cellular materials are built from a mixture of colloids dispersed in water by freeze,drying, thereby using ice crystals as template for the porous structure. An excluded-volume effect armors the "soft"-polymer cell walls with "hard" nanoparticles, thereby enhancing the mechanical robustness of the foams. [source] A lumped mass numerical model for cellular materials deformed by impactINTERNATIONAL JOURNAL FOR NUMERICAL METHODS IN ENGINEERING, Issue 11 2001Z. H. Tu Abstract When impacted by a relatively rigid body, cellular materials undergo severe deformation and extensive material failure. However, such behaviour may not be well described using traditional numerical approaches such as the finite element method. This paper presents a lumped mass numerical model which can accommodate high degrees of deformation and material failure. The essence of this model is to discretize a block of material into contiguous element volumes, each represented by a mass point. Interactions between a node and its neighbours are accounted for by defining ,connections' that represent their interfaces which transmit stresses. Strains at a node are calculated from the co-ordinates of the surrounding nodes; these also determine the stresses on the interfaces. The governing equations for the entire solution domain are then converted into a system of equations of motion with nodal positions as unknowns. Failure criteria and possible combinations of ,connection' breakage are incorporated to model the occurrence of damage. A practical contact algorithm is also developed to describe the contact interactions between cellular materials and rigid bodies. Simulations for normal and oblique impacts of rigid rectangular, cylindrical and wedge-tipped impactors on crushable foam blocks are presented to substantiate the validity of the model. The generally good correlation between the numerical and experimental results demonstrates that the proposed numerical approach is able to model the impact response of the crushable foam. However, some limitations in modelling crack propagation in oblique impacts by a rigid impactor on foam blocks are observed. Copyright © 2001 John Wiley & Sons, Ltd. [source] Extraction Using Moderate Electric FieldsJOURNAL OF FOOD SCIENCE, Issue 1 2004I. SENSOY ABSTRACT: During moderate electric field (MEF) processing, a voltage applied across a food material may affect the permeability of cell membranes. It is known that high electric fields can cause either reversible or irreversible rupture of cell membranes. In this research, the effect of MEF processing on permeability was studied. Effects of frequency and electric field strength were investigated. Cellular structure was investigated by transmission electron microscopy (TEM). Fermented black tea leaves and fresh or dry mint leaves were placed in tea bags or cut in 1 cm2 squares, depending on the experiment, and immersed in an aqueous fluid medium. Control samples were heated on a hot plate. MEF treatments were conducted by applying a voltage across electrodes immersed in opposite sides of the beaker. Control and MEF-treated fresh mint leaf samples heated to 50°C were analyzed by TEM. MEF processing significantly increased the extraction yield for fresh mint leaves because of additional electric field effects during heating. Dried mint leaves and fermented black tea leaves were not affected by the treatment type. Low frequency resulted in higher extraction rates for fresh mint leaves. The electric field strength study showed that electrical breakdown is achieved even at low electric field strengths. MEF treatment shows potential to be used as an alternative to conventional heating for extraction from cellular materials. [source] Design of cellular porous biomaterials for wall shear stress criterionBIOTECHNOLOGY & BIOENGINEERING, Issue 4 2010Yuhang Chen Abstract The microfluidic environment provided by implanted prostheses has a decisive influence on the viability, proliferation and differentiation of cells. In bone tissue engineering, for instance, experiments have confirmed that a certain level of wall shear stress (WSS) is more advantageous to osteoblastic differentiation. This paper proposes a level-set-based topology optimization method to regulate fluidic WSS distribution for design of cellular biomaterials. The topological boundary of fluid phase is represented by a level-set model embedded in a higher-dimensional scalar function. WSS is determined by the computational fluid dynamics analysis in the scale of cellular base cells. To achieve a uniform WSS distribution at the solid,fluid interface, the difference between local and target WSS is taken as the design criterion, which determines the speed of the boundary evolution in the level-set model. The examples demonstrate the effectiveness of the presented method and exhibit a considerable potential in the design optimization and fabrication of new prosthetic cellular materials for bioengineering applications. Biotechnol. Bioeng. 2010;107:737,746. © 2010 Wiley Periodicals, Inc. [source] Quantitative phase microscopy: A new tool for investigating the structure and function of unstained live cellsCLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, Issue 12 2004Claire L Curl SUMMARY 1.,The optical transparency of unstained live cell specimens limits the extent to which information can be recovered from bright-field microscopic images because these specimens generally lack visible amplitude-modulating components. However, visualization of the phase modulation that occurs when light traverses these specimens can provide additional information. 2.,Optical phase microscopy and derivatives of this technique, such as differential interference contrast (DIC) and Hoffman modulation contrast (HMC), have been used widely in the study of cellular materials. With these techniques, enhanced contrast is achieved, which is useful in viewing specimens, but does not allow quantitative information to be extracted from the phase content available in the images. 3.,An innovative computational approach to phase microscopy, which provides mathematically derived information about specimen phase-modulating characteristics, has been described recently. Known as quantitative phase microscopy (QPM), this method derives quantitative phase measurements from images captured using a bright-field microscope without phase- or interference-contrast optics. 4.,The phase map generated from the bright-field images by the QPM method can be used to emulate other contrast image modes (including DIC and HMC) for qualitative viewing. Quantitative phase microscopy achieves improved discrimination of cellular detail, which permits more rigorous image analysis procedures to be undertaken compared with conventional optical methods. 5.,The phase map contains information about cell thickness and refractive index and can allow quantification of cellular morphology under experimental conditions. As an example, the proliferative properties of smooth muscle cells have been evaluated using QPM to track growth and confluency of cell cultures. Quantitative phase microscopy has also been used to investigate erythrocyte cell volume and morphology in different osmotic environments. 6.,Quantitative phase microscopy is a valuable, new, non-destructive, non-interventional experimental tool for structural and functional cellular investigations. [source] | |||||||||||||||||||