Cell Volume Fraction Research Articles

The effect of red blood cells on blood heat transfer

In an attempt to analyze the effect of red blood cells on heat transfer, a two-phase flow heat transfer model of flowing blood was proposed in this paper. In this model, blood is treated as a two-phase fluid composed of red blood cells as the particle phase and plasma as the carrier fluid. The micro-particle dynamics, including aggregation, deformation, mutual collisions of red blood cells and relative movement of red blood cells to plasma, are considered by some equations or simplified methods. The velocity field, temperature field, fluid viscosity and volume fraction of red blood cells in a two-phase blood flow can be calculated using this model. To verify the accuracy of the simulation results of the model, the velocity distribution and heat transfer efficiency calculated by this model were compared with available experimental data from the literature. Good agreement was obtained between these data; thus, this model can accurately simulate the blood flow and heat transfer in a vessel. Then, the model was used to analyze how the micro-particle red blood cells affect the heat transfer of blood, and red blood cells were found to enhance heat transfer efficiency of blood. The viscosity properties of blood, the solid pressure and the lateral movement of red blood cells are the important determinants of this enhancement. The influence of red blood cells on the heat transfer efficiency of pulsatile blood flow was also calculated using this model.

Human CYP2A13 and CYP2F1 Mediate Naphthalene Toxicity in the Lung and Nasal Mucosa of CYP2A13/2F1-Humanized Mice.

Background:The potential carcinogenicity of naphthalene (NA), a ubiquitous environmental pollutant, in human respiratory tract is a subject of intense debate. Chief among the uncertainties in risk assessment for NA is whether human lung CYP2A13 and CYP2F1 can mediate NA’s respiratory tract toxicity.Objectives:We aimed to assess the in vivo function of CYP2A13 and CYP2F1 in NA bioactivation and NA-induced respiratory tract toxicity in mouse models.Methods:Rates of microsomal NA bioactivation and the effects of an anti-CYP2A antibody were determined for lung and nasal olfactory mucosa (OM) from Cyp2abfgs-null, CYP2A13-humanized, and CYP2A13/2F1-humanized mice. The extent of NA respiratory toxicity was compared among wild-type, Cyp2abfgs-null, and CYP2A13/2F1-humanized mice following inhalation exposure at an occupationally relevant dose (10 ppm for 4 hr).Results:In vitro studies indicated that the NA bioactivation activities in OM and lung of the CYP2A13/2F1-humanized mice were primarily contributed by, respectively, CYP2A13 and CYP2F1. CYP2A13/2F1-humanized mice showed greater sensitivity to NA than Cyp2abfgs-null mice, with greater depletion of nonprotein sulfhydryl and occurrence of cytotoxicity (observable by routine histology) in the OM, at 2 or 20 hr after termination of NA exposure, in humanized mice. Focal, rather than gross, lung toxicity was observed in Cyp2abfgs-null and CYP2A13/2F1-humanized mice; however, the extent of NA-induced lung injury (shown as volume fraction of damaged cells) was significantly greater in the terminal bronchioles of CYP2A13/2F1-humanized mice than in Cyp2abfgs-null mice.Conclusion:CYP2F1 is an active enzyme. Both CYP2A13 and CYP2F1 are active toward NA in the CYP2A13/2F1-humanized mice, where they play significant roles in NA-induced respiratory tract toxicity. https://doi.org/10.1289/EHP844

Microstructural effects in drug release by solid and cellular polymeric dosage forms: A comparative study

In recent studies, we have introduced melt-processed polymeric cellular dosage forms to achieve both immediate drug release and predictable manufacture. Dosage forms ranging from minimally-porous solids to highly porous, open-cell and thin-walled structures were prepared, and the drug release characteristics investigated as the volume fraction of cells and the excipient molecular weight were varied. In the present study, both minimally-porous solid and cellular dosage forms consisting of various weight fractions of Acetaminophen drug and polyethylene glycol (PEG) excipient are prepared and analyzed. Microstructures of the solid forms and the cell walls range from single-phase solid solutions of the excipient and a small amount of drug molecules to two-phase composites of the excipient and tightly packed drug particles. Results of dissolution experiments show that the minimally-porous solid forms disintegrate and release drug by slow surface erosion. The erosion rate decreases as the drug weight fraction is increased. By contrast, the open-cell structures disintegrate rapidly by viscous exfoliation, and the disintegration time is independent of drug weight fraction. Drug release models suggest that the solid forms erode by convective mass transfer of the faster-eroding excipient if the drug volume fraction is small. At larger drug volume fractions, however, the slower-eroding drug particles hinder access of the free-flowing fluid to the excipient, thus slowing down erosion of the composite. Conversely, the disintegration rate of the cellular forms is limited by diffusion of the dissolution fluid into the excipient phase of the thin cell walls. Because the wall thickness is of the order of the drug particle size, and the particles are enveloped by the excipient during melt-processing, the drug particles cannot hinder diffusion through the excipient across the walls. Thus the disintegration time of the cellular forms is mostly unaffected by the volume fraction of drug in the walls.

Analysis of histological and immunohistochemical patterns of benign and malignant adrenocortical tumors by computerized morphometry

Diagnosis of benign and purely localized malignant adrenocortical lesions is still a complex issue. Moreover, histology-based diagnosis may suffer of a moment of subjectivity due to inter- and intra-individual variations. The aim of the present study was to assess, by computerized morphometry, the morphological features in benign and malignant adrenocortical neoplasms.Eleven adrenocortical adenomas (ACA) were compared with 18 adrenocortical cancers (ACC). All specimens were stained with H&E, cellular proliferation marker Ki-67 and reticulin. We generated a morphometric model based on the analysis of volume fractions occupied by Ki-67 positive and negative cells (nuclei and cytoplasm), vascular and inflammatory compartment; we also analyzed the surface fraction occupied by reticulin. We compared the quantitative data of Ki-67 obtained by morphometry with the quantification resulting from pathologist’s visual reading.The volume fraction of Ki-67 positive cells in ACCs was higher than in ACAs. The volume fraction of nuclei in unit volume and the nuclear/cytoplasmic ratio in both Ki-67 negative cells and Ki-67 positive cells were prominent in ACCs. The surface fraction of reticulin was considerably lower in ACCs.Our computerized morphometric model is simple, reproducible and can be used by the pathologist in the histological workup of adrenocortical tumors to achieve precise and reader-independent quantification of several morphological characteristics of adrenocortical tumors.

Continuous manufacture of polymeric cellular dosage forms

The most prevalent pharmaceutical dosage forms at present are granular solids in the form of oral tablets and capsules. While effective in releasing drug rapidly upon contact with gastrointestinal fluid, their manufacture, which relies on particulate processing, is fraught with difficulties associated with the unpredictable inter-particle interactions. Such difficulties, however, could be easily overcome by transitioning to a liquid-based process. Therefore, we have recently introduced melt‐processed polymeric cellular dosage forms. The drug release behavior of the cellular forms was tailored by altering the microstructure; yet their preparation relied on an inefficient batch method comprising gas dissolution, and nucleation and growth of microscopic gas bubbles in the melt. In this study, therefore, we present a continuous microfluidic melt extrusion and molding process. The cellular dosage forms are produced by injecting gas bubbles directly into the melt stream in a micro‐ or milli-fluidic channel, followed by molding and solidification of the cellular structure. A model is developed to illustrate the effects of the width, frequency, and pressure of the gas injection pulses, and the flow rate and viscosity of the melt, on the microstructural parameters of the dosage forms produced. Experimental results show that the size and volume fraction of gas-filled cells (or voids) are predictable. They also confirm that the dosage form disintegration rate and density can be tailored by altering the volume fraction of voids. It is thus demonstrated that polymeric cellular dosage forms with predictable drug release properties, and density, can be readily manufactured by a continuous process.

MODELING THE LOWER AND THE UPPER REGIME OF THE BLOOD UNIDIRECTIONAL FLOW IN MICRO-VESSELS

There is a formation of a cell-depleted layer adjacent to micro-vessel walls during blood flow in regime of creeping flow. This biological layer is of vital importance in the transport of oxygen-saturated red cells to the unsaturated tissues. In this work, we first discuss the physical mechanisms in this creeping flow which lead to the formation of a cell-depleted layer. The main non-dimensional physical parameter governing the layer formation are presented from a simple model of predicting the layer thickness in steady state. In particular, we study the blood flow in two different scales (i.e. lower and upper bound limit) of the in vitromicrocirculation. For this end we examine the capillary core flow solution in which the inner fluid is considered a non-Newtonian one facing a small annular gap of a Newtonian plasma. This model is a good approximation for the blood flow occurring in the length scales of venules and arterioles diameters. In addition, we also propose a model for smaller vessels, like capillaries with diameter of few micrometers. In this lower bound limit we consider a periodic configuration of lined up paraboloidal cells moving in a flow under regime of lubrication approximation. So, the boundary condition in this lower flow limit considers the cell velocity and a numerical integration is used to solve the volumetric flux as a function of the pressure drop inside the capillary. The effect of the cell volume fraction in terms of the depleted layer thickness and cell aggregations is also investigated with this model. The influence of the wall irregularities on the flow is studied by using a simple sinusoidal model for the wall. Finally, an intrinsic viscosity of the blood is predicted theoretically for both the lower and upper bound regimes as a function of the non-dimensional vessel diameter, in good agreement with previous experimental works. We compare our theoretical predictions with experimental data and obtain a qualitative good for the classic Fahraeus-Lindqvist effect. A possible application of this work could be in illness diagnosis by evaluating of changes in the intrinsic viscosity due to blood abnormalities. Keywords: blood, hydrodynamic diffusion, non-Newtonian, rheology, cell-depleted layer

Microstructural models for diffusion MRI in breast cancer and surrounding stroma: an ex vivo study.

The diffusion signal in breast tissue has primarily been modelled using apparent diffusion coefficient (ADC), intravoxel incoherent motion (IVIM) and diffusion tensor (DT) models, which may be too simplistic to describe the underlying tissue microstructure. Formalin‐fixed breast cancer samples were scanned using a wide range of gradient strengths, durations, separations and orientations. A variety of one‐ and two‐compartment models were tested to determine which best described the data. Models with restricted diffusion components and anisotropy were selected in most cancerous regions and there were no regions in which conventional ADC or DT models were selected. Maps of ADC generally related to cellularity on histology, but maps of parameters from more complex models suggest that both overall cell volume fraction and individual cell size can contribute to the diffusion signal, affecting the specificity of ADC to the tissue microstructure. The areas of coherence in diffusion anisotropy images were small, approximately 1 mm, but the orientation corresponded to stromal orientation patterns on histology.

The Effect of Hematocrit on Platelet Adhesion: Experiments and Simulations

The volume fraction of red blood cells (RBCs) in a capillary affects the degree to which platelets are promoted to marginate to near a vessel wall and form blood clots. In this work we investigate the relationship between RBC hematocrit and platelet adhesion activity. We perform experiments flowing blood samples through a microfluidic channel coated with type 1 collagen and observe the rate at which platelets adhere to the wall. We compare these results with three-dimensional boundary integral simulations of a suspension of RBCs and platelets in a periodic channel where platelets can adhere to the wall. In both cases, we find that the rate of platelet adhesion varies greatly with the RBC hematocrit. We observe that the relative decrease in platelet activity as hematocrit falls shows a similar profile for simulation and experiment.

Generation of Silicone Poly-HIPEs with Controlled Pore Sizes via Reactive Emulsion Stabilization.

Macrocellular silicone polymers are obtained after solidification of the continuous phase of a poly(dimethylsiloxane) emulsion, which contains poly(ethylene glycol) drops of sub-millimetric dimensions. Coalescence of the liquid template emulsion is prohibited by a reactive blending approach. The relationship is investigated in detail between the interfacial properties and the emulsion stability, and micro- and millifluidic techniques are used to generate macrocellular polymers with controlled structural properties over a wider range of cell sizes (0.2-2 mm) and volume fractions of the continuous phase (0.1%-40%). This approach could easily be transferred to a wide range of polymeric systems.

Condition number analysis and preconditioning of the finite cell method

The (Isogeometric) Finite Cell Method–in which a domain is immersed in a structured background mesh–suffers from conditioning problems when cells with small volume fractions occur. In this contribution, we establish a rigorous scaling relation between the condition number of (I)FCM system matrices and the smallest cell volume fraction. Ill-conditioning stems either from basis functions being small on cells with small volume fractions, or from basis functions being nearly linearly dependent on such cells. Based on these two sources of ill-conditioning, an algebraic preconditioning technique is developed, which is referred to as Symmetric Incomplete Permuted Inverse Cholesky (SIPIC). A detailed numerical investigation of the effectivity of the SIPIC preconditioner in improving (I)FCM condition numbers and in improving the convergence speed and accuracy of iterative solvers is presented for the Poisson problem and for two- and three-dimensional problems in linear elasticity, in which Nitche’s method is applied in either the normal or tangential direction. The accuracy of the preconditioned iterative solver enables mesh convergence studies of the finite cell method.

Taxonomic and Environmental Variability in the Elemental Composition and Stoichiometry of Individual Dinoflagellate and Diatom Cells from the NW Mediterranean Sea.

Here we present, for the first time, the elemental concentration, including C, N and O, of single phytoplankton cells collected from the sea. Plankton elemental concentration and stoichiometry are key variables in phytoplankton ecophysiology and ocean biogeochemistry, and are used to link cells and ecosystems. However, most field studies rely on bulk techniques that overestimate carbon and nitrogen because the samples include organic matter other than plankton organisms. Here we used X-ray microanalysis (XRMA), a technique that, unlike bulk analyses, gives simultaneous quotas of C, N, O, Mg, Si, P, and S, in single-cell organisms that can be collected directly from the sea. We analysed the elemental composition of dinoflagellates and diatoms (largely Chaetoceros spp.) collected from different sites of the Catalan coast (NW Mediterranean Sea). As expected, a lower C content is found in our cells compared to historical values of cultured cells. Our results indicate that, except for Si and O in diatoms, the mass of all elements is not a constant fraction of cell volume but rather decreases with increasing cell volume. Also, diatoms are significantly less dense in all the measured elements, except Si, compared to dinoflagellates. The N:P ratio of both groups is higher than the Redfield ratio, as it is the N:P nutrient ratio in deep NW Mediterranean Sea waters (N:P = 20–23). The results suggest that the P requirement is highest for bacterioplankton, followed by dinoflagellates, and lowest for diatoms, giving them a clear ecological advantage in P-limited environments like the Mediterranean Sea. Finally, the P concentration of cells of the same genera but growing under different nutrient conditions was the same, suggesting that the P quota of these cells is at a critical level. Our results indicate that XRMA is an accurate technique to determine single cell elemental quotas and derived conversion factors used to understand and model ocean biogeochemical cycles.

Numerical calculation of hydrodynamic characteristics of tidal currents for submarine excavation engineering in coastal area

In coastal areas with complicated flow movement, deposition and scour readily occur in submarine excavation projects. In this study, a small-scale model, with a high resolution in the vertical direction, was used to simulate the tidal current around a submarine excavation project. The finite volume method was used to solve Navier-Stokes equations and the Reynolds stress transport equation, and the entire process of the tidal current was simulated with unstructured meshes, generated in the irregular shape area, and structured meshes, generated in other water areas. The meshes near the bottom and free surface were densified with a minimum layer thickness of 0.05 m. The volume of fluid method was used to track the free surface, the volume fraction of cells on the upstream boundary was obtained from the volume fraction of adjacent cells, and that on the downstream boundary was determined by the water level process. The numerical results agree with the observed data, and some conclusions can be drawn: after the foundation trench excavation, the flow velocity decreases quite a bit through the foundation trench, with reverse flow occurring on the lee slope in the foundation trench; the swirling flow impedes inflow, leading to the occurrence of dammed water above the foundation trench; the turbulent motion is stronger during ebbing than in other tidal stages, the range with the maximum value of turbulent viscosity, occurring on the south side of the foundation trench at maximum ebbing, is greater than those in other tidal stages in a tidal cycle, and the maximum value of Reynolds shear stress occurs on the south side of the foundation trench at maximum ebbing in a tidal cycle. The numerical calculation method shows a strong performance in simulation of the hydrodynamic characteristics of tidal currents in the foundation trench, providing a basis for submarine engineering construction in coastal areas.

Intracerebral Cell Implantation: Preparation and Characterization of Cell Suspensions.

Intracerebral cell transplantation is increasingly finding a clinical translation. However, the number of cells surviving after implantation is low (5-10%) compared to the number of cells injected. Although significant efforts have been made with regard to the investigation of apoptosis of cells after implantation, very little optimization of cell preparation and administration has been undertaken. Moreover, there is a general neglect of the biophysical aspects of cell injection. Cell transplantation can only be an efficient therapeutic approach if an optimal transfer of cells from the dish to the brain can be ensured. We therefore focused on the in vitro aspects of cell preparation of a clinical-grade human neural stem cell (NSC) line for intracerebral cell implantation. NSCs were suspended in five different vehicles: phosphate-buffered saline (PBS), Dulbecco's modified Eagle medium (DMEM), artificial cerebral spinal fluid (aCSF), HypoThermosol, and Pluronic. Suspension accuracy, consistency, and cell settling were determined for different cell volume fractions in addition to cell viability, cell membrane damage, and clumping. Maintenance of cells in suspension was evaluated while being stored for 8 h on ice, at room temperature, or physiological normothermia. Significant differences between suspension vehicles and cellular volume fractions were evident. HypoThermosol and Pluronic performed best, with PBS, aCSF, and DMEM exhibiting less consistency, especially in maintaining a suspension and preserving viability under different storage conditions. These results provide the basis to further investigate these preparation parameters during the intracerebral delivery of NSCs to provide an optimized delivery process that can ensure an efficient clinical translation.

Microscopic flows of suspensions of the green non-motile Chlorella micro-alga at various volume fractions: Applications to intensified photobioreactors

An experimental study of flows of the green non-motile Chlorella micro-alga in a plane micro-channel is presented. Depending on the value of the cell volume fraction, three distinct flow regimes are observed. For low values of the cell volume fraction a Newtonian flow regime characterised by a Poiseuille like flow field, absence of wall slip and hydrodynamic reversibility of the flow states is observed. For intermediate values of the cell volume fraction, the flow profiles are consistent with a Poiseuille flow of a shear thinning fluid in the presence of slip at the channel’s wall. For even larger cell volume fractions, a yield stress like behaviour manifested through the presence of a central solid plug is observed. Except for the Newtonian flow regime, a strong hydrodynamic irreversibility of the flow and wall slip are found. The calculation of the wall shear rate and wall stress based on the measured flow fields allows one to identify the mechanisms of wall slip observed in the shear thinning and yield stress regimes.

Nanofiber scaffolds influence organelle structure and function in bone marrow stromal cells.

Recent work demonstrates that osteoprogenitor cell culture on nanofiber scaffolds can promote differentiation. This response may be driven by changes in cell morphology caused by the three-dimensional (3D) structure of nanofibers. We hypothesized that nanofiber effects on cell behavior may be mediated by changes in organelle structure and function. To test this hypothesis, human bone marrow stromal cells (hBMSCs) were cultured on poly(ε-caprolactone) (PCL) nanofibers scaffolds and on PCL flat spuncoat films. After 1 day-culture, hBMSCs were stained for actin, nucleus, mitochondria, and peroxisomes, and then imaged using 3D confocal microscopy. Imaging revealed that the hBMSC cell body (actin) and peroxisomal volume were reduced during culture on nanofibers. In addition, the nucleus and peroxisomes occupied a larger fraction of cell volume during culture on nanofibers than on films, suggesting enhancement of the nuclear and peroxisomal functional capacity. Organelles adopted morphologies with greater 3D-character on nanofibers, where the Z-Depth (a measure of cell thickness) was increased. Comparisons of organelle positions indicated that the nucleus, mitochondria, and peroxisomes were closer to the cell center (actin) for nanofibers, suggesting that nanofiber culture induced active organelle positioning. The smaller cell volume and more centralized organelle positioning would reduce the energy cost of inter-organelle vesicular transport during culture on nanofibers. Finally, hBMSC bioassay measurements (DNA, peroxidase, bioreductive potential, lactate, and adenosine triphosphate (ATP)) indicated that peroxidase activity may be enhanced during nanofiber culture. These results demonstrate that culture of hBMSCs on nanofibers caused changes in organelle structure and positioning, which may affect organelle functional capacity and transport. Published 2016. This article is a U.S. Government work and is in the public domain in the USA. J Biomed Mater Res Part B: Appl Biomater, 2016. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 105B: 989-1001, 2017.

Nutrient uptake in a suspension of squirmers

Nutrient uptake is one of the most important factors in cell growth. Despite the biological importance, little is known about the effect of cell–cell hydrodynamic interactions on nutrient uptake in a suspension of swimming micro-organisms. In this study, we numerically investigate the nutrient uptake in an infinite suspension of squirmers. In the dilute limit, our results are in good agreement with a previous study by Magar et al. (Q. J. Mech. Appl. Maths, vol. 56, 2003, pp. 65–91). When we increased the volume fraction of squirmers, the nutrient uptake of individual cells was enhanced by the hydrodynamic interactions. The average nutrient concentration in the suspension decayed exponentially as a function of time, and the relaxation time could be scaled using the Sherwood number, the Péclet number and the volume fraction of cells. We propose a fitting function for the Sherwood number, which is useful in predicting nutrient uptake in the non-dilute regime. Furthermore, we analyse the swimming energy consumed by individual cells. The results indicate that both the energetic cost and the nutrient uptake increased as the volume fraction of cells was increased, and that the uptake per unit energy was not significantly affected by the volume fraction. These findings are important in understanding the mass transport and metabolism of swimming micro-organisms in nature and for industrial applications.

Rheological manipulation of flocculated algal slurries to achieve high solids processing

Minimising the processing volume of downstream unit operations is critical to the scale-up of algal biorefining operations. This requires the ability to process high solids algal biomass, which relies on understanding the rheology of this material. In this work, the characterisation of particle, microstructural and rheological properties of flocculated and centrifuged Nannochloropsis sp. biomass with a solids concentration of ca. 25% w/w solids were undertaken. This suspension was determined to have a cell volume fraction of ca. 0.73. Continuous networks of cell aggregates arising from flocculant cross-linking and compression during centrifugation resulted in a highly viscous, irreversibly shear-thinning material as determined by stress ramp and oscillatory frequency sweep tests. Understanding that the material is highly sensitive to shear presents the opportunity of manipulating its rheology to enable high solids processing. Mechanical shearing was able to decrease the viscosity of flocculated biomass from ca. 1×105Pas to 1Pas as a result of breaking cell aggregate networks. The reduction of viscosity through shear processing is further demonstrated in a cell disruption process through a bench-scale high pressure homogeniser. The rheological methods described here have the potential to be usefully applied to characterising the bulk flow behaviour of microalgal biomass of different species and processing histories. Overall, this paper provides an accurate description of the underlying mechanisms controlling the flow of high solids algal biomass including the link between microstructure and bulk flow behaviour during processing.

New Proposed Algorithm for Determining the Electrical Characteristics of the Prolates and Oblates RBCs

Shapes and volume fractions (number and volume) of the red blood cells (RBCs) are important indicators for checking the patient cases. Microcytes, macrocytes, Elliptocytosis, oblate, and prolate are different RBCs shapes related to the blood diseases. The structure, the volume and the number of RBCs cell have direct effects on the electrical characteristics of RBCs. Many mathematical algorithms had been proposed for estimating the characteristics of nonspherical shapes. Unfortunately, many assumptions had been imposed to overcome the complexities of these algorithms. Besides these algorithms had been simulated the RBCs with spheres shapes only, where they are very complicated to apply for any other shapes. In this paper, the electrical characteristics of the oblate and the prolate RBCs had been estimated as function of the characteristics of the spherical RBCs. These characteristics include the relaxation time, the membrane capacitance of the cell, the low and very high frequencies permittivity and the conductivity.

Characterising kiwifruit (Actinidia sp.) near skin cellular structures using optical coherence tomography

Pre-harvest growing conditions during the development of fruit have impacts on fruit quality at the time of harvest and during storage. These impacts may result in differences in the skin properties of the fruit and some sub-surface cellular structural changes, which have potential effects on postharvest fruit quality and storability. Optical coherence tomography (OCT) is a non-destructive imaging method that enables acquisition of three-dimensional (3D) images of sub-surface structures of semi-transparent and turbid objects. This technology is a potential tool to provide new information about the structural nature of horticulture products. This work used five commercial kiwifruit cultivars, ‘G3’, ‘G9’, ‘G14’, ‘Hort16A’ and ‘Hayward’, where ‘Hayward’ was also manipulated with different orchard management practices (crop load and girdling), to investigate the properties of the layers of structures immediately underneath the periderm. Fruit samples were harvested at commercial maturity and then 3D OCT images of the skins were captured prior to fruit quality assessment. An automated image processing protocol was established to enable visualisation and characterisation of larger near skin cellular structures in the outer parenchyma tissue. There was no obvious differentiation between the observed large cells and the stone cells that are present in Actinidia chinensis cultivars. Significant differences in the microstructures of the sub-surface cells were found amongst five commercial kiwifruit cultivars. In general ‘G3’, ‘G14’ and ‘Hayward’ had larger and greater numbers of large sub-surface cells than ‘G9’ and ‘Hort16A’. The volume fraction of large cells in the near skin tissue was lower for the yellow-fleshed cultivars (‘G3’, ‘G9’ and ‘Hort16A’) in comparison to the green-fleshed cultivars (‘G14’ and ‘Hayward’). Low crop load increased maximum large cell length. However, no other effects of crop load and girdling were observed on the microstructures of the large cells in ‘Hayward’. Overall, OCT was an efficient non-destructive technique that can be utilised to reveal the structures of skin and sub-surface cellular layers with high resolution. The developed image processing protocol was suitable for the processing of large data sets with acceptable accuracy. However, more work should be carried out to overcome image artefacts caused by surface lenticels and trichomes. Limitations caused by low penetration depth should also be improved to allow better representation of the whole fruit structure.

Understanding particle margination in blood flow – A step toward optimized drug delivery systems

Targeted delivery of drugs and imaging agents is very promising to develop new strategies for the treatment of various diseases such as cancer. For an efficient targeted adhesion, the particles have to migrate toward the walls in blood flow – a process referred to as margination. Due to a huge diversity of available carriers, a good understanding of their margination properties in blood flow depending on various flow conditions and particle properties is required. We employ a particle-based mesoscopic hydrodynamic simulation approach to investigate the margination of different carriers for a wide range of hematocrits (volume fraction of red blood cells) and flow rates. Our results show that margination strongly depends on the thickness of the available free space close to the wall, the so-called red blood cell-free layer (RBC-FL), in comparison to the carrier size. The carriers with a few micrometers in size are comparable with the RBC-FL thickness and marginate better than their sub-micrometer counterparts. Deformable carriers, in general, show worse margination properties than rigid particles. Particle margination is also found to be most pronounced in small channels with a characteristic size comparable to blood capillaries. Finally, different margination mechanisms are discussed.