Electrospun micro/nanodevices for controlled biomolecule release

Controlled biomolecule release technology represents one of the fastest advancing areas of science and engineering. For instance, in drug delivery area, such release system offers numerous advantages compared to conventional dosage drug forms including improved efficiency, reduced toxicity and controlled release profile. Current challenges in this area include biocompatiblity and biodegrability of the materials used in the system, controllablity and effectivity of the control mechanism, easiness of device fabraiction and drug loading loss as well as total cost. In this work, a simple and effective method is adopted to design and fabricate controlled release devices employing smart conmtrol mechanism. Such a technology could be further applied in pharmaceutics, biomeidical science and biotechnologies. Controlled molecule release devices in this work employ the advantage of core-shell structures. In the first design, core-shell microcapsules are developed capable of regulating the release profile of encapsulated molecules. These microcapsules uniquely contain embedded miniature actuators inside their liquid core. The internal actuators are made of stimuli-responsive smart hydrogel beads. The embedded hydrogel beads swell in response to external electric fields, regulating the internal pressure of the liquid core, and thus the diffusion rate, of the encapsulated molecules from the microcapsules. The incorporation of the actuators into the interior of the microcapsules provides an internal control variable to a conventional diffusion-based release process. The microcapsules, which behave much like micro-electro-mechanical systems (MEMS), are fabricated by a simple co-electrospray process. This fabrication technique allows integrating the hydrogel beads, forming the polymer shell, and loading the releasable molecules simultaneously in one step. The other controlled release device is developed by embedding nanofluidic biomolecule reservoirs into a polymer network of a stimuli-responsive hydrogel. The reservoirs are made of liquid core-polymer shell nanofibers using co-electrospinning technique. The mechanism of controlled release is based on buckling instability of the polymer shell under combined axial and radial compression, caused by volume changes of hydrogel responding to a specific external stimulus. The device decouples releasable biomolecules from a hydrogel polymer matrix, avoiding chemical interactions between biomolecules and hydrogel polymer chains, and thus, alleviating nontrivial chemical and biological engineering design of hydrogel formulations. Temperature-sensitive hydrogel is used as a model hydrogel

Study of myocardial fiber length distribution with diffusion tensor MRI

Diffusion tensor MRI (DTI) is a nondestructive method to map myocardial fiber organization. Many studies have been done on myocardial fiber orientation. However, cardiac contraction is also related with myocardial fiber length, but its study is limited so far. The current study aims to provide information of myocardial fiber length distribution in formalin-fixed porcine heart samples. DTI with medium diffusion resolution (15 directions) was performed. Fiber length distribution as a function of fiber helix angle was investigated in multiple short-axis slices located from base to apex of the left ventricles. Results show that longer fibers likely run circumferentially, and fibers located at middle and upper ventricle are generally longer than those near apex. The results provide supplementary structural information on myocardial fiber architecture and cardiac mechanics.published_or_final_versio

Understanding the Epidemiology of Heart Failure to Improve Management Practices: An Asia-Pacific Perspective

published_or_final_versio

Cell number quantification of USPIO-labeled stem cells by MRI: An in vitro study

MRI plays an expanding role in stem cell therapies. The non-invasive nature and high spatial resolution of MR imaging make MR imaging a powerful tool to investigate biologic processes at the molecular and cellular level in vivo longitudinally. Quantitative detection of stem cells after transplantation may allow assessment of stem cell localization and migration, and monitoring of the therapeutic effectiveness of stem cell therapy. In this study, we present a technique for MR quantification of magnetically labeled mouse embryonic stem cells distributed or injected in agarose gel phantoms. Apparent transverse relaxation rate enhancements (ΔR2*) were measured by gradient echo sequences. The linear relationship between ΔR2* and the concentration of USPIO-labeled mouse embryonic stem cells was observed and used for quantifying cell density and cell number after injection or transplantation. The MRI acquisition and analysis protocol were validated by good agreement between actual cell numbers and MRI-estimated cell numbers over a wide range of cell numbers. This MR technique for cell number and cell density quantification is applicable to future in vivo studies. © 2006 IEEE.published_or_final_versio

Detection of ipsilateral and contralateral activation components in unilateral fingers-tapping using spinal BOLD fMR

Ipsilateral activation component has been reported in brain fMRI studies using unilateral finger motion. However, the ipsilateral component is usually taskdependent and sparsely distributed. In this study, spinal BOLD fMRI has been performed on 4 healthy right-handed volunteers performing unilateral fingerstapping to investigate the ipsilateral and contralateral activation inside the cervical spinal cord. Our results showed that more activation were found at the spinal level C5-C6/C7. Bilateral activation was observed in all subjects both in left/right hand fingers-tapping. Spinal fMRI was sensitive to detect bilateral firing in fingers-tapping using dominant or non-dominant hands.published_or_final_versio

Myocardial fiber length mapping with MR diffusion tensor imaging

Diffusion tensor MRI is emerging as a rapid, nondestructive method to map myocardial fiber organization. A precise biological description of myocardial fiber performance requires knowledge of four variables: length, force, velocity and time. However, study of quantification of myocardial fiber length is lacking. The current study aims to show myocardial fiber length maps of formalin-fixed heats. Diffusion tensor MRI with medium diffusion resolution (15 directions) was performed in one isolated pig heart. Fiber length maps were investigated in multiple short-axis slices. The results provide supplementary information of myocardial fiber organization. To our knowledge, the present study is the first report of the myocardial fiber length mapping. © 2005 IEEE.published_or_final_versio

Revisiting stepwise ocean oxygenation with authigenic barium enrichments in marine mudrocks

There are current debates around the extent of global ocean oxygenation, particularly from the late Neoproterozoic to the early Paleozoic, based on analyses of various geochemical indices. We present a temporal trend in excess barium (Ba_{excess}) contents in marine organic-rich mudrocks (ORMs) to provide an independent constraint on global ocean redox evolution. The absence of remarkable Ba_{excess} enrichments in Precambrian (>ca. 541 Ma) ORMs suggests limited authigenic Ba formation in oxygen- and sulfate-deficient oceans. By contrast, in the Paleozoic, particularly the early Cambrian, ORMs are marked by significant Ba_{excess} enrichments, corresponding to substantial increases in the marine sulfate reservoir and oxygenation level. Analogous to modern sediments, the Mesozoic and Cenozoic ORMs exhibit no prominent Ba_{excess} enrichments. We suggest that variations in Ba_{excess} concentrations of ORMs through time are linked to secular changes in the marine dissolved Ba reservoir associated with elevated marine sulfate levels and global ocean oxygenation. Further, unlike Mo, U, and Re abundances, significant Ba_{excess} enrichments in ORMs indicate that the overall ocean oxygenation level in the early Paleozoic was substantially lower than at present

Quantum theory of light diffraction

At present, the theory of light diffraction only has the simple wave-optical approach. In this paper, we study light diffraction with the approach of relativistic quantum theory. We find that the slit length, slit width, slit thickness and wave-length of light have affected to the diffraction intensity and form of diffraction pattern. However, the effect of slit thickness on the diffraction pattern can not be explained by wave-optical approach, and it can be explained in quantum theory. We compare the theoretical results with single and multiple slits experiment data, and find the theoretical results are accordance with the experiment data. Otherwise, we give some theory prediction. We think all the new prediction will be tested by the light diffraction experiment.Comment: 10 page

Evidence for genetic association of TBX21 and IFNG with systemic lupus erythematosus in a Chinese Han population

TBX21 recode T-bet which is an important transcription factor that drives the Th1 immune response primarily by promoting expression of the interferon-gamma (IFNG) gene. Recent studies have shown that genetic variants in TBX21 and IFNG are connected with risk of systemic lupus erythematosus (SLE). The aim of the present study was to replicate these genetic associations with SLE in Anhui Chinese population. Genotyping of 3 variants (rs4794067 in TBX21, rs2069705 and rs2069718 in IFNG) was performed. A total of 3732 subjects were included in the final analysis. The study only identified the association of rs2069705 with SLE susceptibility (T vs. C: odds ratio [OR] = 1.12, 95% confidence interval [CI] = 1.00-1.26, P = 0.046). Combined analysis with Hong Kong GWAS showed that the OR for rs2069705 was 1.10 (95% CI: 1.01-1.21, P = 0.027). Further pooled analysis with Korean populations involving 10498 subjects showed a more significant association between rs2069705 and SLE (T vs. C: OR = 1.11, 95%CI = 1.04-1.19, P = 0.002; TT + TC vs. CC: OR = 1.11, 95%CI = 1.02-1.21, P = 0.012; TT vs. TC + CC: OR = 1.28, 95%CI = 1.07-1.54, P = 0.008; TT vs. CC: OR = 1.33, 95%CI = 1.10-1.60, P = 0.003). In addition, we also identified a significant genetic interaction between rs2069705 and rs4794067 in Anhui Chinese population. Our study suggests that IFNG and IFNG-TBX21 interaction are involved in SLE susceptibility.published_or_final_versio