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1.
Among various transdermal drug delivery (TDD) approaches, utilizing the microneedles (MNs) not only can penetrate the skin but also deliver the drug with reduced tissue damage, reduced pain, and no bleeding. However, the MNs with larger height are required to overcome the skin barrier for effective TDD. Unlike 2D patterning, etching polydimethyl siloxane (PDMS) micropillars for fabrication of 3D microstructures is presented. The PDMS micropillars were first constructed by casting PDMS on the computer numerical control-machined cylindrical microwells, which then went through etching process to obtain the MNs for subsequent fabrication of polymer MNs or high aspect ratio micropillars.  相似文献   

2.
Spheroid culture is a preferable cell culture approach for some cell types, including hepatocytes, as this type of culture often allows maintenance of organ-specific functions. In this study, we describe a spheroid microarray chip (SM chip) that allows stable immobilization of hepatocyte spheroids in microwells and that can be used to evaluate drug metabolism with high efficiency. The SM chip consists of 300-μm-diameter cylindrical wells with chemically modified bottom faces that form a 100-μm-diameter cell adhesion region surrounded by a nonadhesion region. Primary hepatocytes seeded onto this chip spontaneously formed spheroids of uniform diameter on the cell adhesion region in each microwell and these could be used for cytochrome P-450 fluorescence assays. A row of microwells could also be connected to a microchannel for simultaneous detection of different cytochrome P-450 enzyme activities on a single chip. The miniaturized features of this SM chip reduce the numbers of cells and the amounts of reagents required for assays. The detection of four cytochrome P-450 enzyme activities was demonstrated following induction by 3-methylcholantlene, with a sensitivity significantly higher than that in conventional monolayer culture. This microfabricated chip could therefore serve as a novel culture platform for various cell-based assays, including those used in drug screening, basic biological studies, and tissue engineering applications.  相似文献   

3.
In this work, we introduce a method for the soft-lithography-based fabrication of rigid microstructures and a new, simple bonding technique for use as a continuous-flow cell lysis device. While on-chip cell lysis techniques have been reported previously, these techniques generally require a long on-chip residence time, and thus cannot be performed in a rapid, continuous-flow manner. Microstructured microfluidic devices can perform mechanical lysis of cells, enabling continuous-flow lysis; however, rigid silicon-based devices require complex and expensive fabrication of each device, while polydimethylsiloxane (PMDS), the most common material used for soft lithography fabrication, is not rigid and expands under the pressures required, resulting in poor lysis performance. Here, we demonstrate the fabrication of microfluidic microstructures from off-stoichiometry thiol-ene (OSTE) polymer using soft-lithography replica molding combined with a post-assembly cure for easy bonding. With finite element simulations, we show that the rigid microstructures generate an energy dissipation rate of nearly 107, which is sufficient for continuous-flow cell lysis. Correspondingly, with the OSTE device we achieve lysis of highly deformable MDA-MB-231 breast cancer cells at a rate of 85%, while a comparable PDMS device leads to a lysis rate of only 40%.  相似文献   

4.
研究了一种基于正面人脸照片的真实感三维人脸自动重建方法,并运用计算机视觉图OpenCV和图形开发库OpenGL ,在VC++6.0环境下开发了三维人脸自动建模系统。该系统对输入的人脸照片首先进行人脸检测,在检测到的区域进行人脸关键特征提取,并根据检测到的特征点的几何信息对CANDIDE-3模型进行整体和局部调整,得到个性化的三维几何人脸,最后从人脸图像上获取面部纹理信息并得到真实感的三维人脸。  相似文献   

5.
A combination of a microfluidic device with a light modulation system was developed to detect the oxygen consumption rate (OCR) of a single developing zebrafish embryo via phase-based phosphorescence lifetime detection. The microfluidic device combines two components: an array of glass microwells containing Pt(II) octaethylporphyrin as an oxygen-sensitive luminescent layer and a microfluidic module with pneumatically actuated glass lids above the microwells to controllably seal the microwells of interest. The total basal respiration (OCR, in pmol O2/min/embryo) of a single developing zebrafish embryo inside a sealed microwell has been successfully measured from the blastula stage (3 h post-fertilization, 3 hpf) through the hatching stage (48 hpf). The total basal respiration increased in a linear and reproducible fashion with embryonic age. Sequentially adding pharmacological inhibitors of bioenergetic pathways allows us to perform respiratory measurements of a single zebrafish embryo at key developmental stages and thus monitor changes in mitochondrial function in vivo that are coordinated with embryonic development. We have successfully measured the metabolic profiles of a single developing zebrafish embryo from 3 hpf to 48 hpf inside a microfluidic device. The total basal respiration is partitioned into the non-mitochondrial respiration, mitochondrial respiration, respiration due to adenosine triphosphate (ATP) turnover, and respiration due to proton leak. The changes in these respirations are correlated with zebrafish embryonic development stages. Our proposed platform provides the potential for studying bioenergetic metabolism in a developing organism and for a wide range of biomedical applications that relate mitochondrial physiology and disease.  相似文献   

6.
The authors report a feasible and simple microfluidic approach for synthesizing anisotropic gel particles based on template method. By filling arrays of microwells with alginate hydrogel and synthesizing gold nanoparticles (AuNPs) on the gel surface, anisotropic alginate gel particles with single side gold nanoparticles layers were produced in microwells on the polydimethylsiloxan template. AuNPs and the anisotropic feature were characterized using scanning electron microscopy and x-ray photoelectron spectrum analyses. The anisotropic particles made of biocompatible gels could be released from the template and collected with uniform sizes, which might have a powerful potential in biological detection and sensing.  相似文献   

7.
Ordered deposition of elongated DNA molecules was achieved by the forced dewetting of a DNA solution droplet over a microstructured substrate. This technique allows trapping, uncoiling, and deposition of DNA fragments without the need of a physicochemical anchoring of the molecule and results in the combing of double stranded DNA from the edge of microwells on a polydimethylsiloxane (PDMS) substrate. The technique involves scanning a droplet of DNA solution caught between a movable blade and a PDMS substrate containing an array of microwells. The deposition and elongation appears when the receding meniscus dewets microwells, the latter acting here as a perturbation in the dewetting line forcing the water film to break locally. Thus, DNA molecules can be deposited in an ordered manner and elongated conformation based solely on a physical phenomenon, allowing uncoiled DNA molecules to be observed in all their length. However, the exact mechanism that governs the deposition of DNA strands is not well understood. This paper is an analysis of the physical phenomenon occurring in the deposition process and is based on observations made with the use of high frame/second rate video microscopy.  相似文献   

8.
In the 3-D path planning, the undulation of terrain have a significant impact on the roll angle of autonomous vehicle (AV). However, the existing 3-D path planning methods rarely consider the roll angle, which may lead to the rollover of AV. To solve this problem, a 3-D path planning system considering the rollover and path length (3DPPS-CRPL) is presented in this work. The 3DPPS-CRPL can plan a shorter path on the basis of inhibiting the roll angle of AV. In order to inhibit the roll angle, a novel roll angle evaluation model based on the undulation of terrain is developed, and the amount of computation is also greatly reduced because complex dynamics is avoided. In order to optimize the path length, both 2-D and 3-D path length are evaluated synthetically by a path length evaluation model. In order to optimize the parameters of 3DPPS-CRPL, a fuzzy-based optimizer is proposed to determine the weight of roll angle and path length. The simulation results prove that 3DPPS-CRPL has excellent performance for inhibiting roll angle and optimizing the path length in 3-D environment.  相似文献   

9.
This paper studies the two-dimensional (2-D) expected power bound (EPB) for 2-D digital filters with multiplicative noise in the Fornasini-Marchesini local state-space (FMLSS) model. By virtue of a class of linear matrix inequalities (LMIs), the novel existence criterion of 2-D EPB for 2-D digital filters in the considered model is obtained. The corresponding stabilization controller design method is presented based on the above criterion. Finally, two examples are presented to verify the effectiveness of our results.  相似文献   

10.
11.
提出了实数插值并行算法:采用一种高效优化的1-D插值替代经典公式插值,实现2-D插值,使得运算简便迅速,其计算模式类似于"流水"运行,不需要数据记录和数据暂存设施;而且插值运算时间的复杂性同插值单元因子的复杂性互不相关;每个插值计算周期持续时间相当于执行一个相应的加法运算和乘法运算时间;这为实现高速计算、存储共享的并行处理硬件设施提供了设计依据。  相似文献   

12.
针对零件表面质量的要求愈来愈高,而机加工表面微观形貌的粗糙度3-D评定方法却相对滞后。针对这一问题,本文就三维表面微观形貌的等高图的绘制方法、粗糙度3-D评定参数的计算提出了一些具体编程实现方法。重点阐述了三维表面等高图的绘制方法、3-D支承率和液体滞留性能指数的计算方法。利用JB-4C测量仪,开发了粗糙度3-D评定参数计算系统,验证了该方法的可行性。  相似文献   

13.
We developed a new method for releasing viable cells from affinity-based microfluidic devices. The lumen of a microchannel with a U-shape and user-designed microstructures was coated with supported lipid bilayers functionalized by epithelial cell adhesion molecule antibodies to capture circulating epithelial cells of influx solution. After the capturing process, air foam was introduced into channels for releasing target cells and then carrying them to a small area of membrane. The results show that when the air foam is driven at linear velocity of 4.2 mm/s for more than 20 min or at linear velocity of 8.4 mm/s for more than 10 min, the cell releasing efficiency approaches 100%. This flow-induced shear stress is much less than the physiological level (15 dyn/cm2), which is necessary to maintain the intactness of released cells. Combining the design of microstructures of the microfluidic system, the cell recovery on the membrane exceeds 90%. Importantly, we demonstrate that the cells released by air foam are viable and could be cultured in vitro. This novel method for releasing cells could power the microfluidic platform for isolating and identifying circulating tumor cells.  相似文献   

14.
图象分维数的估算技术综述   总被引:1,自引:0,他引:1  
周昌乐  张森 《科技通报》1996,12(3):129-133,138
分维数可以刻划图象的粗糙程度并被广泛应用于图象分割、纹理分析和三维形状恢复的处理,本文综述了国外近年来新出现的图象分维数估算技术,介绍了6种主要的分维数佐算方法,最后给出了这些方法在性能上的比较结果。  相似文献   

15.
The problem factorizing (separating) the transfer function of a given SISO 3-D discrete system, ie of a system depending on three independent variables, is considered. The 3-D system is assumed to be available in its transfer function representation, which is converted to a canonical state-space model by a simple inspection procedure. Then applying state-feedback to this canonical model we choose the feedback matrix gain (under certain conditions) such that the transfer function of the closed-loop system has the desireed factorized form, ie a product of three 1-D transfer functions each one being dependent on a single variable. The method is illustrated by a nontrivial numerical example.  相似文献   

16.
Axon path-finding plays an important role in normal and pathogenic brain development as well as in neurological regenerative medicine. In both scenarios, axonal growth is influenced by the microenvironment including the soluble molecules and contact-mediated signaling from guiding cells and cellular matrix. Microfluidic devices are a powerful tool for creating a microenvironment at the single cell level. In this paper, an asymmetrical-channel-based biochip, which can be later incorporated into microfluidic devices for neuronal network study, was developed to investigate geometric as well as supporting cell control of polarized axonal growth in forming a defined neuronal circuitry. A laser cell deposition system was used to place single cells, including neuron-glia pairs, into specific microwells of the device, enabling axonal growth without the influence of cytophilic∕phobic surface patterns. Phase microscopy showed that a novel "snag" channel structure influenced axonal growth in the intended direction 4:1 over the opposite direction. In heterotypic experiments, glial cell influence over the axonal growth path was observed with time-lapse microscopy. Thus, it is shown that single cell and heterotypic neuronal path-finding models can be developed in laser patterned biochips.  相似文献   

17.
随着塑料制品的日盏普殁,塑料件外形也越来越复杂。对于带有外部侧凹、侧凸、侧孔的塑料件来说,一般采用带有分型抽芯机构的型腔模具生产。本文介绍了型腔模具的特最,并对不同型腔模具的侧抽芯机构的特最进行分析。  相似文献   

18.
Herein, we present a large-area 3D hemispherical perforated microwell structure for a bead based bioassay. Such a unique microstructure enables us to perform the rapid and stable localization of the beads at the single bead level and the facile manipulation of the bead capture and retrieval with high speed and efficiency. The fabrication process mainly consisted of three steps: the convex micropatterned nickel (Ni) mold production from the concave micropatterned silicon (Si) wafer, hot embossing on the polymer matrix to generate the concave micropattened acrylate sheet, and reactive ion etching to make the bottom holes. The large-area hemispherical perforated micropatterned acrylate sheet was sandwiched between two polydimethylsiloxane (PDMS) microchannel layers. The bead solution was injected and recovered in the top PDMS microchannel, while the bottom PDMS microchannel was connected with control lines to exert the hydrodynamic force in order to alter the flow direction of the bead solution for the bead capture and release operation. The streptavidin-coated microbead capture was achieved with almost 100% yield within 1 min, and all the beads were retrieved in 10 s. Lysozyme or thrombin binding aptamer labelled microbeads were trapped on the proposed bead microarray, and the in situ fluorescence signal of the bead array was monitored after aptamer-target protein interaction. The protein-aptamer conjugated microbeads were recovered, and the aptamer was isolated for matrix assisted laser desorption/ionization time-of-flight mass spectrometry analysis to confirm the identity of the aptamer.  相似文献   

19.
In this study, we propose and evaluate a novel low-auto-fluorescence photoresist (SJI photoresist) for bio-application, e.g., in gene analysis and cell assay. The spin-coated SJI photoresist has a wide thickness range of ten to several hundred micrometers, and photoresist microstructures with an aspect ratio of over 7 and micropatterns of less than 2 μm are successfully fabricated. The emission spectrum intensity of the SJI photoresist is found to be over 80% less than that of the widely used SU-8 photoresist. To evaluate the validity of using the proposed photoresist in bio-application for fluorescence observation, we demonstrate a chromosome extension device composed of the SJI photoresist. The normalized contrast ratio of the SJI photoresist exhibits a 50% improvement over that of the SU-8 photoresist; thus, the SJI photoresist is a versatile tool for bio-application.  相似文献   

20.
Embryonic stem cells (ESCs) are pluripotent with multilineage potential to differentiate into virtually all cell types in the organism and thus hold a great promise for cell therapy and regenerative medicine. In vitro differentiation of ESCs starts with a phase known as embryoid body (EB) formation. EB mimics the early stages of embryogenesis and plays an essential role in ESC differentiation in vitro. EB uniformity and size are critical parameters that directly influence the phenotype expression of ESCs. Various methods have been developed to form EBs, which involve natural aggregation of cells. However, challenges persist to form EBs with controlled size, shape, and uniformity in a reproducible manner. The current hanging-drop methods are labor intensive and time consuming. In this study, we report an approach to form controllable, uniform-sized EBs by integrating bioprinting technologies with the existing hanging-drop method. The approach presented here is simple, robust, and rapid. We present significantly enhanced EB size uniformity compared to the conventional manual hanging-drop method.  相似文献   

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