圣和散对胃癌SGC-7901细胞Fas∕FasL表达的影响

Fas∕FasL结合是介导胃癌细胞凋亡的主要方式,圣和散能诱导肿瘤细胞凋亡,其作用是否通来启动Fas∕FasL实现。1,材料与方法1.1,材料人胃低分化腺癌细胞SGC-7901(引自第四军医大学西京医院);RPMI1640(美国Gibco公司),Fas、FasL多抗(北京中山公司),流式细胞仪(美国BD公司),顺铂CDDP,山东齐鲁制药厂)。1.2,方法1.2.1,细胞培养人胃癌SGC-7901细胞常规培养于含10%胎牛血清、100U/ml青霉素、50U/ml庆大霉素的RPMI1640培养液中,在37℃、5%CO2、饱和湿度培养箱内传代培养。中国科技信息20051.2.2,药物处理将中药圣和散SHP)(主要含党参…     

Biomimetic micro∕nanostructured functional surfaces for microfluidic and tissue engineering applications

This paper reviews our work on the application of ultrafast pulsed laser micro∕nanoprocessing for the three-dimensional (3D) biomimetic modification of materials surfaces. It is shown that the artificial surfaces obtained by femtosecond-laser processing of Si in reactive gas atmosphere exhibit roughness at both micro- and nanoscales that mimics the hierarchical morphology of natural surfaces. Along with the spatial control of the topology, defining surface chemistry provides materials exhibiting notable wetting characteristics which are potentially useful for open microfluidic applications. Depending on the functional coating deposited on the laser patterned 3D structures, we can achieve artificial surfaces that are (a) of extremely low surface energy, thus water-repellent and self-cleaned, and (b) responsive, i.e., showing the ability to change their surface energy in response to different external stimuli such as light, electric field, and pH. Moreover, the behavior of different kinds of cells cultured on laser engineered substrates of various wettabilities was investigated. Experiments showed that it is possible to preferentially tune cell adhesion and growth through choosing proper combinations of surface topography and chemistry. It is concluded that the laser textured 3D micro∕nano-Si surfaces with controllability of roughness ratio and surface chemistry can advantageously serve as a novel means to elucidate the 3D cell-scaffold interactions for tissue engineering applications.     

Patterning nanowire and micro-∕nanoparticle array on micropillar-structured surface: Experiment and modeling

DNA molecules in a solution can be immobilized and stretched into a highly ordered array on a solid surface containing micropillars by molecular combing technique. However, the mechanism of this process is not well understood. In this study, we demonstrated the generation of DNA nanostrand array with linear, zigzag, and fork-zigzag patterns and the microfluidic processes are modeled based on a deforming body-fitted grid approach. The simulation results provide insights for explaining the stretching, immobilizing, and patterning of DNA molecules observed in the experiments.     

Thermomodulated cell culture∕harvest in polydimethylsiloxane microchannels with poly(N-isopropylacrylamide)-grafted surface

Cell culture and harvest are the most upstream operation for a completely integrated cell assay chip. In our previous work, thermoresponsive poly(N-isopropylacrylamide) (PNIPAAm) was successfully grafted onto polydimethylsiloxane (PDMS) surface via benzophenone-initiated photopolymerization. In the present work, the PNIPAAm-grafted-PDMS (PNIPAAm-g-PDMS) surface was explored for thermomodulated cell culture and noninvasive harvest in microfluidic channels. Using COS 7 fibroblast from African green monkey kidney as the model cells, the thermomodulated adhering and detaching behaviors of the cells on the PNIPAAm-g-PDMS surfaces were optimized with respect to PNIPAAm-grafting yields and gelatin modification. The viability of the cells cultured on and harvested from the PNIPAAm-g-PDMS surface with the thermomodulated noninvasive protocol was estimated against the traditional cell culture∕harvest method involving trypsin digestion. The configuration of the microchannel on the PNIPAAm-g-PDMS chip was evaluated for static cell culture. Using a pipette-shaped PNIPAAm-g-PDMS microchannel, long-term cell culture could be achieved at 37 °C with periodic change of the culture medium every 12 h. After moving the microchip from the incubator set at 37 °C to the room temperature, the proliferated cells could be spontaneously detached from the PNIPAAm-g-PDMS surface of the upstream chamber and transferred by a gentle fluid flow to the downstream chamber, wherein the transferred cells could be subcultured. The thermomodulated cell culture, harvest, and passage operations on the PNIPAAm-g-PDMS microfluidic channels were demonstrated.     

Single nanopore transport of synthetic and biological polyelectrolytes in three-dimensional hybrid microfluidic∕nanofluidic devices

This paper presents a study of electrokinetic transport in single nanopores integrated into vertically stacked three-dimensional hybrid microfluidic∕nanofluidic structures. In these devices, single nanopores, created by focused ion beam (FIB) milling in thin polymer films, provide fluidic connection between two vertically separated, perpendicular microfluidic channels. Experiments address both systems in which the nanoporous membrane is composed of the same (homojunction) or different (heterojunction) polymer as the microfluidic channels. These devices are then used to study the electrokinetic transport properties of synthetic (i.e., polystyrene sulfonate and polyallylamine) and biological (i.e., DNA) polyelectrolytes across these nanopores using both electrical current measurements and confocal microscopy. Both optical and electrical measurements indicate that electro-osmotic transport is predominant over electrophoresis in single nanopores with d>180 nm, consistent with results obtained under similar conditions for nanocapillary array membranes.     

Electrophoretic separation of neurotransmitters on a polystyrene nano-sphere∕polystyrene sulphonate coated poly(dimethylsiloxane) microchannel

In this paper, a poly(dimethylsiloxane) microchip with amperometric detector was developed for the electrophoretic separation and determination of neurotransmitters. For increasing the separation efficiency, the microchannel is modified by polystyrene sulphonate∕polystyrene nano-sphere self-assembly coating. A stable electro-osmotic flow (EOF) and higher separation efficiency are obtained in proposed modified microchannel. Under optimized conditions, dopamine, epinephrine, catechol, and serotonin are acceptably baseline separated in this 3.5 cm length separation channel with the theoretical plate number from 4.6?×?10(4) to 2.1?×?10(5) per meter and resolution from 1.29 to 12.5. The practicability of proposed microchip is validated by the recovery test with cerebrospinal fluid as real sample which resulted from 91.7% to 106.5%.     

Novel method of generating water-in-oil(W∕O) droplets in a microchannel with grooved walls

We present a novel method of generating and retrieving droplets stored in microfluidic grooves or cavity structures. First we designed and fabricated polydimethylsiloxane microchannels with grooves on the walls and then produced a two-phase flow of oil and aqueous phases to form aqueous phase droplets in an oil state. We propose the following three mechanisms of droplet generation: the contact line on the groove wall continues moving along the wall and descends to the bottom of the cavity, confining the aqueous phase in the cavity; once the interface between the oil and aqueous phases moves into the cavity, the interface contacts the top of the neighboring groove; and a spherical droplet forms at the corner in the cavity due to surface tension. The viscosity of the oil phase and the surface tension of the interface determine whether a droplet can be generated. Then, we could adjust the velocity of the interface and the aspect ratio of the cavity to achieve the optimal conditions for generating the single droplet. We observed that the largest droplet is stably generated without a daughter droplet at typical values of free-stream velocity (10 μl∕min) and groove pitch 110 μm for all three cases with different oil phases (20, 50, and 84 cP). This technique is expected to serve as a platform for droplet-based reaction systems, particularly with regard to monitoring cell behavior, in vitro expression, and possibly even micropolymerase chain reaction chambers.