2006 International Conference on Microtechnologies in Medicine and Biology最新文献_第5页

Characterization of the Membrane Transport Assay System Using Microchamber Array 微室阵列表征膜转运检测系统

2006 International Conference on Microtechnologies in Medicine and Biology Pub Date : 2006-05-09 DOI: 10.1109/MMB.2006.251556

H. Suzuki, K. Tabata, H. Noji, S. Takeuchi

引用次数: 0

Fluid Pressure Measurement in Lacunocanalicular Network of Trabeculae Using MEMS Based Micro-Pressure Transducer 基于MEMS微压力传感器的小梁腔隙网络流体压力测量

2006 International Conference on Microtechnologies in Medicine and Biology Pub Date : 2006-05-09 DOI: 10.1109/MMB.2006.251538

Junghwa Hong, Young Hwan Park, H. Cha

{"title":"Fluid Pressure Measurement in Lacunocanalicular Network of Trabeculae Using MEMS Based Micro-Pressure Transducer","authors":"Junghwa Hong, Young Hwan Park, H. Cha","doi":"10.1109/MMB.2006.251538","DOIUrl":"https://doi.org/10.1109/MMB.2006.251538","url":null,"abstract":"The intraosseous pressure generation and fluid flow in lacunocanalicular network of trabeculae could be important to the remodeling process of cancellous bone. Due to the technical difficulty, experimental information about the amount of intraosseous pressure generation in lacunocanalicular network of trabeculae is never measured. In this study, the maximum intraosseous pressure generation in micro-trabecular specimens within the elastic range was measured in vitro using a specially designed micro-experimental setup representing the most restrictive fluid flow boundaries around microscopic bovine vertebral trabecular specimens. Then, a quasi-static loading (9mum/min) was applied up to the strain of 0.4% with measuring intraosseous pressure generations in the undrained and drained conditions. 49.2plusmn4.45 KPa of intraosseous pressure generation at the 0.4% strain was found in the undrained condition. In contrast, no intraosseous pressure generation was measured in the drained condition. The result could let us know the amount of a possible maximum intraosseous pressure generation in lacunocanalicular network of trabeculae within the elastic range","PeriodicalId":170356,"journal":{"name":"2006 International Conference on Microtechnologies in Medicine and Biology","volume":"197 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2006-05-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"132187611","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 0

Quantitative Evaluation of Micro-motion of Vascular Endothelial Cells in Electrical Cell-substrate Impedance Sensing (ECIS) Method Using a Precision Mathematical Model 用精确数学模型定量评价电-基质阻抗传感(ECIS)方法中血管内皮细胞微运动

2006 International Conference on Microtechnologies in Medicine and Biology Pub Date : 2006-05-09 DOI: 10.1109/MMB.2006.251480

N. Goda, Y. Yamamoto, T. Nakamura, T. Kusuhara, S. Mohri, N. Kataoka, F. Kajiya

引用次数: 3

A Micro-Fluidic Technique for the Evaluation of the Blood Compatibility of Nanostructured Polymer Surfaces 微流体技术评价纳米结构聚合物表面的血液相容性

2006 International Conference on Microtechnologies in Medicine and Biology Pub Date : 2006-05-09 DOI: 10.1109/MMB.2006.251539

C. Minelli, A. Kikuta, A. Yamamoto

引用次数: 1

Novel full platinum nanoprobes suitable for biological SPM experiments 适用于生物SPM实验的新型全铂纳米探针

2006 International Conference on Microtechnologies in Medicine and Biology Pub Date : 2006-05-09 DOI: 10.1109/MMB.2006.251552

J. Stéen, R. Kerkhofs, V. Blech, J. Brugger, B. Kim

引用次数: 0

Flexible Intracortical Neural Probe with Biodegradable Polymer for Delivering Bioactive Components 柔性皮质内神经探针与可生物降解聚合物递送生物活性成分

2006 International Conference on Microtechnologies in Medicine and Biology Pub Date : 2006-05-09 DOI: 10.1109/MMB.2006.251512

Y. Kato, M. Nishino, I. Saito, T. Suzuki, K. Mabuchi

引用次数: 14

In vitro biocompatibility and electrochemical behavior of titanium and its alloys 钛及其合金的体外生物相容性及电化学行为

2006 International Conference on Microtechnologies in Medicine and Biology Pub Date : 2006-05-09 DOI: 10.1109/MMB.2006.251478

M. Popa, D. Iordăchescu, I. Demetrescu, E. Vasilescu, P. Drob, A. Cîmpean, M. Istratescu, C. Vasilescu

{"title":"In vitro biocompatibility and electrochemical behavior of titanium and its alloys","authors":"M. Popa, D. Iordăchescu, I. Demetrescu, E. Vasilescu, P. Drob, A. Cîmpean, M. Istratescu, C. Vasilescu","doi":"10.1109/MMB.2006.251478","DOIUrl":"https://doi.org/10.1109/MMB.2006.251478","url":null,"abstract":"In vitro osteoblasts/Ti-6Al-7Nb bioalloy interactions were characterized in this paper. Also, the electrochemical properties of the passive films on titanium and its Ti-6Al-7Nb bioalloy in Ringer 2 and 3 solutions were determined as an aspect of their biocompatibility. Human osteoblast proliferation and viability are very good. \"Cell effort\" to adhere on metallic support is visualized by some morphologic changes of the osteoblasts. Cytotoxicity effects of Ti-6Al-7Nb alloy appeared after 48 culture hours and decreased in time, demonstrating a very good biocompatibility. In Ringer 2 solution of different pH values (2.5; 5; 6.7 and 9), titanium and Ti-6Al-7Nb alloy presented self-passivation, very large passive potential range, very low passive current densities, confirming a compact, protective, stable layer. The very low corrosion rates and ion release values prove a near imperceptible toxicity. In Ringer 3 solution, open circuit potentials of titanium and its Ti-6Al-7Nb alloy tend to electropositive values, attesting a process of passivity increase by thickening","PeriodicalId":170356,"journal":{"name":"2006 International Conference on Microtechnologies in Medicine and Biology","volume":"5 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2006-05-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"131481435","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 2

Silicon Nanotweezers with Adjustable and Controllable Gap for the Manipulation and Characterization of DNA Molecules 具有可调和可控间隙的硅纳米镊子用于DNA分子的操作和表征

2006 International Conference on Microtechnologies in Medicine and Biology Pub Date : 2006-05-09 DOI: 10.1109/MMB.2006.251507

C. Yamahata, T. Takekawa, K. Ayano, M. Hosogi, M. Kumemura, B. Legrand, D. Collard, G. Hashiguchi, H. Fujita

引用次数: 13

A Sensing Method based on Elastic Instabilities of Swelllng Hydrogels 基于膨胀水凝胶弹性不稳定性的传感方法

2006 International Conference on Microtechnologies in Medicine and Biology Pub Date : 2006-05-09 DOI: 10.1109/MMB.2006.251553

D. Kim, D. Beebe

引用次数: 0

Maskless direct cell patterning by laser writing 激光书写的无掩模直接细胞图案

2006 International Conference on Microtechnologies in Medicine and Biology Pub Date : 2006-05-09 DOI: 10.1109/MMB.2006.251550

J.Y. Cheng, Hsueh-Yi Lee, M. Yen, T. Young

{"title":"Maskless direct cell patterning by laser writing","authors":"J.Y. Cheng, Hsueh-Yi Lee, M. Yen, T. Young","doi":"10.1109/MMB.2006.251550","DOIUrl":"https://doi.org/10.1109/MMB.2006.251550","url":null,"abstract":"A simple and effective method for patterning cell on glass substrate is reported. A passivation layer that is capable of preventing cell adhesion was first coated onto glass surface. The passivation coatings that were tested include 3-[Bis(2-hydroxyethyl)amino]propyl-triethoxysilane, 3-Aminopropyltriethoxysilane, 1H, 1H, 2H, 2H-Perfluorodecyl-triethoxysilane, 3 -Glycidyloxypropyltriethoxysilane, Octade cyltrimethoxysilane, and Octadecyltrichlorosilane. A CO2 laser and a UV laser were used to remove the passivation layer and define patterns according to user design. Cell arrays and arbitrary pattern were demonstrated. The minimal feature attainable by the CO2 laser is about 100 mum. The minimal feature for reliable cell adhesion is found to be about 25 mum. Cells adhere and grow cleanly in the laser defined pattern. The pattern can be re-designed and fabricated easily and rapidly. Living cell staining by CMFDA and antibody staining for epidermal growth factor receptor (EGFR) detection were successfully performed on the surface bound cells. This method can be very useful for developing drug screening tools that utilize cell-based detection","PeriodicalId":170356,"journal":{"name":"2006 International Conference on Microtechnologies in Medicine and Biology","volume":"39 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2006-05-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"116323891","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

引用次数: 1