共查询到20条相似文献,搜索用时 15 毫秒
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Cell Phenotyping: Multiparametric Biomechanical and Biochemical Phenotypic Profiling of Single Cancer Cells Using an Elasticity Microcytometer (Small 17/2016) 下载免费PDF全文
Shuhuan Hu Guangyu Liu Weiqiang Chen Xiang Li Wei Lu Raymond H. W. Lam Jianping Fu 《Small (Weinheim an der Bergstrasse, Germany)》2016,12(17):2247-2247
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Quantum Dots: Linking Subcellular Disturbance to Physiological Behavior and Toxicity Induced by Quantum Dots in Caenorhabditis elegans (Small 23/2016) 下载免费PDF全文
Qin Wang Yanfeng Zhou Bin Song Yiling Zhong Sicong Wu Rongrong Cui Haixia Cong Yuanyuan Su Huimin Zhang Yao He 《Small (Weinheim an der Bergstrasse, Germany)》2016,12(23):3073-3073
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Tumor Cell Phenotyping: Circulating Tumor Cell Phenotyping via High‐Throughput Acoustic Separation (Small 32/2018) 下载免费PDF全文
Mengxi Wu Po‐Hsun Huang Rui Zhang Zhangming Mao Chuyi Chen Gabor Kemeny Peng Li Adrian V. Lee Rekha Gyanchandani Andrew J. Armstrong Ming Dao Subra Suresh Tony Jun Huang 《Small (Weinheim an der Bergstrasse, Germany)》2018,14(32)
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Droplet Microfluidics: Magnetic Suspension Array Technology: Controlled Synthesis and Screening in Microfluidic Networks (Small 33/2016) 下载免费PDF全文
Gungun Lin Dmitriy D. Karnaushenko Gilbert Santiago Cañón Bermúdez Oliver G. Schmidt Denys Makarov 《Small (Weinheim an der Bergstrasse, Germany)》2016,12(33):4580-4580
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Microfluidics: Accelerated Biofluid Filling in Complex Microfluidic Networks by Vacuum‐Pressure Accelerated Movement (V‐PAM) (Small 33/2016) 下载免费PDF全文
Zeta Tak For Yu Mei Ki Cheung Shirley Xiaosu Liu Jianping Fu 《Small (Weinheim an der Bergstrasse, Germany)》2016,12(33):4444-4444
Rapid fluid transport and exchange are critical operations involved in many microfluidic applications. However, conventional mechanisms used for driving fluid transport in microfluidics, such as micropumping and high pressure, can be inaccurate and difficult for implementation for integrated microfluidics containing control components and closed compartments. Here, a technology has been developed termed Vacuum–Pressure Accelerated Movement (V‐PAM) capable of significantly enhancing biofluid transport in complex microfluidic environments containing dead‐end channels and closed chambers. Operation of the V‐PAM entails a pressurized fluid loading into microfluidic channels where gas confined inside can rapidly be dissipated through permeation through a thin, gas‐permeable membrane sandwiched between microfluidic channels and a network of vacuum channels. Effects of different structural and operational parameters of the V‐PAM for promoting fluid filling in microfluidic environments have been studied systematically. This work further demonstrates the applicability of V‐PAM for rapid filling of temperature‐sensitive hydrogels and unprocessed whole blood into complex irregular microfluidic networks such as microfluidic leaf venation patterns and blood circulatory systems. Together, the V‐PAM technology provides a promising generic microfluidic tool for advanced fluid control and transport in integrated microfluidics for different microfluidic diagnosis, organs‐on‐chips, and biomimetic studies. 相似文献
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