Microfabrication techniques or microelectromechanical systems (MEMS) that have revolutionized the electronics industry are now poised to revolutionize the pharmaceutical &biotechnology industries, &basic biomedical sciences. The two leading applications of microfabrication in biology include """"""""genes-on-a-chip"""""""" to monitor the expression level of potentially all genes in humans &organisms simultaneously, &""""""""lab-on-a-chip"""""""" type devices to perform high-throughput biochemistry in very small volumes. Equally exciting is recent advances in the understanding of cellular behavior in microenvironments have started to pave the way towards living micro-devices. The emerging integration of living systems &MEMS are expected to become key technologies in the 21st century of medicine with a broad range of applications varying from diagnostic, therapeutics, cell-based high-throughput drug screening tools, &basic &applied cell biology tools. The mission for the proposed NIH BioMEMS Resource Center is to bridge the gap between MEMS engineering &biomedical community to provide new technologies at the interface of MEMS &living biological systems to biomedical investigators &clinicians. In order to make the tools of BioMEMS available to the biomedical community, we focused our efforts on 2 core technological research &development projects. In Core Project 1, we will use inertial microfluidic technology for high-throughput &precise microscale control of cell &particle motion for sorting &analysis of disease specific """"""""rare"""""""" cells in blood. In Core Project 2, we will develop broad utility """"""""living cell array"""""""" platforms to study the dynamics of cellular &tissue response to a multitude of stimuli. Also, there are 23 collaborative projects that both utilize &help advance the core technologies. The BMRC also provides services to NIH investigators to use the tools of microsystems technology in biology &medicine. The Core, Collaborative, &Service activities are complemented with a rich portfolio of training &dissemination activities. Our collaborators &service users are extremely well-funded NIH investigators. The training activities include ad-hoc training, laboratory courses, &workshops. The dissemination activities are very broad encompassing publications, presentations, web presence, symposia &meetings, visiting faculty program, &technology transfer. We have also been very successful in disseminating our technologies through licensing &spin-off commercialization and the use of MEMS foundries for manufacturing of microchips. BMRC has been very successful in developing cutting-edge, enabling technologies at the Interface of MEMS &biology, &disseminating these technologies to the biomedical community via collaborations, service activities, &organized training &dissemination programs.

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Biotechnology Resource Grants (P41)
Project #
5P41EB002503-10
Application #
8517466
Study Section
Special Emphasis Panel (ZRG1-BST-R (40))
Program Officer
Hunziker, Rosemarie
Project Start
2004-04-01
Project End
2014-07-31
Budget Start
2013-08-01
Budget End
2014-07-31
Support Year
10
Fiscal Year
2013
Total Cost
$1,092,941
Indirect Cost
$474,494
Name
Massachusetts General Hospital
Department
Type
DUNS #
073130411
City
Boston
State
MA
Country
United States
Zip Code
02199
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Jorfi, Mehdi; D'Avanzo, Carla; Kim, Doo Yeon et al. (2018) Three-Dimensional Models of the Human Brain Development and Diseases. Adv Healthc Mater 7:
Otawara, Masayuki; Roushan, Maedeh; Wang, Xiao et al. (2018) Microfluidic Assay Measures Increased Neutrophil Extracellular Traps Circulating in Blood after Burn Injuries. Sci Rep 8:16983
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Huang, Haishui; Yarmush, Martin L; Usta, O Berk (2018) Long-term deep-supercooling of large-volume water and red cell suspensions via surface sealing with immiscible liquids. Nat Commun 9:3201
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ReƔtegui, Eduardo; van der Vos, Kristan E; Lai, Charles P et al. (2018) Engineered nanointerfaces for microfluidic isolation and molecular profiling of tumor-specific extracellular vesicles. Nat Commun 9:175
Gokduman, Kurtulus; Bestepe, Furkan; Li, Lei et al. (2018) Dose-, treatment- and time-dependent toxicity of superparamagnetic iron oxide nanoparticles on primary rat hepatocytes. Nanomedicine (Lond) 13:1267-1284
Muldur, Sinan; Marand, Anika L; Ellett, Felix et al. (2018) Measuring spontaneous neutrophil motility signatures from a drop of blood using microfluidics. Methods Cell Biol 147:93-107

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