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
Wong, Keith H K; Edd, Jon F; Tessier, Shannon N et al. (2018) Anti-thrombotic strategies for microfluidic blood processing. Lab Chip 18:2146-2155
DeVos, Sarah L; Corjuc, Bianca T; Commins, Caitlin et al. (2018) Tau reduction in the presence of amyloid-? prevents tau pathology and neuronal death in vivo. Brain 141:2194-2212
Weng, Lindong; Lee, Gloria Y; Liu, Jie et al. (2018) On-chip oocyte denudation from cumulus-oocyte complexes for assisted reproductive therapy. Lab Chip 18:3892-3902
Irimia, Daniel; Wang, Xiao (2018) Inflammation-on-a-Chip: Probing the Immune System Ex Vivo. Trends Biotechnol 36:923-937
Kim, Jae Jung; ReƔtegui, Eduardo; Hopke, Alex et al. (2018) Large-scale patterning of living colloids for dynamic studies of neutrophil-microbe interactions. Lab Chip 18:1514-1520
Wang, Xiao; Irimia, Daniel (2018) Neutrophil Chemotaxis in One Droplet of Blood Using Microfluidic Assays. Methods Mol Biol 1749:351-360
Wang, Xiao; Jodoin, Emily; Jorgensen, Julianne et al. (2018) Progressive mechanical confinement of chemotactic neutrophils induces arrest, oscillations, and retrotaxis. J Leukoc Biol 104:1253-1261
Weng, Lindong; Stott, Shannon L; Toner, Mehmet (2018) Molecular Dynamics at the Interface between Ice and Poly(vinyl alcohol) and Ice Recrystallization Inhibition. Langmuir 34:5116-5123
Jorfi, Mehdi; D'Avanzo, Carla; Tanzi, Rudolph E et al. (2018) Human Neurospheroid Arrays for In Vitro Studies of Alzheimer's Disease. Sci Rep 8:2450
Boneschansker, Leo; Jorgensen, Julianne; Ellett, Felix et al. (2018) Convergent and Divergent Migratory Patterns of Human Neutrophils inside Microfluidic Mazes. Sci Rep 8:1887

Showing the most recent 10 out of 272 publications