{"title":"Role of fluid shear stress on E-cadherin dynamics and cytoskeletal stresses","authors":"Deepika Verma, N. Ye, S. Hua","doi":"10.1109/NEBEC.2015.7117053","DOIUrl":"https://doi.org/10.1109/NEBEC.2015.7117053","url":null,"abstract":"Adherens junctions (AJs) play an important role in cell-cell mechanical coupling and in maintaining tissue organization. Under chronic flow, epithelial cells adapt by strengthening cell-cell junctions in order to maintain the integrity of epithelia. How forces due to fluid flow are transmitted to E-cadherin and cause the dynamic remodeling of AJs is unclear. In this study we simultaneously measured AJ dynamics and cytoskeletal stresses and reorganization in MDCK cells under flow. The cells were co-expressed with fluorescently labelled E-cadherin and stress sensitive α-actinin FRET sensor for measurements. A fluid shear stress of 0.7dyn/cm2 for 3 hours caused an increase in expression of E-cadherin, formation of new AJs and strengthening of pre-existing AJs leading to a continuous distribution of cell-cell junctions. This increase in cell-cell junctions is correlated with the formation of strong peripheral actin ring due to cytoskeleton reorganization. The average cytoskeletal stress at adherens junctions shows multi-phase changes under flow, which closely links to the dynamic changes of AJs. These results provide the direct evidence that the shear stress induced cytoskeletal forces play an important role on cell-cell adhesions.","PeriodicalId":111398,"journal":{"name":"2015 41st Annual Northeast Biomedical Engineering Conference (NEBEC)","volume":"94 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2015-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"122450150","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}
{"title":"Quantification of entrapped model protein released during electrospun nanofiber degradation","authors":"K. Cummins, K. L. Lee, J. A. Cooper","doi":"10.1109/NEBEC.2015.7117086","DOIUrl":"https://doi.org/10.1109/NEBEC.2015.7117086","url":null,"abstract":"This protein release study investigated the use of poly (ε-caprolactone) (PCL) nanofibrous matrices loaded with bovine serum albumin to model protein delivery. Samples were placed in phosphate buffered saline for an eight week degradation and protein release study. Each week samples were removed, massed, and protein content quantified from the degradation solution. As expected, the PCL samples did not lose substantial mass over 8 weeks, but total protein released was approximately 5.7% by week 1, and 15% by week 8. Results from this study will be used to model the required loading of various growth factors for controlled delivery during future in vitro ligament cell culture studies.","PeriodicalId":111398,"journal":{"name":"2015 41st Annual Northeast Biomedical Engineering Conference (NEBEC)","volume":"104 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2015-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"122452133","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}
M. Lazar, A. Lurski, S. Ghafurian, L. Chen, L. Uko, V. Tan, K. Li
{"title":"In vitro dynamic simulation of elbow motion","authors":"M. Lazar, A. Lurski, S. Ghafurian, L. Chen, L. Uko, V. Tan, K. Li","doi":"10.1109/NEBEC.2015.7117109","DOIUrl":"https://doi.org/10.1109/NEBEC.2015.7117109","url":null,"abstract":"Elbow disorders are a common occurrence; however, our understandings of complex elbow dislocation and the functional anatomy of the elbow joint are still very limited. The efficacy of treatment strategies of this injury is largely unknown. The purpose of this study is to create an active elbow simulator using a new paradigm, In vitro joint simulation driven by in vivo motion, to study how elbow injuries affect joint kinematics. The elbow simulator uses an open source program to calculate muscle-tendon lengths based on elbow joint angles. It then uses five actuators to pull cables attached at five muscle attachment points to create a realistic motion of a cadaver arm. By cutting certain tendons, injury can be simulated and kinematics can be compared to the intact arm. Thus, the effects of injuries and their treatments on elbow kinematics can be better understood.","PeriodicalId":111398,"journal":{"name":"2015 41st Annual Northeast Biomedical Engineering Conference (NEBEC)","volume":"139 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2015-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"127017902","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}
{"title":"Calcaneus stress fractures: A finite element analysis","authors":"A. M. J. Aljabran, D. Piovesan, R. Bortoletto","doi":"10.1109/NEBEC.2015.7117075","DOIUrl":"https://doi.org/10.1109/NEBEC.2015.7117075","url":null,"abstract":"Shock absorption strategies targeted at reducing ground reaction forces during impact have been unsuccessful in decreasing stress fracture development in the calcaneus. We hypothesize that the critical loads on the calcaneus are instead due to muscles forces. We performed a finite element analysis to estimate the time-evolution of stresses in the calcaneus during single support phase of a self-paced walk. Local stresses were found to be higher than the yield stress and located at the interface between the calcaneus and the Achilles' tendon. This supports the hypothesis that stress fractures are likely to be the effect of muscles forces rather than the impact of the foot to the ground.","PeriodicalId":111398,"journal":{"name":"2015 41st Annual Northeast Biomedical Engineering Conference (NEBEC)","volume":"7 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2015-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134033561","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}
Yumiao Zhang, Mansik Jeon, L. Rich, H. Hong, J. Geng, Yin Zhang, Sixiang Shi, T. Barnhart, P. Alexandridis, J. Huizinga, M. Seshadri, W. Cai, C. Kim, J. Lovell
{"title":"Frozen naphthalocyanine micelles for intestinal imaging","authors":"Yumiao Zhang, Mansik Jeon, L. Rich, H. Hong, J. Geng, Yin Zhang, Sixiang Shi, T. Barnhart, P. Alexandridis, J. Huizinga, M. Seshadri, W. Cai, C. Kim, J. Lovell","doi":"10.1109/NEBEC.2015.7117210","DOIUrl":"https://doi.org/10.1109/NEBEC.2015.7117210","url":null,"abstract":"Here we report the development of a family of nanoparticles that can withstand the harsh conditions of the stomach and intestine, avoid systemic absorption, and provide good optical contrast for photoacoustic imaging. The hydrophobicity of naphthalocyanine dyes was exploited to generate frozen micelles (nanonaps), with tunable near-infrared absorption. Nanonaps, following oral administration in mice, passed safely through the gastrointestinal tract. Non-invasive, non-ionizing photoacoustic techniques were used to visualize nanonap intestinal distribution with low background and remarkable resolution, and enabled real-time intestinal functional imaging with ultrasound co-registration.","PeriodicalId":111398,"journal":{"name":"2015 41st Annual Northeast Biomedical Engineering Conference (NEBEC)","volume":"4 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2015-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"131897948","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}
{"title":"Orthogonally tunable solid-state nanopore modifications for improved biosensing","authors":"J. S. Hersey, A. Squires, A. Meller, M. Grinstaff","doi":"10.1109/NEBEC.2015.7117050","DOIUrl":"https://doi.org/10.1109/NEBEC.2015.7117050","url":null,"abstract":"Advances in biosensor sensitivity, specificity, and accessibility are required for the development of next generation diagnostic tools. Solid-state nanopores consisting of sub-10 nm in diameter pores drilled into an insulating material show promise as single-molecule biosensors for detecting both nucleic acid and protein targets. However, this technology is limited by rapid analyte translocation speeds and complex and/or inconsistent device assemblies. To address these limitations, we have developed two orthogonally tunable solid-state nanopore modifications which slow nucleic acid translocation speeds and streamline device assembly and manipulation through the use of a 3-dimensional polymeric nanofiber mesh (NFM) coating and the development of a novel microfluidic device, respectively. A range of translocation speeds from 1x to >100x slower than a bare nanopore were achieved by tuning the chemical composition of the NFM coating. In addition, a microfluidic device was designed to streamline nanopore assembly enabling facile integration of both sample purification protocols and single-molecule detection using optical and electronic readouts simultaneously.","PeriodicalId":111398,"journal":{"name":"2015 41st Annual Northeast Biomedical Engineering Conference (NEBEC)","volume":"16 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2015-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"129092338","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}
{"title":"Biofabrication and 3D localization of multilayered cellular constructs using Laser Direct-Write and Mesoscopic Fluorescent Molecular Tomography","authors":"B. Tricomi, Mehmet S. Ozturk, X. Intes, D. Corr","doi":"10.1109/NEBEC.2015.7117130","DOIUrl":"https://doi.org/10.1109/NEBEC.2015.7117130","url":null,"abstract":"Recent advances in tissue engineering applications demand micro-scale precision in both design and evaluation. Herein, we aim to meet these challenges through a combination of two innovative techniques: gelatin-based Laser Direct-Write (LDW) and Mesoscopic Fluorescence Molecular Tomography (MFMT). LDW was used to precisely pattern cell-loaded, alginate microbeads, in layer-by-layer fashion, to construct thick, multilayered cellular constructs. Then, MFMT was utilized to deeply assess and 3D-model cellular localization. The combination of these two techniques may provide the accuracy and precision needed for the analysis of tissue engineering in 3D.","PeriodicalId":111398,"journal":{"name":"2015 41st Annual Northeast Biomedical Engineering Conference (NEBEC)","volume":"13 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2015-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"133592401","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}
{"title":"Saving navy SEALS: Pressure-activated system for personal flotation device","authors":"N. Miller, J. M. Adams","doi":"10.1109/NEBEC.2015.7117227","DOIUrl":"https://doi.org/10.1109/NEBEC.2015.7117227","url":null,"abstract":"Approximately 2000 operators in the SEAL Teams use a personal flotation device (PFD). While it is a necessary safety measure, the current PFDs in use often deploy prematurely causing the operator to then discard the device. We created a system with changeable modes, allowing the user to retain a fully functional vest with an activation system that is not subject to premature deployment. Implementation of this will reduce the danger for each operator and save lives. Our system is composed of a sensor suite, microcontroller, and actuator. The system has two user chosen modes: automatic and manual. We performed system tests to ensure the system is reliable and validated for use in special operations. Two of these tests included a software functionality test (A) and a valve response test (B). Results for (A) were LED ON for deployment conditions and LED OFF for non-deployment conditions. Results for (B) were a positive result (actuator activated and filled bladder correctly) for each test. The final result was an automatic PFD system that is viable for use in special operations. This will increase the number of lives saved by ensuring that operators can retain their PFDs without premature deployment as well as ensuring that an unconscious victim in the water will be lifted to safety by their automatic PFD.","PeriodicalId":111398,"journal":{"name":"2015 41st Annual Northeast Biomedical Engineering Conference (NEBEC)","volume":"23 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2015-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"131928986","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}
{"title":"Characterization and evaluation of fabricated poly(L-lactic) acid core fibers for ligament fascicle development","authors":"E. Laurilliard, K. L. Lee, J. A. Cooper","doi":"10.1109/NEBEC.2015.7117108","DOIUrl":"https://doi.org/10.1109/NEBEC.2015.7117108","url":null,"abstract":"Poly(L-lactic) acid (PLLA) is a biodegradable thermoplastic aliphatic polyester that has been found to be an excellent material of choice for biomedical applications including tissue engineered implants. This paper will discuss the characterization of PLLA core fibers being developed for tissue engineering applications and its degradation properties which showed that even with a mass loss of ~30 %, the fibers had no significant change in mechanical strength. It is important to understand the degradation of polymer fibers in the design of scaffolds in order to discover the expected temporal loss of mechanical strength and integrity. This will allow for more improved design of fabricated structures and scaffolds that can maintain integrity overtime in the body during the regeneration process.","PeriodicalId":111398,"journal":{"name":"2015 41st Annual Northeast Biomedical Engineering Conference (NEBEC)","volume":"42 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2015-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"117202281","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}
Matthew K. Dion, Colleen P. Healey, S. Giddings, John F. Drazan, Jared T Roberts, N. Cady, E. Ledet
{"title":"Force measurement across the patellofemoral joint using a smart patellar implant following a total knee arthroplasty","authors":"Matthew K. Dion, Colleen P. Healey, S. Giddings, John F. Drazan, Jared T Roberts, N. Cady, E. Ledet","doi":"10.1109/NEBEC.2015.7117087","DOIUrl":"https://doi.org/10.1109/NEBEC.2015.7117087","url":null,"abstract":"Osteoarthritis is one of the leading causes of chronic pain and disability in the United States. The gold standard to treat osteoarthritis of the knee is to perform a total knee replacement. Post-operatively, as high as 21% of total knee replacement patients experience moderate to severe anterior knee pain. The exact mechanism(s) of anterior knee pain remains unknown. Patellofemoral contact forces are believed to play a significant role in the mechanism of anterior knee pain. Yet, measuring contact forces in the patella has remained a challenge. We have developed a “smart patella” to measure force magnitudes and distributions across the patellofemoral joint. We have designed and conducted proof-of-concept experiments demonstrating that our novel force sensing system has the potential to be implanted into the patellofemoral joint space with minimal alterations to modern implant design. Once implanted, our sensors measure in real time, in vivo patellofemoral contact forces.","PeriodicalId":111398,"journal":{"name":"2015 41st Annual Northeast Biomedical Engineering Conference (NEBEC)","volume":"16 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2015-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"117206793","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}