Renormalizable parameters of the sine-Gordon model

The well-known phase structure of the two-dimensional sine-Gordon model is reconstructed by means of its renormalization group flow, the study of the sensitivity of the dynamics on microscopic parameters. Such an analysis resolves the apparent contradiction between the phase structure and the triviality of the effective potential in either phases, provides a case where usual classification of operators based on the linearization of the scaling relation around a fixed point is not available and shows that the Maxwell-cut generates an unusually strong universality at long distances. Possible analogies with four-dimensional Yang-Mills theories are mentioned, too.Comment: 12 pages, 7 figures. Revised form, to appear in Phys. Lett.

Perfused multiwell plate for 3D liver tissue engineering

In vitro models that capture the complexity of in vivo tissue and organ behaviors in a scalable and easy-to-use format are desirable for drug discovery. To address this, we have developed a bioreactor that fosters maintenance of 3D tissue cultures under constant perfusion and we have integrated multiple bioreactors into an array in a multiwell plate format. All bioreactors are fluidically isolated from each other. Each bioreactor in the array contains a scaffold that supports formation of hundreds of 3D microscale tissue units. The tissue units are perfused with cell culture medium circulated within the bioreactor by integrated pneumatic diaphragm micropumps. Electronic controls for the pumps are kept outside the incubator and connected to the perfused multiwell by pneumatic lines. The docking design and open-well bioreactor layout make handling perfused multiwell plates similar to using standard multiwell tissue culture plates. A model of oxygen consumption and transport in the circulating culture medium was used to predict appropriate operating parameters for primary liver cultures. Oxygen concentrations at key locations in the system were then measured as a function of flow rate and time after initiation of culture to determine oxygen consumption rates. After seven days of culture, tissue formed from cells seeded in the perfused multiwell reactor remained functionally viable as assessed by immunostaining for hepatocyte and liver sinusoidal endothelial cell (LSEC) phenotypic markers.National Institute of Environmental Health Sciences (grant number 5P30ES002109-30)National Institutes of Health (U.S.) (NIH grant number 5R01ES015241)DuPont MIT AlliancePfizer Inc.National Science Foundation (U.S.) (NSF grant number EEC-9843342

Mechanical Testing of 3D Printed Prosthetics

The Rapid Orthotics for CURE Kenya team as a whole aims to empower the orthopedic technicians in the CURE Kenya hospital by creating, optimizing, and testing 3D printed prosthetics and orthotics. Our team started in 2016 by creating a 3D printing process for below the knee prosthetic sockets. Since then, we had adapted to the hospital\u27s needs over the years, expanding the capabilities of the system itself. Presently, a section of our team has worked specifically with these leg sockets to ensure the safety and functionality for patients. They have done testing to make sure the sockets are strong enough and to make sure the silicone liners are safe for use in developing countries. In addition to safety testing, over the years we have created ankle-foot orthotics and prosthetic hands. The design part of our team works to create new 3D printed devices to help our clients reach more patients. By 2024 we hope to fully integrate our expanded system in the orthopedic workshop in Kijabe, Kenya.https://mosaic.messiah.edu/engr2020/1018/thumbnail.jp

Pediatric lung transplantation: The years 1985 to 1992 and the clinical trial of FK 506

The application of lung transplantation to the pediatric population was a natural extension of the success realized in our adult transplantation program, which began in 1982. Twenty pediatric patients (age range 3 to 18 years) have had heart-lung (n = 11), double lung (n = 8), and single lung (n = 1) transplantation procedures. The causes of end-stage lung disease were primary pulmonary hypertension (n = 7), congenital heart disease (n = 5), cystic fibrosis (n = 4), pulmonary arteriovenous malformation (n = 2), graft- versus-host disease (n = 1), and desquamative interstitial pneumonitis (n = 1). Four (20%) patients had thoracic surgical procedures before the transplantation operation. The survival was 80% at a mean follow-up of 2 years. Immunosuppressive drugs included cyclosporine (n = 9) or FK 506 (n = 11) based therapy with azathioprine and steroids. Children were followed up by means of spirometry, transbronchial biopsy, and primed lymphocyte testing of bronchoalveolar lavage fluid. The mean number of treated episodes of rejection was 1.4 at 30 days, 0.5 at 30 to 90 days, and 1.4 at more than 90 days, and the first treated rejection episode occurred on average 28 days after the operation. Obliterative bronchiolitis developed in four (25%) of 16 patients surviving more than 100 days. Results of pulmonary function tests have remained good in almost all recipients. The greatest infectious risk was that of cytomegalovirus: one death and one case of pneumonia. Posttransplantation lymphoproliferative disease was diagnosed in two (12.5%) patients; both recovered. The most common complications were hypertension (25%) and postoperative bleeding (15%). Early results indicate that lung transplantation is a most promising therapy for children with severe vascular and parenchymal lung disease

Susceptibility to non-tuberculous mycobacterial disease is influenced by rs1518111 in IL10

Although exposure to potentially pathogenic nontuberculous mycobacteria (NTM) via soil and domestic water supplies is common, pulmonary infection and disease are confined to a small proportion of older individuals. Previously, alleles of a polymorphism in IL10 (rs1800896) were associated with NTM disease and we demonstrated elevated production of IL-10 by blood leukocytes from patients with pulmonary NTM. Here seven additional polymorphisms in IL10 were investigated in a larger cohort of Caucasian controls and patients with pulmonary NTM disease. This demonstrated a significant association between pulmonary NTM disease and one polymorphism (rs1518111) in strong linkage disequilibrium with rs1800896