An automatic control system has been developed to balance and control the output of an artificial heart. The system consisted of 2 linked negative feedback loops. The left ventricle was controlled by a Servo-Stroke Optimizer, which insured complete filling and full stroke operation of the left pump with each beat and changed the beat rate in accord with changes in aortic pressure. The right ventricle was controlled by a Servo-Variable Systolic Duration unit, which changed the stroke of the right ventricle to maintain the left atrial pressure within a preset band. In the initial animal studies, control pressures (aortic and left atrial pressure) were obtained from implanted transducers. More recently, a method has been devised whereby the control pressures were obtained from specific points on the left air line pressure wave, obviating the need for implanted transducers. The control system has been evaluated in a mock circulatory loop and in 9 calves with implanted artificial hearts. The system has provided balance of the 2 implanted ventricles and changes in flow rate in response to changes in peripheral resistance. The need for an operator to make manual adjustment to the power units has been considerably reduced. Further studies are indicated to evaluate the function of the control system in animals performing moderate-to-maximal exercise. Furthermore, the ultimate benefits of full stroke operation vs fill limited mode operation remain to be delineated.
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Nanoscale
January 2025
Transport at Nanoscale Interfaces Laboratory, Empa, Swiss Federal Laboratories for Materials Science and Technology, 8600 Dübendorf, Switzerland.
Magic-angle twisted bilayer graphene (TBLG) has emerged as a versatile platform to explore correlated electron phases driven primarily by low-energy flat bands in moiré superlattices. While techniques for controlling the twist angle between graphene layers have spurred rapid experimental progress, understanding the effects of doping inhomogeneity on electronic transport in correlated electron systems remains challenging. In this work, we investigate the interplay of confinement and doping inhomogeneity on the electrical transport properties of TBLG by leveraging device dimensions and twist angles.
View Article and Find Full Text PDFJ Med Econ
January 2025
UNESCO-TWAS, The World Academy of Sciences, Trieste, Italy.
Aim: Dynamic cancer control is a current health system priority, yet methods for achieving it are lacking. This study aims to review the application of system dynamics modeling (SDM) on cancer control and evaluate the research quality.
Methods: Articles were searched in PubMed, Web of Science, and Scopus from the inception of the study to November 15th, 2023.
Free Radic Res
January 2025
Radiation Biology & Health Sciences Division, Bio-science Group, Bhabha Atomic Research Centre, Trombay, Mumbai-400085, India.
Free radicals have been implicated in the pathogenesis of cancer along with cardiovascular, neurodegenerative, pulmonary and inflammatory disorders. Further, the relationship between oxidative stress and disease is distinctively established. Clinical trials using anti-oxidants for the prevention of disease progression have indicated some beneficial effects.
View Article and Find Full Text PDFInt J Med Robot
February 2025
Department of Urology, The Affiliated Hospital of Qingdao University, Qingdao, China.
Background: The emergence of telesurgery has received global interest, with secure network transmission identified as a crucial determinant of its success. This study aimed to evaluate the safety and viability of employing quantum cryptography communication in remote partial nephrectomy.
Methods: The surgeon operated on the patient from a distance of over 260 km using remote control of a surgical robot.
Therapies against hematological malignancies using chimeric antigen receptors (CAR)-T cells have shown great potential; however, therapeutic success in solid tumors has been constrained due to limited tumor trafficking and infiltration, as well as the scarcity of cancer-specific solid tumor antigens. Therefore, the enrichment of tumor-antigen specific CAR-T cells in the desired region is critical for improving therapy efficacy and reducing systemic on-target/off-tumor side effects. Here, we functionalized human CAR-T cells with superparamagnetic iron oxide nanoparticles (SPIONs), making them magnetically controllable for site-directed targeting.
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