Introduction: In the event of a cardiac arrest during microgravity exposure, external chest compressions (ECCs) which form the main part of basic life support should be carried out while the advanced life support equipment is being deployed. This study was aimed to determine if there was any gender difference in the effectiveness of performing ECCs using a body suspension device to simulate lunar and Martian hypogravity and microgravity.
Methods: The volunteers performed ECCs during simulated microgravity (using the Evetts-Russomano method): lunar, Martian, and Earth/Control. Each volunteer performed 3 sets of 30 compressions with 6 s rest in between. The volunteers had their increase in heart rate measured and used the Borg scale to rate the intensity of work after each protocol.
Results: The mean depth compressions for men during all gravitational simulations were higher than the women, but both sexes performed effective ECCs during the two tested hypogravity states. During simulated microgravity, men performed significantly deeper ECCs (mean +/- SD of 45.07 +/- 4.75 mm) than women (mean +/- SD of 30.37 +/- 4.75 mm). None of the women achieved the required mean depth of ECCs. Though the increase in heart rate was higher in women, no significant difference was seen in the Borg scale scores between genders during or after the performance of ECCs in microgravity.
Discussion: The results suggest both genders can perform effective ECCs during simulated hypogravity. Women, however, cannot perform effective ECCs during microgravity simulation. These findings suggest that there is a gender difference when performing the Evetts-Russomano method.
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http://dx.doi.org/10.3357/asem.3171.2012 | DOI Listing |
Molecules
January 2025
Department of Applied Science and Technology, North Carolina Agricultural and Technical State University, Greensboro, NC 27411, USA.
Fischer-Tropsch synthesis (FTS) in a 3D-printed stainless steel (SS) microchannel microreactor was investigated using Fe@SiO catalysts. The catalysts were prepared by two different techniques: one pot (OP) and autoclave (AC). The mesoporous structure of the two catalysts, Fe@SiO (OP) and Fe@SiO (AC), ensured a large contact area between the reactants and the catalyst.
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Harris Orthopaedics Laboratory, Massachusetts General Hospital, Boston, Massachusetts.
Background: Periprosthetic joint infections (PJIs) are a major complication of total joint replacement surgeries. This study investigated the enhancement of mechanical properties and antibiotic release in ultra-high molecular weight polyethylene (UHMWPE) through the encapsulation of submicron gentamicin sulfate (GS) particles, addressing the critical need for improved implant materials in orthopaedic surgery, particularly in managing PJIs.
Methods: The present study involved embedding submicron GS particles into UHMWPE flakes at concentrations of 2% to 10% by weight.
Inorg Chem
January 2025
State Key Laboratory of Explosion Science and Technology, Beijing Institute of Technology, Beijing 100081, China.
The performance of energetic coordination compounds (ECCs) is influenced by their components and structure. Modifying the chemical structure of the ligands can balance the detonation performance and sensitivity. This study introduced Cu(3-PZCA)(ClO) () and Cu(2-IZCA)(ClO) (), using 3-PZCA and 2-IZCA as ligands.
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January 2025
Department of Nanoscience, Joint School of Nanoscience and Nanoengineering, University of North Carolina at Greensboro, Greensboro, NC, 27401, USA.
The chemistry of the extracellular electron transfer (EET) process in microorganisms can be understood by interfacing them with abiotic materials that act as external redox mediators. These mediators capture and transfer extracellular electrons through redox reactions, bridging the microorganism and the electrode surface. Understanding this charge transfer process is essential for designing biocapacitors capable of modulating and storing charge signatures as capacitance at the electrode interface.
View Article and Find Full Text PDFNat Chem
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Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA, USA.
Atomically precise nanoclusters can be assembled into ordered superlattices with unique electronic, magnetic, optical and catalytic properties. The co-crystallization of nanoclusters with functional organic molecules provides opportunities to access an even wider range of structures and properties, but can be challenging to control synthetically. Here we introduce a supramolecular approach to direct the assembly of atomically precise silver nanoclusters into a series of nanocluster‒organic ionic co-crystals with tunable structures and properties.
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