Michael Kinzel

Dr. Michael Kinzel

Computational Fluids and Aerodynamics Laboratory, University of Central Florida, Orlando, FL 32816, USA
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Research Focus & Metrics

Academic Career Length

8Years (2019-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 February 2021 in Physics of Fluids
Verified
Journal Article
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AFAaron Foster
Aaron Foster
Michael KinzelMichael Kinzel
Michael Kinzel
The COVID-19 pandemic has driven numerous studies of airborne-driven transmission risk primarily through two methods: Wells–Riley and computational fluid dynamics (CFD) models. This effort provides a detailed comparison of the two methods for a classroom scenario with masked habitants and various ventilation conditions. The results of the studies concluded that (1) the Wells–Riley model agrees with CFD results without forced ventilation (6% error); (2) for the forced ventilation cases, there was a significantly higher error (29% error); (3) ventilation with moderate filtration is shown to significantly reduce infection transmission probability in the context of a classroom scenario; (4) for both cases, there was a significant amount of variation in individual transmission route infection probabilities (up to 220%), local air patterns were the main contributor driving the variation, and the separation distance from infected to susceptible was the secondary contributor; (5) masks are shown to have benefits from interacting with the thermal plume created from natural convection induced from body heat, which pushes aerosols vertically away from adjacent students.

29 June 2023 in Bone Research
Verified
Journal Article
Open access
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FWFEI WEI
FEI WEI
ZTZewen Tuong
Zewen Tuong
MOMahmoud Omer
Mahmoud Omer
CNChristopher Ngo
Christopher Ngo
JAJackson Asiatico
Jackson Asiatico
MCMelanie Jean Coathup
Melanie Jean Coathup
Radiotherapy is a critical component of cancer care but can cause osteoporosis and pathological insufficiency fractures in surrounding and otherwise healthy bone. Presently, no effective countermeasure exists, and ionizing radiation-induced bone damage continues to be a substantial source of pain and morbidity. The purpose of this study was to investigate a small molecule aminopropyl carbazole named P7C3 as a novel radioprotective strategy. Our studies revealed that P7C3 repressed ionizing radiation (IR)-induced osteoclastic activity, inhibited adipogenesis, and promoted osteoblastogenesis and mineral deposition in vitro. We also demonstrated that rodents exposed to clinically equivalent hypofractionated levels of IR in vivo develop weakened, osteoporotic bone. However, the administration of P7C3 significantly inhibited osteoclastic activity, lipid formation and bone marrow adiposity and mitigated tissue loss such that bone maintained its area, architecture, and mechanical strength. Our findings revealed significant enhancement of cellular macromolecule metabolic processes, myeloid cell differentiation, and the proteins LRP-4, TAGLN, ILK, and Tollip, with downregulation of GDF-3, SH2B1, and CD200. These proteins are key in favoring osteoblast over adipogenic progenitor differentiation, cell matrix interactions, and shape and motility, facilitating inflammatory resolution, and suppressing osteoclastogenesis, potentially via Wnt/β-catenin signaling. A concern was whether P7C3 afforded similar protection to cancer cells. Preliminarily, and remarkably, at the same protective P7C3 dose, a significant reduction in triple-negative breast cancer and osteosarcoma cell metabolic activity was found in vitro. Together, these results indicate that P7C3 is a previously undiscovered key regulator of adipo-osteogenic progenitor lineage commitment and may serve as a novel multifunctional therapeutic strategy, leaving IR an effective clinical tool while diminishing the risk of adverse post-IR complications. Our data uncover a new approach for the prevention of radiation-induced bone damage, and further work is needed to investigate its ability to selectively drive cancer cell death.

1 February 2023 in Physics of Fluids
Verified
Journal Article
Open access
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RFR. W. Forehand
R. W. Forehand
KNK. C. Nguyen
K. C. Nguyen
CAC. J. Anderson
C. J. Anderson
RSR. Shannon
R. Shannon
SGS. M. Grace
S. M. Grace
Michael KinzelMichael Kinzel
Michael Kinzel
A computational study of the wave phenomenon and probable cavitation that occurs when a droplet interacts with a shock is presented. A volume-of-fluid method with and without a cavitation model activated is employed. The model with no cavitation is used to clarify the droplet's internal wave field. The model is benchmarked using experimental data of a 22 mm water column impacted by a shock wave at Mach 2.4. Good agreement between the computational results for a two-dimensional (2D) circular droplet and the experimental results is demonstrated. A simplified 2D, square droplet is also considered in order to highlight the effects of interface curvature on the internal waves. Comparison of the results for the square and circular drops shows that the circular geometry diffuses the initial pressure wave while focusing the reflected wave. The three-dimensional (3D) spherical droplet was then analyzed. The internal wave behavior is similar to the 2D circular drop with enhanced diffusion and focusing. Two cavitation models were then used to explore the probability that cavitation occurs for a nominal sized raindrop interacting with shock waves, Mach 1.5–5. Two cavitation models, full Rayleigh–Plesset (FRP) and Schnerr-Sauer both predicted vapor formation at the same location with the FRP always predicting slightly higher amounts of vapor. The current setting for number of nuclei ensures that the simulation is not swamped by vapor formation but is unrealistically small. Therefore, while the work demonstrates that cavitation will occur, the full nature of the cavitation along with the impulsive pressure waves it should create is not currently captured.

1 June 2019 in International Journal of Heat and Mass Transfer
Verified
Journal Article
Closed access
DHDavid R. Hanson
David R. Hanson
Michael KinzelMichael Kinzel
Michael Kinzel
SMStephen T. McClain
Stephen T. McClain

1 February 2021 in Ocean Engineering
Verified
Journal Article
Closed access
Michael KinzelMichael Kinzel
Michael Kinzel
JLJules W. Lindau
Jules W. Lindau
RKRobert F. Kunz
Robert F. Kunz

31 July 2022 in Nutrients
Verified
Journal Article
Open access
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MOMahmoud Omer
Mahmoud Omer
HAHessein Ali
Hessein Ali
NONina Orlovskaya
Nina Orlovskaya
ABAmelia Ballesteros-Edwards
Amelia Ballesteros-Edwards
VCVee San Cheong
Vee San Cheong
MCMelanie Jean Coathup
Melanie Jean Coathup
The influence of diet on the development of osteoporosis is significant and not fully understood. This study investigated the effect of diets of varying lipid profiles and ω-3, ω-6 and ω-9 composition on the structural and mechanical properties of bone. The hypothesis studied was that a diet high in saturated fat would induce osteoporosis and produce an overall increased detrimental bony response when compared with a diet high in unsaturated ω-6, or ω-9. Male C57BL/6J mice were fed either a control diet, 50:50 mix (saturated:unsaturated) high in ω-9 (HFD50:50), a diet high in saturated fat (HSF) or a polyunsaturated fat diet high in ω-6 (PUFA) over an 8-week duration. Tibiae were retrieved and evaluated using DMA, 3-point-bending, histomorphometry, and microCT. Mice fed a HSF diet displayed key features characteristic of osteoporosis. The loss tangent was significantly increased in the HFD50:50 diet group compared with control (p = 0.016) and PUFA-fed animals (p = 0.049). HFD50:50-fed mice presented with an increased viscous component, longer tibiae, increased loss modulus (p = 0.009), and ultimate stress, smaller microcracks (p < 0.001), and increased trabecular width (p = 0.002) compared with control animals. A diet high in ω-9 resulted in an overall superior bone response and further analysis of its role in bone health is warranted.