Publications by authors named "A K Haudenschild"

Objective: To establish the pharmacokinetics of the cyclin-dependent kinase-9 inhibitor flavopiridol in equine middle carpal joints, using an extended-release poly lactic-co-glycolic acid (PLGA) microparticle formulation.

Animals: 4 healthy horses without evidence of forelimb lameness.

Methods: A 6-week longitudinal pharmacokinetic study was conducted in 2 phases (6 weeks each) in 4 healthy horses.

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Significance: Cartilage tissue engineering is a promising strategy for effective curative therapies for treatment of osteoarthritis. However, tissue engineers depend predominantly on time-consuming, expensive, and destructive techniques as quality control to monitor the maturation of engineered cartilage. This practice can be impractical for large-scale biomanufacturing and prevents spatial and temporal monitoring of tissue growth, which is critical for the fabrication of clinically relevant-sized cartilage constructs.

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Article Synopsis
  • COVID-19, caused by the SARS-CoV-2 virus, has infected over 650 million people globally, with about 23% experiencing long-term symptoms like fatigue and joint pain.
  • A study using a humanized mouse model has found that SARS-CoV-2 infection results in acute bone loss, an increase in osteoclasts (bone-resorbing cells), and thinner growth plates.
  • Understanding the impact of COVID-19 on bone health is essential to identify at-risk groups and create effective treatments, particularly for older individuals prone to fractures and younger patients who may face growth issues.
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Regulatory guidelines for tissue engineered products require stringent characterization during production and necessitate the development of novel, non-destructive methods to quantify key functional parameters for clinical translation. Traditional assessments of engineered tissues are destructive, expensive, and time consuming. Here, we introduce a non-destructive, inexpensive, and rapid sampling and analysis system that can continuously monitor the mechanical, biochemical, and structural properties of a single sample over extended periods of time.

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Quantification of clinically meaningful tibiofemoral motions requires a coordinate system where motions are free from kinematic crosstalk errors. The objectives were to 1) develop an algorithm for assigning an optimized joint coordinate system (OPT JCS) that minimizes kinematic crosstalk errors based on a kinematic model of the tibiofemoral joint, 2) determine tibiofemoral kinematics of the native (i.e.

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