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Nadim Hallab

Has grant

Professor

Rush University
Country flagUnited States

Research Interests

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Recent Grants

Grant: Close

Determination of excessive immune reactivity to real time implant debris generate

Open Date: 2017-09-30

Close Date: 2019-07-31

Grant: Close

Corrosion Induced Hip Implant Failure: Synergistic Interactions of Patient, Mater

Open Date: 2016-09-19

Close Date: 2022-08-31

Grant: Close

Inflammasome Danger Signaling:A Novel Target to Prevent Debris Induced Osteolysis

Open Date: 2012-09-17

Close Date: 2018-06-30

Grant: Close

Battlefield-Acquired Immunogenicity to Metals Affects Orthopaedic Implant Outcome

Open Date: 2010-09-30

Close Date: 2016-09-29

Grant: Close

Bioreactivity Markers in Total Hip Replacments

Open Date: 2002-03-22

Close Date: 2005-02-28

Articles (5)

Year:

2025

Year:

2025

Past evaluation of particle contamination on packaged implants has typically been conducted using US Pharmacopeia (USP) 788, a 1970s pharmaceutical guideline created to evaluate contaminant particles in injectable fluids and syringes. Our objective was to reestablish relevant acceptance criteria for residual orthopedic and other implant debris, including smaller particles (i.e., <10 μm in diameter). Packaged total hip arthroplasty (THA) titanium (Ti6Al4V)‐alloy femoral stems were used (hydroxyapatite [HA]‐coated and non‐coated stems). Short‐term ultrasonication and longer‐term 24‐hour soak/agitation methods were used to elute surface‐bound contaminant particles, and released particles were analyzed via scanning electron microscopy, energy‐dispersive x‐ray analysis, image analysis, and particle characterization. For HA‐coated THA‐stems, >99% of eluted particles were calcium phosphate. For plain non‐coated THA‐stems, >99% of eluted particles were titanium‐alloy‐based. The number‐based median size of particles in both groups was approximately 1.5 μm in diameter despite being composed of different materials. The total volume of particulate removed from HA‐coated stems was 0.037 mm 3 (671 × 10 3 particles total), which was approximately >50‐fold more volume than that on plain non‐coated stems at 0.0006 mm 3 (89 × 10 3 particles total). Only non‐coated THA stems passed reestablished USP788 acceptance criteria, compared by using equivalent total volumes of contaminant particulate within new and legacy guideline ranges of >10 and >25 μm ECD, that is, <1.0 × 10 7 particles for <1 μm diameter in size, <600,000 for <1–10 μm, <6000 for 10–25 μm and <600 for >25 μm. These results fill a knowledge gap on how much residual debris can be expected to exist on packaged implants and can be used as a basis for updating acceptance criteria (i.e., termed USP788‐Implant [USP788‐I]). Residual implant particulate assessment is critical given the increasing implant complexity and new manufacturing techniques (e.g., additive manufacturing).

Year:

2024

Year:

2024

Year:

2023

Collaborators (5)

Peter Wahl

Deputy Group Leader Biomechanics and Implant Design

University of Basel

SWITZERLAND
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Joshua Jacobs

Professor and Chairman

Rush University Medical Center

UNITED STATES
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Robin Pourzal

Assistant Professor

Rush University Medical Center

UNITED STATES
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Michael Kurtz

Drexel University

UNITED STATES
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Joshua Rainey

University of Utah

UNITED STATES
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