Evidence map›Paper›PMID 34596239›Full record

ArticleBiotechnology and bioengineering2021

Dynamic microfluidic bioreactor-Hip simulator (DMBH) system for implant toxicity monitoring.

Ravindra V Badhe, Divya Bijukumar, Pedro Mesquita, Kai Yuan Cheng, Remya Ampadi Ramachandran, Yang Lin, Mathew T Mathew

Abstract read
In one paragraph

Article in Biotechnology and bioengineering, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Ravindra V BadheDepartment of Biomedical Sciences, University of Illinois College of Medicine at Rockford, Rockford, Illinois, USA.
Divya BijukumarDepartment of Biomedical Sciences, University of Illinois College of Medicine at Rockford, Rockford, Illinois, USA.
Pedro MesquitaDepartment of Mechanical, Industrial and Systems Engineering, University of Rhode Island, Kingston, Rhode Island, USA.
Kai Yuan ChengDepartment of Biomedical Sciences, University of Illinois College of Medicine at Rockford, Rockford, Illinois, USA.
Remya Ampadi RamachandranDepartment of Biomedical Sciences, University of Illinois College of Medicine at Rockford, Rockford, Illinois, USA.
Yang LinDepartment of Mechanical, Industrial and Systems Engineering, University of Rhode Island, Kingston, Rhode Island, USA.
Mathew T MathewDepartment of Biomedical Sciences, University of Illinois College of Medicine at Rockford, Rockford, Illinois, USA.

Funding

Corrosion Induced Hip Implant Failure: Synergistic Interactions of Patient, Material, Design, and Surgical FactorsR01AR070181 · NIAMS · RUSH UNIVERSITY MEDICAL CENTER · PI LUNDBERG, HANNAH JEAN, MATHEW, MATHEW THOPPIL · 2016 to 2020
$2.3M
The role of CoCr nano metal degradation products (DPs) on alteration of DNA replication and repair mechanism in neural cell environment: Toxicology aspectsR03NS111554 · NINDS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI BIJUKUMAR, DIVYA RANI, MATHEW, MATHEW THOPPIL · 2019 to 2020
$160k
Foundation for the National Institutes of Health R01 - AR070181Foundation for the National Institutes of Health R03 - R03NS111554NIAMS NIH HHS R01 AR070181NINDS NIH HHS R03 NS111554
6 · The paper itself

Abstract

The generation of degradation products (DPs) like ions and organo-metallic particles from corroding metallic implants is an important healthcare concern. These DPs generate local and systemic toxicity. The impact on local toxicity is well documented, however, little is known about systemic toxicity. This is mainly due to the limited scope of the current microtiter plate-based (static) toxicity assay techniques. These methods do not mimic the systemic (dynamic) conditions. In this study, it is hypothesized that DPs incubated with cells in static conditions might provide improper systemic toxicity results, as there is no movement mimicking the blood circulation around cells. This study reports the development of a three-chambered prototype microfluidic system connected to the operational hip implant simulator to test the cellular response induced by the DPs. This setup is called a dynamic microfluidic bioreactor-hip simulator system. We hypothesize that a dynamic microfluidic system will provide a realistic toxicology response induced by DPs than a static cell culture plate. To prove the hypothesis, Neuro2a (N2a) cells were used as representative cells to study systemic neurotoxicity by the implant DPs. The microfluidic bioreactor system was validated by comparing the cell toxicity against the traditional static system and using COMSOL modeling for media flow with DPs. The hip implant simulator used in this study was a state-of-the-art sliding hip simulator developed in our lab. The results suggested that static toxicity was significantly more compared to dynamic microfluidic-based toxicity. The newly developed DMBH system tested for in situ systemic toxicity on N2a cells and demonstrated very minimum toxicity level (5.23%) compared to static systems (31.16%). Thus, the new DMBH system is an efficient tool for in situ implant metal systemic toxicity testing.

Indexed as

BioreactorsModels, BiologicalToxicity TestsAnimalsCell LineCell SurvivalEquipment DesignHip ProsthesisMetalsMiceMicrofluidic Analytical TechniquesMetalsbioreactordynamic toxicityhip implant simulatorsmicrofluidicssystemic toxicity

Identifiers

PMID34596239
PMCPMC13271660

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.