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Engineered nanoparticle bio-conjugates toxicity screening: The xCELLigence cells viability impact
Clarence S Yah1,2, Geoffrey S Simate3
1Implementation Science Unit, Wits Reproductive Health and HIV Institute, Faculty of Health Sciences, University of the Witwatersrand, South Africa.
Bioimpacts : BI
|August 15, 2020
Summary
Engineered nanoparticle bio-conjugates (ENPBCs) show limited toxicity data, with most in vitro studies deeming them safe. Further in vitro, in vivo, and clinical trials are crucial for validating ENPBC safety and applications.
Area of Science:
- Biomaterials Science
- Nanotechnology
- Toxicology
Background:
- Engineered nanoparticle bio-conjugates (ENPBCs) have diverse applications, but limited data exists to support risk assessments.
- Ensuring consumer safety and understanding the risks associated with ENPBCs is critical as their market presence grows.
Purpose of the Study:
- To review and analyze existing literature on the in vitro and in vivo toxicity of ENPBCs.
- To identify the extent of data available for risk estimation and consumer safety concerns related to ENPBCs.
Main Methods:
- Systematic literature search for articles published between 2013-2016 using xCELLigence real-time cell analysis (RTCA) for in vitro ENPBC toxicity.
- Literature search for articles published between 2008-2016 on in vivo animal models assessing ENPBC toxicity and safety outcomes.
- Inclusion criteria focused on studies providing in vitro or in vivo toxicity data for ENPBCs.
Main Results:
- Out of 121 identified articles, 32 met the inclusion criteria (23 for in vitro, 9 for in vivo).
- Most in vitro studies (19/23) using xCELLigence technology indicated ENPBCs were non-toxic or partially non-toxic.
- In vivo studies showed limited potential toxicity in one case, with others suggesting ENPBCs as drug therapy candidates but lacking comprehensive toxicity data.
Conclusions:
- Current data on the bioimpacts of ENPBCs, both in vitro and in vivo, remains limited.
- Further in vitro and in vivo assays, clinical trials, and long-term impact studies are necessary to validate ENPBC safety and facilitate their uptake.
- Enhanced real-time analysis using technologies like xCELLigence is needed to generate robust data for subsequent in vivo investigations.

