» Articles » PMID: 29956556

Comparison of Conventional and Advanced in Vitro Models in the Toxicity Testing of Nanoparticles

Overview
Date 2018 Jun 30
PMID 29956556
Citations 48
Authors
Affiliations
Soon will be listed here.
Abstract

Humans are exposed to a wide variety of nanoparticles (NPs) present in the environment, in consumer, health and medical products, and in food. Conventional cytotoxicity testing compared to animal testing is less expensive, faster and avoids ethical problems at the expense of a lower predictive value. New cellular models and exposure conditions have been developed to overcome the limitations of conventional cell culture and obtain more predictive data. The use of three-dimensional culture, co-culture and inclusion of mechanical stimulation can provide physiologically more relevant culture conditions. These systems are particularly relevant for oral, respiratory and intravenous exposure to NPs and it may be assumed that physiologically relevant application of the NPs can improve the predictive value of in vitro testing. Various groups have used advanced culture and exposure systems, but few direct comparisons between data from conventional cultures and from advanced systems exist. In silico models may present another option to predict human health risk by NPs without using animal studies. In the absence of validation, the question whether these alternative models provide more predictive data than conventional testing remains elusive.

Citing Articles

Menadione as Antibiotic Adjuvant Against : Mechanism of Action, Efficacy and Safety.

Shehu K, Schneider M, Kraegeloh A Antibiotics (Basel). 2025; 14(2).

PMID: 40001407 PMC: 11851977. DOI: 10.3390/antibiotics14020163.


New Insights in Microplastic Cellular Uptake Through a Cell-Based Organotypic Rainbow-Trout () Intestinal Platform.

Verdile N, Cattaneo N, Camin F, Zarantoniello M, Conti F, Cardinaletti G Cells. 2025; 14(1.

PMID: 39791745 PMC: 11719976. DOI: 10.3390/cells14010044.


Safety Landscape of Therapeutic Nanozymes and Future Research Directions.

Tagaras N, Song H, Sahar S, Tong W, Mao Z, Buerki-Thurnherr T Adv Sci (Weinh). 2024; 11(46):e2407816.

PMID: 39445544 PMC: 11633477. DOI: 10.1002/advs.202407816.


Bifunctional mesoporous glasses for bone tissue engineering: Biological effects of doping with cerium and polyphenols in 2D and 3D in vitro models.

Menshikh K, Reddy A, Cochis A, Fraulini F, Zambon A, Lusvardi G Biomater Biosyst. 2024; 14:100095.

PMID: 38912165 PMC: 11192985. DOI: 10.1016/j.bbiosy.2024.100095.


Advancing Nanomaterial Toxicology Screening Through Efficient and Cost-Effective Quantitative Proteomics.

Stobernack T, Dommershausen N, Alcolea-Rodriguez V, Ledwith R, Banares M, Haase A Small Methods. 2024; 8(12):e2400420.

PMID: 38813751 PMC: 11671853. DOI: 10.1002/smtd.202400420.


References
1.
Prietl B, Meindl C, Roblegg E, Pieber T, Lanzer G, Frohlich E . Nano-sized and micro-sized polystyrene particles affect phagocyte function. Cell Biol Toxicol. 2013; 30(1):1-16. PMC: 4434214. DOI: 10.1007/s10565-013-9265-y. View

2.
Bourgine J, Billaut-Laden I, Happillon M, Lo-Guidice J, Maunoury V, Imbenotte M . Gene expression profiling of systems involved in the metabolism and the disposition of xenobiotics: comparison between human intestinal biopsy samples and colon cell lines. Drug Metab Dispos. 2012; 40(4):694-705. DOI: 10.1124/dmd.111.042465. View

3.
Geys J, Coenegrachts L, Vercammen J, Engelborghs Y, Nemmar A, Nemery B . In vitro study of the pulmonary translocation of nanoparticles: a preliminary study. Toxicol Lett. 2005; 160(3):218-26. DOI: 10.1016/j.toxlet.2005.07.005. View

4.
Freese C, Schreiner D, Anspach L, Bantz C, Maskos M, Unger R . In vitro investigation of silica nanoparticle uptake into human endothelial cells under physiological cyclic stretch. Part Fibre Toxicol. 2014; 11:68. PMC: 4318365. DOI: 10.1186/s12989-014-0068-y. View

5.
Bregoli L, Chiarini F, Gambarelli A, Sighinolfi G, Gatti A, Santi P . Toxicity of antimony trioxide nanoparticles on human hematopoietic progenitor cells and comparison to cell lines. Toxicology. 2009; 262(2):121-9. DOI: 10.1016/j.tox.2009.05.017. View