TABLE 5 |.
Effects of microplastics in cell viability and uptake.
| End-point | Polymer type | Exposure time | Size | Concentration range | Assay | Cell type | Outcome | Ref |
|---|---|---|---|---|---|---|---|---|
|
| ||||||||
| Cell viability | Polystyrene (PS) | 12 h | 0.1 and 5 um | 1–200 ug/ml | CCK-8 kit | Caco-2 cells | No effect was observed | Wu et al.(2019) |
| 24 h, 48 h | 1.72 ± 0.26 um | 1–1,000 ug/cm2 | Trypan blue | BEAS-2B | Viability decreased to 60–70% at 1,000 ug/cm2 after 24 h exposure and all the concentrations above 10ug/cm2 after 48 h exposure | Dong et al. (2020) | ||
| 1, 4 and 10 um | 1–1,000 ug/ml | CTB and MTT | Caco-2 cells | CTB: 24 h 48 h exposures decrease the viability to 0% only after 1um PS exposure. MTT: Showed the same, results and additionally cell viability decreased to 80% and 70% after 24h and 48 h exposure to 4um | Stock et al. (2019) | |||
| 5 um | 0.00001–100 ug/ml | MTT | Caco-2 cells | No effect was observed | Wu et al. (2020), | |||
| 24 h | 10 um | 0.05–10 mg/L | Hoechst 33258 | T98G and HeLa cells | No effect was observed | Schirinzi et al., (2017) | ||
| COOH-modified polystyrene (PS) | 24 h | 0.5 um | 0.01–100 ug/ml | WST-1 | GIT co culture model | Intestinal cells: PS decreased the metabolic activity only at 0.01 μg/ml. Placental cells: PS increased mitochondrial activity only at concentrations from 0.01–10 μg/ml | Helser et al.,(2019) | |
| MTS | BeWo b30 cells | |||||||
| Polyethylene (PE) | 24 h | 3–16 um | 0.05–10 mg/L | Hoechst 33258 | T98G and HeLa cells | No effect was observed | Schirinzi et al., (2017) | |
| Polypropylene (PP) | 48 h | 20 and 25–200 um | In DMSO 10–1000 ug/ml and in powder 0.1–4.5 mg | CCK-8 colorimetric kit | HDF | HDF cells: only the 20 um PP (in DMSO) caused a reduction in viability (20%) at the highest concentration 1000 ug/ml | Hwang et al., (2019) | |
| Intracellular localization | Polystyrene (PS) | 12 h | 0.1 and 5 um | 1–80 ug/ml | ABC transporter activity (CAM cell probe) | Caco-2 cells | Inhibition of ABC transporter was observed for 0.1 um PS concentrations >20 ug/ml and 5 um PS only at 80 ug/ml | Wu et al., (2019) |
| 24 h | 1, 4 and 10 um | 108/ml (1 and 4 um), 3×106/ml (10 um) | Fluorescence microscopy | Caco-2 cells, mucus co-culture1 model and M-cell model2 | 4 um PS were absorbed the most in Caco-2 cells (3.8%), M cell model and mucus model 4.8%). 1 um PS were significantlyabsorbed by the M cell mode (5.8%)* | Stock et al.,(2019) | ||
| 24 h, 72 h | 1, 4 and 10 um | 100,000/ml (1 um), 250,000/ml (4 um), 60,000/ml (10 um) | Fluorescence microscopy | THP-1 cells derived macrophages | Macrophages contained intracellular 4 um PS (40–80%) and 1 um and 10 um in lower extent | Stock et al., (2019) | ||
| COOH-modified | 24 h | 0.5 um | 100 ug/ml | Confocal microscopy | GIT barrier3 and placental barrier coculture4 models | In the GIT barrier coculture, PS were internalized by intestinal cells and in the placental barrier model the placental cells | Hesler et al., (2019) | |
| Fluorescent polystyrene (PS) | 12 h | 0.1 um and 5 um | 20 ug/ml | Confocal microscopy | Caco-2 cells | Overlap between lysosomes and microplastics. Level of 5 um entering into cells lower than 1 um | Wu et al. (2019) | |
| Polystyrene (PS) and arsenic (As) | 12 h | 0.1 and 5 um | PS: 20 ug/ml (0.1 um), 80 ug/ml (0.5 um). As: 150 mg/L | Intracellular arsenic by ICP-MS | Caco-2 cells | 0.1 um PSs at 20 ug/ml increased the intracellular concentration of As | Wu et al. (2019) | |
extrapolated from the graph. Abbreviations: Polystyrene PS, Polyethylene PE, Polypropylene PP.
Caco-2 cells and HT29-MTX-E12 cells
Caco-2 and RajiB transwell coculture
Caco-2 and HT29-MTX-E12 cells
BeWo b30 and HPEC-A2 cells.