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Tarja Toimela

Researcher at University of Tampere

Publications -  46
Citations -  976

Tarja Toimela is an academic researcher from University of Tampere. The author has contributed to research in topics: Cell culture & Angiogenesis. The author has an hindex of 19, co-authored 42 publications receiving 881 citations. Previous affiliations of Tarja Toimela include National Institute of Chemical Physics and Biophysics.

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The applicability of conventional cytotoxicity assays to predict safety/toxicity of mesoporous silica nanoparticles, silver and gold nanoparticles and multi-walled carbon nanotubes.

TL;DR: Conventional cytotoxicity assays are better suited to rank the order of toxicity of different nanoparticles instead of producing accurate IC50 data and using immune cells, especially macrophages together with fibroblasts, would bring more relevant predictions of ENM cytotoxic as immune cells may discover cytot toxicity that is not captured by BALB/c 3T3 cells alone.
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Retinal Pigment Epithelium Cell Culture as a Model for Evaluation of the Toxicity of Tamoxifen and Chloroquine

TL;DR: In this paper, the effects of tamoxifen and chloroquine on the activity of the lysosomal enzymes N-acetyl-beta-glucosaminidase and cathepsin D in RPE in vitro to evaluate the possible eye toxicity caused by these drugs.
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Effects of Tamoxifen, Toremifene and Chloroquine on the Lysosomal Enzymes in Cultured Retinal Pigment Epithelial Cells

TL;DR: The main lysosomal protease cathepsin D was more sensitive than N-acetyl-beta-D-glucosaminidase to the effects of tamoxifen and toremifene, possibly due to their antioestrogenic properties, and phenol red-free medium with charcoal-stripped serum seemed to make the drugs more effective than the reference medium.
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The combined use of human neural and liver cell lines and mouse hepatocytes improves the predictability of the neurotoxicity of selected drugs

TL;DR: Compared to the use of neurons alone, better estimations of neurotoxicity can be made by the combined use of metabolically competent hepatocytes and glial cells together with neuronal cells (e.g. SH-SY5Y).