Atory or cardiovascular systems were uncovered [7]. At that time, researchers started

Atory or cardiovascular 3-Bromopyruvic acid systems were uncovered [7]. At that time, researchers started to systematically study the effects of (natural) NPs on human health [8,9], especially the association between NP size and its response in lung tissue [10?2]. However, due to their properties, engineered NMs are increasingly often used in consumer products. But the same advantageous sizedependent properties of NMs lead to the possibility of harmful size-dependent biological interactions [13]. Therefore, the need to assess the potential risk of NMs on human health is rapidly growing. NPs can display acute cytotoxic action at the site of entry. Cells important in this regard are epithelial cells of the respective organ, and cells of the innate immune system. Upon exposure to NMs, such as carbon black (CB), carbon nanotubes (CNTs), or zinc oxide, cells may be acutely damaged and their functionality may be compromised [14?7]. Both, bio-persistent (e.g. CNTs) and bio-degradable (e.g. iron oxide) NPs may cause severe problems [2,18]. In addition to acute toxic effects, chronic exposure may result in selective cytotoxicity affecting specific cell functions [19]. However, testing of chronic effects in vitro is rarely done for conventional substances. Drugs are usually metabolized, excretedLong-Term Effects of Nanoparticlesand degraded within cells and cellular accumulation is not expected. Consequently, models to assess chronic toxicity have not been developed and chronic toxicity is usually studied in animals. Nevertheless, data suggest that some NMs are not sufficiently cleared from the organism [20,21]. If an organism is HDAC-IN-3 exposed over a long period to low concentrations of NPs, the function of cells may be compromised. Most indications for organ damage by repeated exposure to 18055761 NPs were obtained in animal studies. Repeated exposure to gold NPs and magnetic NPs caused not only accumulation and histopathological changes in various organs but also weight loss and marked alterations in blood count [22?4]. Therefore, the assessment of toxic effects is becoming of outmost importance. In short-term cytotoxicity studies, cell lines are usually employed, but these generally cannot be studied much longer than 72 hours in conventional culture. Subsequently, the cells need medium change and/or the cultures are in the stationary state. To assess longer time-periods, cells have been sub-cultured and again exposed to the tested compound [21]. Other systems such as bioreactors have to be used when observations over longer time-periods are needed [25,26]. Dependent on their growth characteristics (adherent or in suspension), cells in bioreactors are either dispersed in medium or cultured on scaffolds, matrices or microcarriers. In microcarrier cell cultures, anchorage-dependent cells are grown on the surface of small spheres which are maintained in stirred suspension cultures. In comparison to conventional monolayer cell culture, this technology provides the advantage that high cell densities and higher yields of cellular products such as antibodies can be obtained. Main advantages of the microcarrier system are reduced costs and reduced risk of contamination, increased culture periods without sub-culturing [27] as well as the imitation of the in vivo situation due to a more physiologic environment. This technique is therefore a good choice where cells are used for the production of biologicals, cells, cell products, and viral vaccines. Other applications include studies of ce.Atory or cardiovascular systems were uncovered [7]. At that time, researchers started to systematically study the effects of (natural) NPs on human health [8,9], especially the association between NP size and its response in lung tissue [10?2]. However, due to their properties, engineered NMs are increasingly often used in consumer products. But the same advantageous sizedependent properties of NMs lead to the possibility of harmful size-dependent biological interactions [13]. Therefore, the need to assess the potential risk of NMs on human health is rapidly growing. NPs can display acute cytotoxic action at the site of entry. Cells important in this regard are epithelial cells of the respective organ, and cells of the innate immune system. Upon exposure to NMs, such as carbon black (CB), carbon nanotubes (CNTs), or zinc oxide, cells may be acutely damaged and their functionality may be compromised [14?7]. Both, bio-persistent (e.g. CNTs) and bio-degradable (e.g. iron oxide) NPs may cause severe problems [2,18]. In addition to acute toxic effects, chronic exposure may result in selective cytotoxicity affecting specific cell functions [19]. However, testing of chronic effects in vitro is rarely done for conventional substances. Drugs are usually metabolized, excretedLong-Term Effects of Nanoparticlesand degraded within cells and cellular accumulation is not expected. Consequently, models to assess chronic toxicity have not been developed and chronic toxicity is usually studied in animals. Nevertheless, data suggest that some NMs are not sufficiently cleared from the organism [20,21]. If an organism is exposed over a long period to low concentrations of NPs, the function of cells may be compromised. Most indications for organ damage by repeated exposure to 18055761 NPs were obtained in animal studies. Repeated exposure to gold NPs and magnetic NPs caused not only accumulation and histopathological changes in various organs but also weight loss and marked alterations in blood count [22?4]. Therefore, the assessment of toxic effects is becoming of outmost importance. In short-term cytotoxicity studies, cell lines are usually employed, but these generally cannot be studied much longer than 72 hours in conventional culture. Subsequently, the cells need medium change and/or the cultures are in the stationary state. To assess longer time-periods, cells have been sub-cultured and again exposed to the tested compound [21]. Other systems such as bioreactors have to be used when observations over longer time-periods are needed [25,26]. Dependent on their growth characteristics (adherent or in suspension), cells in bioreactors are either dispersed in medium or cultured on scaffolds, matrices or microcarriers. In microcarrier cell cultures, anchorage-dependent cells are grown on the surface of small spheres which are maintained in stirred suspension cultures. In comparison to conventional monolayer cell culture, this technology provides the advantage that high cell densities and higher yields of cellular products such as antibodies can be obtained. Main advantages of the microcarrier system are reduced costs and reduced risk of contamination, increased culture periods without sub-culturing [27] as well as the imitation of the in vivo situation due to a more physiologic environment. This technique is therefore a good choice where cells are used for the production of biologicals, cells, cell products, and viral vaccines. Other applications include studies of ce.