Many toxicological test methods, including assays of cell viability and function, require an evaluation of concentration-response data. This often involves curve fitting, and the resulting mathematical functions are then used to determine the concentration at which a certain deviation from the control value occurs (e.g. a decrease of cell viability by 15%). Such a threshold is called the benchmark response (BMR). For a toxicological test, it is often of interest to determine the concentration of test compound at which a pre-defined BMR of e.g. 10, 25 or 50% is reached. The concentration at which the modelled curve crosses the BMR is called the benchmark concentration (BMC). We present a user-friendly, web-based tool (BMCeasy), designed for ...
High-throughput in vitro toxicity screening can provide an efficient way to identify potential biolo...
In cell biology, pharmacology and toxicology dose-response and concentration-response curves are fre...
Difficulties arise when extrapolating in vitro derived toxicity data to in vivo acute toxicity data ...
Abstract—Cytotoxic cell assays are performed to asses the toxicity of various compounds or unicellul...
Dose-response assays are a common and increasingly high throughput method of assessing the toxicity ...
In vitro assays and high-throughput screening (HTS) tools are increasingly being employed as replace...
The maximal chemical concentration that causes an acceptably small or no effect in an organism or is...
For hazard classifications of chemicals, continuous data from animal- or nonanimal testing methods a...
High requirements and challenges formed by legislations like REACH and the 7th amendment of cosmetic...
The current bioassay development literature lacks the use of statistically robust methods for calcul...
If in vitro data are to be used as a basis for hazard characterization, a translation of an in vitro...
We investigate several methods commonly used to obtain a benchmark dose and show that those based on...
A paradigm shift is occurring in toxicology following the report of the National Research Council of...
Most tests methods that are accepted by regulatory authorities to assess the safety and toxicity of ...
The half maximal inhibitory concentration (IC50) has several limitations that make it unsuitable for...
High-throughput in vitro toxicity screening can provide an efficient way to identify potential biolo...
In cell biology, pharmacology and toxicology dose-response and concentration-response curves are fre...
Difficulties arise when extrapolating in vitro derived toxicity data to in vivo acute toxicity data ...
Abstract—Cytotoxic cell assays are performed to asses the toxicity of various compounds or unicellul...
Dose-response assays are a common and increasingly high throughput method of assessing the toxicity ...
In vitro assays and high-throughput screening (HTS) tools are increasingly being employed as replace...
The maximal chemical concentration that causes an acceptably small or no effect in an organism or is...
For hazard classifications of chemicals, continuous data from animal- or nonanimal testing methods a...
High requirements and challenges formed by legislations like REACH and the 7th amendment of cosmetic...
The current bioassay development literature lacks the use of statistically robust methods for calcul...
If in vitro data are to be used as a basis for hazard characterization, a translation of an in vitro...
We investigate several methods commonly used to obtain a benchmark dose and show that those based on...
A paradigm shift is occurring in toxicology following the report of the National Research Council of...
Most tests methods that are accepted by regulatory authorities to assess the safety and toxicity of ...
The half maximal inhibitory concentration (IC50) has several limitations that make it unsuitable for...
High-throughput in vitro toxicity screening can provide an efficient way to identify potential biolo...
In cell biology, pharmacology and toxicology dose-response and concentration-response curves are fre...
Difficulties arise when extrapolating in vitro derived toxicity data to in vivo acute toxicity data ...