Toolkit for Exposure Assessment: Beginners Start Here

INTRODUCTION

What is an Exposure Assessment?
How is Exposure Different from Dose?
How is Exposure Different from Risk?
Who Performs Exposure Assessments?


What is an exposure assessment?

Exposure characterization versus exposure assessment
An exposure characterization is viewed as a qualitative description of the exposure potential from the chemical product. A characterization would provide a general explanation as to how the product is used, in what functions, and under what applications; it would not necessarily include measured or calculated values.

Some examples of qualitative exposure reports are provided in the "Examples of Qualitative Exposure Assessment" section of the website.

An exposure assessment determines the level, duration and extent of contact with a particular chemical. In performing an exposure assessment, the following questions should be addressed:

What is the source of the potential exposure?
Examples: industrial operations, pesticide use, consumer products

What potential media, or point of exposure, does the chemical end up in?
Examples: air (indoor, outdoor), water (drinking water, bathing water, river water), food, soil, sediment, plants

Is the chemical changed before it gets to these media?

By what route of exposure does the chemical get to a receptor?
Examples: ingestion, dermal (skin) contact, inhalation

Who is the ultimate receptor that is exposed?
Examples: worker, consumer, community resident, ecological receptor

 

 

The outcome of an exposure assessment is an exposure dose, i.e., an estimate of the concentration of the emitted chemical that is being contacted. Exposure units are expressed as:

  • Mg/liter (mg/l) for liquids
  • Mg/gram (mg/g) for solids
  • Mg/cubic meter (mg/m3) for air/vapor/gas

How is exposure different from dose?
The literature is not consistent in its definition of exposure. Although most people agree that exposure means contact with a chemical or agent, universal agreement has not been reached as to whether that contact takes place at a person's exterior or whether the the exposure means the chemical has penetrated the boundaries and been absorbed through the skin, lungs, or gastrointestinal tract. The following definitions were set forth by EPA's National Center for Environmental Assessment in their Final Guidelines for Exposure Assessment.

"The process of a chemical entering the body can be described in two steps: contact (exposure), followed by actual entry (crossing the boundary). Absorption...leads to the availability of an amount of the chemical to biologically significant sites within the body (internal dose or absorbed dose)."

The definition of terms becomes increasingly murky in the arena of "exposure models". Some developers have viewed "exposure models" as models that determine environmental concentrations that a person or other receptor may come in contact with (external contact). Other developers of "exposure models" are actually referring to models that calculate a dose that the receptor has ingested, inhaled, or has absorbed through the skin. This Web site does its best to distinguish between the two families of models by categorizing them as:

  • FATE AND TRANSPORT MODELS that determine environmental exposures (external contact) to ecological receptors
  • EXPOSURE models that determine predicted doses to humans.

How is exposure different from risk?
Exposure is a component of risk. Exposure occurs through contact with a chemical, either by drinking, inhaling or touching it. The amount of a chemical to which a receptor is exposed does not indicate the risk; the hazard associated with the chemical must also be known. A chemical's hazard describes its potential to cause adverse effects to human, animal or plant life. The risk of a chemical is a function of both the level of exposure and the level of hazard. Often, this is expressed as a "Margin of Exposure" (MOE). The MOE is typically calculated from a threshold concentration for an adverse effect, divided by the estimated exposure. Thus, a very small exposure compared to the adverse effect level results in an MOE > 1 and may represent a low risk situation. Conversely, an MOE < 1 indicates that adverse effects could occur.

Who Performs Exposure Assessments?
Human exposure assessments are developed by toxicologists, industrial hygienists, and others to help assess potential risks associated with exposures to chemicals in consumer products and via other sources. The "science" of exposure assessment has advanced a lot over the past several years, and continues to advance. Key "players" have included U.S. EPA scientists, academicians, experts in consulting companies, and exposure assessors in companies (often via the former Chemical Manufacturers Association, now the American Chemistry Council). Key professional societies include the International Society of Exposure Analysis (ISEA: www.iseaweb.org/) and the Society for Risk Analysis (SRA: www.sra.org/).

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