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Related Concept Videos

Dose-Response Relationship: Overview01:03

Dose-Response Relationship: Overview

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Agonists can bind with and activate receptors, resulting in the formation of drug-receptor complexes. Once formed, these complexes catalyze many biochemical processes at the cellular level and subsequently induce a pharmacologic response. The degree of response is directly proportional to the fraction of activated receptors, which in turn, depends on the concentration of the drug at the receptor site as well as the sensitivity of the receptor. An increase in the administered dose contributes to...
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Dose-Response Relationship: Selectivity and Specificity01:25

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Drugs exert their therapeutic effects by interacting with receptors, enzymes, or ion channels that are present throughout the human body. The strength and duration of the interaction between a drug and its target receptor are characterized by the selectivity and specificity of the drug. Selectivity refers to a drug's strong preference for its intended target over other targets. For instance, isoprenaline, a non-selective β-adrenergic agonist, interacts with both β1- and...
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Response Surface Methodology01:16

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Response Surface Methodology (RSM) is a collection of statistical and mathematical techniques used to develop, improve, and optimize processes. It is particularly valuable when many input variables or factors potentially influence a response variable.
The process of RSM involves several key steps:
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Dose Response Curve: Conventional Versus Nonmonotonic01:21

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The correlation between a drug's dosage and its impact on a biological system is a cornerstone of pharmacology and toxicology. Conventional dose–response curves, which include graded and quantal relationships, are key to this understanding. Graded dose–response curves depict the spectrum of a biological reaction to different doses within an individual, indicating that as the drug dosage increases, so does the intensity of the response. On the other hand, quantal dose–response...
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Dose-Response Relationship: Potency and Efficacy01:22

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The potency of a drug is the measure of its ability to produce a biological response and can be compared by looking at the half-maximum effective concentration or EC50 values of different drugs. A lower EC50 value indicates higher potency of the drug. In the dose–response curve of two antihypertensive drugs, candesartan and irbesartan, a significant difference is observed in their EC50 values. A lower EC50 value for candesartan indicates that it is more potent than irbesartan, as it...
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Factors Affecting Drug Response: Overview01:21

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When it comes to infants and young children, they are typically administered smaller doses of medication in comparison to adults. This is primarily because their organ functions still need to fully develop, meaning their bodies are not as efficient at metabolizing or eliminating drugs. Additionally, their blood-brain barrier is more permeable than in adults. As a result, high concentrations of drugs can easily penetrate the central nervous system (CNS), potentially leading to neurological...
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Wesseling et al. respond

Catharina Wesseling1, Jennifer Crowe, Christer Hogstedt

  • 1Catharina Wesseling and Jennifer Crowe are with the Program on Work, Environment and Health in Central America (SALTRA), Central American Institute for Studies on Toxic Substances (IRET), Universidad Nacional, Heredia, Costa Rica. Christer Hogstedt is with the Institute of Environmental Medicine (IMM), Karolinska Institutet, Stockholm, Sweden. Kristina Jakobsson is with the Department of Occupational and Environmental Medicine, Lund University, Lund, Sweden. Rebekah Lucas is with the Hothaps Program, Umeå International School of Public Health, Umeå University, Umeå, Sweden. David H. Wegman is with Work Environment, University of Massachusetts, Lowell.

American Journal of Public Health
|January 18, 2014
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No abstract available in PubMed .

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