Isothermal Dose Response

Isothermal dose response is a biochemistry method that measures how increasing concentrations of a compound affect a molecular target while the sample is maintained at a constant temperature. In a thermal-shift or cellular thermal shift assay, ligand binding can stabilize or destabilize a protein against heat-induced unfolding and aggregation; researchers quantify the remaining soluble protein to generate a concentration-response profile. These profiles help estimate target engagement, compare compound potency, and assess selectivity in purified systems or cells. By linking concentration-dependent effects with protein stability, isothermal dose response supports drug discovery and the study of molecular interactions in biologically relevant environments.

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JoVE Core - Pharmacology
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Dose-Response Relationship: Overview

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2023

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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JoVE Core - Pharmacology
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Dose-Response Relationship: Potency and Efficacy

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2023

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 produces...

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JoVE Core - Pharmacology
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Dose-Response Relationship: Selectivity and Specificity

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2023

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 β2-adrenergic receptors...

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JoVE Core - Pharmacokinetics and Pharmacodynamics

Dose Response Curve: Conventional Versus Nonmonotonic

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2026

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 relationships...

Isothermal Processes

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2025

A thermodynamic process that occurs at constant temperature is called an isothermal process. Heat slowly flows into the system or out of the system to maintain thermal equilibrium. Processes involving phase changes like water evaporation into steam or freezing water into ice at a constant temperature are examples of Isothermal Processes. An ideal gas can also undergo isothermal expansion or compression. For example, consider 1 mole of an ideal gas inside an isolated cylinder at initial volume V...

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