Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Pharmacokinetics: Drug–Drug Interactions01:25

Pharmacokinetics: Drug–Drug Interactions

376
Drug interactions occur when the pharmacological effect of one drug is altered by another substance, either enhancing or diminishing its activity. The drug whose activity is altered is known as the object drug, and the substance causing the alteration is called the agent drug or the precipitant. The net effects of these interactions are mostly undesirable, leading to decreased effectiveness or increased adverse effects. In rare cases, interactions can be beneficial, such as the enhanced...
376
Pharmacokinetics: Drug–Food and Drug–Viral Interactions01:26

Pharmacokinetics: Drug–Food and Drug–Viral Interactions

222
A drug interaction occurs when the concurrent use of another drug, food, or an external substance alters the pharmacological activity of a drug. This interaction can modify the action of the original drug, affecting its effectiveness and safety.Drug–food interactions are significant as they impact drug absorption, metabolism, and excretion. For example, grapefruit juice is a well-known disruptor of drug metabolism. It inhibits the cytochrome P450 3A4 enzyme, crucial for the metabolism of...
222
Drug-Receptor Interactions01:29

Drug-Receptor Interactions

7.3K
Drug-receptor interaction describes the binding of receptors by drugs, but not all drug-receptor interactions result in activation and tissue response. For instance, the binding of agonists activates the receptor to generate a cellular reaction, while antagonists bind to receptors without causing their activation.
Several parameters, such as the drug's affinity for its receptor and its efficacy, which is its ability to activate the receptor, determine the drug's effect on the tissue....
7.3K
Factors Affecting Protein-Drug Binding: Drug Interactions01:23

Factors Affecting Protein-Drug Binding: Drug Interactions

570
Drug interactions are a critical aspect of pharmacology and can occur when two or more drugs compete for the same binding site. This competition can result in one drug displacing another, altering the effect of the displaced drug. Drug interactions are complex processes that rely heavily on how much of the displacer drug is present and how strongly it can bind to the same sites as the displaced drug.
Displacement interactions can have varying outcomes, ranging from toxicity to virtually...
570
Factors Affecting Renal Clearance: Drug Distribution and Drug Interactions01:09

Factors Affecting Renal Clearance: Drug Distribution and Drug Interactions

516
Renal clearance plays a pivotal role in drug elimination from the body and can be influenced by drug distribution and interactions. Understanding these factors is crucial in pharmacology as they impact the effectiveness and duration of drug therapy.
One important factor is the relationship between renal clearance and the apparent volume of distribution. Renal clearance tends to be inversely proportional to the apparent volume of distribution. Drugs with an extensive distribution volume or those...
516
Drug-Receptor Interaction: Antagonist01:28

Drug-Receptor Interaction: Antagonist

4.9K
An antagonist is a drug that binds strongly to a receptor without activating it. An antagonist prevents other molecules, such as neurotransmitters or hormones, from binding to the receptor and triggering a cellular response. Such interaction effectively hinders the normal physiological processes mediated by the receptor, resulting in various pharmacological effects depending on the specific receptor targeted.
Antagonists can be classified as competitive or noncompetitive based on their...
4.9K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Systemic immunometabolic profiling classifies cisplatin sensitivity states using interpretable machine learning.

iScience·2026
Same author

From stages to states: rethinking sleep from first principles.

Sleep·2025
Same author

Chronic Lymphocytic Thyroiditis Does Not Worsen Early Surgical Outcomes in Papillary Thyroid Cancer.

World journal of surgery·2025
Same author

Automated assessment of laparoscopic pattern cutting skills using computer vision and deep learning.

Surgery·2025
Same author

Weighted Hypoxemia Index: An adaptable method for quantifying hypoxemia severity.

PloS one·2025
Same author

Methodology of murine lung cancer mimics clinical lung adenocarcinoma progression and metastasis.

Scientific reports·2025

Related Experiment Video

Updated: Jan 21, 2026

A Data Integration Workflow to Identify Drug Combinations Targeting Synthetic Lethal Interactions
07:40

A Data Integration Workflow to Identify Drug Combinations Targeting Synthetic Lethal Interactions

Published on: May 27, 2021

4.6K

Semi-Supervised Learning Algorithm for Identifying High-Priority Drug-Drug Interactions Through Adverse Event

Ning Liu, Cheng-Bang Chen, Soundar Kumara

    IEEE Journal of Biomedical and Health Informatics
    |August 10, 2019
    PubMed
    Summary
    This summary is machine-generated.

    This study introduces a machine learning framework to identify high-priority drug-drug interactions (DDIs) from FDA adverse event reports. It aims to reduce alert fatigue and improve patient safety by prioritizing critical DDI alerts.

    More Related Videos

    Supervised Machine Learning for Semi-Quantification of Extracellular DNA in Glomerulonephritis
    09:16

    Supervised Machine Learning for Semi-Quantification of Extracellular DNA in Glomerulonephritis

    Published on: June 18, 2020

    7.3K
    A Computerized Test Battery to Study Pharmacodynamic Effects on the Central Nervous System of Cholinergic Drugs in Early Phase Drug Development
    07:02

    A Computerized Test Battery to Study Pharmacodynamic Effects on the Central Nervous System of Cholinergic Drugs in Early Phase Drug Development

    Published on: February 11, 2019

    10.2K

    Related Experiment Videos

    Last Updated: Jan 21, 2026

    A Data Integration Workflow to Identify Drug Combinations Targeting Synthetic Lethal Interactions
    07:40

    A Data Integration Workflow to Identify Drug Combinations Targeting Synthetic Lethal Interactions

    Published on: May 27, 2021

    4.6K
    Supervised Machine Learning for Semi-Quantification of Extracellular DNA in Glomerulonephritis
    09:16

    Supervised Machine Learning for Semi-Quantification of Extracellular DNA in Glomerulonephritis

    Published on: June 18, 2020

    7.3K
    A Computerized Test Battery to Study Pharmacodynamic Effects on the Central Nervous System of Cholinergic Drugs in Early Phase Drug Development
    07:02

    A Computerized Test Battery to Study Pharmacodynamic Effects on the Central Nervous System of Cholinergic Drugs in Early Phase Drug Development

    Published on: February 11, 2019

    10.2K

    Area of Science:

    • Pharmacovigilance
    • Biomedical Informatics
    • Machine Learning

    Background:

    • Drug-drug interactions (DDIs) pose a significant risk to patient safety, necessitating effective alert systems.
    • Current DDI alerting systems face challenges with alert overload and user fatigue, hindering their clinical utility.
    • Prioritizing high-risk DDIs is crucial for optimizing medication safety alerts.

    Purpose of the Study:

    • To develop and validate a machine learning framework for identifying high-priority DDIs.
    • To leverage FDA adverse event reports for feature extraction and DDI classification.
    • To reduce alert fatigue by focusing on clinically significant drug-drug interactions.

    Main Methods:

    • Utilized a machine learning framework incorporating feature extraction from FDA adverse event reports.
    • Employed an autoencoder-based semi-supervised learning algorithm for DDI identification.
    • Integrated stacked autoencoders and weighted support vector machines for enhanced classification performance.

    Main Results:

    • Demonstrated the effectiveness of adverse event feature representations in distinguishing high-priority DDIs.
    • The proposed algorithm achieved superior performance (F-measure and AUC score) compared to competing methods.
    • Successfully identified potential high-priority DDI candidates for medication alerts.

    Conclusions:

    • The developed framework offers a practical approach for pre-screening high-priority DDI candidates.
    • Integrating multiple data sources and domain knowledge enhances DDI alert system optimization.
    • This method contributes to improving patient safety by refining DDI alert prioritization.