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

Drug Discovery: Overview01:26

Drug Discovery: Overview

Drug discovery is a multifaceted process involving extensive screening, testing, and optimization of lead compounds to identify potential new drugs for therapeutic use. It combines several approaches, including screening large numbers of natural products, chemical modification of known active molecules, identification of new drug targets, and rational design based on biological mechanisms and drug-receptor structure. These approaches are carried out in both academic research laboratories and...
Pharmacokinetic–Pharmacodynamic Relationship: Problems01:24

Pharmacokinetic–Pharmacodynamic Relationship: Problems

The empirical approach to drug therapy optimization relies on correlating pharmacological response with administered dosage. Such an approach can be costly, time-consuming, and often yields poor correlation due to variables like formulation factors and drug elimination characteristics. A more precise approach correlates response with plasma drug concentration or the amount of drug in the body, rather than dosage. This is achieved through pharmacokinetic-pharmacodynamic (PK/PD) modeling, which...
Structure-Activity Relationships and Drug Design01:28

Structure-Activity Relationships and Drug Design

Drug design is a dynamic field that involves discovering and developing new medications based on specific biological targets. This process heavily relies on structure-activity relationships (SAR) and quantitative structure-activity relationships (QSAR) to guide the design and optimization of efficient drugs.
SAR studies the intricate relationship between a drug's chemical structure and biological activity. It focuses on understanding how modifications to a drug's structure can influence its...
Prodrugs01:30

Prodrugs

Prodrugs are a class of pharmaceutical compounds that undergo a biotransformation process within the body to be converted into a pharmacologically active drug. Prodrugs are designed to improve the therapeutic properties of the parent drug, such as enhancing bioavailability, increasing stability, or reducing toxicity. The concept of prodrugs revolves around modifying the chemical structure of the original drug to make it more effective or convenient for administration.
Prodrugs help overcome...
Pharmacogenomics: Identification of New Drug Targets01:29

Pharmacogenomics: Identification of New Drug Targets

Advances in genomics have profoundly influenced drug discovery by increasing both the speed and accuracy of pharmaceutical development. Pharmacogenomics, which examines how genetic variation influences drug response, facilitates the identification of novel therapeutic targets and enables patient stratification for personalized treatment. These strategies contribute to improved drug efficacy, minimized adverse effects, and more efficient clinical trial design.Mapping genetic differences...
Drug Delivery: Overview01:16

Drug Delivery: Overview

The selection of a drug's delivery route depends upon its physicochemical properties, including lipid or water solubility and ionization, as well as the therapeutic requirement, such as immediate or sustained effect. These routes can be divided into three primary categories: enteral, parenteral, and topical.
Enteral delivery involves administering drugs directly through swallowing, sublingual placement, or buccal application. Orally administered drugs predominantly navigate the gastrointestinal...

You might also read

Related Articles

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

Sort by
Same author

Interfacial engineering of montmorillonite clay in an electrospun PVdF-<i>co</i>-HFP nanocomposite separator for high-performance sodium ion batteries.

Nanoscale·2026
Same author

THE SALMONID ONCORHYNCHUS MYKISS AND BRYOZOAN FREDERICELLA BOREALIS SERVE AS ACTIVE HOSTS FOR THE NORTH AMERICAN STRAIN OF TETRACAPSULOIDES BRYOSALMONAE, THE CAUSE OF PROLIFERATIVE KIDNEY DISEASE.

The Journal of parasitology·2026
Same author

Advancing harmful algal bloom predictions using chlorophyll-a as an Indicator: Combining deep learning and EnKF data assimilation method.

Journal of environmental management·2025
Same author

Reirradiation with advanced brachytherapy techniques in recurrent GYN cancers.

Brachytherapy·2023
Same author

Venoms classification and therapeutic uses: a narrative review.

European review for medical and pharmacological sciences·2023
Same author

A comparative assessment of the community frontline health workers for their knowledge and practices of malaria diagnosis and treatment in three contiguous districts Mandla, Balaghat, and Dindori of Madhya Pradesh, India.

Malaria journal·2023
Same journal

Lipid nanoparticles for Cas9 ribonucleoprotein delivery: design and evaluation of ionisable oligoamine-lipidoids.

European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences·2026
Same journal

Synthesis and Biological Evaluation of Novel Carbazole Derivatives as Broad-Spectrum Antibacterial Agents to Fight Antimicrobial Resistance (AMR).

European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences·2026
Same journal

Rheological Modeling and Torque-Based Processability Prediction for Celecoxib/PVPVA Hot-Melt Extruded Amorphous Solid Dispersions.

European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences·2026
Same journal

Design, synthesis, and biological analysis of aurein 1.2 analogues incorporating fluorinated phenylalanine.

European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences·2026
Same journal

Corrigendum to "Early-stage pharmaceutical development of bilayer buccal films with a chitosan backing layer for local pain management in oral mucositis" [European Journal of Pharmaceutical Sciences 221 (2026) 107530].

European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences·2026
Same journal

Mirtazapine identified as a preventive agent against cisplatin-induced nephrotoxicity: Integrating in silico, in vitro, and in vivo analyses.

European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences·2026
See all related articles

Related Experiment Video

Updated: Jun 8, 2026

Drug Repurposing Hypothesis Generation Using the "RE:fine Drugs" System
05:10

Drug Repurposing Hypothesis Generation Using the "RE:fine Drugs" System

Published on: December 11, 2016

Codrug: an efficient approach for drug optimization.

N Das1, M Dhanawat, B Dash

  • 1Department of Pharmaceutics, Institute of Technology, Banaras Hindu University, Varanasi 221 005, Uttar Pradesh, India. nirupam.das.phe05@itbhu.ac.in

European Journal of Pharmaceutical Sciences : Official Journal of the European Federation for Pharmaceutical Sciences
|October 5, 2010
PubMed
Summary
This summary is machine-generated.

Codrugs, or mutual prodrugs, combine drugs to overcome limitations and improve therapeutic properties. This strategy enhances drug delivery and efficacy by leveraging synergistic actions or targeted delivery.

More Related Videos

High-throughput Identification of Synergistic Drug Combinations by the Overlap2 Method
07:51

High-throughput Identification of Synergistic Drug Combinations by the Overlap2 Method

Published on: May 21, 2018

Related Experiment Videos

Last Updated: Jun 8, 2026

Drug Repurposing Hypothesis Generation Using the "RE:fine Drugs" System
05:10

Drug Repurposing Hypothesis Generation Using the "RE:fine Drugs" System

Published on: December 11, 2016

High-throughput Identification of Synergistic Drug Combinations by the Overlap2 Method
07:51

High-throughput Identification of Synergistic Drug Combinations by the Overlap2 Method

Published on: May 21, 2018

Area of Science:

  • Pharmaceutical Sciences
  • Medicinal Chemistry
  • Drug Delivery Systems

Background:

  • Effective drugs often possess drawbacks like poor solubility or targeted delivery challenges.
  • Codrugs offer a strategy to modify existing therapeutics by linking them with other pharmacophores.
  • This approach aims to mitigate limitations and enhance the overall therapeutic profile of drugs.

Purpose of the Study:

  • To explore the concept and applications of codrugs (mutual prodrugs) in pharmaceutical research.
  • To highlight the benefits of combining pharmacophores for improved drug properties.
  • To discuss the role of codrugs in enhancing physicochemical, biopharmaceutical, and drug delivery characteristics.

Main Methods:

  • Literature review on codrug design and synthesis strategies.
  • Analysis of case studies demonstrating codrug efficacy.
  • Examination of the impact of codrugs on drug properties.

Main Results:

  • Codrugs can be formed by direct linkage or through a connecting moiety.
  • Combining pharmacophores can lead to synergistic pharmacological effects.
  • This approach significantly improves physicochemical and biopharmaceutical properties, facilitating targeted drug delivery.

Conclusions:

  • Codrug strategy is a valuable approach for overcoming drug limitations.
  • It enhances drug efficacy, targeting, and delivery properties.
  • Further research into codrugs holds promise for advanced therapeutic agents.