3.29 : Pró-fármacos

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 limitations associated with the parent drug, such as poor solubility, limited permeability, or unfavorable pharmacokinetic properties. By chemically modifying the drug molecule to a prodrug, its absorption, distribution, metabolism, and elimination (ADME) characteristics can be enhanced, leading to improved therapeutic outcomes.

The activation of prodrugs typically occurs through various mechanisms, including enzymatic hydrolysis, oxidation, or reduction, which are inherent biological processes occurring mainly in the liver. In addition, some prodrugs are metabolized at the site of action, while others are transformed extracellularly in blood or gastrointestinal fluids.

Prodrugs offer several advantages in drug development. They can extend the life of a drug and can also enhance patient compliance by offering alternative routes of administration or reducing the frequency of dosing. They have been employed to target specific tissues or cells by utilizing site-specific enzymes or transporters, minimizing off-target effects. As a result, prodrugs offer improved drug efficacy, better safety, and patient convenience.