Prodrug

Source: Wikipedia, the free encyclopedia.

A prodrug is a pharmacologically inactive

pharmacologically active drug.[1][2] Instead of administering a drug directly, a corresponding prodrug can be used to improve how the drug is absorbed, distributed, metabolized, and excreted (ADME).[3][4]

Prodrugs are often designed to improve bioavailability when a drug itself is poorly absorbed from the gastrointestinal tract.[2] A prodrug may be used to improve how selectively the drug interacts with cells or processes that are not its intended target. This reduces adverse or unintended effects of a drug, especially important in treatments like chemotherapy, which can have severe unintended and undesirable side effects.

IUPAC definition

Compound that undergoes biotransformation before exhibiting pharmacological effects.

Note 1: Modified from ref.[5]

Note 2: Prodrugs can thus be viewed as drugs containing specialized nontoxic protective groups used in a transient manner to alter or to eliminate undesirable properties in the parent molecule.[6]

History

Many herbal extracts historically used in medicine contain

glucuronides) that are more active than the parent compound.[2]

The first synthetic antimicrobial drug,

sulfa drug (discovered by Gerhard Domagk in 1932), must be cleaved in the body to release the active molecule, sulfanilamide
. Since that time, many other examples have been identified.

Terfenadine, the first non-sedating antihistamine, had to be withdrawn from the market because of the small risk of a serious side effect. However, terfenadine was discovered to be the prodrug of the active molecule, fexofenadine, which does not carry the same risks as the parent compound. Therefore, fexofenadine could be placed on the market as a safe replacement for the original drug.

Loratadine, another non-sedating antihistamine, is the prodrug of desloratadine, which is largely responsible for the antihistaminergic effects of the parent compound. However, in this case the parent compound does not have the side effects associated with terfenadine, and so both loratadine and its active metabolite, desloratadine, are currently marketed.[9]

Recent prodrugs

Approximately 10% of all marketed drugs worldwide can be considered prodrugs. Since 2008, at least 30 prodrugs have been approved by the

tedizolid phosphate (2014), isavuconazonium (2015), aripiprazole lauroxil (2015), selexipag (2015), latanoprostene bunod (2017), benzhydrocodone (2018), tozinameran (2020) and serdexmethylphenidate
(2021).

Classification

Prodrugs can be classified into two major types,[10] based on how the body converts the prodrug into the final active drug form:

  • Type I prodrugs are bioactivated inside the cells (intracellularly). Examples of these are anti-viral nucleoside analogs that must be phosphorylated and the lipid-lowering statins.
  • Type II prodrugs are bioactivated outside cells (extracellularly), especially in digestive fluids or in the body's circulatory system, particularly in the blood. Examples of Type II prodrugs are salicin (described above) and certain antibody-, gene- or virus-directed enzyme prodrugs used in chemotherapy or immunotherapy.

Both major types can be further categorized into subtypes, based on factors such as (Type I) whether the intracellular bioactivation location is also the site of therapeutic action, or (Type 2) whether or not bioactivation occurs in the gastrointestinal fluids or in the circulation system.

Classification of prodrugs[10][11]
Type Bioactivation site Subtype Tissue location of bioactivation Examples
Type I Intracellular Type IA Therapeutic target tissues/cells
mitomycin, zidovudine
Type IB Metabolic tissues (liver, GI mucosal cell, lung etc.) Carbamazepine, captopril, carisoprodol, heroin, molsidomine, leflunomide, paliperidone, phenacetin, primidone, psilocybin, sulindac, fursultiamine
Type II Extracellular Type IIA GI fluids Loperamide oxide,
oxyphenisatin, sulfasalazine
Type IIB Systemic circulation and other extracellular fluid compartments
dipivefrin, fosphenytoin, lisdexamfetamine, pralidoxime
Type IIC Therapeutic target tissues/cells
VDEPTs

Subtypes

Type IA prodrugs include many antimicrobial and chemotherapy agents (e.g., 5-flurouracil). Type IB agents rely on metabolic enzymes, especially in hepatic cells, to bioactivate the prodrugs intracellularly to active drugs. Type II prodrugs are bioactivated extracellularly, either in the milieu of GI fluids (Type IIA), within the systemic circulation and/or other extracellular fluid compartments (Type IIB), or near therapeutic target tissues/cells (Type IIC), relying on common enzymes such as esterases and phosphatases or target directed enzymes. Importantly, prodrugs can belong to multiple subtypes (i.e., Mixed-Type). A Mixed-Type prodrug is one that is bioactivated at multiple sites, either in parallel or sequential steps. For example, a prodrug, which is bioactivated concurrently in both target cells and metabolic tissues, could be designated as a "Type IA/IB" prodrug (e.g., HMG Co-A reductase inhibitors and some chemotherapy agents; note the symbol " / " applied here). When a prodrug is bioactivated sequentially, for example initially in GI fluids then systemically within the target cells, it is designated as a "Type IIA-IA" prodrug (e.g.,

GDEPTs) and proposed nanoparticle- or nanocarrier-linked drugs can understandably be Sequential Mixed-Type prodrugs. To differentiate these two Subtypes, the symbol dash " - " is used to designate and to indicate sequential steps of bioactivation, and is meant to distinguish from the symbol slash " / " used for the Parallel Mixed-Type prodrugs.[11][12]

See also

References

  1. ^
    S2CID 19489166
    .
  2. ^
    ISBN 978-0080919225
    .
  3. PMID 19835561
    .
  4. S2CID 195692168
    .
  5. doi:10.1351/pac199870051129
    .
  6. S2CID 98107080. Archived from the original
    (PDF) on 2015-03-19. Retrieved 2013-07-29.
  7. PMID 11124191
    .
  8. ISBN 978-3527321094
    .
  9. ^ UK Medicines Information Pharmacists Group. New Medicines on the Market: Desloratadine. Archived 2007-10-11 at the Wayback Machine June 2001.
  10. ^
    PMID 27713225
    .
  11. ^
    PMID 17507137
    .; Table 1
  12. PMID 27713225
    .; Table 1

External links
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