Prodrug approaches for the development of a long-acting drug delivery systems

[Display omitted] •Long-acting prodrugs can improve the compatibility of physicochemically diverse active pharmaceutical ingredients for a variety of drug delivery strategies.•Extended duration of action for long-acting prodrug systems depends on both prodrug release and conversion rates to the acti...

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Veröffentlicht in:Advanced drug delivery reviews 2023-07, Vol.198, p.114860-114860, Article 114860
Hauptverfasser: Chien, Shin-Tian, Suydam, Ian T., Woodrow, Kim A.
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Sprache:eng
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Zusammenfassung:[Display omitted] •Long-acting prodrugs can improve the compatibility of physicochemically diverse active pharmaceutical ingredients for a variety of drug delivery strategies.•Extended duration of action for long-acting prodrug systems depends on both prodrug release and conversion rates to the active metabolite.•Release of active metabolite from macromolecular prodrugs depends primarily on the rate of linker cleavage. Long-acting formulations are designed to reduce dosing frequency and simplify dosing schedules by providing an extended duration of action. One approach to obtain long-acting formulations is to combine long-acting prodrugs (LA-prodrug) with existing or emerging drug delivery technologies (DDS). The design criteria for long-acting prodrugs are distinct from conventional prodrug strategies that alter absorption, distribution, metabolism, and excretion (ADME) parameters. Our review focuses on long-acting prodrug delivery systems (LA-prodrug DDS), which is a subcategory of long-acting formulations where prodrug design enables DDS formulation to achieve an extended duration of action that is greater than the parent drug. Here, we define LA-prodrugs as the conjugation of an active pharmaceutical ingredient (API) to a promoiety group via a cleavable covalent linker, where both the promoiety and linker are selected to enable formulation and administration from a drug delivery system (DDS) to achieve an extended duration of action. These LA-prodrug DDS results in an extended interval where the API is within a therapeutic range without necessarily altering ADME as is typical of conventional prodrugs. The conversion of the LA-prodrug to the API is dependent on linker cleavage, which can occur before or after release from the DDS. The requirement for linker cleavage provides an additional tool to prolong release from these LA-prodrug DDS. In addition, the physicochemical properties of drugs can be tuned by promoiety selection for a particular DDS. Conjugation with promoieties that are carriers or amenable to assembly into carriers can also provide access to formulations designed for extending duration of action. LA-prodrugs have been applied to a wide variety of drug delivery strategies and are categorized in this review by promoiety size and complexity. Small molecule promoieties (typically MW 
ISSN:0169-409X
1872-8294
1872-8294
DOI:10.1016/j.addr.2023.114860