Design of a Long‐Acting Morphine Prodrug for Safe Opioid Delivery

Effective opioid management in neonatal abstinence syndrome (NAS) and opioid use disorder (OUD) requires maintaining low, stable plasma opioid levels to prevent withdrawal without central side effects. Current treatments rely on frequent opioid dosing, such as oral morphine every few hours for up to 3 weeks in NAS, leading to plasma level fluctuations and increased risk of toxicity or withdrawal. Herein, the design and characterization of AG10-L-E2-morphine, a prodrug that forms a zwitterionic subcutaneous depot for sustained morphine release is reported. In rats, a single subcutaneous dose of AG10-L-E2-morphine maintained plasma morphine levels for over 72 h without inducing respiratory depression, even at high doses. The prodrug is stable in human plasma and specifically activated by liver carboxylesterase enzyme 2 (CES2), supporting its safety and translational potential. This long-acting system could improve NAS care by enabling convenient dosing and early integration of nonpharmacologic strategies, ultimately reducing hospital stays and healthcare burden.

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Publication Details

Journal
ChemMedChem
Published
2025-08-18
DOI
https://doi.org/10.1002/cmdc.202500499
Primary Topic
Opioid Use Disorder Treatment
Type
article
Field-Weighted Citation Impact
0.00

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article

Design of a Long‐Acting Morphine Prodrug for Safe Opioid Delivery

Miki Park, Hala Aldawod, Mamoun M. Alhamadsheh, Roshanak Rahimian et al.
ChemMedChem
Opioid Use Disorder Treatment
article

Design of a Long‐Acting Morphine Prodrug for Safe Opioid Delivery

Miki Park, Hala Aldawod, Mamoun M. Alhamadsheh, Roshanak Rahimian, Hana S. Alhamadsheh
article en

Abstract

Effective opioid management in neonatal abstinence syndrome (NAS) and opioid use disorder (OUD) requires maintaining low, stable plasma opioid levels to prevent withdrawal without central side effects. Current treatments rely on frequent opioid dosing, such as oral morphine every few hours for up to 3 weeks in NAS, leading to plasma level fluctuations and increased risk of toxicity or withdrawal. Herein, the design and characterization of AG10-L-E2-morphine, a prodrug that forms a zwitterionic subcutaneous depot for sustained morphine release is reported. In rats, a single subcutaneous dose of AG10-L-E2-morphine maintained plasma morphine levels for over 72 h without inducing respiratory depression, even at high doses. The prodrug is stable in human plasma and specifically activated by liver carboxylesterase enzyme 2 (CES2), supporting its safety and translational potential. This long-acting system could improve NAS care by enabling convenient dosing and early integration of nonpharmacologic strategies, ultimately reducing hospital stays and healthcare burden.

ChemMedChemVol. 20(17)
University of the Pacific (US)
National Science Foundation, University of the Pacific
Openalex Percentile: Top 71%
Opioid Use Disorder Treatment
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