Targeted delivery of mPGES-1 inhibitors to macrophages via the folate receptor-β for inflammatory pain.

ABSTRACT: Activated macrophages overexpress the folate receptor β (FR-β) that can be used for targeted delivery of drugs conjugated to folic acid. FR-expressing macrophages contribute to arthritis progression by secreting prostaglandin E₂ (PGE₂). Non-steroidal anti-inflammatory drugs (NSAIDs) block PGs and thromboxane by inhibiting the cyclooxygenase (COX) enzymes and are used for chronic pain and inflammation despite their well-known toxicity. New NSAIDs target an enzyme downstream of COXs, microsomal prostaglandin E synthase-1 (mPGES-1). Inhibition of mPGES-1 in inflammatory macrophages promises to retain NSAID efficacy while limiting toxicity. We conjugated a potent mPGES-1 inhibitor, MK-7285, to folate, but the construct released the drug inefficiently. Folate conjugation t

SUBMITTER: Mazaleuskaya LL 

PROVIDER: S-EPMC8484072 | biostudies-literature | 2021 Oct

REPOSITORIES: biostudies-literature