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Preparation and evaluation of lactic acid acylated exenatide and its long-acting preparation.

Pharm Dev Technol · 2019

Last updated 2026-05-28

In a study, researchers modified the diabetes drug exenatide by adding lactic acid to create lactic acid acylated exenatide (LA-EX). The modified drug lasted 5.95 hours in the body—2.3 times longer than the original exenatide—and worked as well as the original in lowering blood sugar in mice. When LA-EX was placed into microspheres for slow release, it maintained steadier drug levels and lowered blood sugar more effectively than the original exenatide microspheres.

AI summary of the abstract below.

JournalPharm Dev Technol, 2019
Citations4
Relative citation ratio0.30
NIH percentile19
Molecules exenatide
Conditions studied Type 2 Diabetes

Abstract

Exenatide (EX), a glucagon-like peptide-1 receptor agonist, is used to treat diabetes mellitus. However, its short half-life necessitates frequent administration and fluctuations in its plasma concentration may cause adverse effects. Previously, we developed glycolic acid acylated EX, which showed a good glucose-lowering effect. However, the release of lactic acid (LA) acylated exenatide (LA-EX) as an acylated adduct in EX microspheres has not been studied. Here, we investigated the biological properties of LA-EX. Additionally, LA-EX-loaded microspheres were formulated by an emulsion-solvent evaporation method and their characteristics, pharmacokinetic properties, and antidiabetic activities were evaluated. Pharmacokinetic studies revealed that the of LA-EX (5.95 h) was 2.3-fold longer than that of EX. The antidiabetic activities of LA-EX in / mice were similar to those of EX. LA-EX release from microspheres was fairly well-sustained compared to that of EX microspheres. Additionally, LA-EX-loaded microspheres were more effective in lowering nonfasting blood glucose concentrations than EX microspheres. These findings suggest that LA-EX have the same efficacy as EX and that encapsulating LA-EX into microspheres can achieve better efficacy for the long-term type 2 diabetes mellitus treatment.

Verbatim abstract via PubMed 31368418 ↗

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