Chemical Conjugation of Evans Blue Derivative: A Strategy to Develop Long-Acting Therapeutics through Albumin Binding.
Theranostics · 2016
Last updated 2026-05-28Researchers developed a new version of the diabetes drug Exendin-4, called Abextide, by attaching a molecule that binds to albumin, a protein in the blood. This change made Abextide last longer in the body and improved its ability to control blood sugar compared to the original drug. The approach could potentially be used to create longer-lasting versions of other medications.
AI summary of the abstract below.
| Journal | Theranostics, 2016 |
|---|---|
| Citations | 63 |
| Relative citation ratio | 2.53 |
| NIH percentile | 80 |
| Molecules | — |
Abstract
The efficacy of therapeutic drugs is highly dependent on their optimal in vivo pharmacokinetics. Albumin conjugation is considered to be one of the most effective means of protracting the short lifespan of peptides and proteins. In this study, we proposed a novel platform for developing long lasting therapeutics by conjugating a small molecular albumin binding moiety, truncated Evans blue, to either peptides or proteins. Using the anti-diabetic peptide drug Exendin-4 as a model peptide, we synthesized a new long-acting Exendin-4 derivative (denoted as Abextide). Through complexation with albumin in situ, the biological half-life of Abextide was significantly extended. The hypoglycemic effect of Abextide was also improved remarkably over Exendin-4. Thus, Abextide has considerable potential to treat type 2 diabetes. This strategy as a general technology platform can be applied to other small molecules and biologics for the development of long-acting therapeutic drugs.
Verbatim abstract via PubMed 26877782 ↗