Abstract
In this work, we investigated for the first time the conjugation of gluconolactone to a poly(ethylene oxide)-poly(propylene oxide) block copolymer by a microwave-assisted ring opening reaction. The glucosylated copolymer was obtained with high yield (90%). A conjugation extent of approximately 100% was achieved within 15 min. The modification reduced the critical micellar concentration and increased the size of the micelles. The agglutination of the modified polymeric micelles by a soluble lectin that binds glucose confirmed the recognizability of the modified nanocarrier. Finally, the solubilization of darunavir, an anti-HIV protease inhibitor, showed a sharp increase of the aqueous solubility from 91 microgram/mL to 14.2 and 18.9 mg/mL for 10% w/v pristine and glucosylated polymeric micelles, respectively.
| Original language | English |
|---|---|
| Pages (from-to) | 1639-1651 |
| Number of pages | 13 |
| Journal | Macromolecular Bioscience |
| Volume | 14 |
| Issue number | 11 |
| DOIs | |
| State | Published - 1 Nov 2014 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Glucosylated poly(ethylene oxide)-b-poly(propylene oxide) block copolymers
- darunavir free base
- gluconolactone
- microwave-assisted ring opening conjugation
- polymeric micelles
All Science Journal Classification (ASJC) codes
- Biotechnology
- Bioengineering
- Biomaterials
- Polymers and Plastics
- Materials Chemistry
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