There is more than one way to assemble the two halves of a tethered, urea-substituted calix[4]arene dimer (shown schematically): formation of unimolecular capsules (far left), dimers, or oligomers. By combination of NMR spectroscopy and electrospray mass spectrometry, a hexamethylene spacer was show
Unimolecular micelles: Synthesis and characterization of amphiphilic polymer systems
โ Scribed by Hongbo Liu; Anna Jiang; Jian Guo; Kathryn E. Uhrich
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 153 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0887-624X
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โฆ Synopsis
Unimolecular micelles were successfully synthesized from mucic acid, fatty acids, and poly(ethylene glycols) to create biocompatible polymers. These polymers consist of a core-shell structure that resembles conventional micellar structures but with significant thermodynamic stability in aqueous media. The core of the polymers provide a hydrophobic environment for drug encapsulation via hydrophobic interactions, whereas the shell provides excellent water solubility. The polymers were characterized by nuclear magnetic resonance, infrared and mass spectroscopies, as well as gel permeation chromatography, differential scanning calorimetry, and thermogravimetric and elemental analyses. Encapsulation ability was measured using high-pressure liquid chromatography to monitor lidocaine, a hydrophobic molecule. Encapsulation capabilities increased as lipophilicity of the core increased. To verify that encapsulation was caused by individual unimolecular micelles, surface tension and dynamic light scattering measurements were performed. The results indicated that these unimolecular micelles have great potential as drug carriers.
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