## Abstract This study aims to investigate the rheological properties of self‐assembling gels containing cyclodextrins with potential application as injectable matrix for the sustained delivery of poorly soluble drugs. The ability of these gels to entrap two hydrophobic molecules, benzophenone (BZ)
Self-Assembled Nanogel of Hydrophobized Dendritic Dextrin for Protein Delivery
✍ Scribed by Yayoi Ozawa; Shin-ichi Sawada; Nobuyuki Morimoto; Kazunari Akiyoshi
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 498 KB
- Volume
- 9
- Category
- Article
- ISSN
- 1616-5187
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✦ Synopsis
Abstract
Highly branched cyclic dextrin derivatives (CH‐CDex) that are partly substituted with cholesterol groups have been synthesized. The CH‐CDex forms monodisperse and stable nanogels with a hydrodynamic radii of ≈10 nm by the self‐assembly of 4–6 CH‐CDex macromolecules in water. The CH‐CDex nanogels spontaneously trap 10–16 molecules of fluorescein isothiocyanate‐labeled insulin (FITC‐Ins). The complex shows high colloidal stability: no dissociation of trapped insulin is observed after at least 1 month in phosphate buffer (0.1 M, pH 8.0). In the presence of bovine serum albumin (BSA, 50 mg · mL^−1^), which is a model blood system, the FITC‐Ins trapped in the nanogels is continuously released (≈20% at 12 h) without burst release. The high‐density nanogel structure derived from the highly branched CDex significantly affects the stability of the nanogel–protein complex.
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