| Literature DB >> 19951730 |
Tai Hirakura1, Kenji Yasugi, Takayuki Nemoto, Mika Sato, Tsuyoshi Shimoboji, Yoshinori Aso, Nobuyuki Morimoto, Kazunari Akiyoshi.
Abstract
Novel hybrid hyaluronan (HA) hydrogel encapsulating nanogels was designed for sustained delivery of protein. HA modified with 2-aminoethyl methacrylate was cross-linked via Michael addition in the presence of cholesteryl group-bearing pullulan (CHP) nanogels. The nanogels were physically entrapped and well dispersed in a three-dimensional network of chemically cross-linked HA (HA gel). Therapeutic peptides and proteins, such as glucagon-like peptide-1, insulin and erythropoietin, were spontaneously trapped in the CHP nanogels in the HA gel just by immersing hybrid hydrogels into the drug solutions. CHP/protein complex nanogels were released from the hybrid hydrogels in a sustained manner both in vitro and in vivo. The release was controlled by the cross-linking density and the degradability of the HA gel, modulated by the initial gelation condition. The synergy between the CHP nanogel as a drug reservoir and the HA gel as a nanogel-releasing matrix of the hybrid hydrogel system simultaneously achieved both simple drug loading and controlled release with no denaturation of the protein drugs. This is a new method of fabricating biodegradable controlled release matrix with molecular chaperone-like activity for therapeutic proteins. (c) 2009 Elsevier B.V. All rights reserved.Entities:
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Year: 2009 PMID: 19951730 DOI: 10.1016/j.jconrel.2009.11.023
Source DB: PubMed Journal: J Control Release ISSN: 0168-3659 Impact factor: 9.776