Institute of Biomaterial and Bioengineering, Tokyo Medical and Dental University, Chiyoda-ku, Tokyo, 101-0062, Japan.
J Control Release. 2010 Mar 19;142(3):483-9. doi: 10.1016/j.jconrel.2009.11.023. Epub 2009 Nov 29.
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.
新型杂化透明质酸 (HA) 水凝胶包埋纳米凝胶被设计用于蛋白质的持续递送。通过迈克尔加成反应,将带有 2-氨基乙基甲基丙烯酸酯的 HA 进行交联,同时存在带有胆固醇基团的普鲁兰 (CHP) 纳米凝胶。纳米凝胶在化学交联的 HA(HA 凝胶)的三维网络中被物理包埋并良好分散。治疗性肽和蛋白质,如胰高血糖素样肽-1、胰岛素和促红细胞生成素,只需将杂化水凝胶浸入药物溶液中,就可自发地被捕获在 HA 凝胶中的 CHP 纳米凝胶中。CHP/蛋白质复合纳米凝胶在体外和体内均以持续方式从杂化水凝胶中释放。释放受 HA 凝胶的交联密度和降解性控制,可通过初始凝胶形成条件进行调节。CHP 纳米凝胶作为药物储库和 HA 凝胶作为杂化水凝胶系统的纳米凝胶释放基质之间的协同作用,同时实现了蛋白质药物的简单药物加载和控制释放,而不会导致蛋白质药物变性。这是一种用于治疗性蛋白质的具有分子伴侣样活性的可生物降解控制释放基质的新方法。