Liu Pingsheng, Skelly Jordan D, Song Jie
Department of Orthopedics & Physical Rehabilitation, Department of Cell & Developmental Biology, University of Massachusetts Medical School, Worcester, MA 01655, USA.
Department of Orthopedics & Physical Rehabilitation, Department of Cell & Developmental Biology, University of Massachusetts Medical School, Worcester, MA 01655, USA.
Acta Biomater. 2014 Oct;10(10):4296-303. doi: 10.1016/j.actbio.2014.06.024. Epub 2014 Jun 20.
Zwitterions are well known for their anti-biofouling properties. Past investigations of zwitterionic materials for biomedical uses have been centered on exploiting their ability to inhibit non-specific adsorption of proteins. Here, we report that zwitterionic motifs, when presented in three dimensions (e.g. in crosslinked hydrogels), could effectively sequester osteogenic bone morphogenetic protein-2 (rhBMP-2). The ionic interactions between rhBMP-2 and the 3-D zwitterionic network enabled dynamic sequestering and sustained release of the protein with preserved bioactivity. We further demonstrated that the zwitterionic hydrogel confers high-efficiency in vivo local delivery of rhBMP-2. It can template the functional healing of critical-size femoral segmental defects in rats with rhBMP-2 at a loading dose substantially lower than those required for current natural or synthetic polymeric carriers. These findings reveal a novel function of zwitterionic materials beyond their commonly perceived anti-biofouling property, and may establish 3-D zwitterionic matrices as novel high-efficiency vehicles for protein/ionic drug therapeutic delivery.
两性离子因其抗生物污损特性而广为人知。过去对用于生物医学用途的两性离子材料的研究主要集中在利用其抑制蛋白质非特异性吸附的能力上。在此,我们报告,当以三维形式呈现(例如在交联水凝胶中)时,两性离子基序可以有效地螯合成骨骨形态发生蛋白-2(rhBMP-2)。rhBMP-2与三维两性离子网络之间的离子相互作用能够实现该蛋白的动态螯合和持续释放,并保留其生物活性。我们进一步证明,两性离子水凝胶能够高效地在体内局部递送rhBMP-2。它可以在比当前天然或合成聚合物载体所需剂量低得多的负载剂量下,引导rhBMP-2对大鼠临界尺寸股骨节段性缺损进行功能性愈合。这些发现揭示了两性离子材料超出其通常被认为的抗生物污损特性的一种新功能,并可能将三维两性离子基质确立为用于蛋白质/离子药物治疗递送的新型高效载体。