McCarthy Donald A, Nazem Ahmad A, McNeilan James, Shakerley Nicole L, Clark Ryan R, Idelchik María D, Yigit Mehmet, Melendez J Andrés
1 SUNY Polytechnic Institute, Colleges of Nanoscale Science and Engineering, Albany, NY 12203, USA.
2 University at Albany, Albany, NY 12222, USA.
Exp Biol Med (Maywood). 2016 Dec;241(18):2023-2032. doi: 10.1177/1535370216662534. Epub 2016 Jul 29.
The wide array of proteases, including matrix metalloproteinases, produced in response to many pathogenic insults, confers a unique proteolytic signature which is often disease specific and provides a potential therapeutic target for drug delivery. Here we propose the use of collagen-based nanoenhanced matrix metalloproteinase-responsive delivery vehicles that display matrix metalloproteinase-specific degradation in diverse in vitro models of proteolysis. We demonstrate that collagen particles comprised of protease substrates (primarily collagen) can be made of uniform size and loaded efficiently with assorted cargo including fluorescently labeled mesoporous silica, magnetic nanoparticles, proteins and antioxidants. We also demonstrate that pathologic concentrations of proteases produced in situ or in vitro display protease-specific cargo release. Additionally, we show that the collagen-based particles display bright fluorescence when loaded with a fluorophore, and have the potential to be used as vehicles for targeted delivery of drugs or imaging agents to regions of high proteolytic activity.
多种蛋白酶,包括基质金属蛋白酶,在应对许多致病损伤时产生,赋予了一种独特的蛋白水解特征,这种特征通常具有疾病特异性,并为药物递送提供了潜在的治疗靶点。在此,我们提出使用基于胶原蛋白的纳米增强型基质金属蛋白酶响应性递送载体,其在多种体外蛋白水解模型中表现出基质金属蛋白酶特异性降解。我们证明,由蛋白酶底物(主要是胶原蛋白)组成的胶原蛋白颗粒可以制成均匀大小,并能有效地负载各种货物,包括荧光标记的介孔二氧化硅、磁性纳米颗粒、蛋白质和抗氧化剂。我们还证明,原位或体外产生的病理浓度的蛋白酶表现出蛋白酶特异性的货物释放。此外,我们表明,基于胶原蛋白的颗粒在负载荧光团时会发出明亮的荧光,并且有潜力用作将药物或成像剂靶向递送至蛋白水解活性高的区域的载体。