Qi Hongzhao, Yang Lijun, Shan Peipei, Zhu Sujie, Ding Han, Xue Sheng, Wang Yin, Yuan Xubo, Li Peifeng
Institute for Translational Medicine, Qingdao University, Qingdao 266021, China.
College of Materials Science and Engineering, Qingdao University of Science and Technology, Qingdao 266042, China.
Pharmaceutics. 2020 Feb 1;12(2):115. doi: 10.3390/pharmaceutics12020115.
Protein drugs are often loaded on scaffolds with organic coatings to realize a spatiotemporal controlled release. The stability or activity of protein drugs, however, is largely affected by the organic coating, particularly with organic solvents, which can dramatically reduce their delivery efficiency and limit their application scope. In spite of this, little attention has been paid to maintaining the stability of protein drugs in organic coatings, to date. Here, we used catalase as a model protein drug to exploit a kind of chemically cross-linked nanogel that can efficiently encapsulate protein drugs. The polymeric shells of nanogels can maintain the surface hydration shell to endow them with a protein protection ability against organic solvents. Furthermore, the protection efficiency of nanogels is higher when the polymeric shell is more hydrophilic. In addition, nanogels can be dispersed in polylactic acid (PLA) solution and subsequently coated on scaffolds to load catalase with high activity. To the best of our knowledge, this is the first use of hydrophilic nanogels as a protection niche to load protein drugs on scaffolds through an organic coating, potentially inspiring researchers to exploit new methods for protein drug loading.
蛋白质药物通常负载于带有有机涂层的支架上,以实现时空控制释放。然而,蛋白质药物的稳定性或活性在很大程度上受到有机涂层的影响,尤其是有机溶剂,这会显著降低其递送效率并限制其应用范围。尽管如此,迄今为止,很少有人关注在有机涂层中维持蛋白质药物的稳定性。在此,我们以过氧化氢酶作为模型蛋白质药物,开发了一种能够有效包封蛋白质药物的化学交联纳米凝胶。纳米凝胶的聚合物壳层可以维持表面水化层,赋予它们对有机溶剂的蛋白质保护能力。此外,当聚合物壳层更具亲水性时,纳米凝胶的保护效率更高。此外,纳米凝胶可以分散在聚乳酸(PLA)溶液中,随后涂覆在支架上,以高活性负载过氧化氢酶。据我们所知,这是首次使用亲水性纳米凝胶作为保护微环境,通过有机涂层将蛋白质药物负载到支架上,这可能会激发研究人员开发蛋白质药物负载的新方法。