Department of NanoEngineering, Chemical Engineering Program, and Moores Cancer Center, University of California San Diego, La Jolla, California 92093, United States.
Department of Pediatric Research, MD Anderson Cancer Center, Houston, Texas 77030, United States.
Nano Lett. 2020 May 13;20(5):4051-4058. doi: 10.1021/acs.nanolett.0c01654. Epub 2020 May 4.
Therapeutic enzymes used for genetic disorders or metabolic diseases oftentimes suffer from suboptimal pharmacokinetics and stability. Nanodelivery systems have shown considerable promise for improving the performance of enzyme therapies. Here, we develop a cell membrane-camouflaged metal-organic framework (MOF) system with enhanced biocompatibility and functionality. The MOF core can efficiently encapsulate enzymes while maintaining their bioactivity. After the introduction of natural cell membrane coatings, the resulting nanoformulations can be safely administered . The surface receptors on the membrane can also provide additional functionalities that synergize with the encapsulated enzyme to target disease pathology from multiple dimensions. Employing uricase as a model enzyme, we demonstrate the utility of this approach in multiple animal disease models. The results support the use of cell membrane-coated MOFs for enzyme delivery, and this strategy could be leveraged to improve the usefulness of enzyme-based therapies for managing a wide range of important human health conditions.
治疗遗传疾病或代谢疾病的酶制剂通常存在药代动力学和稳定性不理想的问题。纳米递药系统在改善酶治疗效果方面显示出巨大的潜力。在这里,我们开发了一种具有增强的生物相容性和功能性的细胞膜伪装金属有机骨架(MOF)系统。MOF 核可以有效地包封酶,同时保持其生物活性。在引入天然细胞膜涂层后,所得的纳米制剂可以安全地给药。膜上的表面受体还可以提供额外的功能,与包封的酶协同作用,从多个维度靶向疾病病理。我们以尿酸酶作为模型酶,在多种动物疾病模型中证明了这种方法的实用性。结果支持使用细胞膜包被的 MOF 进行酶传递,并且可以利用这种策略来提高基于酶的治疗方法在治疗广泛的重要人类健康状况方面的有效性。