Tianjin Key Laboratory on Technologies Enabling Development of Clinical Therapeutics and Diagnostics (Theranostics), School of Pharmacy, Tianjin Medical University, Tianjin, 300072, P.R. China.
Key Laboratory of Smart Drug Delivery, Ministry of Education (Fudan University), Shanghai, 201203, China.
J Control Release. 2014 Feb 28;176:123-132. doi: 10.1016/j.jconrel.2013.12.019. Epub 2013 Dec 27.
Red blood cells (RBCs) based drug carrier appears to be the most appealing for protein drugs due to their unmatched biocompatability, biodegradability, and long lifespan in the circulation. Numerous methods for encapsulating protein drugs into RBCs were developed, however, most of them induce partial disruption of the cell membrane, resulting in irreversible alterations in both physical and chemical properties of RBCs. Herein, we introduce a novel method for encapsulating proteins into intact RBCs, which was meditated by a cell penetrating peptide (CPP) developed in our lab-low molecular weight protamine (LMWP). l-asparaginase, one of the primary drugs used in treatment of acute lymphoblastic leukemia (ALL), was chosen as a model protein to illustrate the encapsulation into erythrocytes mediated by CPPs. In addition current treatment of ALL using different l-asparaginase delivery and encapsulation methods as well as their associated problems were also reviewed.
基于红细胞(RBC)的药物载体似乎是蛋白质药物最具吸引力的载体,因为它们具有无与伦比的生物相容性、可生物降解性和在循环中的长寿命。已经开发出许多将蛋白质药物封装到 RBC 中的方法,然而,大多数方法都会导致细胞膜部分破坏,从而导致 RBC 的物理和化学性质发生不可逆的改变。在此,我们介绍了一种将蛋白质封装到完整 RBC 中的新方法,该方法是由我们实验室开发的细胞穿透肽(CPP)介导的-低分子量鱼精蛋白(LMWP)。天冬酰胺酶,是治疗急性淋巴细胞白血病(ALL)的主要药物之一,被选为模型蛋白,以说明 CPP 介导的将蛋白质封装到红细胞中。此外,还综述了目前使用不同的天冬酰胺酶递送和封装方法治疗 ALL 以及它们相关的问题。