| Literature DB >> 24374002 |
Huining He1,2, Junxiao Ye3, Yinsong Wang1, Quan Liu3, Hee Sun Chung4, Young Min Kwon5, Meong Cheol Shin4, Kyuri Lee4, Victor C Yang1,4,6.
Abstract
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.Entities:
Keywords: Acute lymphoblastic leukemia; Cell penetrating peptide; Encapsulation; Erythrocytes; Red blood cells
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Year: 2013 PMID: 24374002 PMCID: PMC3939723 DOI: 10.1016/j.jconrel.2013.12.019
Source DB: PubMed Journal: J Control Release ISSN: 0168-3659 Impact factor: 9.776