Effect of shear stress on structure and function of polyplex micelles from poly(ethylene glycol)-poly(l-lysine) block copolymers as systemic gene delivery carrier. (May 2017)

• Record Type: Journal Article
• Authors: Takeda, Kaori M.; Yamasaki, Yuichi; Dirisala, Anjaneyulu; Ikeda, Sorato; Tockary, Theofilus A.; Toh, Kazuko; Osada, Kensuke; Kataoka, Kazunori
• Is Part Of: Biomaterials. Volume 126(2017)
• Page Start: 31
• Page End: 38
• Publication Date: 2017-05
• Subjects: Polyplex micelle -- Poly(ethylene glycol) -- Shear stress -- Systemic administration -- Nonviral gene delivery; Biomedical materials -- Periodicals; Biocompatible Materials -- Periodicals; Biomatériaux -- Périodiques; 610.28
• DOI: 10.1016/j.biomaterials.2017.02.012
• Languages: English
• ISSNs: 0142-9612

Abstract

Abstract: Structural stability of polyplex micelles (PMs), prepared from plasmid DNA (pDNA) and poly(ethylene glycol)- b -poly(l -lysine) block catiomer (PEG−PLys), was evaluated in terms of their resistance against shear stress. When exposed to shear stress at magnitudes typically present in the blood stream, structural deterioration was observed in PMs owing to the partial removal of PEG−PLys strands. Eventually, impaired PEG coverage of the polyplex core led to accelerated degradation by nucleases, implying that structural deterioration by shear stress in blood stream may be a major cause of rapid clearance of PMs from blood circulation. To address this issue, introduction of disulfide crosslinking into the PM core was shown to be an efficient strategy, which successfully mitigated unfavorable effects of shear stress. Furthermore, improved in vivo blood retention profile and subsequently enhanced antitumor efficacy in systemic treatment of pancreatic adenocarcinoma were confirmed for the crosslinked PMs loaded with pDNA encoding an anti-angiogenic protein, suggesting that high stability under the shear stress during blood circulation may be a critical factor in systemically applicable gene delivery systems.