Protein delivery nanosystem of six-arm copolymer poly for long-term sustained release

Background: To address the issue of delivery of proteins, a six-arm copolymer, six-arm poly ([epsilon]-caprolactone)-poly(ethylene glycol) (6S-PCL-PEG), was synthesized by a simple two-step reaction. Thereafter, the application of 6S-PCL-PEG as a protein carrier was evaluated. Materials and methods:...

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Veröffentlicht in:International journal of nanomedicine 2018-01, Vol.13, p.2743
Hauptverfasser: Duan, Jianwei, Liu, Chao, Liang, Xiaoyu, Li, Xuanling, Chen, Youlu, Chen, Zuoguan, Wang, Xiaoli, Kong, Deling, Li, Yongjun, Yang, Jing
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Sprache:eng
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Zusammenfassung:Background: To address the issue of delivery of proteins, a six-arm copolymer, six-arm poly ([epsilon]-caprolactone)-poly(ethylene glycol) (6S-PCL-PEG), was synthesized by a simple two-step reaction. Thereafter, the application of 6S-PCL-PEG as a protein carrier was evaluated. Materials and methods: A six-arm copolymer, six-arm poly([epsilon]-caprolactone) (6S-PCL), was synthesized by ring-opening polymerization, with stannous octoate as a catalyst and inositol as an initiator. Then, poly(ethylene glycol) (PEG) was linked with 6S-PCL by oxalyl chloride to obtain 6S-PCL-PEG. Hydrogen-1 nuclear magnetic resonance spectrum, Fourier-transform infrared spectroscopy, and gel-permeation chromatography were conducted to identify the structure of 6S-PCL-PEG. The biocompatibility of the 6S-PCL-PEG was evaluated by a cell counting kit-8 assay. Polymeric nanoparticles (NPs) were prepared by a water-in-oil-in-water double emulsion ([W.sub.1]/O/[W.sub.2]) solvent evaporation method. The size distribution and zeta potential of NPs were determined by dynamic light scattering. Transmission electron microscopy was used to observe the morphology of NPs. Drug-loading capacity, encapsulation efficiency, and the release behavior of ovalbumin (OVA)-loading NPs were tested by the bicinchoninic acid assay kit. The stability and activity of OVA released from NPs were detected and the uptake of NPs was evaluated by NIH-3T3 cells. Results: All results indicated the successful synthesis of amphiphilic copolymer 6S-PCL-PEG, which possessed excellent biocompatibility and could formulate NPs easily. High drug-loading capacity and encapsulation efficiency of protein NPs were observed. In vitro, OVA was released slowly and the bioactivity of OVA was maintained for over 28 days. Conclusion: 6S-PCL-PEG NPs prepared in this study show promising potential for use as a protein carrier. Keywords: six-arm PCL-PEG, copolymer synthesis, protein carrier, sustained release
ISSN:1178-2013
DOI:10.2147/IJN.S161006