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 |
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description | 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 |
doi_str_mv | 10.2147/IJN.S161006 |
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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</description><identifier>ISSN: 1178-2013</identifier><identifier>DOI: 10.2147/IJN.S161006</identifier><language>eng</language><publisher>Dove Medical Press Limited</publisher><subject>Albumin ; Biomedical laboratory equipment ; Caprolactone ; Chromatography ; Copolymers ; Electron microscopy ; Ethylene glycols ; Glycols (Class of compounds) ; Hydrogen ; Infrared spectroscopy ; Inositol ; Microscopy ; Nanoparticles ; Nuclear magnetic resonance spectroscopy ; Polymerization ; Proteins ; Spectroscopy</subject><ispartof>International journal of nanomedicine, 2018-01, Vol.13, p.2743</ispartof><rights>COPYRIGHT 2018 Dove Medical Press Limited</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,860,27901,27902</link.rule.ids></links><search><creatorcontrib>Duan, Jianwei</creatorcontrib><creatorcontrib>Liu, Chao</creatorcontrib><creatorcontrib>Liang, Xiaoyu</creatorcontrib><creatorcontrib>Li, Xuanling</creatorcontrib><creatorcontrib>Chen, Youlu</creatorcontrib><creatorcontrib>Chen, Zuoguan</creatorcontrib><creatorcontrib>Wang, Xiaoli</creatorcontrib><creatorcontrib>Kong, Deling</creatorcontrib><creatorcontrib>Li, Yongjun</creatorcontrib><creatorcontrib>Yang, Jing</creatorcontrib><title>Protein delivery nanosystem of six-arm copolymer poly for long-term sustained release</title><title>International journal of nanomedicine</title><description>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</description><subject>Albumin</subject><subject>Biomedical laboratory equipment</subject><subject>Caprolactone</subject><subject>Chromatography</subject><subject>Copolymers</subject><subject>Electron microscopy</subject><subject>Ethylene glycols</subject><subject>Glycols (Class of compounds)</subject><subject>Hydrogen</subject><subject>Infrared spectroscopy</subject><subject>Inositol</subject><subject>Microscopy</subject><subject>Nanoparticles</subject><subject>Nuclear magnetic resonance spectroscopy</subject><subject>Polymerization</subject><subject>Proteins</subject><subject>Spectroscopy</subject><issn>1178-2013</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNptjMtKxDAUhrNQcBxd-QIB161Jk54ky2HwMjKo4LgeQnMyRNpEkir27a3owoX8iw_-GyEXnNUNl-pqc_9QP3PgjMERWXCudNUwLk7IaSmvjLVKg1mQl6ecRgyROuzDB-aJRhtTmcqIA02elvBZ2TzQLr2lfhow029SnzLtUzxUI85heS-jDREdzdijLXhGjr3tC57_ckl2N9e79V21fbzdrFfb6gDKVMZ5qY0y3DYdWKUAHIIRwK1nTkmhreCcNUx4J6xUzHAJ0AIHCZbJRoslufy5Pdge9yH6NGbbDaF0-1WrhdRKGzO36n9asxwOoUsRfZj9P4MvGHte0Q</recordid><startdate>20180101</startdate><enddate>20180101</enddate><creator>Duan, Jianwei</creator><creator>Liu, Chao</creator><creator>Liang, Xiaoyu</creator><creator>Li, Xuanling</creator><creator>Chen, Youlu</creator><creator>Chen, Zuoguan</creator><creator>Wang, Xiaoli</creator><creator>Kong, Deling</creator><creator>Li, Yongjun</creator><creator>Yang, Jing</creator><general>Dove Medical Press Limited</general><scope/></search><sort><creationdate>20180101</creationdate><title>Protein delivery nanosystem of six-arm copolymer poly for long-term sustained release</title><author>Duan, Jianwei ; Liu, Chao ; Liang, Xiaoyu ; Li, Xuanling ; Chen, Youlu ; Chen, Zuoguan ; Wang, Xiaoli ; Kong, Deling ; Li, Yongjun ; Yang, Jing</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g679-9df489791a2c6a7766de69361af0d7438a3110203fd3a47091466561646a04283</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Albumin</topic><topic>Biomedical laboratory equipment</topic><topic>Caprolactone</topic><topic>Chromatography</topic><topic>Copolymers</topic><topic>Electron microscopy</topic><topic>Ethylene glycols</topic><topic>Glycols (Class of compounds)</topic><topic>Hydrogen</topic><topic>Infrared spectroscopy</topic><topic>Inositol</topic><topic>Microscopy</topic><topic>Nanoparticles</topic><topic>Nuclear magnetic resonance spectroscopy</topic><topic>Polymerization</topic><topic>Proteins</topic><topic>Spectroscopy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Duan, Jianwei</creatorcontrib><creatorcontrib>Liu, Chao</creatorcontrib><creatorcontrib>Liang, Xiaoyu</creatorcontrib><creatorcontrib>Li, Xuanling</creatorcontrib><creatorcontrib>Chen, Youlu</creatorcontrib><creatorcontrib>Chen, Zuoguan</creatorcontrib><creatorcontrib>Wang, Xiaoli</creatorcontrib><creatorcontrib>Kong, Deling</creatorcontrib><creatorcontrib>Li, Yongjun</creatorcontrib><creatorcontrib>Yang, Jing</creatorcontrib><jtitle>International journal of nanomedicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Duan, Jianwei</au><au>Liu, Chao</au><au>Liang, Xiaoyu</au><au>Li, Xuanling</au><au>Chen, Youlu</au><au>Chen, Zuoguan</au><au>Wang, Xiaoli</au><au>Kong, Deling</au><au>Li, Yongjun</au><au>Yang, Jing</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Protein delivery nanosystem of six-arm copolymer poly for long-term sustained release</atitle><jtitle>International journal of nanomedicine</jtitle><date>2018-01-01</date><risdate>2018</risdate><volume>13</volume><spage>2743</spage><pages>2743-</pages><issn>1178-2013</issn><abstract>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</abstract><pub>Dove Medical Press Limited</pub><doi>10.2147/IJN.S161006</doi></addata></record> |
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subjects | Albumin Biomedical laboratory equipment Caprolactone Chromatography Copolymers Electron microscopy Ethylene glycols Glycols (Class of compounds) Hydrogen Infrared spectroscopy Inositol Microscopy Nanoparticles Nuclear magnetic resonance spectroscopy Polymerization Proteins Spectroscopy |
title | Protein delivery nanosystem of six-arm copolymer poly for long-term sustained release |
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