Nanomicelle with long-term circulation and enhanced stability of camptothecin based on mPEGylated α, β-poly ( l-aspartic acid)-camptothecin conjugate
To enhance the stability and long-term circulation of camptothecin (CPT), mPEGylated α, β-poly ( l-aspartic acid)-CPT conjugates were synthesized, and used to fabricate nanomicelle. Firstly, α, β-poly ( l-aspartic acid) derivative (PAA-der) containing alkyne groups was synthesized via the ring-openi...
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Veröffentlicht in: | Colloids and surfaces, B, Biointerfaces B, Biointerfaces, 2010-11, Vol.81 (1), p.297-303 |
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creator | Zhang, Weilu Huang, Jin Fan, Naiqian Yu, Jiahui Liu, Yongbiao Liu, Shiyuan Wang, Daxin Li, Yaping |
description | To enhance the stability and long-term circulation of camptothecin (CPT), mPEGylated
α,
β-poly (
l-aspartic acid)-CPT conjugates were synthesized, and used to fabricate nanomicelle. Firstly,
α,
β-poly (
l-aspartic acid) derivative (PAA-der) containing alkyne groups was synthesized via the ring-opening of PSI with propargyl amine. And then, azide-functionalized CPT derivatives (CPT-N
3) and azide-terminated poly (ethylene glycol) methyl ether (mPEG-N
3) were conjugated with PAA-der by click cycloaddition to give mPEG-
graft-PAA-CPT conjugates. The formation of mPEG-
graft-PAA-CPT nanomicelles was confirmed by fluorescence spectrophotoscopy and particle size measurements. It was found that all the nanomicelles showed spherical shapes with size about 178
nm. MPEG-
graft-PAA-CPT nanomicelles showed good storage stability, even incubation at 37
°C for 60 days, and improved the stability of CPT lactone form in aqueous media. A steady release rate of CPT was kept for 72
h, suggested the great potential of mPEG-
graft-PAA-CPT nanomicelles as polymer prodrug of CPT. |
doi_str_mv | 10.1016/j.colsurfb.2010.07.019 |
format | Article |
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α,
β-poly (
l-aspartic acid)-CPT conjugates were synthesized, and used to fabricate nanomicelle. Firstly,
α,
β-poly (
l-aspartic acid) derivative (PAA-der) containing alkyne groups was synthesized via the ring-opening of PSI with propargyl amine. And then, azide-functionalized CPT derivatives (CPT-N
3) and azide-terminated poly (ethylene glycol) methyl ether (mPEG-N
3) were conjugated with PAA-der by click cycloaddition to give mPEG-
graft-PAA-CPT conjugates. The formation of mPEG-
graft-PAA-CPT nanomicelles was confirmed by fluorescence spectrophotoscopy and particle size measurements. It was found that all the nanomicelles showed spherical shapes with size about 178
nm. MPEG-
graft-PAA-CPT nanomicelles showed good storage stability, even incubation at 37
°C for 60 days, and improved the stability of CPT lactone form in aqueous media. A steady release rate of CPT was kept for 72
h, suggested the great potential of mPEG-
graft-PAA-CPT nanomicelles as polymer prodrug of CPT.</description><identifier>ISSN: 0927-7765</identifier><identifier>EISSN: 1873-4367</identifier><identifier>DOI: 10.1016/j.colsurfb.2010.07.019</identifier><identifier>PMID: 20674289</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Antineoplastic Agents, Phytogenic - chemistry ; Antineoplastic Agents, Phytogenic - pharmacokinetics ; Aspartic Acid - chemistry ; Camptothecin ; Camptothecin - chemistry ; Camptothecin - pharmacokinetics ; Click cycloaddition ; Drug Compounding ; Drug Stability ; Long-term circulation ; Micelles ; Microscopy, Electron, Transmission ; Models, Chemical ; Molecular Structure ; Nanostructures ; Particle Size ; Polyethylene Glycols - chemistry ; Polymeric nanomicelles ; Polymers - chemistry ; Spectroscopy, Fourier Transform Infrared ; Stability ; Time Factors</subject><ispartof>Colloids and surfaces, B, Biointerfaces, 2010-11, Vol.81 (1), p.297-303</ispartof><rights>2010 Elsevier B.V.</rights><rights>Copyright (c) 2010 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c367t-bbd764b8ebabe837fd560bb8fb5427523d5d4fb640fa5c51709b8d61d661614f3</citedby><cites>FETCH-LOGICAL-c367t-bbd764b8ebabe837fd560bb8fb5427523d5d4fb640fa5c51709b8d61d661614f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.colsurfb.2010.07.019$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,45974</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20674289$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhang, Weilu</creatorcontrib><creatorcontrib>Huang, Jin</creatorcontrib><creatorcontrib>Fan, Naiqian</creatorcontrib><creatorcontrib>Yu, Jiahui</creatorcontrib><creatorcontrib>Liu, Yongbiao</creatorcontrib><creatorcontrib>Liu, Shiyuan</creatorcontrib><creatorcontrib>Wang, Daxin</creatorcontrib><creatorcontrib>Li, Yaping</creatorcontrib><title>Nanomicelle with long-term circulation and enhanced stability of camptothecin based on mPEGylated α, β-poly ( l-aspartic acid)-camptothecin conjugate</title><title>Colloids and surfaces, B, Biointerfaces</title><addtitle>Colloids Surf B Biointerfaces</addtitle><description>To enhance the stability and long-term circulation of camptothecin (CPT), mPEGylated
α,
β-poly (
l-aspartic acid)-CPT conjugates were synthesized, and used to fabricate nanomicelle. Firstly,
α,
β-poly (
l-aspartic acid) derivative (PAA-der) containing alkyne groups was synthesized via the ring-opening of PSI with propargyl amine. And then, azide-functionalized CPT derivatives (CPT-N
3) and azide-terminated poly (ethylene glycol) methyl ether (mPEG-N
3) were conjugated with PAA-der by click cycloaddition to give mPEG-
graft-PAA-CPT conjugates. The formation of mPEG-
graft-PAA-CPT nanomicelles was confirmed by fluorescence spectrophotoscopy and particle size measurements. It was found that all the nanomicelles showed spherical shapes with size about 178
nm. MPEG-
graft-PAA-CPT nanomicelles showed good storage stability, even incubation at 37
°C for 60 days, and improved the stability of CPT lactone form in aqueous media. A steady release rate of CPT was kept for 72
h, suggested the great potential of mPEG-
graft-PAA-CPT nanomicelles as polymer prodrug of CPT.</description><subject>Antineoplastic Agents, Phytogenic - chemistry</subject><subject>Antineoplastic Agents, Phytogenic - pharmacokinetics</subject><subject>Aspartic Acid - chemistry</subject><subject>Camptothecin</subject><subject>Camptothecin - chemistry</subject><subject>Camptothecin - pharmacokinetics</subject><subject>Click cycloaddition</subject><subject>Drug Compounding</subject><subject>Drug Stability</subject><subject>Long-term circulation</subject><subject>Micelles</subject><subject>Microscopy, Electron, Transmission</subject><subject>Models, Chemical</subject><subject>Molecular Structure</subject><subject>Nanostructures</subject><subject>Particle Size</subject><subject>Polyethylene Glycols - chemistry</subject><subject>Polymeric nanomicelles</subject><subject>Polymers - chemistry</subject><subject>Spectroscopy, Fourier Transform Infrared</subject><subject>Stability</subject><subject>Time Factors</subject><issn>0927-7765</issn><issn>1873-4367</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU-OFCEUh4nROG3rFSbs1MRqoYqCqp1mMo4mE3Wha8LfaToUlEBp-iSeQw8yZ5JKz5i4kg0Bfh8v730AnGO0wwjT14edij4vycpdi-olYjuExwdggwfWNaSj7CHYoLFlDWO0PwNPcj4ghFqC2WNw1iLKSDuMG_Dzowhxcsp4b-APV_bQx3DTFJMmqFxSixfFxQBF0NCEvQjKaJiLkM67coTRQiWmucSyN8oFKEWu7zU_fb68Ola2nm5_vYK3v5s5-iN8AX0j8ixScQoK5fTL5h9exXBYbir2FDyywmfz7G7fgq_vLr9cvG-uP119uHh73ajaYmmk1IwSORgppBk6ZnVPkZSDlT1pWd92utfESkqQFb3qMUOjHDTFmlJMMbHdFjw__Tun-G0xufDJ5XUaIpi4ZM7IiHC3ri2gp6RKMedkLJ-Tm0Q6coz46oQf-L0TvjrhiPHqpILndyUWORn9F7uXUANvTgFTG_3uTOJZObNO2iWjCtfR_a_GH34MpXY</recordid><startdate>20101101</startdate><enddate>20101101</enddate><creator>Zhang, Weilu</creator><creator>Huang, Jin</creator><creator>Fan, Naiqian</creator><creator>Yu, Jiahui</creator><creator>Liu, Yongbiao</creator><creator>Liu, Shiyuan</creator><creator>Wang, Daxin</creator><creator>Li, Yaping</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20101101</creationdate><title>Nanomicelle with long-term circulation and enhanced stability of camptothecin based on mPEGylated α, β-poly ( l-aspartic acid)-camptothecin conjugate</title><author>Zhang, Weilu ; Huang, Jin ; Fan, Naiqian ; Yu, Jiahui ; Liu, Yongbiao ; Liu, Shiyuan ; Wang, Daxin ; Li, Yaping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c367t-bbd764b8ebabe837fd560bb8fb5427523d5d4fb640fa5c51709b8d61d661614f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Antineoplastic Agents, Phytogenic - chemistry</topic><topic>Antineoplastic Agents, Phytogenic - pharmacokinetics</topic><topic>Aspartic Acid - chemistry</topic><topic>Camptothecin</topic><topic>Camptothecin - chemistry</topic><topic>Camptothecin - pharmacokinetics</topic><topic>Click cycloaddition</topic><topic>Drug Compounding</topic><topic>Drug Stability</topic><topic>Long-term circulation</topic><topic>Micelles</topic><topic>Microscopy, Electron, Transmission</topic><topic>Models, Chemical</topic><topic>Molecular Structure</topic><topic>Nanostructures</topic><topic>Particle Size</topic><topic>Polyethylene Glycols - chemistry</topic><topic>Polymeric nanomicelles</topic><topic>Polymers - chemistry</topic><topic>Spectroscopy, Fourier Transform Infrared</topic><topic>Stability</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Weilu</creatorcontrib><creatorcontrib>Huang, Jin</creatorcontrib><creatorcontrib>Fan, Naiqian</creatorcontrib><creatorcontrib>Yu, Jiahui</creatorcontrib><creatorcontrib>Liu, Yongbiao</creatorcontrib><creatorcontrib>Liu, Shiyuan</creatorcontrib><creatorcontrib>Wang, Daxin</creatorcontrib><creatorcontrib>Li, Yaping</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Colloids and surfaces, B, Biointerfaces</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Weilu</au><au>Huang, Jin</au><au>Fan, Naiqian</au><au>Yu, Jiahui</au><au>Liu, Yongbiao</au><au>Liu, Shiyuan</au><au>Wang, Daxin</au><au>Li, Yaping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Nanomicelle with long-term circulation and enhanced stability of camptothecin based on mPEGylated α, β-poly ( l-aspartic acid)-camptothecin conjugate</atitle><jtitle>Colloids and surfaces, B, Biointerfaces</jtitle><addtitle>Colloids Surf B Biointerfaces</addtitle><date>2010-11-01</date><risdate>2010</risdate><volume>81</volume><issue>1</issue><spage>297</spage><epage>303</epage><pages>297-303</pages><issn>0927-7765</issn><eissn>1873-4367</eissn><abstract>To enhance the stability and long-term circulation of camptothecin (CPT), mPEGylated
α,
β-poly (
l-aspartic acid)-CPT conjugates were synthesized, and used to fabricate nanomicelle. Firstly,
α,
β-poly (
l-aspartic acid) derivative (PAA-der) containing alkyne groups was synthesized via the ring-opening of PSI with propargyl amine. And then, azide-functionalized CPT derivatives (CPT-N
3) and azide-terminated poly (ethylene glycol) methyl ether (mPEG-N
3) were conjugated with PAA-der by click cycloaddition to give mPEG-
graft-PAA-CPT conjugates. The formation of mPEG-
graft-PAA-CPT nanomicelles was confirmed by fluorescence spectrophotoscopy and particle size measurements. It was found that all the nanomicelles showed spherical shapes with size about 178
nm. MPEG-
graft-PAA-CPT nanomicelles showed good storage stability, even incubation at 37
°C for 60 days, and improved the stability of CPT lactone form in aqueous media. A steady release rate of CPT was kept for 72
h, suggested the great potential of mPEG-
graft-PAA-CPT nanomicelles as polymer prodrug of CPT.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>20674289</pmid><doi>10.1016/j.colsurfb.2010.07.019</doi><tpages>7</tpages></addata></record> |
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source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Antineoplastic Agents, Phytogenic - chemistry Antineoplastic Agents, Phytogenic - pharmacokinetics Aspartic Acid - chemistry Camptothecin Camptothecin - chemistry Camptothecin - pharmacokinetics Click cycloaddition Drug Compounding Drug Stability Long-term circulation Micelles Microscopy, Electron, Transmission Models, Chemical Molecular Structure Nanostructures Particle Size Polyethylene Glycols - chemistry Polymeric nanomicelles Polymers - chemistry Spectroscopy, Fourier Transform Infrared Stability Time Factors |
title | Nanomicelle with long-term circulation and enhanced stability of camptothecin based on mPEGylated α, β-poly ( l-aspartic acid)-camptothecin conjugate |
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