β‑Cyclodextrin-poly(β-Amino Ester) Nanoparticles for Sustained Drug Delivery across the Blood–Brain Barrier
Novel biodegradable polymeric nanoparticles composed of β-cyclodextrin and poly(β-amino ester) segments have been developed for sustained drug delivery across the blood–brain barrier (BBB). The nanoparticles have been synthesized by cross-linking β-cyclodextrin with poly(β-amino ester) via the Micha...
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Veröffentlicht in: | Biomacromolecules 2012-11, Vol.13 (11), p.3533-3541 |
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description | Novel biodegradable polymeric nanoparticles composed of β-cyclodextrin and poly(β-amino ester) segments have been developed for sustained drug delivery across the blood–brain barrier (BBB). The nanoparticles have been synthesized by cross-linking β-cyclodextrin with poly(β-amino ester) via the Michael addition method. The chemical, physical, and degradation properties of the nanoparticles have been characterized by matrix-assisted laser desoption/ionization time-of-flight, attenuated total reflectance Fourier transform infrared spectroscopy, nuclear magnetic resonance, dynamic light scattering, and atomic force microscopy techniques. Bovine and human brain microvascular endothelial cell monolayers have been constructed as in vitro BBB models. Preliminary results show that the nanoparticles do not affect the integrity of the in vitro BBB models, and the nanoparticles have much higher permeability than dextran control across the in vitro BBB models. Doxorubicin has been loaded into the nanoparticles with a loading efficiency of 86%, and can be released from the nanoparticles for at least one month. The developed β-cyclodextrin-poly(β-amino ester) nanoparticles might be useful as drug carriers for transporting drugs across the BBB to treat chronic diseases in the brain. |
doi_str_mv | 10.1021/bm3008633 |
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The nanoparticles have been synthesized by cross-linking β-cyclodextrin with poly(β-amino ester) via the Michael addition method. The chemical, physical, and degradation properties of the nanoparticles have been characterized by matrix-assisted laser desoption/ionization time-of-flight, attenuated total reflectance Fourier transform infrared spectroscopy, nuclear magnetic resonance, dynamic light scattering, and atomic force microscopy techniques. Bovine and human brain microvascular endothelial cell monolayers have been constructed as in vitro BBB models. Preliminary results show that the nanoparticles do not affect the integrity of the in vitro BBB models, and the nanoparticles have much higher permeability than dextran control across the in vitro BBB models. Doxorubicin has been loaded into the nanoparticles with a loading efficiency of 86%, and can be released from the nanoparticles for at least one month. The developed β-cyclodextrin-poly(β-amino ester) nanoparticles might be useful as drug carriers for transporting drugs across the BBB to treat chronic diseases in the brain.</description><identifier>ISSN: 1525-7797</identifier><identifier>EISSN: 1526-4602</identifier><identifier>DOI: 10.1021/bm3008633</identifier><identifier>PMID: 23066958</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Animals ; Applied sciences ; beta-Cyclodextrins - chemistry ; beta-Cyclodextrins - metabolism ; Biological and medical sciences ; Biological Transport ; Blood-Brain Barrier - metabolism ; Brain - blood supply ; Cattle ; Cells, Cultured ; Doxorubicin - administration & dosage ; Doxorubicin - pharmacokinetics ; Drug Carriers - chemistry ; Endothelial Cells ; Exact sciences and technology ; General pharmacology ; Humans ; Magnetic Resonance Spectroscopy ; Medical sciences ; Microscopy, Atomic Force ; Microvessels ; Nanoparticles - chemistry ; Organic polymers ; Particle Size ; Permeability ; Pharmaceutical technology. Pharmaceutical industry ; Pharmacology. Drug treatments ; Physicochemistry of polymers ; Polymers - chemistry ; Polymers - metabolism ; Polymers with particular properties ; Preparation, kinetics, thermodynamics, mechanism and catalysts ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization ; Spectroscopy, Fourier Transform Infrared</subject><ispartof>Biomacromolecules, 2012-11, Vol.13 (11), p.3533-3541</ispartof><rights>Copyright © 2012 American Chemical Society</rights><rights>2014 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a378t-98acd73342e1dfbfaf031edd2585223411e38707215987e1d567d979724633f13</citedby><cites>FETCH-LOGICAL-a378t-98acd73342e1dfbfaf031edd2585223411e38707215987e1d567d979724633f13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/bm3008633$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/bm3008633$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2763,27075,27923,27924,56737,56787</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26603273$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23066958$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gil, Eun Seok</creatorcontrib><creatorcontrib>Wu, Linfeng</creatorcontrib><creatorcontrib>Xu, Lichong</creatorcontrib><creatorcontrib>Lowe, Tao Lu</creatorcontrib><title>β‑Cyclodextrin-poly(β-Amino Ester) Nanoparticles for Sustained Drug Delivery across the Blood–Brain Barrier</title><title>Biomacromolecules</title><addtitle>Biomacromolecules</addtitle><description>Novel biodegradable polymeric nanoparticles composed of β-cyclodextrin and poly(β-amino ester) segments have been developed for sustained drug delivery across the blood–brain barrier (BBB). The nanoparticles have been synthesized by cross-linking β-cyclodextrin with poly(β-amino ester) via the Michael addition method. The chemical, physical, and degradation properties of the nanoparticles have been characterized by matrix-assisted laser desoption/ionization time-of-flight, attenuated total reflectance Fourier transform infrared spectroscopy, nuclear magnetic resonance, dynamic light scattering, and atomic force microscopy techniques. Bovine and human brain microvascular endothelial cell monolayers have been constructed as in vitro BBB models. Preliminary results show that the nanoparticles do not affect the integrity of the in vitro BBB models, and the nanoparticles have much higher permeability than dextran control across the in vitro BBB models. Doxorubicin has been loaded into the nanoparticles with a loading efficiency of 86%, and can be released from the nanoparticles for at least one month. The developed β-cyclodextrin-poly(β-amino ester) nanoparticles might be useful as drug carriers for transporting drugs across the BBB to treat chronic diseases in the brain.</description><subject>Animals</subject><subject>Applied sciences</subject><subject>beta-Cyclodextrins - chemistry</subject><subject>beta-Cyclodextrins - metabolism</subject><subject>Biological and medical sciences</subject><subject>Biological Transport</subject><subject>Blood-Brain Barrier - metabolism</subject><subject>Brain - blood supply</subject><subject>Cattle</subject><subject>Cells, Cultured</subject><subject>Doxorubicin - administration & dosage</subject><subject>Doxorubicin - pharmacokinetics</subject><subject>Drug Carriers - chemistry</subject><subject>Endothelial Cells</subject><subject>Exact sciences and technology</subject><subject>General pharmacology</subject><subject>Humans</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Medical sciences</subject><subject>Microscopy, Atomic Force</subject><subject>Microvessels</subject><subject>Nanoparticles - chemistry</subject><subject>Organic polymers</subject><subject>Particle Size</subject><subject>Permeability</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. Drug treatments</subject><subject>Physicochemistry of polymers</subject><subject>Polymers - chemistry</subject><subject>Polymers - metabolism</subject><subject>Polymers with particular properties</subject><subject>Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</subject><subject>Spectroscopy, Fourier Transform Infrared</subject><issn>1525-7797</issn><issn>1526-4602</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0T1uFTEQB3ALgUgIFFwAuUFKigV_e7fMe0kAKYICqFd-61lw5F2_jHcRr8sVUG6Sg-QQOQkmeSQNEtVM8dOM5j-EvOTsDWeCv10NkrHaSPmI7HItTKUME49ve11Z29gd8iznM8ZYI5V-SnaEZMY0ut4l59dXNxe_lpsuJg8_JwxjtU5xs399VR0OYUz0OE-AB_SjG9Pa4RS6CJn2CennOU8ujODpEc7f6BHE8ANwQ12HKWc6fQe6iCn5m4vLBRZIFw4xAD4nT3oXM7zY1j3y9eT4y_J9dfrp3Yfl4WnlpK2nqqld562USgD3_ap3PZMcvBe61kJIxTnI2jIruG5qW4w21jflVqFKED2Xe2T_bu4a0_kMeWqHkDuI0Y2Q5tyWcJRiihv7f8o1t0xzrgo9uKO3VyL07RrD4HDTctb-eUZ7_4xiX23HzqsB_L38m34Br7fA5c7FHt3YhfzgjGFSWPngXJfbszTjWIL7x8LfniKe0g</recordid><startdate>20121112</startdate><enddate>20121112</enddate><creator>Gil, Eun Seok</creator><creator>Wu, Linfeng</creator><creator>Xu, Lichong</creator><creator>Lowe, Tao Lu</creator><general>American Chemical Society</general><scope>IQODW</scope><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><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20121112</creationdate><title>β‑Cyclodextrin-poly(β-Amino Ester) Nanoparticles for Sustained Drug Delivery across the Blood–Brain Barrier</title><author>Gil, Eun Seok ; Wu, Linfeng ; Xu, Lichong ; Lowe, Tao Lu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a378t-98acd73342e1dfbfaf031edd2585223411e38707215987e1d567d979724633f13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Animals</topic><topic>Applied sciences</topic><topic>beta-Cyclodextrins - chemistry</topic><topic>beta-Cyclodextrins - metabolism</topic><topic>Biological and medical sciences</topic><topic>Biological Transport</topic><topic>Blood-Brain Barrier - metabolism</topic><topic>Brain - blood supply</topic><topic>Cattle</topic><topic>Cells, Cultured</topic><topic>Doxorubicin - administration & dosage</topic><topic>Doxorubicin - pharmacokinetics</topic><topic>Drug Carriers - chemistry</topic><topic>Endothelial Cells</topic><topic>Exact sciences and technology</topic><topic>General pharmacology</topic><topic>Humans</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Medical sciences</topic><topic>Microscopy, Atomic Force</topic><topic>Microvessels</topic><topic>Nanoparticles - chemistry</topic><topic>Organic polymers</topic><topic>Particle Size</topic><topic>Permeability</topic><topic>Pharmaceutical technology. Pharmaceutical industry</topic><topic>Pharmacology. Drug treatments</topic><topic>Physicochemistry of polymers</topic><topic>Polymers - chemistry</topic><topic>Polymers - metabolism</topic><topic>Polymers with particular properties</topic><topic>Preparation, kinetics, thermodynamics, mechanism and catalysts</topic><topic>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</topic><topic>Spectroscopy, Fourier Transform Infrared</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gil, Eun Seok</creatorcontrib><creatorcontrib>Wu, Linfeng</creatorcontrib><creatorcontrib>Xu, Lichong</creatorcontrib><creatorcontrib>Lowe, Tao Lu</creatorcontrib><collection>Pascal-Francis</collection><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><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Biomacromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gil, Eun Seok</au><au>Wu, Linfeng</au><au>Xu, Lichong</au><au>Lowe, Tao Lu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>β‑Cyclodextrin-poly(β-Amino Ester) Nanoparticles for Sustained Drug Delivery across the Blood–Brain Barrier</atitle><jtitle>Biomacromolecules</jtitle><addtitle>Biomacromolecules</addtitle><date>2012-11-12</date><risdate>2012</risdate><volume>13</volume><issue>11</issue><spage>3533</spage><epage>3541</epage><pages>3533-3541</pages><issn>1525-7797</issn><eissn>1526-4602</eissn><abstract>Novel biodegradable polymeric nanoparticles composed of β-cyclodextrin and poly(β-amino ester) segments have been developed for sustained drug delivery across the blood–brain barrier (BBB). The nanoparticles have been synthesized by cross-linking β-cyclodextrin with poly(β-amino ester) via the Michael addition method. The chemical, physical, and degradation properties of the nanoparticles have been characterized by matrix-assisted laser desoption/ionization time-of-flight, attenuated total reflectance Fourier transform infrared spectroscopy, nuclear magnetic resonance, dynamic light scattering, and atomic force microscopy techniques. Bovine and human brain microvascular endothelial cell monolayers have been constructed as in vitro BBB models. Preliminary results show that the nanoparticles do not affect the integrity of the in vitro BBB models, and the nanoparticles have much higher permeability than dextran control across the in vitro BBB models. Doxorubicin has been loaded into the nanoparticles with a loading efficiency of 86%, and can be released from the nanoparticles for at least one month. The developed β-cyclodextrin-poly(β-amino ester) nanoparticles might be useful as drug carriers for transporting drugs across the BBB to treat chronic diseases in the brain.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>23066958</pmid><doi>10.1021/bm3008633</doi><tpages>9</tpages></addata></record> |
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subjects | Animals Applied sciences beta-Cyclodextrins - chemistry beta-Cyclodextrins - metabolism Biological and medical sciences Biological Transport Blood-Brain Barrier - metabolism Brain - blood supply Cattle Cells, Cultured Doxorubicin - administration & dosage Doxorubicin - pharmacokinetics Drug Carriers - chemistry Endothelial Cells Exact sciences and technology General pharmacology Humans Magnetic Resonance Spectroscopy Medical sciences Microscopy, Atomic Force Microvessels Nanoparticles - chemistry Organic polymers Particle Size Permeability Pharmaceutical technology. Pharmaceutical industry Pharmacology. Drug treatments Physicochemistry of polymers Polymers - chemistry Polymers - metabolism Polymers with particular properties Preparation, kinetics, thermodynamics, mechanism and catalysts Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization Spectroscopy, Fourier Transform Infrared |
title | β‑Cyclodextrin-poly(β-Amino Ester) Nanoparticles for Sustained Drug Delivery across the Blood–Brain Barrier |
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