Development and characterization of a novel drug nanocarrier for oral delivery, based on self-assembled β-casein micelles
β-casein is an amphiphilic protein that self-organizes into well-defined core–shell micelles. We developed these micelles as efficient nanocarriers for oral drug delivery. Our model drug is celecoxib, an anti-inflammatory hydrophobic drug utilized for treatment of rheumatoid arthritis and osteoarthr...
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Veröffentlicht in: | Journal of controlled release 2012-06, Vol.160 (2), p.164-171 |
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creator | Bachar, Michal Mandelbaum, Amitai Portnaya, Irina Perlstein, Hadas Even-Chen, Simcha Barenholz, Yechezkel Danino, Dganit |
description | β-casein is an amphiphilic protein that self-organizes into well-defined core–shell micelles. We developed these micelles as efficient nanocarriers for oral drug delivery. Our model drug is celecoxib, an anti-inflammatory hydrophobic drug utilized for treatment of rheumatoid arthritis and osteoarthritis, now also evaluated as a potent anticancer drug. This system is unique as it enables encapsulation loads >100-fold higher than other β-casein/drug formulations, and does not require additives as do other formulations that have high loadings. This is combined with the ability to lyophilize the formulation without a cryoprotectant, long-term physical and chemical stability of the resulting powder, and fully reversible reconstitution of the structures by rehydration. The dry dosage form, in which >95% of the drug is encapsulated, meets the daily dose. Cryo-TEM and DLS prove that drug encapsulation results in micelle swelling, and X-ray diffraction shows that the encapsulated drug is amorphous. Altogether, our novel dosage form is highly advantageous for oral administration.
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doi_str_mv | 10.1016/j.jconrel.2012.01.004 |
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[Display omitted]</description><identifier>ISSN: 0168-3659</identifier><identifier>EISSN: 1873-4995</identifier><identifier>DOI: 10.1016/j.jconrel.2012.01.004</identifier><identifier>PMID: 22266050</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>additives ; Administration, Oral ; Amphiphilic block copolymers ; anti-inflammatory activity ; Anti-Inflammatory Agents, Non-Steroidal - administration & dosage ; Anti-Inflammatory Agents, Non-Steroidal - chemistry ; antineoplastic agents ; beta-casein ; Caseins - chemistry ; Celecoxib ; Chemistry, Pharmaceutical ; Cryoelectron Microscopy ; Drug Carriers - chemistry ; Drug Compounding ; Drug delivery ; Drug Design ; drug formulations ; encapsulation ; Freeze Drying ; Hydrophobic and Hydrophilic Interactions ; hydrophobicity ; Micelles ; Microscopy, Electron, Transmission ; Molecular Structure ; nanocarriers ; Nanomedicine ; Nanoparticles - chemistry ; oral administration ; osteoarthritis ; Protein micelles ; Pyrazoles - administration & dosage ; Pyrazoles - chemistry ; rehydration ; rheumatoid arthritis ; Solubility ; Sulfonamides - administration & dosage ; Sulfonamides - chemistry ; Surface Properties ; Surface-Active Agents - chemistry ; X-Ray Diffraction</subject><ispartof>Journal of controlled release, 2012-06, Vol.160 (2), p.164-171</ispartof><rights>2012 Elsevier B.V.</rights><rights>Copyright © 2012 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c389t-a4af3a723ddb0625190fbef2aa68872ea8d4c037cfc178e78bb108dadcf72ce03</citedby><cites>FETCH-LOGICAL-c389t-a4af3a723ddb0625190fbef2aa68872ea8d4c037cfc178e78bb108dadcf72ce03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jconrel.2012.01.004$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22266050$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bachar, Michal</creatorcontrib><creatorcontrib>Mandelbaum, Amitai</creatorcontrib><creatorcontrib>Portnaya, Irina</creatorcontrib><creatorcontrib>Perlstein, Hadas</creatorcontrib><creatorcontrib>Even-Chen, Simcha</creatorcontrib><creatorcontrib>Barenholz, Yechezkel</creatorcontrib><creatorcontrib>Danino, Dganit</creatorcontrib><title>Development and characterization of a novel drug nanocarrier for oral delivery, based on self-assembled β-casein micelles</title><title>Journal of controlled release</title><addtitle>J Control Release</addtitle><description>β-casein is an amphiphilic protein that self-organizes into well-defined core–shell micelles. We developed these micelles as efficient nanocarriers for oral drug delivery. Our model drug is celecoxib, an anti-inflammatory hydrophobic drug utilized for treatment of rheumatoid arthritis and osteoarthritis, now also evaluated as a potent anticancer drug. This system is unique as it enables encapsulation loads >100-fold higher than other β-casein/drug formulations, and does not require additives as do other formulations that have high loadings. This is combined with the ability to lyophilize the formulation without a cryoprotectant, long-term physical and chemical stability of the resulting powder, and fully reversible reconstitution of the structures by rehydration. The dry dosage form, in which >95% of the drug is encapsulated, meets the daily dose. Cryo-TEM and DLS prove that drug encapsulation results in micelle swelling, and X-ray diffraction shows that the encapsulated drug is amorphous. Altogether, our novel dosage form is highly advantageous for oral administration.
[Display omitted]</description><subject>additives</subject><subject>Administration, Oral</subject><subject>Amphiphilic block copolymers</subject><subject>anti-inflammatory activity</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - administration & dosage</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - chemistry</subject><subject>antineoplastic agents</subject><subject>beta-casein</subject><subject>Caseins - chemistry</subject><subject>Celecoxib</subject><subject>Chemistry, Pharmaceutical</subject><subject>Cryoelectron Microscopy</subject><subject>Drug Carriers - chemistry</subject><subject>Drug Compounding</subject><subject>Drug delivery</subject><subject>Drug Design</subject><subject>drug formulations</subject><subject>encapsulation</subject><subject>Freeze Drying</subject><subject>Hydrophobic and Hydrophilic Interactions</subject><subject>hydrophobicity</subject><subject>Micelles</subject><subject>Microscopy, Electron, Transmission</subject><subject>Molecular Structure</subject><subject>nanocarriers</subject><subject>Nanomedicine</subject><subject>Nanoparticles - chemistry</subject><subject>oral administration</subject><subject>osteoarthritis</subject><subject>Protein micelles</subject><subject>Pyrazoles - administration & dosage</subject><subject>Pyrazoles - chemistry</subject><subject>rehydration</subject><subject>rheumatoid arthritis</subject><subject>Solubility</subject><subject>Sulfonamides - administration & dosage</subject><subject>Sulfonamides - chemistry</subject><subject>Surface Properties</subject><subject>Surface-Active Agents - chemistry</subject><subject>X-Ray Diffraction</subject><issn>0168-3659</issn><issn>1873-4995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEuO1DAQhi0EYpqBIwBesiCNH4njrBAantJILGDWVsUuD24ldmOnW5o5FgfhTLiVhi2rkqq-v6r0EfKcsy1nXL3ZbXc2xYzTVjAutoxvGWsfkA3XvWzaYegekk3ldCNVN1yQJ6XsGGOdbPvH5EIIoRTr2Ibcv8cjTmk_Y1woREftD8hgF8zhHpaQIk2eAo2pUtTlwy2NEJOFnANm6lOmKUOd4BSOmO9e0xEKOlpzBSffQCk4j1Pt_P7V2DoKkc7B4jRheUoeeZgKPjvXS3Lz8cP3q8_N9ddPX67eXTdW6mFpoAUvoRfSuZEp0fGB-RG9AFBa9wJBu9Yy2Vtvea-x1-PImXbgrO-FRSYvyat17z6nnwcsi5lDOb0AEdOhmKpTKymrvop2K2pzKiWjN_scZsh3FTpxyuzMWbs5aTeMmzX34nziMM7o_qX-eq7AyxXwkAzc5lDMzbe6oWOM90oNqhJvVwKrimOVa4oNGC26kNEuxqXwnyf-AO6qouM</recordid><startdate>20120610</startdate><enddate>20120610</enddate><creator>Bachar, Michal</creator><creator>Mandelbaum, Amitai</creator><creator>Portnaya, Irina</creator><creator>Perlstein, Hadas</creator><creator>Even-Chen, Simcha</creator><creator>Barenholz, Yechezkel</creator><creator>Danino, Dganit</creator><general>Elsevier B.V</general><scope>FBQ</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></search><sort><creationdate>20120610</creationdate><title>Development and characterization of a novel drug nanocarrier for oral delivery, based on self-assembled β-casein micelles</title><author>Bachar, Michal ; Mandelbaum, Amitai ; Portnaya, Irina ; Perlstein, Hadas ; Even-Chen, Simcha ; Barenholz, Yechezkel ; Danino, Dganit</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-a4af3a723ddb0625190fbef2aa68872ea8d4c037cfc178e78bb108dadcf72ce03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>additives</topic><topic>Administration, Oral</topic><topic>Amphiphilic block copolymers</topic><topic>anti-inflammatory activity</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - administration & dosage</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - chemistry</topic><topic>antineoplastic agents</topic><topic>beta-casein</topic><topic>Caseins - chemistry</topic><topic>Celecoxib</topic><topic>Chemistry, Pharmaceutical</topic><topic>Cryoelectron Microscopy</topic><topic>Drug Carriers - chemistry</topic><topic>Drug Compounding</topic><topic>Drug delivery</topic><topic>Drug Design</topic><topic>drug formulations</topic><topic>encapsulation</topic><topic>Freeze Drying</topic><topic>Hydrophobic and Hydrophilic Interactions</topic><topic>hydrophobicity</topic><topic>Micelles</topic><topic>Microscopy, Electron, Transmission</topic><topic>Molecular Structure</topic><topic>nanocarriers</topic><topic>Nanomedicine</topic><topic>Nanoparticles - chemistry</topic><topic>oral administration</topic><topic>osteoarthritis</topic><topic>Protein micelles</topic><topic>Pyrazoles - administration & dosage</topic><topic>Pyrazoles - chemistry</topic><topic>rehydration</topic><topic>rheumatoid arthritis</topic><topic>Solubility</topic><topic>Sulfonamides - administration & dosage</topic><topic>Sulfonamides - chemistry</topic><topic>Surface Properties</topic><topic>Surface-Active Agents - chemistry</topic><topic>X-Ray Diffraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bachar, Michal</creatorcontrib><creatorcontrib>Mandelbaum, Amitai</creatorcontrib><creatorcontrib>Portnaya, Irina</creatorcontrib><creatorcontrib>Perlstein, Hadas</creatorcontrib><creatorcontrib>Even-Chen, Simcha</creatorcontrib><creatorcontrib>Barenholz, Yechezkel</creatorcontrib><creatorcontrib>Danino, Dganit</creatorcontrib><collection>AGRIS</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><jtitle>Journal of controlled release</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bachar, Michal</au><au>Mandelbaum, Amitai</au><au>Portnaya, Irina</au><au>Perlstein, Hadas</au><au>Even-Chen, Simcha</au><au>Barenholz, Yechezkel</au><au>Danino, Dganit</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Development and characterization of a novel drug nanocarrier for oral delivery, based on self-assembled β-casein micelles</atitle><jtitle>Journal of controlled release</jtitle><addtitle>J Control Release</addtitle><date>2012-06-10</date><risdate>2012</risdate><volume>160</volume><issue>2</issue><spage>164</spage><epage>171</epage><pages>164-171</pages><issn>0168-3659</issn><eissn>1873-4995</eissn><abstract>β-casein is an amphiphilic protein that self-organizes into well-defined core–shell micelles. We developed these micelles as efficient nanocarriers for oral drug delivery. Our model drug is celecoxib, an anti-inflammatory hydrophobic drug utilized for treatment of rheumatoid arthritis and osteoarthritis, now also evaluated as a potent anticancer drug. This system is unique as it enables encapsulation loads >100-fold higher than other β-casein/drug formulations, and does not require additives as do other formulations that have high loadings. This is combined with the ability to lyophilize the formulation without a cryoprotectant, long-term physical and chemical stability of the resulting powder, and fully reversible reconstitution of the structures by rehydration. The dry dosage form, in which >95% of the drug is encapsulated, meets the daily dose. Cryo-TEM and DLS prove that drug encapsulation results in micelle swelling, and X-ray diffraction shows that the encapsulated drug is amorphous. Altogether, our novel dosage form is highly advantageous for oral administration.
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subjects | additives Administration, Oral Amphiphilic block copolymers anti-inflammatory activity Anti-Inflammatory Agents, Non-Steroidal - administration & dosage Anti-Inflammatory Agents, Non-Steroidal - chemistry antineoplastic agents beta-casein Caseins - chemistry Celecoxib Chemistry, Pharmaceutical Cryoelectron Microscopy Drug Carriers - chemistry Drug Compounding Drug delivery Drug Design drug formulations encapsulation Freeze Drying Hydrophobic and Hydrophilic Interactions hydrophobicity Micelles Microscopy, Electron, Transmission Molecular Structure nanocarriers Nanomedicine Nanoparticles - chemistry oral administration osteoarthritis Protein micelles Pyrazoles - administration & dosage Pyrazoles - chemistry rehydration rheumatoid arthritis Solubility Sulfonamides - administration & dosage Sulfonamides - chemistry Surface Properties Surface-Active Agents - chemistry X-Ray Diffraction |
title | Development and characterization of a novel drug nanocarrier for oral delivery, based on self-assembled β-casein micelles |
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