Click chemistry-based novel albumin nanoparticles for anticancer treatment via H 2 O 2 generation
Glucose oxidase (GOD) exerts anticancer effects by producing hydrogen peroxide (H O ). However, the use of GOD is limited by its short half-life and low stability. Systemic H O production following systemic absorption of GOD can also cause serious toxicity. GOD-conjugated bovine serum albumin nanopa...
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Veröffentlicht in: | Colloids and surfaces, B, Biointerfaces B, Biointerfaces, 2023-06, Vol.226, p.113335 |
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description | Glucose oxidase (GOD) exerts anticancer effects by producing hydrogen peroxide (H
O
). However, the use of GOD is limited by its short half-life and low stability. Systemic H
O
production following systemic absorption of GOD can also cause serious toxicity. GOD-conjugated bovine serum albumin nanoparticles (GOD-BSA NPs) may be useful for overcoming these limitations. Here, bioorthogonal copper-free click chemistry was employed to develop GOD-BSA NPs that are non-toxic and biodegradable and can effectively and rapidly conjugate proteins. These NPs retained their activity, unlike conventional albumin NPs. NPs using dibenzyl cyclooctyne (DBCO)-modified albumin, azide-modified albumin, and azide-modified GOD were fabricated in 10 min. After intratumoral administration, GOD-BSA NPs remained in the tumor for a longer period and displayed better anticancer activity than the effects of GOD alone. GOD-BSA NPs were approximately 240 nm in size and inhibited tumor growth to 40 mm
, whereas tumors treated with phosphate-buffered saline or albumin NPs had sizes of 1673 and 1578 mm
, respectively. GOD-BSA NPs prepared using click chemistry may be useful as a drug delivery system for protein enzymes. |
doi_str_mv | 10.1016/j.colsurfb.2023.113335 |
format | Article |
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O
). However, the use of GOD is limited by its short half-life and low stability. Systemic H
O
production following systemic absorption of GOD can also cause serious toxicity. GOD-conjugated bovine serum albumin nanoparticles (GOD-BSA NPs) may be useful for overcoming these limitations. Here, bioorthogonal copper-free click chemistry was employed to develop GOD-BSA NPs that are non-toxic and biodegradable and can effectively and rapidly conjugate proteins. These NPs retained their activity, unlike conventional albumin NPs. NPs using dibenzyl cyclooctyne (DBCO)-modified albumin, azide-modified albumin, and azide-modified GOD were fabricated in 10 min. After intratumoral administration, GOD-BSA NPs remained in the tumor for a longer period and displayed better anticancer activity than the effects of GOD alone. GOD-BSA NPs were approximately 240 nm in size and inhibited tumor growth to 40 mm
, whereas tumors treated with phosphate-buffered saline or albumin NPs had sizes of 1673 and 1578 mm
, respectively. GOD-BSA NPs prepared using click chemistry may be useful as a drug delivery system for protein enzymes.</description><identifier>EISSN: 1873-4367</identifier><identifier>DOI: 10.1016/j.colsurfb.2023.113335</identifier><identifier>PMID: 37148665</identifier><language>eng</language><publisher>Netherlands</publisher><ispartof>Colloids and surfaces, B, Biointerfaces, 2023-06, Vol.226, p.113335</ispartof><rights>Copyright © 2023 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37148665$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Changkyu</creatorcontrib><title>Click chemistry-based novel albumin nanoparticles for anticancer treatment via H 2 O 2 generation</title><title>Colloids and surfaces, B, Biointerfaces</title><addtitle>Colloids Surf B Biointerfaces</addtitle><description>Glucose oxidase (GOD) exerts anticancer effects by producing hydrogen peroxide (H
O
). However, the use of GOD is limited by its short half-life and low stability. Systemic H
O
production following systemic absorption of GOD can also cause serious toxicity. GOD-conjugated bovine serum albumin nanoparticles (GOD-BSA NPs) may be useful for overcoming these limitations. Here, bioorthogonal copper-free click chemistry was employed to develop GOD-BSA NPs that are non-toxic and biodegradable and can effectively and rapidly conjugate proteins. These NPs retained their activity, unlike conventional albumin NPs. NPs using dibenzyl cyclooctyne (DBCO)-modified albumin, azide-modified albumin, and azide-modified GOD were fabricated in 10 min. After intratumoral administration, GOD-BSA NPs remained in the tumor for a longer period and displayed better anticancer activity than the effects of GOD alone. GOD-BSA NPs were approximately 240 nm in size and inhibited tumor growth to 40 mm
, whereas tumors treated with phosphate-buffered saline or albumin NPs had sizes of 1673 and 1578 mm
, respectively. GOD-BSA NPs prepared using click chemistry may be useful as a drug delivery system for protein enzymes.</description><issn>1873-4367</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNqFjkFOwzAQRS0k1JaWK1RzgQQ7TpPuK1B3bNhXE3cCLvY4GjuVenu6gDWLr6cnvcVXamt0bbTpXi61SyHPMg51oxtbG2Ot3T2oldn3tmpt1y_VU84XrXXTmn6hlrY37b7rdiuFh-DdN7gvij4XuVUDZjoDpysFwDDM0TMwcppQineBMoxJAPkuyI4EihCWSFzg6hGO0MD7fZ_EJFh84o16HDFkev7lWm3fXj8Ox2qah0jn0yQ-otxOf5_sv8EPpclKQA</recordid><startdate>202306</startdate><enddate>202306</enddate><creator>Lee, Changkyu</creator><scope>NPM</scope></search><sort><creationdate>202306</creationdate><title>Click chemistry-based novel albumin nanoparticles for anticancer treatment via H 2 O 2 generation</title><author>Lee, Changkyu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-pubmed_primary_371486653</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Changkyu</creatorcontrib><collection>PubMed</collection><jtitle>Colloids and surfaces, B, Biointerfaces</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Changkyu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Click chemistry-based novel albumin nanoparticles for anticancer treatment via H 2 O 2 generation</atitle><jtitle>Colloids and surfaces, B, Biointerfaces</jtitle><addtitle>Colloids Surf B Biointerfaces</addtitle><date>2023-06</date><risdate>2023</risdate><volume>226</volume><spage>113335</spage><pages>113335-</pages><eissn>1873-4367</eissn><abstract>Glucose oxidase (GOD) exerts anticancer effects by producing hydrogen peroxide (H
O
). However, the use of GOD is limited by its short half-life and low stability. Systemic H
O
production following systemic absorption of GOD can also cause serious toxicity. GOD-conjugated bovine serum albumin nanoparticles (GOD-BSA NPs) may be useful for overcoming these limitations. Here, bioorthogonal copper-free click chemistry was employed to develop GOD-BSA NPs that are non-toxic and biodegradable and can effectively and rapidly conjugate proteins. These NPs retained their activity, unlike conventional albumin NPs. NPs using dibenzyl cyclooctyne (DBCO)-modified albumin, azide-modified albumin, and azide-modified GOD were fabricated in 10 min. After intratumoral administration, GOD-BSA NPs remained in the tumor for a longer period and displayed better anticancer activity than the effects of GOD alone. GOD-BSA NPs were approximately 240 nm in size and inhibited tumor growth to 40 mm
, whereas tumors treated with phosphate-buffered saline or albumin NPs had sizes of 1673 and 1578 mm
, respectively. GOD-BSA NPs prepared using click chemistry may be useful as a drug delivery system for protein enzymes.</abstract><cop>Netherlands</cop><pmid>37148665</pmid><doi>10.1016/j.colsurfb.2023.113335</doi></addata></record> |
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source | Elsevier ScienceDirect Journals Complete |
title | Click chemistry-based novel albumin nanoparticles for anticancer treatment via H 2 O 2 generation |
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