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Evaluation of the stability of cucurbit[8]uril-based ternary host-guest complexation in physiological environment and the fabrication of a supramolecular theranostic nanomedicine
Supramolecular theranostics have exhibited promising potentials in disease diagnosis and therapy by taking advantages of the dynamic and reversible nature of non-covalent interactions. It is extremely important to figure out the stability of the driving forces in physiological environment for the pr...
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Published in: | Journal of nanobiotechnology 2021-10, Vol.19 (1), p.330-13, Article 330 |
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creator | Wu, Han Chen, Zuobing Qi, Shaolong Bai, Bing Ye, Jiajun Wu, Dan Shen, Jie Kang, Fei Yu, Guocan |
description | Supramolecular theranostics have exhibited promising potentials in disease diagnosis and therapy by taking advantages of the dynamic and reversible nature of non-covalent interactions. It is extremely important to figure out the stability of the driving forces in physiological environment for the preparation of theranostic systems.
The host-guest complexation between cucurbit[8]uril (CB[8]), 4,4'-bipyridinium, and napththyl guest was fully studied using various characterizations, including nuclear magnetic resonance spectroscopy, ultraviolet-visible (UV-vis) spectroscopy, isothermal titration calorimetry (ITC). The association constants of this ternary complex were determined using isothermal titration calorimetry. The stability of the non-covalent interactions and self-assemblies form from this molecular recognition was confirmed by UV-vis spectroscopy and dynamic light scattering (DLS). A supramolecular nanomedicine was constructed on the basis of this 1:1:1 ternary recognition, and its in vitro and in vivo anticancer efficacy were thoroughly evaluated. Positron emission tomography (PET) imaging was used to monitor the delivery and biodistribution of the supramolecular nanomedicine.
Various experiments confirmed that the ternary complexation between 4,4'-bipyridinium, and napththyl derivative and CB[8] was stable in physiological environment, including phosphate buffered solution and cell culture medium. Supramolecular nanomedicine (SNM@DOX) encapsulating a neutral anticancer drug (doxrubincin, DOX) was prepared based on this molecular recognition that linked the hydrophobic poly(ε-caprolactone) chain and hydrophilic polyethylene glycol segment. The non-covalent interactions guaranteed the stability of SNM@DOX during blood circulation and promoted its tumor accumulation by taking advantage of the enhanced permeability and retention effect, thus greatly improving the anti-tumor efficacy as compared with the free drug.
Arising from the host-enhanced charge-transfer interactions, the CB[8]-based ternary recognition was stable enough in physiological environment, which was suitable for the fabrication of supramolecular nanotheranostics showing promising potentials in precise cancer diagnosis and therapy. |
doi_str_mv | 10.1186/s12951-021-01076-z |
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The host-guest complexation between cucurbit[8]uril (CB[8]), 4,4'-bipyridinium, and napththyl guest was fully studied using various characterizations, including nuclear magnetic resonance spectroscopy, ultraviolet-visible (UV-vis) spectroscopy, isothermal titration calorimetry (ITC). The association constants of this ternary complex were determined using isothermal titration calorimetry. The stability of the non-covalent interactions and self-assemblies form from this molecular recognition was confirmed by UV-vis spectroscopy and dynamic light scattering (DLS). A supramolecular nanomedicine was constructed on the basis of this 1:1:1 ternary recognition, and its in vitro and in vivo anticancer efficacy were thoroughly evaluated. Positron emission tomography (PET) imaging was used to monitor the delivery and biodistribution of the supramolecular nanomedicine.
Various experiments confirmed that the ternary complexation between 4,4'-bipyridinium, and napththyl derivative and CB[8] was stable in physiological environment, including phosphate buffered solution and cell culture medium. Supramolecular nanomedicine (SNM@DOX) encapsulating a neutral anticancer drug (doxrubincin, DOX) was prepared based on this molecular recognition that linked the hydrophobic poly(ε-caprolactone) chain and hydrophilic polyethylene glycol segment. The non-covalent interactions guaranteed the stability of SNM@DOX during blood circulation and promoted its tumor accumulation by taking advantage of the enhanced permeability and retention effect, thus greatly improving the anti-tumor efficacy as compared with the free drug.
Arising from the host-enhanced charge-transfer interactions, the CB[8]-based ternary recognition was stable enough in physiological environment, which was suitable for the fabrication of supramolecular nanotheranostics showing promising potentials in precise cancer diagnosis and therapy.</description><identifier>ISSN: 1477-3155</identifier><identifier>EISSN: 1477-3155</identifier><identifier>DOI: 10.1186/s12951-021-01076-z</identifier><identifier>PMID: 34670552</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Animals ; Antibiotics, Antineoplastic - chemistry ; Antibiotics, Antineoplastic - pharmacokinetics ; Anticancer properties ; Antitumor agents ; Aqueous solutions ; Blood circulation ; Bridged-Ring Compounds - chemistry ; Bridged-Ring Compounds - pharmacokinetics ; Bridged-Ring Compounds - toxicity ; Calorimetry ; Cancer ; Caproates - chemistry ; Cell culture ; Charge transfer ; Chemical properties ; Chemotherapy ; Complexation ; Covalence ; Diagnosis ; Doxorubicin - chemistry ; Doxorubicin - pharmacokinetics ; Drug delivery ; Drug Delivery Systems - methods ; Drug Stability ; Emission analysis ; Fabrication ; Female ; Health aspects ; Heat measurement ; Hep G2 Cells ; Host–guest molecular recognition ; Humans ; Hydrophobicity ; Imidazoles - chemistry ; Imidazoles - pharmacokinetics ; Imidazoles - toxicity ; Lactones - chemistry ; Light scattering ; Macrocycles ; Magnetic resonance spectroscopy ; Medical research ; Medicine, Experimental ; Mice ; Mice, Nude ; Microscopy ; Nanomedicine ; Nanoparticles ; Nanotechnology ; NMR ; NMR spectroscopy ; Nuclear magnetic resonance ; Peptides ; Permeability ; Photon correlation spectroscopy ; Physiology ; Polycaprolactone ; Polyethylene glycol ; Polyethylene terephthalate ; Positron emission tomography ; Precision medicine ; Production processes ; Recognition ; Spectroscopy ; Spectrum Analysis ; Stability analysis ; Supramolecular chemistry ; Theranostic Nanomedicine - methods ; Tissue Distribution ; Titration ; Titration calorimetry ; Tumors ; Xenograft Model Antitumor Assays</subject><ispartof>Journal of nanobiotechnology, 2021-10, Vol.19 (1), p.330-13, Article 330</ispartof><rights>2021. The Author(s).</rights><rights>COPYRIGHT 2021 BioMed Central Ltd.</rights><rights>2021. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c597t-672b26fc5a8301a5a17983b4df25c72747ffb4415ff6271cd6d76e8b75fb2ce03</citedby><cites>FETCH-LOGICAL-c597t-672b26fc5a8301a5a17983b4df25c72747ffb4415ff6271cd6d76e8b75fb2ce03</cites><orcidid>0000-0003-1157-4184</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8529793/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2599097881?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25732,27903,27904,36991,44569,53769,53771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34670552$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wu, Han</creatorcontrib><creatorcontrib>Chen, Zuobing</creatorcontrib><creatorcontrib>Qi, Shaolong</creatorcontrib><creatorcontrib>Bai, Bing</creatorcontrib><creatorcontrib>Ye, Jiajun</creatorcontrib><creatorcontrib>Wu, Dan</creatorcontrib><creatorcontrib>Shen, Jie</creatorcontrib><creatorcontrib>Kang, Fei</creatorcontrib><creatorcontrib>Yu, Guocan</creatorcontrib><title>Evaluation of the stability of cucurbit[8]uril-based ternary host-guest complexation in physiological environment and the fabrication of a supramolecular theranostic nanomedicine</title><title>Journal of nanobiotechnology</title><addtitle>J Nanobiotechnology</addtitle><description>Supramolecular theranostics have exhibited promising potentials in disease diagnosis and therapy by taking advantages of the dynamic and reversible nature of non-covalent interactions. It is extremely important to figure out the stability of the driving forces in physiological environment for the preparation of theranostic systems.
The host-guest complexation between cucurbit[8]uril (CB[8]), 4,4'-bipyridinium, and napththyl guest was fully studied using various characterizations, including nuclear magnetic resonance spectroscopy, ultraviolet-visible (UV-vis) spectroscopy, isothermal titration calorimetry (ITC). The association constants of this ternary complex were determined using isothermal titration calorimetry. The stability of the non-covalent interactions and self-assemblies form from this molecular recognition was confirmed by UV-vis spectroscopy and dynamic light scattering (DLS). A supramolecular nanomedicine was constructed on the basis of this 1:1:1 ternary recognition, and its in vitro and in vivo anticancer efficacy were thoroughly evaluated. Positron emission tomography (PET) imaging was used to monitor the delivery and biodistribution of the supramolecular nanomedicine.
Various experiments confirmed that the ternary complexation between 4,4'-bipyridinium, and napththyl derivative and CB[8] was stable in physiological environment, including phosphate buffered solution and cell culture medium. Supramolecular nanomedicine (SNM@DOX) encapsulating a neutral anticancer drug (doxrubincin, DOX) was prepared based on this molecular recognition that linked the hydrophobic poly(ε-caprolactone) chain and hydrophilic polyethylene glycol segment. The non-covalent interactions guaranteed the stability of SNM@DOX during blood circulation and promoted its tumor accumulation by taking advantage of the enhanced permeability and retention effect, thus greatly improving the anti-tumor efficacy as compared with the free drug.
Arising from the host-enhanced charge-transfer interactions, the CB[8]-based ternary recognition was stable enough in physiological environment, which was suitable for the fabrication of supramolecular nanotheranostics showing promising potentials in precise cancer diagnosis and therapy.</description><subject>Animals</subject><subject>Antibiotics, Antineoplastic - chemistry</subject><subject>Antibiotics, Antineoplastic - pharmacokinetics</subject><subject>Anticancer properties</subject><subject>Antitumor agents</subject><subject>Aqueous solutions</subject><subject>Blood circulation</subject><subject>Bridged-Ring Compounds - chemistry</subject><subject>Bridged-Ring Compounds - pharmacokinetics</subject><subject>Bridged-Ring Compounds - toxicity</subject><subject>Calorimetry</subject><subject>Cancer</subject><subject>Caproates - chemistry</subject><subject>Cell culture</subject><subject>Charge transfer</subject><subject>Chemical properties</subject><subject>Chemotherapy</subject><subject>Complexation</subject><subject>Covalence</subject><subject>Diagnosis</subject><subject>Doxorubicin - chemistry</subject><subject>Doxorubicin - pharmacokinetics</subject><subject>Drug delivery</subject><subject>Drug Delivery Systems - methods</subject><subject>Drug Stability</subject><subject>Emission analysis</subject><subject>Fabrication</subject><subject>Female</subject><subject>Health aspects</subject><subject>Heat measurement</subject><subject>Hep G2 Cells</subject><subject>Host–guest molecular recognition</subject><subject>Humans</subject><subject>Hydrophobicity</subject><subject>Imidazoles - chemistry</subject><subject>Imidazoles - pharmacokinetics</subject><subject>Imidazoles - toxicity</subject><subject>Lactones - chemistry</subject><subject>Light scattering</subject><subject>Macrocycles</subject><subject>Magnetic resonance spectroscopy</subject><subject>Medical research</subject><subject>Medicine, Experimental</subject><subject>Mice</subject><subject>Mice, Nude</subject><subject>Microscopy</subject><subject>Nanomedicine</subject><subject>Nanoparticles</subject><subject>Nanotechnology</subject><subject>NMR</subject><subject>NMR spectroscopy</subject><subject>Nuclear magnetic resonance</subject><subject>Peptides</subject><subject>Permeability</subject><subject>Photon correlation spectroscopy</subject><subject>Physiology</subject><subject>Polycaprolactone</subject><subject>Polyethylene glycol</subject><subject>Polyethylene terephthalate</subject><subject>Positron emission tomography</subject><subject>Precision medicine</subject><subject>Production processes</subject><subject>Recognition</subject><subject>Spectroscopy</subject><subject>Spectrum Analysis</subject><subject>Stability analysis</subject><subject>Supramolecular chemistry</subject><subject>Theranostic Nanomedicine - methods</subject><subject>Tissue Distribution</subject><subject>Titration</subject><subject>Titration calorimetry</subject><subject>Tumors</subject><subject>Xenograft Model Antitumor Assays</subject><issn>1477-3155</issn><issn>1477-3155</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptUltrFDEUHkSxtfoHfJABn3yYOslMLvMilFJ1oSB4eRIJZzLJbJZMsiaZpduf5S80u9vWLkg45HDyne9c8hXFa1SfI8Tp-4hwR1BV42yoZrS6fVKcopaxqkGEPH3knxQvYlzVNcYtbp8XJ01LWU0IPi3-XG3AzpCMd6XXZVqqMibojTVpuwvIWc6hN-kn_zUHY6seohrKpIKDsC2XPqZqnFVMpfTT2qqbA5Nx5Xq5jcZbPxoJtlRuY4J3k3KpBDfs62joQ368Lw1lnNcBJm-VnC2EHSaAyxWMLF12JjUYaZx6WTzTYKN6dXefFT8-Xn2__Fxdf_m0uLy4riTpWKoowz2mWhLgTY2AAGIdb_p20JhIhlnLtO7bFhGtKWZIDnRgVPGeEd1jqermrFgceAcPK7EOZsojCw9G7AM-jAJCbs4qAV0PdKBA25q2FDQfVDbeNEw3vKU0c304cK3nPs8h8x4C2CPS4xdnlmL0G8EJ7ljXZIK3dwTB_94tXKz8nD_BRoFJ19Ud4xz9Q42QuzJO-0wmJxOluKAc0YazhmXU-X9Q-QxqMtI7pU2OHyW8O0rImKRu0ghzjGLx7esxFh-wMvgYg9IPQ6Ja7GQrDrIVWbZiL1txm5PePF7PQ8q9Tpu_OsbtKg</recordid><startdate>20211020</startdate><enddate>20211020</enddate><creator>Wu, Han</creator><creator>Chen, Zuobing</creator><creator>Qi, Shaolong</creator><creator>Bai, Bing</creator><creator>Ye, Jiajun</creator><creator>Wu, Dan</creator><creator>Shen, Jie</creator><creator>Kang, Fei</creator><creator>Yu, Guocan</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</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>ISR</scope><scope>3V.</scope><scope>7QO</scope><scope>7TB</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>P64</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-1157-4184</orcidid></search><sort><creationdate>20211020</creationdate><title>Evaluation of the stability of cucurbit[8]uril-based ternary host-guest complexation in physiological environment and the fabrication of a supramolecular theranostic nanomedicine</title><author>Wu, Han ; Chen, Zuobing ; Qi, Shaolong ; Bai, Bing ; Ye, Jiajun ; Wu, Dan ; Shen, Jie ; Kang, Fei ; Yu, Guocan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c597t-672b26fc5a8301a5a17983b4df25c72747ffb4415ff6271cd6d76e8b75fb2ce03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Animals</topic><topic>Antibiotics, Antineoplastic - chemistry</topic><topic>Antibiotics, Antineoplastic - pharmacokinetics</topic><topic>Anticancer properties</topic><topic>Antitumor agents</topic><topic>Aqueous solutions</topic><topic>Blood circulation</topic><topic>Bridged-Ring Compounds - chemistry</topic><topic>Bridged-Ring Compounds - pharmacokinetics</topic><topic>Bridged-Ring Compounds - toxicity</topic><topic>Calorimetry</topic><topic>Cancer</topic><topic>Caproates - chemistry</topic><topic>Cell culture</topic><topic>Charge transfer</topic><topic>Chemical properties</topic><topic>Chemotherapy</topic><topic>Complexation</topic><topic>Covalence</topic><topic>Diagnosis</topic><topic>Doxorubicin - chemistry</topic><topic>Doxorubicin - pharmacokinetics</topic><topic>Drug delivery</topic><topic>Drug Delivery Systems - methods</topic><topic>Drug Stability</topic><topic>Emission analysis</topic><topic>Fabrication</topic><topic>Female</topic><topic>Health aspects</topic><topic>Heat measurement</topic><topic>Hep G2 Cells</topic><topic>Host–guest molecular recognition</topic><topic>Humans</topic><topic>Hydrophobicity</topic><topic>Imidazoles - chemistry</topic><topic>Imidazoles - pharmacokinetics</topic><topic>Imidazoles - toxicity</topic><topic>Lactones - chemistry</topic><topic>Light scattering</topic><topic>Macrocycles</topic><topic>Magnetic resonance spectroscopy</topic><topic>Medical research</topic><topic>Medicine, Experimental</topic><topic>Mice</topic><topic>Mice, Nude</topic><topic>Microscopy</topic><topic>Nanomedicine</topic><topic>Nanoparticles</topic><topic>Nanotechnology</topic><topic>NMR</topic><topic>NMR spectroscopy</topic><topic>Nuclear magnetic resonance</topic><topic>Peptides</topic><topic>Permeability</topic><topic>Photon correlation spectroscopy</topic><topic>Physiology</topic><topic>Polycaprolactone</topic><topic>Polyethylene glycol</topic><topic>Polyethylene terephthalate</topic><topic>Positron emission tomography</topic><topic>Precision medicine</topic><topic>Production processes</topic><topic>Recognition</topic><topic>Spectroscopy</topic><topic>Spectrum Analysis</topic><topic>Stability analysis</topic><topic>Supramolecular chemistry</topic><topic>Theranostic Nanomedicine - methods</topic><topic>Tissue Distribution</topic><topic>Titration</topic><topic>Titration calorimetry</topic><topic>Tumors</topic><topic>Xenograft Model Antitumor Assays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Han</creatorcontrib><creatorcontrib>Chen, Zuobing</creatorcontrib><creatorcontrib>Qi, Shaolong</creatorcontrib><creatorcontrib>Bai, Bing</creatorcontrib><creatorcontrib>Ye, Jiajun</creatorcontrib><creatorcontrib>Wu, Dan</creatorcontrib><creatorcontrib>Shen, Jie</creatorcontrib><creatorcontrib>Kang, Fei</creatorcontrib><creatorcontrib>Yu, Guocan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale in Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Health & Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Materials Science Database</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Materials science collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of nanobiotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Han</au><au>Chen, Zuobing</au><au>Qi, Shaolong</au><au>Bai, Bing</au><au>Ye, Jiajun</au><au>Wu, Dan</au><au>Shen, Jie</au><au>Kang, Fei</au><au>Yu, Guocan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of the stability of cucurbit[8]uril-based ternary host-guest complexation in physiological environment and the fabrication of a supramolecular theranostic nanomedicine</atitle><jtitle>Journal of nanobiotechnology</jtitle><addtitle>J Nanobiotechnology</addtitle><date>2021-10-20</date><risdate>2021</risdate><volume>19</volume><issue>1</issue><spage>330</spage><epage>13</epage><pages>330-13</pages><artnum>330</artnum><issn>1477-3155</issn><eissn>1477-3155</eissn><abstract>Supramolecular theranostics have exhibited promising potentials in disease diagnosis and therapy by taking advantages of the dynamic and reversible nature of non-covalent interactions. It is extremely important to figure out the stability of the driving forces in physiological environment for the preparation of theranostic systems.
The host-guest complexation between cucurbit[8]uril (CB[8]), 4,4'-bipyridinium, and napththyl guest was fully studied using various characterizations, including nuclear magnetic resonance spectroscopy, ultraviolet-visible (UV-vis) spectroscopy, isothermal titration calorimetry (ITC). The association constants of this ternary complex were determined using isothermal titration calorimetry. The stability of the non-covalent interactions and self-assemblies form from this molecular recognition was confirmed by UV-vis spectroscopy and dynamic light scattering (DLS). A supramolecular nanomedicine was constructed on the basis of this 1:1:1 ternary recognition, and its in vitro and in vivo anticancer efficacy were thoroughly evaluated. Positron emission tomography (PET) imaging was used to monitor the delivery and biodistribution of the supramolecular nanomedicine.
Various experiments confirmed that the ternary complexation between 4,4'-bipyridinium, and napththyl derivative and CB[8] was stable in physiological environment, including phosphate buffered solution and cell culture medium. Supramolecular nanomedicine (SNM@DOX) encapsulating a neutral anticancer drug (doxrubincin, DOX) was prepared based on this molecular recognition that linked the hydrophobic poly(ε-caprolactone) chain and hydrophilic polyethylene glycol segment. The non-covalent interactions guaranteed the stability of SNM@DOX during blood circulation and promoted its tumor accumulation by taking advantage of the enhanced permeability and retention effect, thus greatly improving the anti-tumor efficacy as compared with the free drug.
Arising from the host-enhanced charge-transfer interactions, the CB[8]-based ternary recognition was stable enough in physiological environment, which was suitable for the fabrication of supramolecular nanotheranostics showing promising potentials in precise cancer diagnosis and therapy.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>34670552</pmid><doi>10.1186/s12951-021-01076-z</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0003-1157-4184</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1477-3155 |
ispartof | Journal of nanobiotechnology, 2021-10, Vol.19 (1), p.330-13, Article 330 |
issn | 1477-3155 1477-3155 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_a9ba6d6a640646af8def8d8337f38466 |
source | Open Access: PubMed Central; Publicly Available Content Database |
subjects | Animals Antibiotics, Antineoplastic - chemistry Antibiotics, Antineoplastic - pharmacokinetics Anticancer properties Antitumor agents Aqueous solutions Blood circulation Bridged-Ring Compounds - chemistry Bridged-Ring Compounds - pharmacokinetics Bridged-Ring Compounds - toxicity Calorimetry Cancer Caproates - chemistry Cell culture Charge transfer Chemical properties Chemotherapy Complexation Covalence Diagnosis Doxorubicin - chemistry Doxorubicin - pharmacokinetics Drug delivery Drug Delivery Systems - methods Drug Stability Emission analysis Fabrication Female Health aspects Heat measurement Hep G2 Cells Host–guest molecular recognition Humans Hydrophobicity Imidazoles - chemistry Imidazoles - pharmacokinetics Imidazoles - toxicity Lactones - chemistry Light scattering Macrocycles Magnetic resonance spectroscopy Medical research Medicine, Experimental Mice Mice, Nude Microscopy Nanomedicine Nanoparticles Nanotechnology NMR NMR spectroscopy Nuclear magnetic resonance Peptides Permeability Photon correlation spectroscopy Physiology Polycaprolactone Polyethylene glycol Polyethylene terephthalate Positron emission tomography Precision medicine Production processes Recognition Spectroscopy Spectrum Analysis Stability analysis Supramolecular chemistry Theranostic Nanomedicine - methods Tissue Distribution Titration Titration calorimetry Tumors Xenograft Model Antitumor Assays |
title | Evaluation of the stability of cucurbit[8]uril-based ternary host-guest complexation in physiological environment and the fabrication of a supramolecular theranostic nanomedicine |
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