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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
Main Authors: Wu, Han, Chen, Zuobing, Qi, Shaolong, Bai, Bing, Ye, Jiajun, Wu, Dan, Shen, Jie, Kang, Fei, Yu, Guocan
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container_title Journal of nanobiotechnology
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creator Wu, Han
Chen, Zuobing
Qi, Shaolong
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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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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. 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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 - 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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>
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identifier ISSN: 1477-3155
ispartof Journal of nanobiotechnology, 2021-10, Vol.19 (1), p.330-13, Article 330
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1477-3155
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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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