2022
DOI: 10.1007/s00249-022-01597-x
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Interceptor potential of C60 fullerene aqueous solution: a comparative analysis using the example of the antitumor antibiotic mitoxantrone

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Cited by 2 publications
(5 citation statements)
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“…Inspection of the calculated parameters in Table evidences their general compliance with the complexation parameters reported before for other related drug molecules with C 60 fullerene. ,, For instance, the relation K h1 > K h2 noted previously for various ligands (see refs , for details) also holds for the TPT-C 60 case indicating the predominance of the stacking-type complexation over the adsorption into clusters. The double inequality ε h2 > ε m > ε h1 previously reported for doxorubicin and proflavine, appears to be valid for the TPT case as well.…”
Section: Resultssupporting
confidence: 77%
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“…Inspection of the calculated parameters in Table evidences their general compliance with the complexation parameters reported before for other related drug molecules with C 60 fullerene. ,, For instance, the relation K h1 > K h2 noted previously for various ligands (see refs , for details) also holds for the TPT-C 60 case indicating the predominance of the stacking-type complexation over the adsorption into clusters. The double inequality ε h2 > ε m > ε h1 previously reported for doxorubicin and proflavine, appears to be valid for the TPT case as well.…”
Section: Resultssupporting
confidence: 77%
“…The titration curve was fitted according to the procedure thoroughly described in ref using the “upscaled” model briefly described in Appendix A. The fitting curve (blue line in Figure B) agrees well with the experimental data (red dots in Figure B) and complies with the values of equilibrium parameters of complexation, calculated in this work and outlined in Table .…”
Section: Resultssupporting
confidence: 71%
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