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1.
Anal Chem ; 96(17): 6643-6651, 2024 Apr 30.
Article de Anglais | MEDLINE | ID: mdl-38626411

RÉSUMÉ

Visualizing the distribution of small-molecule drugs in living cells is an important strategy for developing specific, effective, and minimally toxic drugs. As an alternative to fluorescence imaging using bulky fluorophores or cell fixation, stimulated Raman scattering (SRS) imaging combined with bisarylbutadiyne (BADY) tagging enables the observation of small molecules closer to their native intracellular state. However, there is evidence that the physicochemical properties of BADY-tagged analogues of small-molecule drugs differ significantly from those of their parent drugs, potentially affecting their intracellular distribution. Herein, we developed a modified BADY to reduce deviations in physicochemical properties (in particular, lipophilicity and membrane permeability) between tagged and parent drugs, while maintaining high Raman activity in live-cell SRS imaging. We highlight the practical application of this approach by revealing the nuclear distribution of a modified BADY-tagged analogue of JQ1, a bromodomain and extra-terminal motif inhibitor with applications in targeted cancer therapy, in living HeLa cells. The modified BADY, methoxypyridazyl pyrimidyl butadiyne (MPDY), revealed intranuclear JQ1, while BADY-tagged JQ1 did not show a clear nuclear signal. We anticipate that the present approach combining MPDY tagging with live-cell SRS imaging provides important insight into the behavior of intracellular drugs and represents a promising avenue for improving drug development.


Sujet(s)
Noyau de la cellule , Humains , Cellules HeLa , Noyau de la cellule/composition chimique , Noyau de la cellule/métabolisme , Microscopie optique non linéaire/méthodes , Alcynes/composition chimique , Analyse spectrale Raman/méthodes , Bibliothèques de petites molécules/composition chimique , Bibliothèques de petites molécules/pharmacologie
2.
Nanoscale ; 5(23): 11755-60, 2013 Dec 07.
Article de Anglais | MEDLINE | ID: mdl-24121541

RÉSUMÉ

Sc3N@C80 fullerenes are inserted inside carbon nanotubes (CNTs). The results show that the thermal stability of Sc3N@C80 fullerenes is around 1200 °C for the fullerenes resting on the wall of CNTs. Internal fullerenes show stability up to 1300 °C, which portrays them as one of most stable types of fullerenes. Electron irradiation of the peapods at 90 kV leads to the formation of capsules inside the CNTs at 5 × 10(9) e nm(-2) electron dosage. This value is an order of magnitude higher than the threshold of electron-induced damage in C60 molecules. Electron energy loss spectroscopy confirms the presence of Sc atoms in capsules. Encapsulation of fullerenes and capsule formation changes the oxidation state of Sc atoms from +2.5 towards +3. This is an evidence of charge transfer between the fullerene/capsule cage and CNT walls.

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