Characterization of Locally Excited and Charge-Transfer States of the Anticancer Drug Lapatinib by Ultrafast Spectroscopy and Computational Studies.

Fecha de publicación: Fecha Ahead of Print:

Autores de IIS La Fe

Participantes ajenos a IIS La Fe

  • Lence E
  • González-Bello C
  • Navarrete-Miguel M
  • Roca-Sanjuán D

Grupos

Abstract

Lapatinib (LAP) is an anticancer drug, which is metabolized to the N- and O-dealkylated products (N-LAP and O-LAP, respectively). In view of the photosensitizing potential of related drugs, a complete experimental and theoretical study has been performed on LAP, N-LAP and O-LAP, both in solution and upon complexation with human serum albumin (HSA). In organic solvents, coplanar locally excited (LE) emissive states are generated; they rapidly evolve towards twisted intramolecular charge-transfer (ICT) states. By contrast, within HSA only LE states are detected. Accordingly, femtosecond transient absorption reveals a very fast switching (ca. 2 ps) from LE (? max =550 nm) to ICT states (? max =480 nm) in solution, whereas within HSA the LE species become stabilized and live much longer (up to the ns scale). Interestingly, molecular dynamics simulation studies confirm that the coplanar orientation is preferred for LAP (or to a lesser extent N-LAP) within HSA, explaining the experimental results.

Datos de la publicación

ISSN/ISSNe:
0947-6539, 1521-3765

CHEMISTRY-A EUROPEAN JOURNAL  WILEY-V C H VERLAG GMBH

Tipo:
Article
Páginas:
15922-15930
Factor de Impacto:
1,687 SCImago
Cuartil:
Q1 SCImago

Citas Recibidas en Web of Science: 11

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Keywords

  • anticancer drugs, femtosecond transient absorption, fluorescence, lapatinib, molecular dynamics simulations

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Investigador Principal: MIGUEL ÁNGEL MIRANDA ALONSO

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