Abstract
A glucopyranose functionalized star-shaped oligomer, N-tris{4,4',4"- [(1E)-2-(2-{(E)-2-[4-(benzo[d]thiazol-2-yl)phenyl]vinyl}-9,9-bis(6-2-amido-2- deoxy-1-thio-β-D-glucopyranose-hexyl)-9H-fluoren-7-yl)vinyl]phenyl} phenylamine (TVFVBN-S-NH2), is synthesized for two-photon fluorescence imaging. In water, TVFVBN-S-NH2 self-assembles into nanoparticles with an average diameter of ∼49 nm and shows a fluorescence quantum yield of 0.21. Two-photon fluorescence measurements reveal that TVFVBN-S-NH2 has a two-photon absorption cross-section of ∼1100 GM at 780 nm in water. The active amine group on the glucopyranose moiety allows further functionalization of TVFVBN-S-NH2 with folic acid to yield TVFVBN-S-NH2FA with similar optical and physical properties as those for TVFVBN-S-NH2. Cellular imaging studies reveal that TVFVBN-S-NH2FA has increased uptake by MCF-7 cells relative to that for TVFVBN-S-NH2, due to specific interactions between folic acid and folate receptors on the MCF-7 cell membrane. This study demonstrates the effectiveness of glycosylation as a molecular engineering strategy to yield water-soluble materials with a large two-photon absorption (TPA) cross-section for targeted cancer-cell imaging. Biological imaging: A star-shaped two-photon absorbing material (see scheme) with folic acid functionalization has been synthesized for targeted two-photon fluorescence imaging of MCF-7 cancer cells.
Original language | English |
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Pages (from-to) | 9705-9713 |
Number of pages | 9 |
Journal | Chemistry - A European Journal |
Volume | 18 |
Issue number | 31 |
DOIs | |
Publication status | Published - Jul 27 2012 |
Externally published | Yes |
ASJC Scopus Subject Areas
- Catalysis
- General Chemistry
- Organic Chemistry
Keywords
- fluorescence
- glucopyranose
- oligomers
- self-assembly
- targeted imaging