posted on 2016-06-10, 00:00authored bySudeshna
Das Chakraborty, Abhishek Sau, Denis V. Kuznetsov, Amrita Banerjee, Munmun Bardhan, Maireyee Bhattacharya, Dipak Dasgupta, Samita Basu, Dulal Senapati
Triplet–triplet (T–T)
absorption spectroscopy has
been used successfully as a molecular ruler to understand the actual
release process of sanguinarine as a drug molecule from a gold nanoparticle
surface in the presence of cell components, that is, DNA and chromatin.
The obtained results have been verified by fluorescence and surface-enhanced
Raman spectroscopy (SERS), and a plausible explanation has been put
forward to describe the underestimation and overestimation of the
percentage (%) of the release of drug molecules measured by fluorescence-
and SERS-based techniques, respectively, over the highlighted T–T
absorption spectroscopy. Because of the intrinsic nature of absorption,
the reported T–T absorption spectroscopic assay overpowers
fluorescence- and SERS-based assays, which are limited by the long-range
interaction and nonlinear dependence of the concentration of analytes,
respectively.