Affiliations: College of Integrated Traditional Chinese and Western Medicine, Fujian University of Traditional Chinese Medicine, Fuzhou, China | Key Laboratory of Optoelectronic Science and Technology for Medicine, Ministry of Education, Fujian Provincial Key Laboratory of Photonic Technology, Fujian Normal University, Fuzhou, China | Fujian Provincial Cancer Hospital, Fuzhou, China | Fujian Provincial Tumor Hospital, Fuzhou, China
Note: [] Corresponding author: Dr. Shangyuan Feng, Key Laboratory of Optoelectronic Science and Technology for Medicine, Ministry of Education, Fujian Provincial Key Laboratory for Photonics Technology, Fujian Normal University, Fuzhou 350007, China. Tel.: +86 591 83489919; Fax: +86 591 83465373; E-mail: [email protected].
Abstract: The intracellularly-grown-Au-nanoparticles (IGAuNs) technique was employed to analyze the surface-enhanced Raman scattering (SERS) spectra of nasopharyngeal carcinoma cells (CNE-1 cell line). There are only six obvious Raman bands (718, 1001, 1123, 1336, 1446, 1660 cm−1) in the normal Raman spectrum of living CNE-1 cells. However, over twenty SERS Raman bands have been detected in the SERS spectra of IGAuNs-induced cells, among which five bands are of the DNA backbone (673, 1097, 1306, 1336 and 1585 cm−1). There are four vibrations of the DNA backbone (1026, 1097, 1336 and 1585 cm−1) in the SERS spectra of living CNE-1 cells induced by the passive uptake gold nanoparticles (PUAuNS), but one more DNA backbone and many nucleus Raman peaks appeared in the IGAuNs-induced SERS spectra. Many Raman peaks in the PUAuNs-induced SERS spectra are stronger than those in the IGAuNs-induced ones. This study has shown that the PUAuNs technique can achieve stronger Raman signals, and that the IGAuNs technique can enable the gold element to access to the nucleus more easily, which could help to obtain more surface-enhanced Raman signals of the intracellular biochemical molecules. Thus, the two techniques can work together to attain the Raman spectral information of the cytoplasm and the nucleus in a better way, which might provide a sensitive method for broad biomedical applications such as intracellular SERS analysis of living cells.
