ABSTRACT
There is a continued interest in the development of new on-chip protocols for the determination of the causes of infectious disease. In this paper, we demonstrate the use of surface-enhanced resonance Raman scattering (SERRS) for detecting the clinically relevant nucleic acid sequences of Chlamydia trachomatis in a bead-based lab-on-a-chip format, incorporating a solid-phase sample clean-up on-chip. The assay uses streptavidinated polymer microspheres to capture a biotinylated PCR product of the oligonucleotide sequence, which was subsequently hybridized against a complementary rhodamine-labeled, Raman active probe. Central to the assay is an in-channel integrated microfilter, which was used to retain the microspheres, enabling the bound target to be separated from the rest of the sample as part of a solid-phase clean-up (thereby removing any contributions from the background). After washing, the bound Rhodamine labeled detection probe was released thermally from the microspheres by heating and was subsequently mixed on-chip with a stream of silver nanoparticles. The signal was detected downstream using a Raman spectrometer to collect the SERRS response. The assay offers several advantages over traditional laboratory methods, including: the speed of the assay on-chip, the potential for sample clean-up; and the low volume of sample required.
Subject(s)
Chlamydia trachomatis/chemistry , DNA/analysis , Nanoparticles/chemistry , Oligonucleotide Array Sequence Analysis/methods , Spectrum Analysis, Raman/methods , Streptavidin/chemistry , Base Sequence , Equipment Design , Polymerase Chain Reaction/methods , Sensitivity and Specificity , Silver/chemistry , Surface PropertiesABSTRACT
Silica particles were partially coated with silver, and a suitable chromophore, such that they could be simultaneously trapped within an optical tweezers system, and emit a surface-enhanced resonance Raman scattering (SERRS) response. A standard 1064 nm TEM00 mode laser was used to trap the bead whilst a frequency doubling crystal inserted into the beam gave several microwatts of 532 nm co-linear light to excite the SERRS emission. The con fi guration has clear applications in providing apparatus that can simultaneously manipulate a particle whilst obtaining surface sensitive sensory information.
ABSTRACT
Remote nanoparticle detection is required for the development of in situ biological probes. Here we describe the labelling of silver nanoparticles to produce multiply coded particles which can be detected by surface enhanced resonance Raman scattering (SERRS). There is a potential for thousands of codes to be written and read without the need for spatial resolution of components of the code. The use of these systems in bioanlaysis and in situ detection is discussed.
Subject(s)
Microspheres , Oligonucleotides/chemistry , Buffers , Colloids , DNA Primers , Fluorescent Dyes , Scattering, Radiation , Spectrum Analysis, RamanABSTRACT
The first simultaneous detection of three dye-labelled oligonucleotides in a microfluidics chip by SERRS is reported.
