In spite of the fact that the original Raman microscope was designed in the early 1970's for Raman imaging,
wide-spread practical use of the technology did not appear until the last 5 years. The instruments are smaller,
faster, easier-to-use, promoting reports of a variety of interesting applications in fields as diverse as
nanomaterials, pharmaceuticals, composites, semiconductors, bio-clinical studies, polymers, ceramics and
glasses. While the information content in Raman analysis is quite high, the time to acquire an image has been
a deterrent to its application. Recent innovations including Swift and DUO Scan have addressed and are
addressing these issues. SWIFT (Scanning with Incredibly Fast Times) is a rapid CCD read-out technique
that is based on the synchronization between the XY motion of the motorized or piezo stage and the CCD
readout. DUO scanning uses a set of scanning mirrors above the microscope objective to raster rapidly the
laser beam across a sample area. This can be used to create a "giant pixel" in the map without compromising
the NA of the light collection, or to create a map with step sizes as small as 10nm. Swift, in combination with
DUO scan, as been used to produce full spectral maps of pharmaceutical tablets in times as short as 10
minutes, something that was previously believed to be near impossible. Off-line analysis of such a map using
multivariate techniques produces Raman images indicating the quality of component mixing, and also the
presence of minor, difficult-to-detect components (such as Mgstearate in pharmaceutical tablets).
KEYWORDS: Raman spectroscopy, Data processing, Smoothing, Seaborgium, Hyperspectral imaging, Raman scattering, Chemical analysis, Data acquisition, Charge-coupled devices, Chemical compounds
Raman maps, when acquired and processed successfully, produce Raman chemical images, which provide detailed
information on the spatial distribution and morphology of individual chemical species in samples. The advantages of
Raman chemical images are most significant when the sample is chemically and structurally complicated. In
pharmaceutical applications, these Raman chemical images can be used to understand and develop drug formulations,
drug delivery mechanisms, and drug-cellular interactions. Studies using Raman hyperspectral imaging - the term that
encompasses the entire procedure from data measurement to processing and interpretation - is increasing and gaining a
wider acceptance due to recent improvements in Raman instrumentation and software.
Since Raman maps are a collection of numerous Raman spectra of different chemical species, within a single data set,
spectral characteristics such as the scattering strength, fluorescence level, and baselines vary a great deal. To acquire and
process a Raman map successfully, this heterogeneity must be taken into the consideration. This paper will show the
impact of signal-to-noise ratio (S/N) on data processing strategies and their results. It will be demonstrated that the S/N
of original data is critical for good classification and scientifically meaningful results regardless of the processing
strategies.
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