@article {1628,
	title = {On-line content uniformity determination of tablets using low-resolution Raman spectroscopy},
	journal = {Applied Spectroscopy},
	volume = {60},
	number = {6},
	year = {2006},
	note = {ISI Document Delivery No.: 055FDTimes Cited: 5Cited Reference Count: 31},
	month = {Jun},
	pages = {672-681},
	type = {Article},
	abstract = {Analytical techniques for rapid and nondestructive content uniformity determination of pharmaceutical solid dosage forms have been studied for several years in an effort to replace the traditional wet chemistry procedures, which are labor intensive and time consuming. Both Raman spectroscopy and near-infrared spectroscopy have been used for this purpose, and predictability errors are approaching those of the traditional techniques. In this study, a low-resolution Raman spectrometer was utilized to demonstrate the feasibility of both rapid at-line and on-line determination of tablet content uniformity. Additionally, sampling statistics were reviewed in an effort to determine how many tablets should be assayed for specific. batch sizes. A good correlation was observed between assay values determined by high-performance liquid chromatography and Raman analysis. Due. to rapid acquisition times for the Raman data, it was possible to analyze far more samples than with wet chemistry methods, leading to a better statistical description of variation within the batch. For at-line experiments, the sampling volume was increased by rotating the laser beam during the acquisition period. For the on-line experiments, the sampling volume was increased by sampling from a stream of tablets moving underneath the Raman probe on a conveyor system. Finally, an approach is proposed for monitoring content uniformity immediately following the compaction process. In conclusion, Raman spectroscopy has potential as a rapid, nondestructive technique for at- or on-line determination of tablet content uniformity.},
	keywords = {ACTIVE-SUBSTANCE, central limit theorem, COATED TABLETS, content uniformity, FORMS, INTACT TABLETS, NEAR-INFRARED SPECTROSCOPY, PARACETAMOL, process analytical technology, Raman spectroscopy, sampling, SPECTRA, STATE, TRANSMITTANCE SPECTROSCOPY},
	isbn = {0003-7028},
	url = {<Go to ISI>://000238434500013},
	author = {Wikstrom, H. and Romero-Torres, S. and Wongweragiat, S. and Williams, J. A. S. and Grant, E. R. and Taylor, L. S.}
}
@article {1630,
	title = {Plastic separation planning for end-of-life electronics},
	journal = {Ieee Transactions on Electronics Packaging Manufacturing},
	volume = {29},
	number = {2},
	year = {2006},
	note = {ISI Document Delivery No.: 046PLTimes Cited: 3Cited Reference Count: 34},
	month = {Apr},
	pages = {110-118},
	type = {Article},
	abstract = {Important challenges remain for sustainable design, manufacture, use, and recycling of electronics including materials selection and disassembly time. This paper examines the value relationship between the quantity of plastics separated and the time required for disassembly and segregation. Labor,costs for disassembly can constitute a large portion of the total acquisition cost for a recycled material. We report work measurement studies conducted on the disassembly of 21 computers, 22 printers, and 32 monitors manufactured by 27 producers in the years from 1984 to 2001. Results include the weight per total separation time for each plastic part. Each recovered part is identified according to polymer resin using laser Raman spectroscopy by chemometric reference to a library of standards. We extrapolate time as well as the product input required to accumulate various specific types of plastic. We develop disassembly policies and show that they are effective for a variety of computer, printer, or monitor models, which is typical of the random product streams that arrive at electronics recycling facilities. The results demonstrate how new laser identification tech- nology and work measurement can be used for plastics separation planning.},
	keywords = {DESIGN, disassembly, electronics recycling, measurement, plastics, Raman spectroscopy, work},
	isbn = {1521-334X},
	url = {<Go to ISI>://000237823400006},
	author = {Williams, J. A. S. and Grant, E. R. and Rios, P. and Blyler, L. and Tieman, L. and Twining, L. and Bonawi-Tan, W. and Madden, M. and Guthrie, N. R. M.}
}
@article {1530,
	title = {Raman spectroscopy for tablet coating thickness quantification and coating characterization in the presence of strong fluorescent interference},
	journal = {Journal of Pharmaceutical and Biomedical Analysis},
	volume = {41},
	number = {3},
	year = {2006},
	note = {ISI Document Delivery No.: 051CCTimes Cited: 22Cited Reference Count: 27},
	month = {Jun},
	pages = {811-819},
	type = {Article},
	abstract = {We report a novel approach to the measurement of colored tablet coating thickness, which employs Raman spectroscopy with univariate and multivariate data analysis. Our results suggest that Raman sensing can serve as a viable non-invasive means to quantify tablet coating thickness in the presence of a fluorescent ingredient in the coating formulation (food colorant Alphazurine FG or D\&C Blue No. 4). This study comparatively tests the advantage of several data transformation approaches, including mean centering, standard normal variate, and Savitzky-Golay smoothed second derivative as means of improving predictive models in the presence of fluorescence. By application of the partial least squares (PLS) calibration algorithm to establish optimum covariance between transformed spectral data and measured tablet coating thicknesses, we have been able to create predictive models with calibration errors as small as 4 mu m for a training set that spans colored coating thicknesses from 50 to 151 mu m. (c) 2006 Elsevier B.V. All rights reserved.},
	keywords = {film coating, FLUORESCENCE, FORMS, INDUCED BREAKDOWN SPECTROSCOPY, near infrared spectroscopy, QUANTITATIVE-ANALYSIS, Raman spectroscopy, REFLECTANCE, SPECTRA, SPECTROMETRY},
	isbn = {0731-7085},
	url = {<Go to ISI>://000238137100019},
	author = {Romero-Torres, S. and Perez-Ramos, J. D. and Morris, K. R. and Grant, E. R.}
}
@inbook {1447,
	title = {Surface science studies of the effect of Al alloy microstructure on the formation of chromate coatings},
	booktitle = {Aluminium Alloys 2006, Pts 1 and 2 - Research through Innovation and Technology},
	series = {Materials Science Forum},
	volume = {519-521},
	year = {2006},
	note = {ISI Document Delivery No.: BEZ41Times Cited: 3Cited Reference Count: 22Kulinich, S. A. Akhtar, A. S. Susac, D. Wong, K. C. Wong, P. C. Mitchell, K. A. R.Proceedings Paper10th International Conference on Aliminium Alloys (ICAA-10)JUL 09-13, 2006Vancouver, CANADABRANDRAIN 6, CH-8707 ZURICH-UETIKON, SWITZERLAND},
	pages = {621-628},
	publisher = {Trans Tech Publications Ltd},
	organization = {Trans Tech Publications Ltd},
	address = {Zurich-Uetikon},
	abstract = {Surface science methods including scanning Auger microscopy (SAM), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and Raman spectroscopy have been used to study the initial growth of chromate conversion coatings on aluminum 2024-T3 alloy, using a coating bath formed by dissolving CrO3, Na2Cr2O7 and NaF in water. The objective is to learn more about growth mechanism on the different microstructural regions of this alloy surface, including the second-phase particles and the alloy matrix.},
	keywords = {2024-T3 ALUMINUM-ALLOY, AA2024-T3, aluminum alloy, ATOMIC-FORCE MICROSCOPY, CHEMISTRY, chromate conversion coating, CONVERSION COATINGS, corrosion, NUCLEATION, PAINT ADHESION, photoelectron, Raman spectroscopy, scanning Auger microscopy, scanning electron microscopy, SPECTROSCOPY},
	isbn = {0255-54760-87849-408-1},
	url = {<Go to ISI>://000240309000097},
	author = {Kulinich, S. A. and Akhtar, A. S. and Susac, D. and Wong, K. C. and Wong, P. C. and Mitchell, K. A. R.},
	editor = {Poole, W. J. and Wells, M. A. and Lloyd, D. J.}
}
@article {1270,
	title = {Lewis adducts of the side-on end-on dinitrogen-bridged complex [{(NPN)Ta}(2)(mu-H)(2)(mu-eta(1):eta(2)-N-2)] with AlMe3, GaMe3, and B(C6F5)(3): Synthesis, structure, and spectroscopic properties},
	journal = {Chemistry-a European Journal},
	volume = {11},
	number = {2},
	year = {2005},
	note = {ISI Document Delivery No.: 887VLTimes Cited: 12Cited Reference Count: 49},
	month = {Jan},
	pages = {604-618},
	type = {Article},
	abstract = {{Reaction of the side-on end-on dinitrogen complex [{(NPN)Ta}(2)(mu- H)(2)(mu-eta(1):eta(2)-N-2)] (1; in which NPN= (PhNSiMe2CH2)(2)PPh), with the Lewis acids XR3 results in the adducts [{(NPN)Ta}(2)(mu-H)(2)(mu-eta(1):eta(2)-NNXR3)]},
	keywords = {CHEMISTRY, CLEAVAGE, COORDINATED, density functional calculations, DINITROGEN, DINITROGEN COMPLEXES, DINUCLEAR TANTALUM COMPLEX, EFFECTIVE CORE POTENTIALS, FIXATION, MOLECULAR CALCULATIONS, MOLYBDENUM CENTER, N-2 LIGAND, NITROGEN, Raman spectroscopy, REACTIVITY, tantalum, TRIS(PENTAFLUOROPHENYL)BORANE},
	isbn = {0947-6539},
	url = {<Go to ISI>://000226333500014},
	author = {Studt, F. and MacKay, B. A. and Johnson, S. A. and Patrick, B. O. and Fryzuk,Michael D. and Tuczek, F.}
}
@article {648,
	title = {Revealing system dynamics through decomposition of the perturbation domain in two-dimensional correlation spectroscopy},
	journal = {Applied Spectroscopy},
	volume = {57},
	number = {12},
	year = {2003},
	note = {ISI Document Delivery No.: 753MHTimes Cited: 5Cited Reference Count: 36},
	month = {Dec},
	pages = {1551-1560},
	type = {Article},
	abstract = {A technique is presented to simply and effectively decompose the perturbation domain in two-dimensional (2D) correlation maps calculated on a given set of vibrational spectra. Decomposition of the perturbation domain exposes a wealth of kinetic information complementary to the information extracted from conventional 2D correlation spectroscopy. It is shown that the technique produces "perturbation profile maps" that can be utilized in both the interpretation of the conventional 2D correlation maps and the independent kinetic analysis of the given system. Discrimination between spectral features exhibiting similar, but not identical, dynamics is facilitated by the decomposition, and spectral features exhibiting identical dynamics over the perturbation interval are quickly identified. Spectral features exhibiting similar dynamics over only a sub-range of the full perturbation are also identifiable. Interpretation of phase information illuminated in synchronous and asynchronous maps is simplified. Comparison between similar spectral features present in different samples is facilitated with the technique. The simplicity and ease of implementation of the technique make decomposition of the perturbation domain a valuable addition to the tools available in 2D correlation analysis.},
	keywords = {cross-correlation, FT-RAMAN, HUMAN, INFRARED CORRELATION SPECTROSCOPY, multivariate data, POLYACRYLAMIDE GELS, POLYMER GEL DOSIMETERS, RADIATION-DOSIMETRY, Raman spectroscopy, SAMPLE-SAMPLE, SECONDARY STRUCTURE, SERUM-ALBUMIN, SPECTRA, STRUCTURAL-CHANGES, two-dimensional correlation spectroscopy},
	isbn = {0003-7028},
	url = {<Go to ISI>://000187234800013},
	author = {Jirasek, A. and Schulze, G. and Blades, M. W. and Turner, R. F. B.}
}
@article {648,
	title = {Revealing system dynamics through decomposition of the perturbation domain in two-dimensional correlation spectroscopy},
	journal = {Applied Spectroscopy},
	volume = {57},
	number = {12},
	year = {2003},
	note = {ISI Document Delivery No.: 753MHTimes Cited: 5Cited Reference Count: 36},
	month = {Dec},
	pages = {1551-1560},
	type = {Article},
	abstract = {A technique is presented to simply and effectively decompose the perturbation domain in two-dimensional (2D) correlation maps calculated on a given set of vibrational spectra. Decomposition of the perturbation domain exposes a wealth of kinetic information complementary to the information extracted from conventional 2D correlation spectroscopy. It is shown that the technique produces "perturbation profile maps" that can be utilized in both the interpretation of the conventional 2D correlation maps and the independent kinetic analysis of the given system. Discrimination between spectral features exhibiting similar, but not identical, dynamics is facilitated by the decomposition, and spectral features exhibiting identical dynamics over the perturbation interval are quickly identified. Spectral features exhibiting similar dynamics over only a sub-range of the full perturbation are also identifiable. Interpretation of phase information illuminated in synchronous and asynchronous maps is simplified. Comparison between similar spectral features present in different samples is facilitated with the technique. The simplicity and ease of implementation of the technique make decomposition of the perturbation domain a valuable addition to the tools available in 2D correlation analysis.},
	keywords = {cross-correlation, FT-RAMAN, HUMAN, INFRARED CORRELATION SPECTROSCOPY, multivariate data, POLYACRYLAMIDE GELS, POLYMER GEL DOSIMETERS, RADIATION-DOSIMETRY, Raman spectroscopy, SAMPLE-SAMPLE, SECONDARY STRUCTURE, SERUM-ALBUMIN, SPECTRA, STRUCTURAL-CHANGES, two-dimensional correlation spectroscopy},
	isbn = {0003-7028},
	url = {<Go to ISI>://000187234800013},
	author = {Jirasek, A. and Schulze, G. and Blades, M. W. and Turner, R. F. B.}
}
@article {4474,
	title = {The carbonyl chlorine(I) cation [ClCO](+)},
	journal = {Angewandte Chemie-International Edition},
	volume = {38},
	number = {6},
	year = {1999},
	note = {ISI Document Delivery No.: 177VXTimes Cited: 11Cited Reference Count: 28},
	pages = {823-825},
	type = {Article},
	keywords = {CATIONS, GAS-PHASE, INFRARED-SPECTRUM, IR spectroscopy, OCS, Raman spectroscopy, SPECTROSCOPIC CHARACTERIZATION, SUPERACID SYSTEMS},
	isbn = {1433-7851},
	url = {<Go to ISI>://000079232700020},
	author = {Bernhardt, E. and Willner, H. and Aubke, F.}
}
@article {3685,
	title = {Rational design of fiber-optic probes for visible and pulsed-ultraviolet resonance Raman spectroscopy},
	journal = {Applied Optics},
	volume = {35},
	number = {21},
	year = {1996},
	note = {ISI Document Delivery No.: VA608Times Cited: 16Cited Reference Count: 24OSA 1995 Annual Meeting1995PORTLAND, OROpt Soc Amer},
	month = {Jul},
	pages = {4086-4095},
	type = {Proceedings Paper},
	abstract = {The investigated the performance of fiber-optic resonance Raman probes with a series of experiments to determine the working curves of such probes using model analytes and to investigate the effects of absorbing media. A computer model designed to simulate these experiments is presented, and numerical results are found to be in agreement with the experimental data. Design considerations resulting from these studies are discussed, and novel designs for overcoming problems of coupling efficiency, damage threshold, and sensitivity in absorbing samples are presented. These findings are applied to the design of fiber-optic probes for ultraviolet resonance Raman spectroscopy involving nanosecond pulsed-ultraviolet excitation (225 and 266 nm). These probes have been used to collect what is, to our knowledge, the first reported fiber-optic-linked ultraviolet resonance Raman spectra of tryptophan and DNA. (C) 1996 Optical Society of America},
	keywords = {AROMATIC-AMINO-ACIDS, EFFECTIVE DEPTH, fiber-optic probes, LASER EXCITATION, numerical modeling of, optical fibers, OPTIMIZATION, Raman spectroscopy, remote Raman, resonance Raman spectroscopy, SCATTERING, sensors, SPECTROSCOPY},
	isbn = {0003-6935},
	url = {<Go to ISI>://A1996VA60800014},
	author = {Greek, L. S. and Schulze, H. G. and Haynes, C. A. and Blades, M. W. and Turner, R. F. B.}
}
@article {3685,
	title = {Rational design of fiber-optic probes for visible and pulsed-ultraviolet resonance Raman spectroscopy},
	journal = {Applied Optics},
	volume = {35},
	number = {21},
	year = {1996},
	note = {ISI Document Delivery No.: VA608Times Cited: 16Cited Reference Count: 24OSA 1995 Annual Meeting1995PORTLAND, OROpt Soc Amer},
	month = {Jul},
	pages = {4086-4095},
	type = {Proceedings Paper},
	abstract = {The investigated the performance of fiber-optic resonance Raman probes with a series of experiments to determine the working curves of such probes using model analytes and to investigate the effects of absorbing media. A computer model designed to simulate these experiments is presented, and numerical results are found to be in agreement with the experimental data. Design considerations resulting from these studies are discussed, and novel designs for overcoming problems of coupling efficiency, damage threshold, and sensitivity in absorbing samples are presented. These findings are applied to the design of fiber-optic probes for ultraviolet resonance Raman spectroscopy involving nanosecond pulsed-ultraviolet excitation (225 and 266 nm). These probes have been used to collect what is, to our knowledge, the first reported fiber-optic-linked ultraviolet resonance Raman spectra of tryptophan and DNA. (C) 1996 Optical Society of America},
	keywords = {AROMATIC-AMINO-ACIDS, EFFECTIVE DEPTH, fiber-optic probes, LASER EXCITATION, numerical modeling of, optical fibers, OPTIMIZATION, Raman spectroscopy, remote Raman, resonance Raman spectroscopy, SCATTERING, sensors, SPECTROSCOPY},
	isbn = {0003-6935},
	url = {<Go to ISI>://A1996VA60800014},
	author = {Greek, L. S. and Schulze, H. G. and Haynes, C. A. and Blades, M. W. and Turner, R. F. B.}
}
@article {3510,
	title = {ARTIFICIAL NEURAL-NETWORK AND CLASSICAL LEAST-SQUARES METHODS FOR NEUROTRANSMITTER MIXTURE ANALYSIS},
	journal = {Journal of Neuroscience Methods},
	volume = {56},
	number = {2},
	year = {1995},
	note = {ISI Document Delivery No.: QH949Times Cited: 5Cited Reference Count: 28},
	month = {Feb},
	pages = {155-167},
	type = {Article},
	abstract = {Identification of individual components in biological mixtures can be a difficult problem regardless of the analytical method employed. In this work, Raman spectroscopy was chosen as a prototype analytical method due to its inherent versatility and applicability to aqueous media, making it useful for the study of biological samples. Artificial neural networks (ANNs) and the classical least-squares (CLS) method were used to identify and quantify the Raman spectra of the small-molecule neurotransmitters and mixtures of such molecules. The transfer functions used by a network, as well as the architecture of a network, played an important role in the ability of the network to identify the Raman spectra of individual neurotransmitters and the Raman spectra of neurotransmitter mixtures. Specifically, networks using sigmoid and hyperbolic tangent transfer functions generalized better from the mixtures in the training data set to those in the testing data sets than networks using sine functions. Networks with connections that permit the local processing of inputs generally performed better than other networks on all the testing data sets, and better than the CLS method of curve fitting, on novel spectra of some neurotransmitters. The CLS method was found to perform well on noisy, shifted, and difference spectra.},
	keywords = {ARTIFICIAL NEURAL, BACTERIA, CLASSICAL LEAST-SQUARES ANALYSIS, INVIVO VOLTAMMETRY, MIXTURE ANALYSIS, NETWORK, Raman spectroscopy, REGRESSION, SMALL-MOLECULE NEUROTRANSMITTER, SPECTRA, SYSTEM, UV RESONANCE RAMAN},
	isbn = {0165-0270},
	url = {<Go to ISI>://A1995QH94900006},
	author = {Schulze, H. G. and Greek, L. S. and Gorzalka, B. B. and Bree, A. V. and Blades, M. W. and Turner, R. F. B.}
}
@article {3510,
	title = {ARTIFICIAL NEURAL-NETWORK AND CLASSICAL LEAST-SQUARES METHODS FOR NEUROTRANSMITTER MIXTURE ANALYSIS},
	journal = {Journal of Neuroscience Methods},
	volume = {56},
	number = {2},
	year = {1995},
	note = {ISI Document Delivery No.: QH949Times Cited: 5Cited Reference Count: 28},
	month = {Feb},
	pages = {155-167},
	type = {Article},
	abstract = {Identification of individual components in biological mixtures can be a difficult problem regardless of the analytical method employed. In this work, Raman spectroscopy was chosen as a prototype analytical method due to its inherent versatility and applicability to aqueous media, making it useful for the study of biological samples. Artificial neural networks (ANNs) and the classical least-squares (CLS) method were used to identify and quantify the Raman spectra of the small-molecule neurotransmitters and mixtures of such molecules. The transfer functions used by a network, as well as the architecture of a network, played an important role in the ability of the network to identify the Raman spectra of individual neurotransmitters and the Raman spectra of neurotransmitter mixtures. Specifically, networks using sigmoid and hyperbolic tangent transfer functions generalized better from the mixtures in the training data set to those in the testing data sets than networks using sine functions. Networks with connections that permit the local processing of inputs generally performed better than other networks on all the testing data sets, and better than the CLS method of curve fitting, on novel spectra of some neurotransmitters. The CLS method was found to perform well on noisy, shifted, and difference spectra.},
	keywords = {ARTIFICIAL NEURAL, BACTERIA, CLASSICAL LEAST-SQUARES ANALYSIS, INVIVO VOLTAMMETRY, MIXTURE ANALYSIS, NETWORK, Raman spectroscopy, REGRESSION, SMALL-MOLECULE NEUROTRANSMITTER, SPECTRA, SYSTEM, UV RESONANCE RAMAN},
	isbn = {0165-0270},
	url = {<Go to ISI>://A1995QH94900006},
	author = {Schulze, H. G. and Greek, L. S. and Gorzalka, B. B. and Bree, A. V. and Blades, M. W. and Turner, R. F. B.}
}
@article {3347,
	title = {SNR ENHANCEMENT AND DECONVOLUTION OF RAMAN-SPECTRA USING A 2-POINT ENTROPY REGULARIZATION METHOD},
	journal = {Applied Spectroscopy},
	volume = {49},
	number = {4},
	year = {1995},
	note = {ISI Document Delivery No.: QV637Times Cited: 24Cited Reference Count: 20},
	month = {Apr},
	pages = {425-431},
	type = {Article},
	abstract = {A new method for Raman signal recovery, the two-point maximum entropy method (TPMEM), based on a regularization method using two-point entropy is presented, The method can be used for signal-to-noise ratio (SNR) enhancement in very low SNR measurements or for deconvolution, in order to remove the effects of the instrumental line shape on the measured spectrum, Unlike most SNR enhancement schemes, TPMEM requires no filter parameters and no a priori knowledge of the expected signal. A rigorous test on a randomly produced set of convolved and/or noise-corrupted simulated Raman spectra is presented in order to validate the method and compare it to Savitzky-Golay filtering and the maximum entropy method. The method is evaluated on the basis of the root mean square (rms) error and correlation coefficients of the recovered data with the original data, as well as on the basis of SNR improvement, and showed significant improvements in both performance and speed over conventional methods. The method is demonstrated in an application involving fiber-optic-linked Raman and resonance Raman spectroscopy.},
	keywords = {DECONVOLUTION, FILTERS, NOISE FILTERING, Raman spectroscopy, SNR ENHANCEMENT, TO-NOISE RATIOS},
	isbn = {0003-7028},
	url = {<Go to ISI>://A1995QV63700005},
	author = {Greek, L. S. and Schulze, H. G. and Blades, M. W. and Bree, A. V. and Gorzalka, B. B. and Turner, R. F. B.}
}
@article {3347,
	title = {SNR ENHANCEMENT AND DECONVOLUTION OF RAMAN-SPECTRA USING A 2-POINT ENTROPY REGULARIZATION METHOD},
	journal = {Applied Spectroscopy},
	volume = {49},
	number = {4},
	year = {1995},
	note = {ISI Document Delivery No.: QV637Times Cited: 24Cited Reference Count: 20},
	month = {Apr},
	pages = {425-431},
	type = {Article},
	abstract = {A new method for Raman signal recovery, the two-point maximum entropy method (TPMEM), based on a regularization method using two-point entropy is presented, The method can be used for signal-to-noise ratio (SNR) enhancement in very low SNR measurements or for deconvolution, in order to remove the effects of the instrumental line shape on the measured spectrum, Unlike most SNR enhancement schemes, TPMEM requires no filter parameters and no a priori knowledge of the expected signal. A rigorous test on a randomly produced set of convolved and/or noise-corrupted simulated Raman spectra is presented in order to validate the method and compare it to Savitzky-Golay filtering and the maximum entropy method. The method is evaluated on the basis of the root mean square (rms) error and correlation coefficients of the recovered data with the original data, as well as on the basis of SNR improvement, and showed significant improvements in both performance and speed over conventional methods. The method is demonstrated in an application involving fiber-optic-linked Raman and resonance Raman spectroscopy.},
	keywords = {DECONVOLUTION, FILTERS, NOISE FILTERING, Raman spectroscopy, SNR ENHANCEMENT, TO-NOISE RATIOS},
	isbn = {0003-7028},
	url = {<Go to ISI>://A1995QV63700005},
	author = {Greek, L. S. and Schulze, H. G. and Blades, M. W. and Bree, A. V. and Gorzalka, B. B. and Turner, R. F. B.}
}
