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dc.creatorLewis, Christopher Bryan
dc.date.accessioned2012-06-07T22:56:33Z
dc.date.available2012-06-07T22:56:33Z
dc.date.created1999
dc.date.issued1999
dc.identifier.urihttps://hdl.handle.net/1969.1/ETD-TAMU-1999-THESIS-L47
dc.descriptionDue to the character of the original source materials and the nature of batch digitization, quality control issues may be present in this document. Please report any quality issues you encounter to digital@library.tamu.edu, referencing the URI of the item.en
dc.descriptionIncludes bibliographical references (leaves 61-63).en
dc.descriptionIssued also on microfiche from Lange Micrographics.en
dc.description.abstractCurrent techniques used to monitor glucose concentration of cell culture media require invasive and tedious handling of the sample for sterile media removal and nutrient replacement. In order to maximize cell culture growth in bioreactors, biosensors must be developed that are capable of monitoring the cell culture processes non-invasively and continuously. Non-invasive determinations of glucose and lactate in cell culture media were investigated via near-infrared spectroscopy (NIR) across the 2.0-2.5 []m combination region. A system was developed using a Fourier Transform Infrared (FHR) spectrometer to characterize glucose and lactate single beam spectra collected from cell culture media. Spectra recorded from a three-day fibroblast culture using a fiber-optic coupled culture flask with an FTIR spectrometer have been analyzed and compared with standard clinical chemistry techniques. Partial least squares regression has been used to extract the analyte-dependent information and to build a successful multivariate calibration model. Calibration, using a combination of spectra from cell culture media and prepared media mixtures, was performed and applied to an independent validation set, resulting in a prediction error of 14.8 mg/dl. Critical parameters surround the application of NIR spectroscopy to most biologically based samples, such as cell culture media. In addition to temperature and humidity, pH stability plays an essential role in the investigator's ability to accurately quantify concentrations of analyses of interest. It has been shown here that absorbable spectra of glucose may drastically deviate from "normal'' in the presence of pH-varying sample and a pH-constant reference spectrum. Because cell culture ranges of PH extend beyond the comparatively tight control of human physiological pH, it was necessary to seek out these implications and report them. For quantification studies, results indicate that potential interference due to varying pH values must be accounted for.en
dc.format.mediumelectronicen
dc.format.mimetypeapplication/pdf
dc.language.isoen_US
dc.publisherTexas A&M University
dc.rightsThis thesis was part of a retrospective digitization project authorized by the Texas A&M University Libraries in 2008. Copyright remains vested with the author(s). It is the user's responsibility to secure permission from the copyright holder(s) for re-use of the work beyond the provision of Fair Use.en
dc.subjectbiomedical engineering.en
dc.subjectMajor biomedical engineering.en
dc.titleInvestigation of near-infrared spectroscopy for periodic in situ cell culture media determination of glucose and lactateen
dc.typeThesisen
thesis.degree.disciplinebiomedical engineeringen
thesis.degree.nameM.S.en
thesis.degree.levelMastersen
dc.type.genrethesisen
dc.type.materialtexten
dc.format.digitalOriginreformatted digitalen


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