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Algal Cells, Cartilage, and IRENI    51









                                 Synovial Fluid



                 Absorbance      BCP Standard






                                 Synovial Fluid




                              M-CPPD Standard


                 4000  3500  3000  2500  2000  1500  1000  500
                                            –1
                              Wavenumbers (cm )
        FIGURE 2.15  Representative synchrotron-based FTIR microspectroscopy
        spectra from human synovial fl uid demonstrating CPPD and BCP crystals.
        (Printed with permission from Ref. 47.)



        spectrum. The chondrocyte spectrum was collected with 12 × 12 μm 2
        and 64 scans.
            Our initial success with this methodology allowed us to make
        some important observations about these crystals that prompted fur-
        ther studies.
            We noted that the spectra of the biologic crystals often did not
        exactly match the spectra of synthetic crystals. We asked whether
        this could be due to contamination of the crystals with biologic mate-
        rial such as proteoglycans. As shown in Fig. 2.17, spectra generated
        with combinations of synthetic CPPD crystals and cartilage proteo-
        glycans, mimicked some of the changes observed in spectra from
        biologically generated CPPD crystals. The synchrotron-based FTIR
        microspectroscopy spectrum from a crystal generated by chondro-
        cyte monolayers was compared with an FTIR spectrum generated
        by  a combination of 50 percent cartilage proteoglycans, 30 percent
        M-CPPD, and 20 percent BCP.
            We also noted that CPPD and BCP crystals were frequently found
        together in a single crystal deposit. This occurred in native crystals
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