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Original

FLUOROALKYLATED POLYETHYLENE GLYCOL AS POTENTIAL SURFACTANT FOR PERFLUOROCARBON EMULSION

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Pages 483-492 | Published online: 11 Jul 2009

Figures & data

Figure 1. Morphological changes of J774A.1 macrophage cells after the engulfment of PFC emulsions manufactured by (b) EYP and (c) RF-PEG 8000, respectively. The cells shown in (a) were the normal cells without the treatment of PFC emulsions. Compared with EYP-mediated PFC emulsions, the degree of phagocytosis was ameliorated to a large extent for RF-PEG 8000 mediated ones. Photomicrographs were taken after 9-h incubation (Magnification × 100).

Figure 1. Morphological changes of J774A.1 macrophage cells after the engulfment of PFC emulsions manufactured by (b) EYP and (c) RF-PEG 8000, respectively. The cells shown in (a) were the normal cells without the treatment of PFC emulsions. Compared with EYP-mediated PFC emulsions, the degree of phagocytosis was ameliorated to a large extent for RF-PEG 8000 mediated ones. Photomicrographs were taken after 9-h incubation (Magnification × 100).

Figure 2. 19F-NMR spectrum of FC-40 emulsions. The CF3 absorption peak of the FC-40 was located at −86.2 ppm.

Figure 2. 19F-NMR spectrum of FC-40 emulsions. The CF3 absorption peak of the FC-40 was located at −86.2 ppm.

Figure 3. 19F-NMR spectra of fluorine contained within the macrophages that engulfed emulsified PFC microparticles made by EYP and RF-PEG 8000, respectively. All the chemical shifts were referenced to the internal standard CF3SO3Na at −81.4 ppm.

Figure 3. 19F-NMR spectra of fluorine contained within the macrophages that engulfed emulsified PFC microparticles made by EYP and RF-PEG 8000, respectively. All the chemical shifts were referenced to the internal standard CF3SO3Na at −81.4 ppm.

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