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In-vivo NIR autofluorescence imaging of rat mammary tumors

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Abstract

We investigate in vivo detection of mammary tumors in a rat model using autofluorescence imaging in the red and far-red spectral regions. The objective was to explore this method for non-invasive detection of malignant tumors and correlation between autofluorescence properties of tumors and their pathologic status. Eighteen tumor-bearing rats, bearing eight benign and seventeen malignant tumors were imaged. Autofluorescence images were acquired using spectral windows centered at 700-nm, 750-nm and 800-nm under laser excitation at 632.8-nm and 670-nm. Intensity in the autofluorescence images of malignant tumors under 670-nm excitation was higher than that of the adjacent normal tissue. whereas intensity of benign tumors was lower compared to normal tissue.

©2006 Optical Society of America

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Figures (4)

Fig. 1.
Fig. 1. Schematic layout of the key components of the optical imaging system.
Fig. 2.
Fig. 2. (a) Light scattering image under ambient light and (b) corresponding autofluorescence image under 670-nm excitation showing a rat containing malignant tumors in supine position (tumors #2 and 3). The spectral window for image formation was at 800-nm in both images. The hair represents the very bright regions visible on the fluorescence image outside the area of interest. On the fluorescence image (b), the tumor (indicated by the black arrow), spontaneously emits more fluorescence than adjacent normal mammary tissue (white arrow).
Fig. 3.
Fig. 3. (a) Light scattering image under ambient light and (b) corresponding autofluorescence image under 670-nm excitation and detection at 800-nm showing a rat containing a benign tumor in supine position (tumor #7). In the fluorescence image (b), the tumor (white arrow) is on the contrary to Fig. 2, much less fluorescent than the adjacent normal mammary tissue (black arrow). This tumor was shown to be a benign fibroadenoma on pathology. The signal intensity ratio T/N was in this case 0.22. Note the visibility of a blood vessel, absorbing light (black arrowheads), outlined by the brighter normal tissue. Small variation in the autofluorescence intensity in the normal tissue area is attributed to the presence of various organs of the animal located below the surface that exhibit different autofluorescence intensities under the deeply propagating excitation light.
Fig. 4.
Fig. 4. Tumor-to-normal signal intensity ratio plotted according to size for benign (엯) and malignant (Δ) tumors.

Tables (3)

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Table 1. Tumor-to-normal average signal intensity ratios at different laser excitation and detection spectral bands, for benign and malignant tumors.

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Table 2. Tumor-to-normal autofluorescence intensity ratios measured using laser excitation at 670 nm and detection spectral window of 750±20 nm 800±20 nm.

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Table 3. Diagnostic value of NIR autofluorescence imaging under 670-nm excitation and 800-nm detection for the differentiation of benign and malignant breast tumors.

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