For tissue illumination with endomicroscopic low-power laser (488-nm blue laser light) application of fluorescence agents are necessary. Most studies in humans have been performed with intravenous fluorescein sodium (5 mL, 10%). Fluorescein quickly distributes within all compartments of the tissue, and CLE is possible within seconds after injection. It contrasts cellular and subcellular details, connective tissue, and vessel architecture at high resolution, but does not stain nuclei.12 Intravenous fluorescein is a nontoxic agent that is safe and mostly well tolerated, and only transient discoloration of the skin has been described.12

CLE with intravenous fluorescein sodium allows analysis of cellular structure, connective tissue, and blood cells of the colonic mucosa in vivo. However, the nuclei of the intestinal epithelium are not readily http://www.selleckchem.com/products/LBH-589.html visible because of the pharmacokinetic properties of fluorescein. Acriflavine and cresyl violet are alternative dyes that are applied topically and highlight

nuclei, cell membranes, cytoplasm, and to a lesser extent vessels. Acriflavine accumulates in nuclei and therefore carries a potential mutagenic risk. Cresyl violet, which enriches in the cytoplasm and visualizes nuclear morphology negatively, is an alternative. A 2-step study approach made in 2007 by Goetz and colleagues21 evaluated the staining characteristics and optimal concentration of a single topical contrast agent, cresyl violet (Merck, Darmstadt, Germany) for simultaneous chromoendoscopy and CLE for straightforward and reliable recognition of lesions and their immediate characterization Tenoxicam buy DAPT in vivo. After establishing the optimal cresyl violet dye concentration of 0.13% with a pH of 3.8 in an animal preclinical study, 67 sites in 36 patients in a prospective clinical study were topically stained and subsurface serial images were generated at different depths using CLE. The results showed a good resolution with chromoendoscopy for pit pattern classification and good fluorescent contrast for endomicroscopy. Imaging at variable

penetration depths permitted high-resolution visualization of tissue architecture and subcellular details, such as mucin in goblet cells, and, more importantly, cell nuclei so that in vivo distinction of low-grade versus high-grade intraepithelial neoplasia was possible for the first time. Endomicroscopic targeting of biopsies to a region of altered nucleus/cytoplasm ratio on intravital staining with cresyl violet has resulted in the diagnosis of 1 additional case of high-grade intraepithelial neoplasia, and the overall prediction rate of neoplastic changes by CLE was excellent, although the small number of sites investigated may limit the significance of this finding.21 Endomicroscopy is a new imaging tool for gastrointestinal endoscopy. In vivo histology becomes possible at subcellular resolution during ongoing colonoscopy.