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Study of dynamic process of acetic acid induced-whitening in epithelial tissues at cellular level

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Abstract

Acetic acid, inducing transient whitening (acetowhitening) when applied to epithelial tissues, is a commonly used contrast agent for detecting early cervical cancer. The goals of this research are to investigate the temporal characteristics of acetowhitening process in cervical epithelial tissue at cellular level and develop a clear understanding of the diagnostic information carried in the acetowhitening signal. A system measuring time-resolved reflectance was built to study the rising and decay processes of acetowhitening signal from the monolayered cell cultures of normal and cancerous cervical squamous cells. It is found that the dynamic processes of acetowhitening in normal and cancerous cells are significantly different. The results of this study provide insight valuable to further understand the acetowhitening process in epithelial cells and to encourage the development of an objective procedure to detect the early cervical cancers based on quantitative monitoring of the dynamic process of acetowhitening.

©2005 Optical Society of America

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Supplementary Material (3)

Media 1: MOV (1228 KB)     
Media 2: MOV (961 KB)     
Media 3: MOV (203 KB)     

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Figures (8)

Fig. 1.
Fig. 1. Schematic of time-resolved reflectance measurement system. L1: Focus Lens (f=35mm); C1: Fiber Optic Collimator; A1: Aperture Stop; M1, M2: Mirrors.
Fig. 2.
Fig. 2. Acetowhitening signals (right) and phase-contrast images (left) recorded from cancer cell samples in rising and decay courses. (a) (1.228MB) Concentration of acetic acid in medium: 0.3%; (b) (962KB) Concentration of acetic acid in medium: 1.2%.
Fig. 3.
Fig. 3. Wavelength-dependence of acetowhitening signal. (a) RGB reflectance signals recorded from a cancer cell sample with the application of 0.6% acetic acid solution; (b) Comparison of RGB signals in the rising course; (c) Comparison of signals in the decay course.
Fig. 4.
Fig. 4. Acetowhitening signals of cancer cell samples at different acetic acid concentrations. (a) (203KB) Movie of the acetowhitening signals as a function of acetic acid concentration; (b) The peak value of acetowhitening signals as a function of acetic acid concentration.
Fig. 5.
Fig. 5. Comparison of the acetowhitening signals of cancer cell samples when applying the medium with different acetic acid concentrations. (a) Normalized signals in the rising courses; (b) Normalized signals in the decay courses.
Fig. 6.
Fig. 6. Acetowhitening signals of normal cell samples at different acetic acid concentrations. (a) The acetowhitening signals as a function of acetic acid concentration; (b) The peak value of acetowhitening signals as a function of acetic acid concentration.
Fig. 7.
Fig. 7. Comparison of single and dual-exponential models in fitting the decay of acetowhitening signals. (a) Cancer cell sample, 0.6% acetic acid; (b) Normal cell sample, 0.6% acetic acid.
Fig. 8.
Fig. 8. (a) pH value and (b) H+ concentration (mol/L) of the acetic acid solution as a function of the concentration of acetic acid at room temperature 25°C.

Tables (2)

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Table 1. The decay time constants for normal and cancer cell samples calculated from a single exponential model.

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Table 2. Analyses of decay process of acetowhitening effect in normal and cancer cells using dual-exponential model.

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