1998
DOI: 10.1016/s0016-5107(98)70349-9
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Immunoscopy—a technique combining endoscopy and immunofluorescence for diagnosis of colorectal carcinoma

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Cited by 30 publications
(27 citation statements)
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“…Several attempts using labeled CEAantibodies have also been reported (2). Fluorescence that is specific to gastrointestinal lesions has been observed in studies using isolated specimens (4,5). However, the use of fluorescence of ultraviolet-range wavelength result in interference from strong background noise (7) and possible damage the living tissue (6).…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Several attempts using labeled CEAantibodies have also been reported (2). Fluorescence that is specific to gastrointestinal lesions has been observed in studies using isolated specimens (4,5). However, the use of fluorescence of ultraviolet-range wavelength result in interference from strong background noise (7) and possible damage the living tissue (6).…”
Section: Discussionmentioning
confidence: 99%
“…In the field of gastroenterology (4,5), attempts have been made to check for lesions using carcinoembryonic antigen (CEA) antibody labeled with fluorescent material. However, since the wavelength of fluorescence used in those studies was in the ultraviolet range, its use in vivo is limited due to safety concerns (6) and due to interference from some other sources of fluorescence (7).…”
Section: Introductionmentioning
confidence: 99%
“…Similarly, in the field of GI endoscopy, the authors propose rapid development of 'endoscopic molecular imaging', which is considered to be divided into three categories: (a) visualization of cell morphology on the micro to nano level; (b) reflection of spectroscopic characteristics; and (c) visualization of molecular characteristics. The future of endoscopic diagnosis is likely to be affected by a combination of biomarkers and technology (Takayama et al, 1998), and 'endoscopic molecular imaging' would be defined as (c), which has been described as 'immunoscopy' (Keller et al, 1998), 'bioendoscopy' (Pasricha & Motamedi, 2002), and 'optical biopsy' (Fujimoto et al, 1995). These innovations will allow us not only to locate a tumor but also useful to 1) differentiate malignant and benign polyps and ulcers, 2) minimize number of biopsies and frequency of surveillance, 3) accurate preoperative identification of tumor margin, 4) evaluate effectiveness of pharmacological therapy, 5) detect local dysplasia in Barrett's mucosa or ulcerative colitis.…”
Section: Introductionmentioning
confidence: 99%
“…Further, fluorescence imaging can permit monitoring of the progress of accumulation and destruction of the photosensitiser both before and during PDT treatments, which can aid in the clinical assessment of the appropriateness of drug and light dosing at the time of treatment [9]. ALA-based PD and PDT is used in a variety of applications [1], including endoscopic detection of lesions [12][13][14] and on-line determination of treatment end-points by kinetic fluorescence measurements [15].…”
Section: Introductionmentioning
confidence: 99%
“…Various devices suitable for this application have already been developed [9,12,14]. We have assembled an a#ordable, portable fluorescence imaging prototype for skin lesion detection.…”
Section: Introductionmentioning
confidence: 99%