Near-infrared fluorescence enhanced optical imaging: an analysis of penetration depth

Due to the character of the original source materials and the nature of batch digitization, quality control issues may be present in this document. Please report any quality issues you encounter to digital@library.tamu.edu, referencing the URI of the item.Includes bibliographical references (leaves 131-140).Issued also on microfiche from Lange Micrographics.Non-invasive, in vivo imaging modalities are valuable diagnostic indicators of tissue abnormalities, disease, metabolic changes, and other cellular anomalies that occur beneath the skin's surface. Imaging tools have become particularly valuable for the diagnosis of cancer and abnormal cell growth in tissues. Although many established imaging modalities are heavily relied upon by patients undergoing oncology treatment, new techniques are developing that may not only provide tumor detection methods, but also may facilitate cancer staging and increase our understanding of tumor progression. Frequency domain photon migration imaging (FDPM) is a maturing optical tool that is based upon the propagation of near infrared (NIR) radiation through tissue and scattering media. Within the scope of applications for breast cancer detection, fluorescence-enhanced FDPM has seen many milestones, although it is still in a developmental stage. Fluorescence-enhanced FDPM exploits a NIR light source for the excitation of a fluorescent contrast agent for detection. The research presented in this M.S. thesis seeks to further develop fluorescence-enhanced FDPM for cancer screening via sentinel lymph node mapping. Sentinel lymph node mapping involves the localization and resection for biopsy of the sentinel node, or the first node to receive metastatic drainage from the primary tumor. Investigating the propagation of NIR fluorescence deep within tissue-like scattering media will provide evidence to support the sensitivity of NIR imaging for sentinel lymph node localization, particularly when the sentinel lymph node is located up to 4 cm below the skin surface. The work summarized by this thesis thus provides a systematic examination of FDPM detection of signals originating from deeply embedded fluorescent inclusions within a tissue-mimicking phantom. Two dimensional multipixel images of embedded fluorescent targets are examined to determine if detection of fluorescence is possible over a reflectance geometry provided using an intensified charge coupled device camera system (ICCD). Data collected show fluorescence from targets containing 1 M, 0.01 M and 1 nM can be located when originating from 1 to 4-cm below the imaged surface, and as few as 0.01 femtomoles of ICG can be detected by the ICCD system, with proper choice of rejection filters