Gawedzinski John, Schmeler Kathleen M, Milbourne Andrea, Ramalingam Preetha, Moghaddam Parnian A, Richards-Kortum Rebecca, Tkaczyk Tomasz S
Department of Bioengineering, Rice University, 6100 Main Street, Houston, TX 77005, USA.
Departments of Gynecologic Oncology and Pathology, The University of Texas M.D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030, USA.
Biomed Opt Express. 2019 Nov 6;10(12):6145-6159. doi: 10.1364/BOE.10.006145. eCollection 2019 Dec 1.
Cervical cancers are primarily diagnosed via colposcopy, in which the tissue is visually assessed by a clinician for abnormalities, followed by directed biopsies and histologic analysis of excised tissue. Optical biopsy technologies offer a less invasive method of imaging such that subcellular features can be resolved without removing tissue. These techniques, however, are limited in field-of-view by the distal end of the probe. We present a prototype that incorporates a rigid, machinable waveguide that is in direct contact with a fluorescently-labeled sample paired with a scanning fluorescent microscope. The system is capable of imaging large areas of tissue without the need to re-position the tissue-probe interface. A mosaicing algorithm was developed to quantify scanning shifts and stitch neighboring frames together to increase the field-of-view. Our prototype can yield a maximum axial resolution of <5 µm for individual frames and can produce mosaiced images with a field-of-view greater than 15 mm x 15 mm without sacrificing resolution. We validated the system with a 1951 USAF resolution target, fluorescent in vitro standards, and a patient study where conization samples of squamous cervical epithelium were imaged. The results of the patient study indicate that architectural features of subcellular components could be detected and differentiated between normal tissue and precancerous lesions.
宫颈癌主要通过阴道镜检查来诊断,在此过程中临床医生通过肉眼评估组织是否存在异常,随后进行定向活检以及对切除组织进行组织学分析。光学活检技术提供了一种侵入性较小的成像方法,能够在不切除组织的情况下分辨亚细胞特征。然而,这些技术的视野受到探头远端的限制。我们展示了一个原型,它包含一个刚性的、可加工的波导,该波导与荧光标记的样本直接接触,并与扫描荧光显微镜配合使用。该系统能够对大面积组织进行成像,而无需重新定位组织 - 探头界面。我们开发了一种拼接算法来量化扫描偏移并将相邻帧拼接在一起,以扩大视野。我们的原型对于单个帧能够产生小于5微米的最大轴向分辨率,并且能够生成视野大于15毫米×15毫米的拼接图像,同时不牺牲分辨率。我们用1951年美国空军分辨率靶标、荧光体外标准以及一项对宫颈鳞状上皮锥切样本进行成像的患者研究对该系统进行了验证。患者研究结果表明,可以检测到亚细胞成分的结构特征,并区分正常组织和癌前病变。