Duke University, Department of Biomedical Engineering, Durham, North Carolina 27708, USA.
J Biomed Opt. 2012 Nov;17(11):116014. doi: 10.1117/1.JBO.17.11.116014.
ABSTRACT. We used a probe-based dual-modality optical imaging instrument to measure in vivo coating thickness distributions of a gel distributed along the vaginal lumen, in a clinical study. The gel was a surrogate for one delivering an anti-HIV topical microbicide. Imaging data from Fourier-domain multiplexed low-coherence interferometry (mLCI) and fluorimetric measurements were compared to assess the feasibility and accuracy of mLCI in measuring in vivo gel coating thickness distributions. In each study session, 3.5 mL of Replens gel was inserted to the vaginal fornix while the participant was supine. The participant either: 1. remained supine (10 or 60 min); or 2. sat up (1 min), stood up (1 min), sat down (1 min) and returned to the supine position; net elapsed time was 10 or 60 min after which the gel distribution was imaged. Local coating thickness distributions were qualitatively and quantitatively similar. Here mLCI did not accurately measure thicker gel coatings (>0.8 mm), a limitation not seen with fluorimetry. However, mLCI is capable of measuring in vivo microbicide gel distributions with resolution on the order of 10 μm, without the need for exogenous contrast agents, and can accurately capture relevant summary coating measures in good agreement with fluorimetry.
摘要。我们使用基于探头的双模式光学成像仪器,在一项临床研究中,测量了阴道腔内分布的凝胶的活体涂层厚度分布。该凝胶是一种用于递送抗 HIV 局部杀微生物剂的替代物。比较了傅里叶域复用低相干干涉测量 (mLCI) 和荧光测量的成像数据,以评估 mLCI 测量活体凝胶涂层厚度分布的可行性和准确性。在每个研究时段中,将 3.5 毫升 Replens 凝胶插入阴道穹窿,而参与者仰卧。参与者:1. 保持仰卧(10 或 60 分钟);或 2. 坐起来(1 分钟)、站起来(1 分钟)、坐下来(1 分钟),然后回到仰卧位;在 10 或 60 分钟后,凝胶分布被成像。局部涂层厚度分布在定性和定量上相似。在这里,mLCI 不能准确测量较厚的凝胶涂层(>0.8 毫米),而荧光测量则没有这种限制。然而,mLCI 能够以 10 微米量级的分辨率测量活体杀微生物剂凝胶分布,无需使用外源性造影剂,并且可以准确捕获与荧光测量一致的相关涂层综合测量值。