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利用偏振增强光声技术对手性分子进行深层组织传感。

Deep tissue sensing of chiral molecules using polarization-enhanced photoacoustics.

作者信息

Padmanabhan Swathi, Prakash Jaya

机构信息

Department of Instrumentation and Applied Physics, Indian Institute of Science, Bengaluru 560012, India.

出版信息

Sci Adv. 2025 Mar 21;11(12):eado8012. doi: 10.1126/sciadv.ado8012. Epub 2025 Mar 19.

Abstract

Chiral molecule sensing is typically performed using techniques like chromatography, electrophoresis, enzymatic assays, mass spectrometry, and chiroptical methods. While polarimetry allows for in vivo sensing up to 1 mm depth using ultraviolet-visible light, it is limited by dominant light scattering beyond this depth. We propose that photoacoustic sensing in the near-infrared II (NIR-II) window can enable deep tissue sensing as acoustic waves scatter less than light. To achieve this, we developed a photoacoustic polarization-enhanced optical rotation sensing (PAPEORS) system, capable of estimating optical rotation from photoacoustic signals and correlating it with chiral molecular concentration for depths up to 3.5 mm. Experiments were conducted using aqueous glucose solutions, naproxen, serum-based glucose samples, and ex vivo chicken tissue. PAPEORS achieved a detection limit of 80 mg/dl while using circularly polarized light with serum samples, demonstrating the potential for deep-tissue chiral molecular sensing. PAPEORS holds promise for in vivo sensing and easy miniaturization using single wavelength.

摘要

手性分子传感通常使用色谱法、电泳法、酶分析法、质谱法和旋光方法等技术来进行。虽然旋光测定法能够利用紫外-可见光在体内对深度达1毫米的区域进行传感,但超过这个深度后,它会受到主要的光散射的限制。我们提出,近红外II(NIR-II)窗口的光声传感能够实现深层组织传感,因为声波的散射比光少。为实现这一点,我们开发了一种光声偏振增强旋光传感(PAPEORS)系统,该系统能够从光声信号中估计旋光,并将其与深度达3.5毫米的手性分子浓度相关联。使用葡萄糖水溶液、萘普生、血清基葡萄糖样本和离体鸡组织进行了实验。在对血清样本使用圆偏振光时,PAPEORS实现了80毫克/分升的检测限,证明了深层组织手性分子传感的潜力。PAPEORS在体内传感以及使用单波长进行简易小型化方面具有前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d786/11922051/3f36ddb1bd7c/sciadv.ado8012-f1.jpg

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