High-resolution high-contrast mid-infrared imaging of fresh biological samples with ultraviolet-localized photoacoustic microscopy (Conference Presentation)

Junhui Shi, T. T. Wong, Yun He, Lei Li, Ruiying Zhang, Jeeseong Hwang, K. Maslov, Lihong V. Wang
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引用次数: 3

Abstract

Label-free mid-infrared (MIR) imaging provides rich chemical and structural information of biological tissues without staining. Conventionally, the long MIR wavelength severely limits the lateral resolution owing to optical diffraction; moreover, the strong MIR absorption of water ubiquitous in fresh biological samples results in high background and low contrast. Here, we present a novel approach, called ultraviolet-localized MIR photoacoustic microscopy (ULM-PAM), to achieve high-resolution and water-background–free MIR imaging of fresh biological samples. In our approach, a pulsed MIR laser thermally excites the sample at the focal spot, and a pulsed ultraviolet (UV) laser photoacoustically detects the resulting transient temperature rise owing to the Gruneisen relaxation effect, thereby reporting the intensity of the MIR absorption by the sample. The imaging resolution of our method is determined by the wavelength of the UV laser, which is one order of magnitude shorter than that of the mid-IR laser (2.5 μm to 12 μm). In addition, in the UV region from 200 nm to 230 nm, most important organic molecules in biological tissues, including proteins, lipids and nuclei acids, have strong absorption, while water is transparent. Therefore, our method can achieve high resolution and water-background free IR imaging of fresh biological samples. For cell cultures, our method achieved high-resolution and high-contrast infrared imaging of lipids, proteins. The capability of label-free histology of this method is also demonstrated in thick biological tissues, such as brain slices. Our approach provides convenient high-resolution and high-contrast MIR imaging, which can benefit diagnosis of fresh biological samples.
利用紫外定位光声显微镜对新鲜生物样品进行高分辨率、高对比度中红外成像(会议报告)
无标记中红外(MIR)成像无需染色即可提供丰富的生物组织化学和结构信息。通常,由于光学衍射,较长的MIR波长严重限制了横向分辨率;此外,新鲜生物样品中普遍存在的水的强MIR吸收导致高背景和低对比度。在这里,我们提出了一种新的方法,称为紫外定位MIR光声显微镜(ULM-PAM),以实现新鲜生物样品的高分辨率和无水背景的MIR成像。在我们的方法中,脉冲MIR激光在焦点点处热激发样品,脉冲紫外(UV)激光光声检测由于Gruneisen弛豫效应而产生的瞬态温升,从而报告样品对MIR的吸收强度。该方法的成像分辨率由紫外激光的波长决定,它比中红外激光的波长(2.5 μm ~ 12 μm)短一个数量级。此外,在200 ~ 230 nm的紫外波段,生物组织中最重要的有机分子,包括蛋白质、脂质、核酸等都有很强的吸收,而水则是透明的。因此,我们的方法可以实现新鲜生物样品的高分辨率和无水背景的红外成像。对于细胞培养,我们的方法实现了脂质和蛋白质的高分辨率和高对比度红外成像。这种方法的无标记组织学的能力也被证明在厚的生物组织,如脑切片。我们的方法提供了方便的高分辨率和高对比度MIR成像,有利于新鲜生物样品的诊断。
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