Abdelrahman Mona H, Shen Jerry, Fisher Nicholas C, Losert Wolfgang, Fourkas John T
Department of Chemistry and Biochemistry, University of Maryland, College Park, MD, United States.
Pharmaceutical Analytical Chemistry Department, Faculty of Pharmacy, Ain Shams University, Cairo, Egypt.
Front Bioeng Biotechnol. 2024 Aug 13;12:1409735. doi: 10.3389/fbioe.2024.1409735. eCollection 2024.
Photomodifiable azopolymer nanotopographies represent a powerful means of assessing how cells respond to rapid changes in the local microenvironment. However, previous studies have suggested that azopolymers are readily photomodified under typical fluorescence imaging conditions over much of the visible spectrum. Here we assess the stability of azopolymer nanoridges under 1-photon and 2-photon imaging over a broad range of wavelengths.
Azopolymer nanoridges were created via microtransfer molding of master structures that were created using interference lithography. The effects of exposure to a broad range of wavelengths of light polarized parallel to the ridges were assessed on both a spinning-disk confocal microscope and a 2-photon fluorescence microscope. Experiments with live cells were also performed using alternating cycles of 514-nm light for photomodification and 561-nm light for fluorescence imaging.
We find that for both 1-photon and 2-photon imaging, only a limited range of wavelengths of light leads to photomodification of the azopolymer nanotopography. These results indicate that nondestructive 1-photon and 2-photon fluorescence imaging can be performed over a considerably broader range of wavelengths than would be suggested by previous research.
可光改性的偶氮聚合物纳米拓扑结构是评估细胞如何响应局部微环境快速变化的有力手段。然而,先前的研究表明,在典型的荧光成像条件下,偶氮聚合物在大部分可见光谱范围内很容易被光改性。在此,我们评估了偶氮聚合物纳米脊在广泛波长范围内单光子和双光子成像下的稳定性。
通过微转移模塑由干涉光刻制造的母版结构来制备偶氮聚合物纳米脊。在旋转盘共聚焦显微镜和双光子荧光显微镜上评估了暴露于与脊平行偏振的广泛波长光的影响。还使用用于光改性的514纳米光和用于荧光成像的561纳米光的交替循环对活细胞进行了实验。
我们发现,对于单光子和双光子成像,只有有限范围的波长光会导致偶氮聚合物纳米拓扑结构的光改性。这些结果表明,与先前研究所表明的相比,无损单光子和双光子荧光成像可以在相当宽的波长范围内进行。