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基于单壁碳纳米管的组织工程支架的多尺度光声显微镜研究。

Multiscale photoacoustic microscopy of single-walled carbon nanotube-incorporated tissue engineering scaffolds.

机构信息

Department of Biomedical Engineering, Washington University in St. Louis, St. Louis, MO 63130, USA.

出版信息

Tissue Eng Part C Methods. 2012 Apr;18(4):310-7. doi: 10.1089/ten.TEC.2011.0519. Epub 2011 Dec 22.

DOI:10.1089/ten.TEC.2011.0519
PMID:22082018
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3311878/
Abstract

Three-dimensional polymeric scaffolds provide structural support and function as substrates for cells and bioactive molecules necessary for tissue regeneration. Noninvasive real-time imaging of scaffolds and/or the process of tissue formation within the scaffold remains a challenge. Microcomputed tomography, the widely used technique to characterize polymeric scaffolds, shows poor contrast for scaffolds immersed in biological fluids, thereby limiting its utilities under physiological conditions. In this article, multiscale photoacoustic microscopy (PAM), consisting of both acoustic-resolution PAM (AR-PAM) and optical-resolution PAM (OR-PAM), was employed to image and characterize single-walled carbon-nanotube (SWNT)-incorporated poly(lactic-co-glycolic acid) polymer scaffolds immersed in biological buffer. SWNTs were incorporated to reinforce the mechanical properties of the scaffolds, and to enhance the photoacoustic signal from the scaffolds. By choosing excitation wavelengths of 570 and 638 nm, multiscale PAM could spectroscopically differentiate the photoacoustic signals generated from blood and from carbon-nanotube-incorporated scaffolds. OR-PAM, providing a fine lateral resolution of 2.6 μm with an adequate tissue penetration of 660 μm, successfully quantified the average porosity and pore size of the scaffolds to be 86.5%±1.2% and 153±15 μm in diameter, respectively. AR-PAM further extended the tissue penetration to 2 mm at the expense of lateral resolution (45 μm). Our results suggest that PAM is a promising tool for noninvasive real-time imaging and monitoring of tissue engineering scaffolds in vitro, and in vivo under physiological conditions.

摘要

三维聚合物支架为细胞和生物活性分子提供结构支撑,并作为其必要的基质,以促进组织再生。非侵入性实时成像支架和/或支架内组织形成的过程仍然是一个挑战。微计算机断层扫描是一种广泛用于表征聚合物支架的技术,但对于浸入生物流体中的支架对比度较差,从而限制了其在生理条件下的应用。在本文中,我们采用多尺度光声显微镜(PAM),包括声学分辨率光声显微镜(AR-PAM)和光学分辨率光声显微镜(OR-PAM),对浸入生物缓冲液中的单壁碳纳米管(SWNT)掺入的聚(乳酸-共-羟基乙酸)聚合物支架进行成像和表征。SWNTs 被掺入以增强支架的机械性能,并增强支架的光声信号。通过选择 570nm 和 638nm 的激发波长,多尺度 PAM 可以从血液和碳纳米管掺入的支架产生的光声信号进行光谱区分。OR-PAM 提供了 2.6μm 的精细横向分辨率和 660μm 的适当组织穿透深度,成功地定量了支架的平均孔隙率和孔径分别为 86.5%±1.2%和 153±15μm。AR-PAM 进一步将组织穿透深度扩展到 2mm,但代价是横向分辨率(45μm)降低。我们的结果表明,PAM 是一种有前途的工具,可用于非侵入性实时成像和监测组织工程支架在体外,以及在生理条件下的体内。

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