Yonghong ShaoHeng LiQiao WenYan WangJunle QuHanben Niu
We present a miniature fluorescence sectioning microscope which uses a diode-pumped solid-state (DPSS) laser as the light source and a fast translating diffuser to produce dynamically changing speckle patterns onto the back aperture of the objective to illuminate the sample.Optical sectioning, which originates from the statistical characteristics of laser speckles, is obtained by calculating the contrast of a series of fluorescence images.High contrast fluorescence sectioning images of bovine pulmonary artery endothelial (BPAE) cells are obtained.The image quality is similar to that of the images acquired by standard laser scanning confocal microscope (LSCM).Compared with LSCM, the laser speckle fluorescence microscope (LSFM) presented in this letter has many advantages, such as simple configurations, low cost, compact, and easy to operate, which makes it possible to have wide spread applications in biomedicine.
吴越前 Wu Yueqian徐欣 Xu Xin王吉祥 Wang Jixiang张欣 Zhang Xin史国华 Shi Guohua
蓝凯秋 LAN Kaiqiu杨西斌 YANG Xibin徐宝腾 XU Baoteng刘家林 LIU Jialin周伟 ZHOU Wei熊大曦 XIONG Daxi
Jianwei FuXiaoquan YangGuotao QuanHui Gong