光学相干层析用于牙齿病变的检测

阐述了适用于牙齿结构成像的光学相干层析成像(OCT)系统。系统光源中心波长为1 310 nm,成像分辨率10μm,在牙内成像深度2 mm,成像速度1幅/秒,系统信噪比100 dB。利用此OCT仪清晰检测到牙齿样品的牙釉质和牙本质,观察到牙釉质与牙本质的分界面以及正常牙齿牙釉质与龋齿牙齿牙釉质OCT图像的区别。进一步设计研制了适用于口腔内探测的小型OCT探头。     

人手部皮下微循环特性随深度变化的研究

本研究使用手持式扫频光学相干层析(SSOCT)系统分别在人左手无名指指甲上方、无名指指腹和手掌大拇指根部选取3 mm×3 mm区域进行了在体成像,使用指数补偿方法还原血流信息,获取不同深度的血流正面光学断层图像(en face图像),从血管灌注密度(PD)、血管直径(VD)两个方面分析了微循环随深度的变化特性。试验结果证明,在上述三个成像位置中,随着成像深度的增加,血管PD与血管VD均增大,血流信息的丰富程度增加,但同时en face图像的清晰度有所下降。其中左掌大拇指根部微血管最为细密,血流信息较为丰富,比较适宜作为微循环疾病诊断研究的成像部位。分层投影结果显示,左手无名指指甲上方部位在成像深度较浅(220～660μm)时,血管PD明显小于其他两个成像部位,说明此处在该范围内血流信息丰富程度不够。本文测量了随深度变化的手部血流几何学特征,验证了光学相干层析(OCT)技术基于手部皮下微循环光学断层图像进行疾病诊断的可行性。许多微循环疾病早期就已经产生了微血管病变,因此对这种微循环变化的探测在疾病的早期诊断方面具有临床指导意义。     

基于自适应光学的视网膜单细胞光学相干层析成像技术

介绍了一种基于CCD相机的并行光学相干层析成像技术,将所建立的层析成像系统和自适应光学视网膜相机结合。利用一维光学相干层析系统对人眼视网膜进行追踪并控制相干门在视网膜内的位置,利用基于CCD相机的二维光学相干层析成像系统记录视网膜的干涉图像。用眼模型和牛眼视网膜组织对系统进行了测试,通过将4幅干涉图像的获取时间控制在7 ms以内来减少视网膜运动对成像的影响;系统的轴向点扩展函数和灵敏度分别达到10 μm和76 dB。实验结果表明,所建立的基于自适应光学的视网膜光学相干层析成像系统的空间分辨率和灵敏度远远高于其它基于自适应光学的视网膜成像技术。     

基于OCT技术的鼠皮肤激光热损伤修复过程的监测

采用Er:YAG激光(波长为2 940 nm,能量密度为:2.5 J/cm2单光斑,扫描次数为4)照射活体小白鼠皮肤,利用光学相干层析成像(optical coherence tomography,OCT)技术在活体小鼠上观察其皮肤组织在激光作用之前及作用之后光热损伤修复的整个过程,得到了激光光热作用下引起损伤的皮肤组织在此过程中皮肤光学特性参数的变化情况,发现皮肤修复过程中光学参数有显著差异,并分析了这些差异引起的原因,以揭示激光美容中并发症主要因素。     

传统光学相干断层成像:软骨双折射特性的研究

传统光学相干断层成像可实现无损伤在体检测,具有较高的分辨率和灵敏度。获取生物组织的双折射信息可望是其应用之一。本文用传统光学相干断层成像系统以动物模型对关节软骨进行了研究,对软骨组织的传统光学相干断层图像的层结构随脱水和机械作用的变化进行了分析。结果表明,传统光学相干断层成像系统在一定程度上可用于监测由其胶原质纤维排列决定的软骨组织的双折射和密度。     

大鼠乙酸性胃溃疡模型的光学相干层析成像研究

应用光学相干层析成像技术对大鼠乙酸胃溃疡模型的愈合过程进行初步检测,探讨光学层析成像技术在消化性溃疡疾病中的诊断价值及其意义.实验中应用乙酸局部刺激法建立大鼠胃溃疡模型,应用光学相干层析成像系统于模型复制后不同时期进行扫描,观察在其自然愈合过程中溃疡组织的变化情况,并且对其图像进行比较分析.结果显示:利用光学相干层析成像技术能够很准确的区别正常和非正常的胃组织,并且能够区分不同的愈合时期胃溃疡组织的图像,以及对病变组织进行一定深度的扫描.研究表明:光学相干层析成像系统对乙酸胃溃疡的愈合和复发情况的观察是一种很有发展潜力的检测手段,对其愈合质量判定亦具有一定的价值.     

基于光学相干层析图像的离体牙三维重建

利用shear-warp算法对离体牙的光学相干层析图像进行三维重建,通过不透明度传递函数的合理设置及光照模型的引入实现牙齿内部组织结构的可视化,便于医生在早期龋齿诊断中定位病变.介绍了shear-warp算法的原理、用于龋齿检测的全光纤光学相干层析成像系统及其二维层析图,以及利用离体牙牙冠的二维层析图重建获得三维结构图.     

用于全眼段成像和视轴参数测量的四焦点开关光学相干断层扫描

本文演示了四焦点开关傅里叶域光学相干断层扫描系统用于全眼段成像和体内视轴参数（VAP）测量的可行性. 使用包括不同厚度平行玻璃板的两个同步转盘来将探测光束的焦点位置从角膜以及晶状体的前部和后部切换到视网膜. 该过程同时增加了参考光束的深度范围. 这种多级聚焦的方法可以使探测光束完全聚焦在人眼的每个部分. 初步实验表明,该方法可以实现全眼段成像和包括中央角膜厚度、前房深度、晶状体厚度和轴长在内的VAP测量.     

位相分辨偏振灵敏光学相干层析术:组织双折射特性的成像与定量分析

我们研制了一种基于光纤的位相分辨偏振灵敏光学相干层析成像系统。该系统中的偏振状态控制设量在参考臂而非光源臂上,因而使得光抵达样品的传输效率大大提高。鉴于光源的部分偏振性,入射于样品上的光含有任意偏振状态的分量,通过对参考光偏振状态的调制,就可相干地提取对应于入射光四种正交偏振状态并经样品后向散射的光信号。基于斯托克斯矢量夹角在无损光纤系统传输的变换不变性,我们能利用测量臂中光信号的斯托克斯参数来确定双折射样品深度分辨的位相延迟信息。利用所研制的偏振灵敏光学相干层析成像系统,不仅确认了韧带和软骨的双折射性质,而且定量分析了不同条件下韧带的双折射变化．研究结果表明：韧带松弛可使其双折射特性明显减弱,而韧带经拉伸后,其双折射特性的变化却不明显。     

宽场光学相干层析成像技术在眼科学中的研究进展

宽场光学相干层析成像技术(WF-OCT)是光学相干成像技术领域的一个新方向。其接收干涉信号获得样品的二维信息,一次性建立样品整个断面的图像,可快速高效地获得样品的成像信息,以实现对物体特质的研究。本文就WF-OCT的基本原理、系统的基本构成及特点,以及近年来在眼科疾病诊断方面的应用进行了综述,可为WF-OCT仪器的设计及其在眼科医学中的应用提供思路和参考。     

A Unique Protease Cleavage Site Predicted in the Spike Protein of the Novel Pneumonia Coronavirus (2019-nCoV) Potentially Related to Viral Transmissibility

正Dear Editor,In December 2019, a novel human coronavirus caused an epidemic of severe pneumonia(Coronavirus Disease 2019,COVID-19) in Wuhan, Hubei, China(Wu et al. 2020; Zhu et al. 2020). So far, this virus has spread to all areas of China and even to other countries. The epidemic has caused 67,102 confirmed infections with 1526 fatal cases     

Curcuminoids as inhibitors of thioredoxin reductase: A receptor based pharmacophore study with distance mapping of the active site

Curcumin is the yellow pigment of turmeric that interacts irreversibly forming an adduct with thioredoxin reductase (TrxR), an enzyme responsible for redox control of cell and defence against oxidative stress. Docking at both the active sites of TrxR was performed to compare the potency of three naturally occurring curcuminoids, namely curcumin, demethoxy curcumin and bis-demethoxy curcumin. Results show that active sites of TrxR occur at the junction of E and F chains. Volume and area of both cavities is predicted. It has been concluded by distance mapping of the most active conformations that Se atom of catalytic residue SeCYS498, is at a distance of 3.56 from C13 of demethoxy curcumin at the E chain active site, whereas C13 carbon atom forms adduct with Se atom of SeCys 498. We report that at least one methoxy group in curcuminoids is necessary for interation with catalytic residues of thioredoxin. Pharmacophore of both active sites of the TrxR receptor for curcumin and demethoxy curcumin molecules has been drawn and proposed for design and synthesis of most probable potent antiproliferative synthetic drugs.     

Comparative morphology of the carpel in the Liliaceae: Hewardieae, Petrosavieae, and Tricyrteae

The young pistils in the melanthioid tribes, Hewardieae, Petrosavieae and Tricyrteae, are uniformly tricarpellate and syncarpous. They lack raphide idioblasts. All are multiovulate, with bitegmic ovules. The Petrosavieae are marked by the presence of septal glands and incomplete syncarpy. Tepals and stamens adhere to the ovary in the Hewardieae and the Petrosavieae but not in the Tricyrteae. Two vascular bundles occur in the stamens of the Hewartlieae and Tricyrtis latifolia. Ventral bundles in the upper part of the ovary of the Hewardieae are continuous with compound septal bundles and placental bundles in the lower part. Putative ventral bundles occur in the alternate position in the Tricyrteae and putative placental bundles in the opposite. position in the Petrosavieae. The dichtomously branched stigma in each carpel of the Tricyrteae is supplied by a bifurcated dorsal bundle.     

Enterovirus 71 3C proteolytically processes the histone H3 N-terminal tail during infection

Highlights
1. The N-terminal tail of histone H3 is specifically cleaved during EV71 infection.
2. Viral protease 3C is identified as a protease responsible for proteolytically processing the N-terminal H3 tail.
3. Our finding reveals a new epigenetic regulatory mechanism for Enterovirus 71 in virus-host interactions.     

Detection of EBV and HHV6 in the Brain Tissue of Patients with Rasmussen’s Encephalitis

Rasmussen’s encephalitis (RE) is a rare pediatric neurological disorder, and the exact etiology is not clear. Viral infection may be involved in the pathogenesis of RE, but conflicting results have reported. In this study, we evaluated the expression of both Epstein-Barr virus (EBV) and human herpes virus (HHV) 6 antigens in brain sections from 30 patients with RE and 16 control individuals by immunohistochemistry. In the RE group, EBV and HHV6 antigens were detected in 56.7% (17/30) and 50% (15/30) of individuals, respectively. In contrast, no detectable EBV and HHV6 antigen expression was found in brain tissues of the control group. The co-expression of EBV and HHV6 was detected in 20.0% (6/30) of individuals. In particular, a 4-year-old boy had a typical clinical course, including a medical history of viral encephalitis, intractable epilepsy, and hemispheric atrophy. The co-expression of EBV and HHV6 was detected in neurons and astrocytes in the brain tissue, accompanied by a high frequency of CD8⁺ T cells. Our results suggest that EBV and HHV6 infection and the activation of CD8⁺ T cells are involved in the pathogenesis of RE.