Study on the mean trabecular bone spacing based on fundamental frequency estimation method

Ultrasonic backscatter signals from the cancellous bone can be used to diagnose osteoporosis effectively due to its ability to provide the information of bone microstructure. Mean trabecular bone spacing(MTBS)is one of the important parameters for characterization of bone microstructure.This paper proposed a MTBS estimating method based on the fundamental frequency estimation,which was applied to backscatter signals from simulations, and in vitro bovine trabeculae.The estimated MTBS were compared with those of simplified inverse filter tracking(SIFT)algorithm and autoregressive(AR)cepstrum method.The results demonstrated that the proposed method is very robust for the MTBS estimation with more precise estimates and smaller estimated variance in the presence of a small signal-to-noise ratio (SNR),and a large scattering strength ratio of diffuse scatterers to regular ones.     

时频方法分析长骨中的超声导波及皮质骨厚度

超声导波在长骨中传播时,接收信号中含有相互叠加的多个导波模式。本文提出将希尔伯特-黄变换(HHT)用于分析叠加的多模式导波信号,将其分解成许多单个独立的模式,然后对分解出的模式求得其对应频率下的群速度,并与短时傅里叶变换所得的结果进行比较。通过与理论计算结果比较,可得到长骨皮质骨的厚度。研究结果表明,实验得到的厚度与实际厚度一致。说明通过测量导波模式的速度可以评价皮质骨的厚度,也说明HHT方法是一种识别叠加多模式导波信号的有效方法。     

长骨裂纹宽度和角度对低阶超声导波的影响

超声导波检测长骨骨折和监测骨折愈合已成为一种极具前景的课题,但高频厚积下导波多模式混叠带来的模式识别和分离问题一直是一个难点。为避免上述问题,在低频下仅激励两个低阶兰姆波SO和AO模式,采用二维时域有限差分(2DFDTD)法定量分析裂纹宽度和骨折角度对SO和AO幅度的影响。结果表明,SO与AO模式的幅度均随裂纹宽度的增加而下降;AO的幅度随骨折角度增大而上升,SO幅度随骨折角度增大先下降后上升,转折点约为45°。SO与AO的幅度比值在不同骨折角度下均能较好地表征裂纹宽度的变化,可为横断型和斜切型长骨骨折状况的超声评价及骨折愈合监测提供依据。     

Barker码激励超声导波在长骨检测中的应用

单脉冲激励的超声导波在长骨中传播时,信号的衰减大,导致接收信号的幅度很小,且噪声严重。Barker码激励能有效增大接收信号幅度,提高信噪比(SNR)。将其应用到超声导波长骨检测中,进行仿真和长骨实验,得到的信号分别用加权匹配滤波器和有限冲激响应-最小均方误差(FIR-LS)逆滤波器进行压缩,并与单脉冲激励的结果进行了对比。结果表明,对于13位的Barker码,采用加权匹配滤波器进行解码时,压缩信号幅度是单脉冲激励接收信号的13倍;而FIR-LS逆滤波器则达到-63.59 dB的峰值旁瓣水平(PSL),更好地抑制噪声。说明可以将Barker码激励超声导波应用于长骨的检测中。     

基于离散随机介质平均散射声功率的无损测温方法

生物组织中超声散射回波的平均功率与其温度有关.该理论包含:(1)生物组织近似为离散随机介质.(2)离散随机介质的平均散射功率与组织的衰减系数α和声速c有关。对于似水生物组织(如:猪肝),当温度升高时,衰减系数的减小使平均散射声功率增加,但其影响大小与时间窗△t有关,而声速的增大则使平均散射声功率减小。实验结果表明:生物组织的平均散射声功率随温度变化趋势明显,该结果提供一种肿瘤热疗无损伤检测温度的新方法。     

3D-Non-destructive Imaging through Heavy-Metal Eosin Salt Contrast Agents

Conventional histology is a destructive technique based on the evaluation of 2D slices of a 3D biopsy. By using 3D X-ray histology these obstacles can be overcome, but their application is still restricted due to the inherently low attenuation properties of soft tissue. In order to solve this problem, the tissue can be stained before X-ray computed tomography imaging (CT) to enhance the soft tissue X-ray contrast. Evaluation of brominated fluorescein salts revealed a mutual influence of the number of bromine atoms and the cations applied on the achieved contrast enhancement. The dibromo fluorescein barium salt turned out to be the ideal X-ray contrast agent, allowing for 3D imaging and subsequent complementing counterstaining applying standard histological techniques.     

Strained cyclophane natural products: macrocyclization at its limits

Cyclophane natural products comprise an intriguing class of structurally diverse compounds. As inherent for all cyclic compounds regardless of their origin, macrocyclization is naturally the most decisive step, which defines the overall efficiency of the synthetic pathway. Especially in small cyclophane molecules, this key step constitutes an even greater challenge. Due to the strain imparted by the macrocyclic system, free rotation of the benzene ring(s) is often restricted depending on both the constitution of the tether and the aromatic portions. Not surprisingly, the synthesis of natural cyclophanes with their often outstanding pharmaceutical activities and the inherent issues associated with their preparation has attracted much attention among the synthetic community. In particular, it stimulated the development of new strategies for the ring-closing step, as often otherwise well established and robust reactions fail to perform effectively. In this review, we describe the challenges synthetic chemists are facing during the synthesis of this small, but structurally and biologically fascinating class of natural products, concentrating on the representatives exhibiting configurational stability. The main focus will be on the different concepts for the installation of the macrocyclic system, in most cases the central problem in assembling these extremely rigid molecules.     

骨折长骨中超声导波传播特性的仿真研究

采用超声导波评价长骨骨折已成为近两年来的一个研究热点.本文采用混合边界元方法(HBEM)对超声导波在骨裂长骨中的传播情况以及各导波模式的反射系数和透射系数进行了数值分析.研究结果表明,入射导波模式经由裂纹处模式转换后依然保持为主要接收模式不变.对某一裂纹,各模式透射系数常在相近的频率点上达到局部峰值.对于不同深宽比(d/w)裂纹,某些模式透射系数曲线局部峰值所对应的频率存在着相互错开的现象,这些结果可用于选择最优入射导波模式和频率,以便更好地定量评价骨质以及骨裂状况.     

Hydrothermal Synthesis and Crystal Structure of a Novel Polyoxometalate K(C_4N_2H_(12))_4(C_4N_2H_(11))_(2-)[Mo_8~ⅤMo_4~ⅥCdP_8O_(54)(OH)_8]F·6H_2O

The title compound 1 has been synthesized by the reaction of H_2MoO_4, CdCl_2, H_3PO_4, KF, piperazine hexahydrate and water in aqueous solution under mild hydrothermal conditions. Single-crystal X-ray analysis reveals that the title compound crystallizes in the triclinic system, space group P(-1) with a = 14.049(3), b = 15.972(3), c = 20.043(4) (A), α = 85.82(3), β = 81.28(3),γ = 67.15(3)°, V= 4095.9(14) (A)~3, M_r = 3204.62, Z=2,D_c = 2.598 g/cm~3,μ = 2.360 mm~(-1), F(000) = 3124, the final R = 0.0314, wR = 0.0826 and S = 0.989 for 18592 observed reflections with I > 2σ(I). The crystal packing is stabilized by N-H…O and O-H…O intra- and intermolecular hydrogen bonds to form an infinite 3D network.     

A Simple and Rapid Label-free Fluorimetric “Turn Off-on” Sensor for Cadmium Detection Using Glutathione-capped CdS Quantum Dots

A convenient label-free fluorescence(FL) nanoprobe for rapid detection of cadmium(Cd) was established using glutathione-capped CdS quantum dots(QDs) and 1,10-phenanthroline(phen). The prepared CdS QDs exhibited a strong FL emission at 536 nm, which could be quenched by phen due to the photoinduced hole transfer(PHT) mechanism. The existence of Cd effectively recovered the FL intensity of CdS QDs, which was due to the easy detachment of phen from the surface of QDs to form[Cd(phen)₂(H₂O)₂]²⁺ in solution. Cd concentrations were linearly correlated with the FL intensity in the range of 0.0625-1.25 μmol/L under the optimized conditions and the detection limit was 0.01 μmol/L. Finally, the Cd concentration was accurately quantified in real water sample using the proposed sensor.