Concurrent detection of cabozantinib as an anticancer agent and its major metabolites in human serum using fluorescence-coupled micellar liquid chromatography

A novel, highly sensitive, simple, and rapid strategy was designed and developed for simultaneous determination of cabozantinib (CBZ) as an anticancer agent and its main metabolites including monohydroxy sulfate (EXEL-1646), N-oxide (EXEL-5162(, amide cleavage product (EXEL-5366), and 6-desmethyl amide cleavage product sulfate) EXEL-1644). Measurements were done through a micellar liquid chromatography (MLC) method coupled with fluorescence detection. The high-performance liquid chromatography (HPLC) was performed using a Kinetex C18 100 Å column as well as acetonitrile, cetyltrimethylammonium bromide (CTAB; 0.2 mol.L^?1), and tris buffer (pH 8.5) solutions as the mobile phase at a 40:50:10 (v/v) ratio. The method’s linearity (20 to 700 ng.mL^?1), limit of detection (LOD; 2.11 to 3.69 ng.mL^?1), limit of quantification (LOQ; 20 to 30 ng.mL^?1), intra- and inter-day precisions (RSD < 4.00%), selectivity, recovery, and robustness were fully evaluated. According to the obtained results, the developed method can be used for simple and rapid (~35 min) quantification of CBZ as an anticancer drug and its major metabolites in human serum samples with high sensitivity and low cost.     

Comparison of Two Rhodamine-Polyamine Polystyrene Solid-phase Fluorescence Sensors for Hg(II) Detection Based on Theoretical Calculation

Two novel rhodamine-based polystyrene solid-phase fluorescence sensors PS-PA-I and PS-PA-II with different lengths of polyamines were synthesized for Hg(II) determination. The detection mechanism involving the Hg(II) chelation-induced spirocycle open of rhodamine was proposed with the aid of theoretical calculation. The stronger N-Hg bond and the longer polyamine chain in PS-PA-II led to a better selectivity, much higher and more quickly fluorescence response to Hg(II).     

Voltammetric Label‐free Immunosensors for the Diagnosis of Cystic Echinococcosis

Cystic echinococcosis (CE) or hydatid disease is a parasitic infection caused by Echinococcus granulosus. Early serodiagnosis and continuous monitoring of the disease is very important for medical treatment. Here, we report the detecting of both echinococcus antigen and antibody for the diagnosis of hydatid disease using square wave voltammetry (SWV)‐based immunosensors. The gold electrodes were functionalized using cysteamine/phenylene diisothiocyanate linkers and used for the immunosensors fabrication. The hydatid antigen and antibody immunosensors were constructed by the immobilization of either purified rabbit polyclonal antibody or recombinant antigen B (AgB), respectively on the functionalized gold electrodes surfaces. The detection in both cases was achieved by following the change in the SWV reduction peak current of the ferro/ferricyanide redox couple upon antibody or antigen binding. These immunosensors enabled the detection of echinococcus antigen and antibody within a concentration range of 1 pg.mL^?1 to 1 μg.mL^?1 with detection limits of 0.4 pg.mL^?1 and 0.3 pg.mL^?1, respectively. A preliminary application of the developed immunosensor was performed in spiked serum sample showing good recovery percentages ranging from 102 to 110 % for both hydatid antibody and antigen detection. This easy‐to‐use, sensitive, and low cost quantitative method holds great promise for the early diagnosis of hydatid disease and thus, better managements and treatment outcomes.     

基于庞加莱截面的语音基音检测

提出了利用庞加莱截面检测语音信号基音的方法,通过延时重构语音信号的相空间,在相空间内计算通过某点的庞加莱截面,根据相轨迹穿过截面上初始点邻域交点进行基音检测;实验表明,基于庞加莱截面的语音信号的方法,描述语音信号的非线性特性具有较高的准确性和时间分辨率。     

Adjusting the selectivity of inorganic anion separation by capillary electrophoresis

The separation of the principal inorganic anions (bromide, carbonate, chlorate, chloride, fluoride, nitrate, nitrite, sulfate, phosphate) has been achieved using a capillary electrophoresis system with indirect UV detection at 260 nm. Several types of cationic surfactants (quaternary ammonium, phosphonium or methonium) were tested as electroosmotic flow modifiers and added to a chromatebased buffer prepared from potassium dichromate. The influence of many physicochemical parameters such as nature and concentration of cationic surfactant, buffer pH, dichromate concentration buffer, voltage and temperature upon the migration time of an analyte anion, peak efficiency, asymmetry factor, and finally resolution has been investigated. A linear relationship between the corrected area and the anion concentration in the 2.5–50 ppm range was obtained, thus allowing the quantitative analysis of anions in mineral water. Finally, by increasing the hydrodynamic injection time, the separation of inorganic anions at a low concentration level of 50 ng/ml was achieved without any loss of resolution.     

Capillary zone electrophoresis with UV-scanning detection for the analysis of metal species and their organic binding partners in biological systems

A capillary zone electrophoretic method with UV-scanning detection for the separation and identification of both free ligands and metal species is presented. The electrophoretic behavior of naturally occurring binding partners such as organic acids and amino acids was studied and compared with their metal-complexes. Copper(II) complexes of citrate and amino acids showed decreased electrophoretic mobilities and altered UV spectra. The optimized method was validated on ultrafiltered cow's milk and human milk samples. In cow's milk six low molecular weight substances, including citrate, orotate, and hippurate, could be separated. Metal supplementation with Cu(II), Ni(II), or Zn(II) decreased not only the citrate peak but also the orotate signal and in the case of copper(II) supplementation a new signal for the copper(II)-citrate complex appeared. In human milk samples various amino acids such as glutamate, phenylalanine, tyrosine, and tryptophan could be identified besides citrate. The electrophoretic mobilites and peak areas of the amino acids were also influenced by the metal supplementation.     

心音心电检测仪电磁兼容问题的测试分析及整改方法

现代医疗器械更偏向于高精确度、高敏感度和小型化,其所处的电磁环境越来越复杂。外界电磁干扰对医疗设备会产生影响,严重时甚至影响医生的诊断。本文结合心音心电检测仪,基于医疗器械测试标准对传导发射测试、辐射发射测试和静电放电这3个测试项目进行了研究,提出了壳体整改,增加滤波电路、磁环、电荷释放电路等整改方法。对其他类型相关医疗器械的电磁兼容问题分析和整改,有一定的参考借鉴作用。     

基于THz-TDR的芯片金属微带线缺陷检测

针对体积小、走线密集、集成度高的封装芯片缺陷检测,目前的主要检测手段存在精度低、周期长等缺点。为弥补传统检测方法的不足,作者结合太赫兹技术与时域反射技术,探究对芯片上金属导线缺陷检测的可行性。首先在不同宽度的金属微带线上加工了不同比例的凸起、凹槽缺陷,模拟集成芯片中金属导线的不完全开/短路等阻抗不匹配情况,利用太赫兹时域反射计采集其时域反射信号。然后根据时域反射脉冲对应的时间分别对不同缺陷程度、不同缺陷类型进行定性分析,并精确计算出了芯片上金属微带线的缺陷位置。最后利用有限元分析法对硅基底上存在缺陷的金属微带线进行仿真分析,与实验结果具有良好的一致性。该研究表明,太赫兹技术与时域反射技术结合能够实现对芯片上金属导线缺陷的诊断检测,为集成芯片的缺陷检测提供了经验参考。     

Fluorogenic Detection of Human Serum Albumin Using Curcumin-Capped Mesoporous Silica Nanoparticles

Mesoporous silica nanoparticles loaded with rhodamine B and capped with curcumin are used for the selective and sensitive fluorogenic detection of human serum albumin (HSA). The sensing mesoporous silica nanoparticles are loaded with rhodamine B, decorated with aminopropyl moieties and capped with curcumin. The nanoparticles selectively release the rhodamine B cargo in the presence of HSA. A limit of detection for HSA of 0.1 mg/mL in PBS (pH 7.4)-acetonitrile 95:5 v/v was found, and the sensing nanoparticles were used to detect HSA in spiked synthetic urine samples.