Poly(ferrocenyldimethylsilane) and poly(ferrocenylmethylphenylsilane) have been prepared via the thermal ring-opening polymerization of the corresponding strained, silicon-bridged ferrocenophanes. It was found that the molecular weights of resultant polymers depend on the polymerization time. Their electrochemical behavior in aqueous electrolytes was investigated by cyclic voltammetry. 相似文献
The electrochemical behavior of ciprofloxacin (CFX) and its interaction with the natural calf thymus DNA (ctDNA) is studied
by using pulse difference voltammetry on a carbon electrode. CFX shows a well-defined oxidative peak at + 0.88 V. As a result
of reaction with ctDNA,the oxidative peak of CFX decreased markedly. According to the electrochemical equation deduced in
this paper, the binding constant of 1.36 × 105 (mol/L)−1 and the binding size of 1.94 (base pairs) of CFX with ctDNA were obtained by nonlinear fit analysis of the electrochemical
data. The mechanism of the interaction was explored.
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Translated from Journal of Zhejiang University (Science Edition), 2007, 34(3): 330–334 [译自: 浙江大学学报(自然科学版)] 相似文献
Chemotherapy side effects are minimized, and therapeutic results are enhanced by combination therapy, which is extensively utilized in cancer therapy. MTT experiment showed that compared to the free drugs calreticulin (CRT) and gemcitabine (GEM), GEM-CRT@NPs significantly increased the cytotoxicity of endometrial cancer (Ishikawa cells and KLE cells). These drugs were conjugated to a tri-block copolymeric framework. GEM-CRT@NPs were studied using HR-TEM and DLS analysis to determine particle size and zeta potential. Biochemical staining analyses were also used to investigate the morphological characteristics of endometrial cancer cell lines. After KLE and Ishikawa cancer cells were treated with GEM-CRT@NPs, endometrial cell shape was altered, as evidenced by nuclear fragmentation and nuclear condensation (apoptosis hallmarks). Additionally, the most significant apoptosis ratio to mitochondrial membrane potential indicates that the mitochondrial membrane potential is responsible for the cell's death. Upon treatment with GEM-CRT@NPs, systemic toxicity analysis revealed minimal histological abnormalities and significant blood chemistry alterations, and a near-normal look of the organs. Endometrial cancer treatment may be enhanced with the use of the targeted combination therapeutic system.
In this paper, an absolute‐phase unwrapping and speckle suppression approach to reconstruct a three‐dimensional (3‐D) image of an object with laser digital holography is described. This method offers three advantages to enhance the performance of the phase reconstruction technique. First, both speckle suppression and phase unwrapping are processed in the complex amplitude domain rather than in the single phase or amplitude domain. With this approach, the phase details of the object are better preserved upon phase reconstruction. Second, the proposed algorithm requires no threshold determination and thus achieves self‐adaptive speckle suppression and robust phase unwrapping, in contrast to other methods. Finally, an improved dual‐domain image denoising method is applied to further remove speckle‐remnant‐induced phase distortion. Ideal 3‐D phase reconstruction results are obtained both theoretically and experimentally for the first time. 相似文献
In the present study, ionic liquid (IL)‐modified Fe3O4 magnetic nanoparticles (Fe3O4) were synthesized by the thiol‐ene click reaction for magnetic solid‐phase extraction (MSPE) of polycyclic aromatic hydrocarbons (PAHs) in water and smoked meat samples. An IL 1‐vinyl‐3‐butylimidazolium bromide was firstly synthesized, and then immobilized on the surface of thiol group‐functionalized Fe3O4 via a thiol‐ene click reaction. The as‐synthesized Fe3O4@ILs were characterized using Fourier transform infrared spectroscopy, X‐ray diffraction, and transmission electron microscopy. Various parameters (including the amount of adsorbent, extraction time, sample volume, and desorption conditions) affecting MSPE were optimized. Under the optimum conditions, the limits of detection of four PAHs in the range of 0.6–7.2 ng/L were obtained using high‐performance liquid chromatography–ultraviolet detection. The accuracy of the method was assessed by recovery measurements on spiked real samples and good recovery of 80–108% with relative standard deviations lower than 8.16% was achieved. The enrichment factors ranging from 699 to 858 were obtained for the analytes. This result indicated that the proposed method had great potential for sample preparation. 相似文献