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Hai-Feng Yang

Publications and source records attributed to Hai-Feng Yang.

5 recordsLinked to original sources

Characterization of chloramphenicol palmitate drug polymorphs by Raman mapping with multivariate image segmentation using a spatial directed agglomeration clustering method.

Chemical imaging analysis holds great potential in probing the chemical heterogeneity of samples with high spatial resolution and molecular specificity. This paper demonstrates the implementation of Raman mapping for microscopic characterization of tablets containing chloramphenicol palmitate polymorphs with the aid of a new multivariate image segmentation approach based on spatial directed agglomeration clustering. This approach performs the agglomeration clustering by stepwise merging the pixels possessing both spatial closeness and spectral similarity into clusters that define the image segmentation. The incorporation of spatial closeness into the clustering process enables the approach to improve the robustness and avoid poorly defined image segmentation arising from clusters with highly separated pixels. Additionally, the stepwise merging of clusters offers an F-statistic-based procedure to automatically ascertain the number of image segments. Raman mapping analysis of tablets containing two polymorphs of chloramphenicol palmitate followed by multivariate image segmentation reveals that the proposed technique offers the identification of each polymorph and a quantitative visualization of the spatial distribution of the polymorphs identified. This technique holds promise in rapid, noninvasive, and quantitative polymorph analysis for pharmaceutical production processes.

Chloramphenicol↗

[Surface enhanced Raman scattering spectra of phytic acid in the sol silver oxide].

Surface enhanced Raman scattering spectra of phytic acid were recorded in the sol oxide silver. Based on ab-initio/ STO-3 quantum calculations results, assignments to the vibrational modes of phytic acid were carried out. On the basis of the mechanism of SERS, the adsorption modes were suggested that phytic acid chemically adsorbed on the oxide silver surface through four phosphate bonds.

English Abstract↗

Quartz crystal microbalance bioaffinity sensor for biotin based on mixed self-assembled monolayers and metastable molecular complex receptor.

A quartz crystal microbalance (QCM) sensor was proposed for the detection of small molecule biotin based on the mixed self-assembled monolayer (SAM) of thiols on gold substrate and the bioaffinity difference between an analyte (biotin) and an analogue compound (HABA) in binding avidin. Avidin formed a metastable complex with 2-[(4-hydroxyphenyl)azo]benzoic acid (HABA) immobilized on the crystal surface. When the sensor contacts a sample solution containing biotin, the avidin was released from the sensor surface to form a more stable complex with biotin in solution. The frequency change recorded is proportional to the desorbed mass of avidin, and there is a clear mathematic relationship between the frequency change and the biotin concentration. The use of mixed SAMs allows the stable attachment of bioreceptor molecules on the QCM, and enhances the amount of the immobilized molecules on the QCM, as a longer "space arm" in the mixed SAMs makes this monolayer membrane more accessible to capture the immobilized molecules. The proposed bioaffinity sensor has nice response to biotin in the range of 0.017-1.67 microg/mL. The sensor could be regenerated under very mild conditions simply by reimmersion of the sensor into a biotin solution to desorb the surplus avidin.

Azo Compounds↗

Nanosized flower-like ZnO synthesized by a simple hydrothermal method and applied as matrix for horseradish peroxidase immobilization for electro-biosensing.

Nanosized flower-like ZnO was synthesized by a simple hydrothermal method which is a convenient, environment friendly, inexpensive and efficient process. Raman spectroscopy, X-ray diffraction (XRD) and scanning electron microscope (SEM) were used to confirm the material structure and the crystallite microstructure. Then ZnO was dispersed in the chitosan solution to form a ZnO/chitosan composite matrix for the fabrication of H2O2 biosensor. This composite combined the advantages of inorganic species (ZnO) and organic polymer (chitosan). The parameters affecting the fabrication and experimental conditions of biosensors were optimized. Using hydroquinone as the mediator, the biosensor showed a fast response of less than 5s with the linear range of 1.0x10(-5) to 1.8x10(-3) M H2O2 with a correlation coefficient of 0.995 (n=20). The detection limit of the sensor was found to be 2.0 microM, based on a signal-to-noise ratio of 3. The biosensor exhibited satisfactory reproducibility and stability and retained about 78% of its original response after 40 days storage in a phosphate buffer at 4 degrees C.

Biosensing Techniques↗

[Vascular endothelial growth factor gene expression in nasopharyngeal carcinoma cell line induced by hypoxia in vitro].

BACKGROUND & OBJECTIVE: Hypoxia is a common phenomenon in the tumor microenvironment of most solid tumors including human nasopharyngeal neoplasms. Hypoxia can induces vascular endothelial growth factor (VEGF) gene expression in some tumor cells like glioma cell line C6. The present investigations were conducted to study the effect of hypoxia on the VEGF gene expression in cultured nasopharyngeal carcinoma (NPC) cell line CNE-2Z in vitro and to discuss its impact on tumor metastasis. METHODS: Hypoxic culture model in vitro was established to test the VEGF gene expression in CNE-2Z cell line. After cultured in the hypoxia circumstance for 24 hours, VEGF expression were tested in mRNA level and protein level by RT-PCR and Western-blot analysis, respectively. RESULTS: VEGF mRNA isoforms VEGF189, VEGF165, VEGF145,and VEGF121 were identified by RT-PCR in cultured CNE-2Z cell line. All of the four VEGF mRNA isoforms expression were increased after treated under hypoxia for 24 hours. The mRNA level of four VEGF isoforms were 2.67+/-0.30, 2.05+/-0.03, 2.73+/-0.15, and 1.65+/-0.01 folds as those in normoxic cells,respectively. Western blot analysis showed that VEGF protein expression in CNE-2Z cells was 2.20+/-0.07 folds as that in normoxic cells. CONCLUSION: VEGF gene expresses in CNE-2Z cell line and can be induced by hypoxia in vitro, this mechanism may be involve in metastasis process of NPC by inproved neoplasm angiogenesis.

Cell Hypoxia↗