Biomedical subjects

Jing Teng

Publications and source records attributed to Jing Teng.

5 recordsLinked to original sources

PubMed2006

Community surveys and risk factor analysis of human alveolar and cystic echinococcosis in Ningxia Hui Autonomous Region, China.

OBJECTIVE: To determine the true community prevalence of human cystic (CE) and alveolar (AE) echinococcosis (hydatid disease) in a highly endemic region in Ningxia Hui, China, by detecting asymptomatic cases. METHODS: Using hospital records and "AE-risk" landscape patterns we selected study communities predicted to be at risk of human echinococcosis in Guyuan, Longde and Xiji counties. We conducted community surveys of 4773 individuals from 26 villages in 2002 and 2003 using questionnaire analysis, ultrasound examination and serology. FINDINGS: Ultrasound and serology showed a range of prevalences for AE (0-8.1%; mean 2%) and CE (0-7.4%; mean 1.6%), with the highest prevalence in Xiji (2% for CE, 2.5% for AE). There were significant differences in the prevalence of CE, AE and total echinococcosis between the three counties and villages (with multiple degrees of freedom). While hospital records showed 96% of echinococcosis cases attributable to CE, our survey showed a higher prevalence of human AE (56%) compared to CE (44%). Questionnaire analysis revealed that key risk factors for infection were age and dog ownership for both CE and AE, and Hui ethnicity and being female for AE. Drinking well-water decreased the risk for both AE and CE. CONCLUSION: Echinococcosis continues to be a severe public health problem in this part of China because of unhygienic practices/habits and poor knowledge among the communities regarding this disease.

Adolescent↗

PubMed2005

In-situ observation of switchable nanoscale topography for y-shaped binary brushes in fluids.

Direct, in-fluid observation of the surface morphology and nanomechanical properties of the mixed brushes composed of Y-shaped binary molecules PS-PAA revealed nanoscale network-like surface topography formed by coexisting stretched soluble PAA arms and collapsed insoluble PS chains in water. Placement of Y-shaped brushes in different fluids resulted in dramatic reorganization ranging from soft repellent layer covered by swollen PS arms in toluene to an adhesive, mixed layer composed of coexisting swollen PAA and collapsed PS arms in water. These binary layers with the overall nanoscale thickness can serve as adaptive nanocoatings with stimuli-responsive properties.

Acrylic Resins↗

PubMed2004

Interfacial micellar structures from novel amphiphilic star polymers.

An amphiphilic heteroarm star polymer containing 12 alternating hydrophobic/hydrophilic arms of polystyrene (PS) and poly(acrylic acid) (PAA) connected to a well-defined rigid aromatic core was studied at the air-water and the air-solid interfaces. At the air-water interface, the molecules spontaneously form pancakelike micellar aggregates which measure up to several microns in diameter and 5 nm in thickness. Upon reduction of the surface area per molecule to 7 nm2, the two-dimensional micelles merged into a dense monolayer. We suggest that confined phase separation of dissimilar polymer arms occurred upon their segregation on the opposite sides of the rigid disklike aromatic core, forcing the rigid cores to adopt a face-on orientation with respect to the interface. Upon transfer onto solid supports the PS chains face the air-film interface making it completely hydrophobic, and the PAA chains were found to collapse and form a thin flattened underlayer. This study points toward new strategies to create large 2D microstructures with facial amphiphilicity and suggests a profound influence of star molecular architecture on the self-assembly of amphiphiles at the air-water interface.

Acrylic Resins↗

PubMed2003

Y-shaped amphiphilic brushes with switchable micellar surface structures.

We observed novel nanoscale surface structures of segregated pinned micelles and craterlike micelles formed by grafted Y-shaped molecules and their reversible reorganization in selective solvents. The Y-shaped molecules have two incompatible polymer chains (polystyrene and poly(tert-butyl acrylate)) attached to a functional stemlike segment capable of covalent grafting to a functionalized silicon surface. Postgrafting hydrolysis of poly(tert-butyl acrylate) arms imparts amphiphilicity to the brush. We demonstrated that spatial constraints induced by a chemical junction of two relatively short (6-10 nm) dissimilar arms in such Y-shaped molecules lead to the formation of segregated micellar surface nanostructures in the grafted layer. We proposed a model of these segregated pinned micelles and the corresponding reverse micelles (craterlike structures) featuring different segregation states of hydrophobic polystyrene and hydrophilic poly(acrylic acid) arms. The arms undergo conformational rearrangements in selective solvents in a controlled and reversible fashion. These nanoscale structural reorganizations define adaptive macroscopic wetting surface properties of the amphiphilic Y-shaped brushes. This surface structure and switchable behavior can be considered as a promising way toward the patterning of solid substrates with adaptive nanowells, which could be used for trapping of adsorbing nanoscale objects.

Journal Article↗

PubMed2003

Synthesis and self-assembly of a heteroarm star amphiphile with 12 alternating arms and a well-defined core.

We report on a stepwise synthesis of a heteroarm starlike amphiphile containing 12 alternating arms (six polystyrene and six poly(acrylic acid)) connected to a hexabiphenyl aromatic core. The synthesis does not involve polymerization, and only commercially available precursors are used. Most importantly, this amphiphile undergoes self-assembly into spherical and wormlike cylindrical micelles in aqueous and methanol solutions, and forms reverse 1D micellar structures in chloroform. This remarkable morphological diversity of the reported amphiphile 1 is believed to be a direct consequence of its well-defined molecular architecture.

Journal Article↗