Application of metabolomics in toxicity evaluation of traditional Chinese medicines.

Traditional Chinese medicines (TCM) have a long history of use because of its potential complementary therapy and fewer adverse effects. However, the toxicity and safety issues of TCM have drawn considerable attention in the past two decades. Metabolomics is an "omics" approach that aims to comprehensively analyze all metabolites in biological samples.

Fabrication of a Flexible Gold Nanorod Polymer Metafilm via a Phase Transfer Method as a SERS Substrate for Detecting Food Contaminants.

Surface enhanced Raman scattering (SERS) has been widely used in detection of food safety due to the nondestructive examination property. Here, we reported a flexible SERS film based on a polymer-immobilized gold nanorod polymer metafilm. Polystyrene-polyisoprene-polystyrene (SIS), a transparent and flexible, along with having excellent elasticity, polymer, was chosen as the main support of gold nanorods.

Rapid fabrication of flexible and transparent gold nanorods/poly (methyl methacrylate) membrane substrate for SERS nanosensor application.

Flexible substrates have been proposed for daily-life applications in SERS detection due to the prominent sample collection properties such as they can be wrapped around non-planar object surface. Combining the noble metals with polymers, flexible SERS substrates could be fabricated with advantages of light weight, transparency and high SERS sensitivity. Herein, we prepare a gold nanorods (AuNRs)/poly(methyl methacrylate) (PMMA) film as flexible SERS substrate by self-assembling a uniformly AuNRs array layer on PMMA template.

[Identification of ubiquitously expressed transcript as the potential interactor of hepatitis B virus polymerase].

Objective: To investigate the function of hepatitis B virus polymerase (HBV Pol) in the viral life cycle by screening the proteins interacting with HBV polymerase.

Methods: The HBV Pol gene was constructed into the pGBKT7 vector. GAL4 yeast two-hybrid system was used to screen the human liver cDNA library to obtain proteins which interacted with HBV Pol.