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In this work, zein nanofiber membranes loaded with ε-polylysine-polyphenol-polyaspartic acid were prepared using electrospinning for the controlled delivery of polyphenols. The loading efficiency (LE) and loading capacity (LC) of polyphenols in ε-polylysine/polyaspartic acid hydrogels were determined. Characterization of the films was carried out using water contact angle (WCA) measurement, thermal analysis (DSC/TG), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). The study showed that the embedding rates of all samples reached more than 80%. The structural characterization results showed that the nanofiber membranes loaded with hydrophobic polyphenols were more stable and no new compounds formed during electrostatic spinning. The in vitro release study of phlorotannin, kaempferol and tannic acid indicated that about 62.35%, 63.51% and 73.65% of polyphenol release occurred at pH 6.8 for 8 h. The result of cytotoxicity assay in human colon cancer cells (HT-29) showed good biocompatibility of the zein nanofiber membranes. The investigation suggested that polyphenols can be successfully entrapped in the ε-polylysine-polyaspartic acid-zein nanofiber membranes for targeted delivery.

Graphene quantum dots (GQDs), which have high photostability, anti-photobleaching and scintillation, good biocompatibility and low toxicity, are important member of the fluorescent material family, and have attracted extensive research interest. In this paper, a fluorescence resonance energy transfer (FRET) biosensor based on protoporphyrin IX (PpIX) and GQDs was developed for melamine detection. PpIX was bound to the surface of GQDs to produce self-assembled nanosensors, and a FRET process occurred between GQDs and PpIX. However, due to the combination of melamine and PpIX, the FRET process was shut down in the presence of melamine. The FRET system could quickly and accurately detect melamine with a detection range of 1.0 × 10 -8 to 2.0 × 10 -6  mol/L based on the fluorescence intensity ratio of PpIX and GQDs, and the detection limit was 3.6 × 10 -9  mol/L. This method obtained satisfactory results when it was employed to the determination of melamine in milk samples.

A sensitive and selective quantum dot (QD)-based fluorescence resonance energy transfer (FRET) biosensor was successfully fabricated for the detection of organophosphorus pesticides (OPs). 5,10,15,20-Tetra(4-pyridyl)porphyrin (TPyP) with meso-pyridyl substituents was bound to the surface of CdTe QDs to produce self-assembled nanosensors, and the process of FRET between QDs and TPyP occurred. However, the process of FRET was switched off with the addition of OPs, due to the combination between TPyP and OPs. The fluorescence intensity of TPyP (donor) would decrease gradually with the increasing concentration of OPs. Under optimal conditions, a linear correlation was established between the fluorescence intensity ratio ITPyP/IQDs and the concentration of paraoxon in the range of 9.09 × 10(-12)-1.09 × 10(-6) mol L(-1) with a detection limit of 3.15 × 10(-12) mol L(-1). The attractive sensitivity was obtained due to the efficient FRET and the superior fluorescence properties of QDs. The proposed method was successfully applied to the determination of the OPs in real fruit samples with satisfactory results.

An optical biosensing method using CdTe quantum dots (QDs) and bi-enzyme-immobilized eggshell membranes for the determination of organophosphorus pesticides (OPs) has been developed. Increasing amounts of OPs led to a decrease of the enzymatic activity and thus a decrease in the production of hydrogen peroxide (H2O2), which can quench the fluorescence of the CdTe QDs. Under the optimum conditions, there was a good linear relationship between the enzyme inhibition percentage and the logarithm of paraoxon or parathion concentration in the range of 1.0 × 10(-11)-1.0 × 10(-6) mol L(-1). The detection limit (S/N = 3) of the proposed biosensors were as low as 4.30 × 10(-12) mol L(-1) for paraoxon and 2.47 × 10(-12) mol L(-1) for parathion. The bi-enzyme-immobilized eggshell membrane demonstrated a long shelf-life of at least 2 months and the results showed good repeatability. The proposed method was successfully applied to the determination of the OPs in real fruit samples with satisfactory results.

Background: Some patients with conotruncal heart defects (CTDs) have a chromosome 22q11.2 deletion, but we do not know whether patients with CTDs who are missing the peripheral blood-cell chromosome 22q11.2 deletion are also missing the 22q11.2 deletion in myocardial cells, and whether patients with the 22q11.2 deletion can show a different 22q11.2 deletion in peripheral blood cells and myocardial cells due to a postzygotic mutation during the embryonic period., Methods: A total of 32 Chinese pediatric nonsyndromic CTD patients (21 with tetralogy of fallot [TOF], 9 with double outlet right ventricle [DORV], 1 with pulmonary artery atresia with ventricular septal defect [PAA/VSD], and 1 with congenitally corrected transposition of the great arteries [CCTGA]), 12 females and 20 males ranging in age from 5 months to 7 years, were included in our study. We used fluorescence in situ hybridization (FISH) to find the chromosome 22q11.2 deletion in peripheral blood cells and compared genotypes of 15 short tandem repeat (STR) markers within 22q11.2 between peripheral blood cells and myocardial cells to search for genetic mosaicism of the chromosome 22q11.2 deletion., Results: Three patients, 2 with TOF and 1 with DORV, were determined to have the peripheral blood cell chromosome 22q11.2 deletion. There was no STR genotypic difference observed between peripheral blood cells and myocardial cells in patients with or without the chromosome 22q11.2 deletion., Conclusions: Genetic mosaicism may not play a major role in the etiology of isolated CTDs., (Copyright 2006 Wiley-Liss, Inc.)