A thin film polyethylene terephthalate (PET) electrochemical sensor for detection of glucose in sweat.

In this work, a thin film PET based gold electrode (PGE) glucose sensor was fabricated through ultraviolet mediated chemical plating technique. Compared with the most existing wearable thin film gold electrode sensors, the PGE-glucose sensor is simple, low cost and minimum instrumentation was required. The proposed glucose sensor revealed a sensitivity of 22.05 µA mM-1 cm-2 in a linear range from 0.02 to 1.11 mM with a low detection limit of 2.7 µM (S/N = 3). The PGE-glucose sensor had a good selectivity and was not interfered by lactic acid, urea, acetaminophen, uric acid, dopamine and ascorbic acid. Additionally, it exhibited good reproducibility and long-term stability over four weeks. Finally, the disposable PGE-glucose sensor was successfully applied to determine the glucose in sweat and commercial beverage accurately.

Self-primed isothermal amplification for genomic DNA detection of human papillomavirus.

Rolling circle amplification (RCA) is an isothermal amplification technique with high efficiency and perfect accuracy for nucleic acids detection. However, RCA technique suffers the limitation to detect short DNA or RNA molecules. For long nucleic acid molecules, enzymatic restriction as well as heat denaturation process is usually required, which makes the amplification not effective and strictly isothermal. In this article, a simple and efficient one-pot self-primed isothermal amplification (SIA) was developed for detection of genomic DNA directly based on the combination of nicking endonuclease assisted strand displacement amplification (SDA) and exponential RCA. In virtue of numerous nicking sites on the genome, a pre-amplification of the whole genome was performed through SDA with the specific cleaving of nicking endonuclease. Meanwhile, the single strand DNA with HPV target sequence generated from SDA could hybrid with the circle probe as a primer and trigger the exponential RCA as a result of the existence of nicking endonuclease. As the reaction temperature and enzyme were the same, the amplification could be operated in one pot. The reaction solution after amplification was added on the electrode for hybridization with the sulfydryl probe to achieve the electrochemical signal. Based on the isothermal amplification, genotyping of HPV 11, 16, 18 and the detection of HPV 18 in Hela cell line were attempted with satisfied results. This approach should be a promising tool for pathogene detection in clinical diagnostics and research.

High specific surface gold electrode on polystyrene substrate: Characterization and application as DNA biosensor.

In the past decades, many efforts have been made to improve the sensitivity and specificity of electrochemical DNA biosensors. However, it is still strongly required to develop disposable and reliable DNA biosensors for wide and practical application. In this article, we reported superior electrochemical properties of an integrated plastic-gold electrode (PGE) fabricated in-house by chemical plating on polystyrene substrate. PGEs were found having extremely high capacity of DNA immobilization compared with gold electrodes fabricated by standard sputtering based photolithography. Unique nano-structured surface was observed on PGEs through morphology techniques, which would to some extend give an explanation to higher capacity of DNA immobilization on PGEs. A probable mechanism of carboxylic acid produced on polystyrene substrate after exposure to UV irradiation was proposed and discussed for the first time. This biosensor was applied to detection and manipulate of DNA hybridization. Detection limit of 7.2×10(-11) M and 1-500 nM of linearity range was obtained.

Gathering nanorings via Fe(2+)-bipyridine coordination.

Spontaneously precise organization of small structures into complex superstructures is ubiquitous and important in nature. But using small building blocks to mimic this process remains a challenge to scientists. Herein, we report the rational design of a bipyridine-derivative and applied it for the self-assembly of nanorings. The addition of Fe(2+) to the nanorings resulted in the assembly of the nanorings into supernanostructures via Fe(2+)-bipyridine coordination. HPLC, HR-ESI/MS, UV-vis, DLS, and TEM analyses clearly validated the intramolecular cyclization, self-assembly of the nanorings, and the additional self-assembly of the superstructures via Fe(2+)-bipyridine coordination. We envision our strategy to be a new approach of precisely assembling nanostructures of ring shape into more complex superstructures.

Discriminative fluorescence sensing of biothiols in vitro and in living cells.

Simultaneous discriminative sensing of biothiols in vitro and in living cells has remained challenging. Herein, we report a new sulfonamide-based self-quenched fluorescent probe 1 for this purpose with high sensitivity and good selectivity. Treatment of 1 with cysteine (Cys), homocysteine (Hcy), or glutathione (GSH) yields aminoluciferin, 2-cyano-6-aminobenzothiazole homocysteine (CBTHcy), or 2-cyano-6-aminobenzothiazole (CBT), turning "on" the fluorescence at wavelengths of 522, 517, or 490 nm, respectively. Kinetic study indicated that 1 reacts with Cys faster than with Hcy or GSH. With these unique properties of 1, we applied 1 for highly sensitive sensing of Cys, Hcy, and GSH among other 19 natural amino acids (AAs) with good selectivity. Confocal fluorescence microscopic imaging of 1-treated HepG2 cells at two channels (522 ± 8 and 490 ± 8 nm), together with quantitative analysis, indicated that the "turn-on" fluorescence was induced by intracellular Cys-dominating condensation and reduction of 1 but not by intracellular GSH-dominating reduction of 1. This suggests that 1 could be applied for discriminative sensing of intracellular Cys from the abundant GSH. Further development of 1 might bring about an efficient tool for probing cellular functions that relate to biothiols.

Bipyridine hydrogel for selective and visible detection and absorption of Cd(2+).

Herein, we report for the first time the use of bipyridine-based hydrogel for selective and visible detection and absorption of Cd(2+). At low concentrations, hydrogelator 1 was applied for selective detection of Cd(2+) in vitro and in living cells with high sensitivity. In the absence of metal ions, 1 is nonfluorescent at 470 nm. Upon addition of metal ions, 1 selectively coordinates to Cd(2+), causing an 86-fold increase of fluorescence intensity at 470 nm via the chelation enhanced fluorescence (CHEF) effect, as revealed by first-principles simulations. At 1.5 wt% and pH 5.5, 1 self-assembles into nanofibers to form hydrogel Gel I. Since Cd(2+) could actively participate in the hydrogelation and promote the self-assembly, we also successfully applied Gel I for visible detection and absorption of Cd(2+). With these excellent properties, Gel I is expected to be explored as one type of versatile biomaterial for not only environmental monitoring but also for pollution treatment in the near future.

A fluorescent switch for sequentially and selectively sensing copper(II) and L-histidine in vitro and in living cells.

Herein, we report the development of a new fluorescent switch for sequential and selective sensing of Cu(2+) and L-histidine (L-His) in vitro and in living cells for the first time. In the absence of metal ions, Ac-SAACQ-Gly-Gly-Gly-Lys (FITC) (1) exhibits comparable fluorescence to that of free FITC. In the presence of metal ions, 1 selectively coordinates to Cu(2+) , causing its fluorescence emission to be quenched via photoinduced electron transfer. Interestingly, the as-formed 1­Cu(2+) complex selectively responds to L-His among the 20 natural amino acids by turning its fluorescence on. This property of fluorescence switch of 1 was successfully applied for qualitatively and quantitatively sensing Cu(2+) and L-His in vitro. Using this dual functional probe, we also sequentially imaged Cu(2+) and L-His in living HepG2 cells. Our new probe 1 could be applied for not only environmental monitoring but also biomolecule detection in the near future.