In this work, the water-soluble fluorescent Ag nanoclusters (DPA@Ag NCs) were first prepared based on D-Penicillamine (DPA) as a stabilizer, however, the fluorescence quantum yield (QY) of DPA@Ag NCs was very low, then Cu2+ was employed to improve the fluorescence QY and the doped Ag nanoclusters with Cu2+ (DPA@Ag/Cu NCs) were obtained. The study showed that the QY increased fourfold and the emission of nanoclusters changed from red to yellow after addition of Cu2+. The reasonfor change of fluorescent properties wasattributed to the change of self-assembly structures caused by adding Cu2+ into reaction system, leading to the aggregation-induced emission enhancement (AIEE) effect and enhancing the band gap (Eg) between the HOMO and LUMO in nanoclusters. Subsequently, a fluorescent Ag+ sensor with high sensitivity and selectivity was established based on the DPA@Ag/Cu NCs as probes in aqueous solution. Experiments showed that the Ag+ could significantly quench the fluorescence of DPA@Ag/Cu NCs under experimental conditions, and there was a good linear relationship between the fluorescent intensity quenching value and Ag+ concentration in the range of 0.05-800 μM, and the limit of detection (LOD) was 0.03 μM (3σ/k). Meanwhile, most of common ions had no effect on the experimental results under the same conditions. In addition, the sensor was successfully applied on the detection of Ag+ in real water samples, and the recovery rate was 80.3-99.0%.Vibrational spectroscopy, based on either infrared absorption or Raman scattering, has attracted increasing attention for biomedical applications. Proof of concept explorations for diagnosis of oral potentially malignant disorders and cancer are reviewed, and recent advances critically appraised. Specific examples of applications of Raman microspectroscopy for analysis of histological, cytological and saliva samples are presented for illustrative purposes, and the future prospects, ultimately for routine, chairside in vivo screening are discussed. Estimating patient specific annual risk of rupture of abdominal aortic aneurysm (AAA) is currently based only on population. Remodelin solubility dmso More accurate knowledge based on patient specific data would allow surgical treatment of only those AAAs with significant risk of rupture. This would be beneficial for both patients and health care system. A methodology for estimating annual risk of rupture (EARR) of abdominal aortic aneurysms (AAA) that utilizes Bayesian statistics, mechanics and patient-specific blood pressure monitoring data is proposed. EARR estimation takes into consideration, peak wall stress in AAA computed by patient-specific finite element modeling, the probability distributions of wall thickness, wall strength, systolic blood pressure and the period of time that the patient is known to have already survived with the intact AAA. Initial testing of proposed approach was performed on fifteen patients with intact AAA (mean maximal diameter 51mm±8mm). They were equipped with a pressure holter and their blood pr generally low and in good agreement with confirmed survival time of investigated patients so proposed method should be further clinically validated.Methodology for computing annual risk of rupture of AAA was developed for the first time. Sensitivity analyses showed respecting patient specific blood pressure is important factor and should be included in the AAA rupture risk assessment. Obtained EARR values were generally low and in good agreement with confirmed survival time of investigated patients so proposed method should be further clinically validated. Physicians have prescribed anticholinergic agents as monotherapy or adjuvant therapy in patients with Parkinson's disease for decades. However, these medications can cause many adverse effects including gait freezing and falling. Herein we assessed the effects of anticholinergic medications on motor function, freezing of gait and falling in a group of patients with PD. This prospective study evaluated the effect of gradual discontinuation of anticholinergics on motor function in 131 outpatients with Parkinson's disease. We assessed patients' motor function at baseline six and twelve months later using the UPDRS-III. We also evaluated freezing of gait and falling in patients using UPDRS-II part 14 and 13 respectively. The anticholinergics were tapered and gradually discontinued and additional levodopa doses were added as patients needed. 131patients successfully discontinued their anticholinergic medications. Stopping anticholinergics significantly improved the motor symptoms in PD patients as reflected heir treatment strategies.Pickering emulsion-based photocatalysis is considered to be a promising system due to its large active surface area and water/oil spatial separation capability for enrichment of substrates and products. In this work, a novel hierarchical structure composed of calcium alginate gel sphere wrapped ionic liquid-in-water Pickering emulsion with TiO2 in the water phase, which are stabilized by graphene oxide, is prepared via a facile one-step emulsion gelation method. Such subtle combination of Pickering emulsion, hydrogel and TiO2 with a multi-stage solid-liquid assemblage structure shows enhanced degradation activity of 2-naphthol into small molecular alkanes under simulated solar irradiation. The photodegradation activity is attributed to the ionic liquid as adsorption medium for 2-naphthol, and the high-efficient charge separation at graphene oxide/TiO2 interface superior to that of pure TiO2. More importantly, the as-prepared millimeter-sized assembled gel spheres can be directly used as the column filler to construct continuous flow photocatalytic system, maintaining the promising performance in removing pollutants from water with ~100% remove ability of 2-naphthol on stream. A charge transfer mechanism of the photocatalyst is proposed, i.e. photogenerated charges are separated in TiO2/graphene oxide p-n heterostructure at the interface of Pickering emulsion droplets.Human pluripotent stem cells (hPSCs), like embryonic (hESCs) and induced pluripotent stem cells (hiPSCs), exhibit an unusual cell cycle structure characterized by a short G1 phase and cells being most of time in S phase. hPSCs are receptive to differentiation cues during their transition through G1 phase when lineage determination is decided. Although several MicroRNAs (miRNAs) have been shown to target transcripts that directly or indirectly coordinate the cell cycle of pluripotent cells, its temporal expression profile along hPSCs cell cycle remains poorly characterized. miR-145 and miR-296 are induced during differentiation and silence the self-renewal and pluripotency program. miR-302 family is essential for hPSCs stemness and its expression decreases during differentiation. We aimed to study how the aforementioned miRNAs are regulated along the cell cycle of hPSCs. We demonstrated by pharmacological synchronization and block and release experiments that miR-145, miR-296 and miR-302 family are periodically expressed in hPSCs.