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Quantifying Solvophobic Outcomes within Organic and natural Chemicals Employing a Hydrocarbon Molecular Equilibrium.
Lateral flow immunoassay (LFIA) biosensor is a paper-based tool and widely utilized in various fields. Here, we developed a novel LFIA biosensor by introducing Co3O4 nanoparticles (NPs) as signal labels for highly sensitive detection of 3-amino-2-oxazolidinone (AOZ), a metabolite of furazolidone. The characteristic brown color of Co3O4 NPs enabled AOZ to be visually detected by the LFIA. Significantly, the size of Co3O4 NPs is relatively small compared with most of other signal labels, which could remarkably reduce steric hindrance, increase immunoreaction probability and shorten the analysis time. Under optimal conditions, the novel Co3O4 NPs-LFIA could possess high sensitivity for the detection of AOZ with a detection limit of 0.4 ng mL-1 by naked eyes, which was at least 3-fold improved than that of the conventional gold nanoparticles (GNPs) based LFIA. Moreover, the detection could be achieved within 6 min and without cross-reactions with other analogue small molecules. Taking merits of convenience, rapid and sensitivity, the proposed Co3O4 NPs-LFIA may be readily adapted for the detection of other small molecules. V.The combined LIBS and ICP HRMS analysis of 13 tea samples are studied in view of identification of tea geographical origin. The elemental signature provided by LIBS spectra is treated by principal component analysis followed by partial least square discriminant analysis and factorial discriminant analysis. Selected element lines are found efficient to discriminate most sample groups. Data analysis model is improved by variable selection and the isotopic ratio 11B/10B was employed to improve the prediction capacity of the model. The alkaline earth Ba, Ca, Mg, Sr and alkaline Rb, Na are easily detected by the LIBS system and these elements are important to classify sample according to their geographical origin. Minor elements like P, S, Fe, B … also bring discriminant information. A five clusters model gave best correct identification in a cross validation test (94.2%). This method also allowed to identify the origin of four unknown teas. In this study the use of FDA or PLS DA after the PCA examination of the LIBS/ICP MS data led to similar conclusions for fast classification of the tea samples and identification of the geographical origin of the four unknown teas. MiRNAs are known to be involved in a series of diseases, including breast cancer, and they have the potential to serve as diagnostic/prognostic markers and therapeutic targets. A prerequisite for miRNAs to be applied in clinical practice is the quantitative profiling of their expression. However, the majority of current assays used in miRNA detection are highly enzyme-dependent. In this study, a novel enzyme-free assay was developed that relies on stacking hybridization and a photocleavable DNA-PL-peptide probe, which contains a reporter peptide (AVLGVDPFR), a photocleavable o-nitrobenzyl derivative linker and a detection DNA sequence that is complementary to a part of the target miRNA (e.g., miR-21, miR-125a or miR-200c). Stacking hybridization enabled the DNA-PL-peptide probe to capture DNA in a contiguous tandem arrangement to generate a long DNA single strand complementary to the target miRNA. Then, photolysis was initiated to rapidly release the reporter peptide, and the reporter peptide was ultimately monitored by liquid chromatography-tandem mass spectrometry (LC-MS/MS). In this experiment, the parameters linked with photorelease, binding, conjugation and hybridization were characterized. The results showed that the assay time was significantly shortened, and the detection specificity was improved. After validation of the assay, the target miRNA level was determined in human breast cells and tissue samples. The results demonstrated that photocleavable materials coupled with mass spectrometric detection have great potential in clinical practice. Online measuring end-tidal propofol concentration during balanced anesthesia is important for anesthetists to learn the patient's anesthesia depth as exhaled propofol concentration is well related to blood propofol concentration. In previous work, exhaled propofol was detected using acetone assisted negative photoionization ion mobility spectrometer, however, the existence of high concentration sevoflurane interfered the response of propofol. In this work, an anisole assisted photoionization ion mobility spectrometer operated in positive mode was developed to sensitively and selectively measure the end-tidal propofol by eliminating the interferences of exhaled humidity and sevoflurane during balanced anesthesia. Anisole molecular ion is stable enough not to go under proton transfer reaction with water presents in the exhaled breath. Hence, the exhaled humidity related peaks were eliminated and only one propofol product ion peak (K0 = 1.50 cm2 V-1 s-1) was observed. The relative standard deviation (RSD) ranging from 0.64%-0.91% showed good repeatability and the quantitative range was 0.2-40 ppbv with a response time of 4 s. Finally, the performance of the proposed method was demonstrated by monitoring end-tidal propofol of balanced anesthetized patients during gastric cancer surgery. Biochanin A is one of the most common phytoestrogens, occurring in high concentrations in soy and red clover, for instance, which shows a wide spectrum of biological activity. Prunetin is an isomer of biochanin A, and even though it is not very common, its structural relationship to the latter makes it interesting, regarding its biological activity. Nowadays, LC/ESI-MS methods are widely used for identification of natural compounds, including biochanin A and prunetin. However, we found that the published data concerning the identification of biochanin A and prunetin are sometimes disputable. Namely, the identification is based on the product ions which cannot be regarded as characteristic of biochanin A or prunetin. The reported retention times sometimes may be also disputable. Molecularly imprinted polymer (MIP)-based optosensing materials capable of direct, reliable, and highly selective detection of small organic analytes in complex aqueous samples hold great promise in many bioanalytical applications, but their development remains a challenging task. CM272 Addressing this issue, well-defined hydrophilic "turn-on"-type ratiometric fluorescent MIP microspheres are developed via a versatile and modular strategy based on the controlled/"living" radical polymerization method. Its general principle was demonstrated by the synthesis of red CdTe quantum dot (QD)-labeled silica particles with surface-bound atom transfer radical polymerization (ATRP)-initiating groups via the one-pot sol-gel reaction and their successive grafting of a thin fluorescent 2,4-D (an organic herbicide)-MIP layer (labeled with green organic fluorophores bearing both nitrobenzoxadiazole (NBD) and urea interacting groups) and hydrophilic poly(glyceryl monomethacrylate) (PGMMA) brushes via surface-initiated ATRP. The introduction of PGMMA brushes and rationally selected dual fluorescence labeling (i.e., red CdTe QDs being inert to 2,4-D and green NBD showing fluorescence "light-up" upon binding 2,4-D) onto MIP particles afforded them excellent complex aqueous sample-compatibility (due to their largely enhanced hydrophilicity) and analyte binding-induced "turn-on"-type ratiometric fluorescence changes, respectively. Such advanced MIP particles proved to be promising optosensing materials, which had a detection limit of 0.13 μM and showed obvious fluorescent color change upon binding different concentrations of 2,4-D in the undiluted pure milk. Moreover, they were successfully applied for direct and highly selective quantification of 2,4-D in the undiluted pure goat and bovine milks with good recoveries (97.9%-104.5%), even in the presence of several analogues of 2,4-D. In this study, a colorimetric sensing assay of isoniazid based on excellent oxidase-like activity of heparin sodium stabilized platinum nanoparticles (HS-PtNPs) has been demonstrated. The newly prepared HS-PtNPs exhibit a great dispersion with an average size distribution of 4.8 ± 0.6 nm, and maintain more than 90% catalytic activity under strong acid and alkali or long-term storage conditions, indicating a robust nanomaterial with attractive potential. The HS-PtNPs show distinct oxidase-like activity with an ultrahigh affinity (Km = 0.01012 mM) for 3, 3', 5, 5'-tetramethylbenzidine (TMB). More significantly, we found that the pyridine ring of isoniazid has a strong reductive hydrazyl substitution, which can compete with TMB for the catalytic site of HS-PtNPs resulting in a colorless solution. Accordingly, a colorimetric sensing of isoniazid was fabricated. A linear relationship for isoniazid was achieved in 2.5 × 10-6 to 2.5 × 10-4 M (R2 = 0.998) with a low limit of detection 1.7 × 10-6 M (S/N = 3). Recovery experiments in drug tablets show that the standard recovery rates were 95%-103%. The quantitative detection data for isoniazid in drug tablets calculated respectively from the standard method and this method exhibited a high correlation coefficient (a slope of 0.9995), suggesting that high accuracy in isoniazid detection. A challenge in turn-on mode operating optodes application is elimination of pH sensitivity. The polyoctylthiophene based optodes response mechanism is not involving hydrogen ions exchange, thus paves the way for optodes applicable for sensing in wide pH range. We report on nanoptodes that can be used both in alkaline and in acidic pH range inaccessible for classical systems using pH sensitive dyes as transducers. The proposed sensors offer 6 orders of magnitude broad, linear dependence of emission intensity on logarithm of analyte (K+ or Ca2+) concentration, in turn on mode. However, the slopes of calibration plots are to some extent dependent on solution pH and oxygen presence/absence. It is shown that this effect is resulting from changes of solution redox potential maintained mainly by dissolved oxygen. The solution redox potential affects the oxidation state of the polymer and thus amount of the neutral, fluorescent form of polyoctylthiophene, ultimately affecting performance of the sensor especially in acidic pH. Tailoring composition of polyoctylthiophene optodes, including hydrogen binding compound in the polymer phase, effectively diminishes the effect of pH change on sensitivity of proposed optodes, as shown on model examples of potassium and calcium sensors. Thus polyoctylthiophene based nanosensors show equally high sensitivity for analyte cations concentration change both in acidic (pH = 4) and alkaline (pH = 9.2) media. Protein function is modulated via different levels including their structure and chemical modifications, but method for monitoring of protein structures and their modifications on a large scale is far from mature. In this study, we present a shot-gun proteomic method, which combine ultrafiltration with limited tryptic proteolysis (FLiP) to enrich the surface accessible peptides and modification sites on protein structures. FLiP enable high throughput confirmation of the structural information of 1939 proteins. Based on this, we identified 120 types of modifications located on the surface accessible regions of proteins, including some rare modification types like phosphorylation of asparagine and acetylation of threonine. Our data provides a comprehensive picture of the spatial distribution of multiple modification types on protein structures. Collectively, our work provides a promising tool for large-scale confirmation of protein structures and unbiased discovery of multiple proteins surface assessable post-translational modifications, which may also benefits the study of rare modification types.
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