Identification of Possible Milk Adulteration Using Physicochemical Data and Multivariate Analysis

Milk is one the most widely consumed foods in the world, with an average annual production of 723 million tons in the second half of the past decade. However, to increase milk’s profitability, some actors in the dairy chain may adulterate it, altering its chemical composition, and reducing the nutritional value of this food. The quality of milk is therefore assessed through chemical and physical analyses such as total dry matter, total Kjeldahl nitrogen, ash, acidity, fat, reducing sugars, depression of freezing point, and relative density. In this work, we have used Principal Components Analysis (PCA) and supervised methods (PLS-DA, SIMCA, kNN, and SVM-DA) to explore physicochemical data from milk and to classify and discriminate between samples that were compliant or not to the parameters set in the Brazilian Regulation for the Inspection of Animal Products and other national regulations. Classification results regarding specificity and selectivity for PLS-DA, SIMCA, kNN, and SVM-DA for noncompliant samples in the test group were, respectively, the following: 91, 88; 100, 97; 78, 67; 78, and 71%.     

Combining mass spectrometry and pull-down techniques for the study of receptor heteromerization. Direct epitope-epitope electrostatic interactions between adenosine A2A and dopamine D2 receptors

Previous results from FRET and BRET experiments and computational analysis (docking simulations) have suggested that a portion of the third intracellular loop (I3) of the human dopamine D2 receptor (D2R) and the C-tail from the human adenosine A2A receptor (A2AR) are involved in A2AR-D2R heteromerization. The results of the present studies, using pull-down and mass spectrometry experiments, suggest that A2AR-D2R heteromerization depends on an electrostatic interaction between an Arg-rich epitope from the I3 of the D2R (217RRRRKR222) and two adjacent Asp residues (DD401-402) or a phosphorylated Ser (S374) residue in the C-tail of the A2AR. A GST-fusion protein containing the C-terminal domain of the A2AR (GST-A2ACT) was able to pull down the whole D2R solubilized from D2R-tranfected HEK-293 cells. Second, a peptide corresponding to the Arg-rich I3 region of the D2R (215VLRRRRKRVN224) and bound to Sepharose was able to pull down both GST-A2ACT and the whole A2AR solubilized from A2AR-tranfected HEK-293 cells. Finally, mass spectometry and pull-down data showed that the Arg-rich D2R epitope binds to two different epitopes from the C-terminal part of the A2AR, containing the two adjacent Asp residues or the phosphorylated Ser residue (388HELKGVCPEPPGLDDPLAQDGAVGS412 and 370SAQEpSQGNT378). The present results are the first example of epitope-epitope electrostatic interaction underlying receptor heteromerization, a new, expanding area of protein-protein interactions.     

Fuzzy logic for identifying pigments studied by Raman spectroscopy

Fuzzy logic and linguistic variables are used for the automatic interpretation of Raman spectra obtained from pigments found in cultural heritage art objects. Featured bands are extracted from a Raman spectrum of a reference pigment and the methodology for constructing the library is illustrated. An unknown spectrum is then interpreted automatically and a process for identifying the corresponding pigment is described. A reference library consisting of 32 pigments was built and the effectiveness of the algorithm was tested by the Raman spectroscopic analysis of 10 pigments that are known to have been extensively used in Byzantine hagiography. Binary mixtures of these pigments were also tested. The algorithm's level of identification was good even though extra peaks, noise, and background signals were encountered in the spectra.     

Microencapsulation of ADN with HTPB-based membrane in the presence of the bonding agents Tepan or Tepanol**

Ammonium dinitramide (ADN) has appeared as a promising oxidizer for green propellants and thereby a potential substitute for ammonium perchlorate, largely in use in composite propellants for tactical and strategic long-range missiles. The novelty lies in replacing ammonium perchlorate with a chlorine-free oxidizer less harmful to the health and environment. However, ADN is hygroscopic and can potentially react with other chemical components, which could be overcome by microencapsulating the particles. The simple coacervation method was tested herein to microencapsulate ADN with a membrane made of hydroxyl-terminated polybutadiene as pre-polymer and methylene diphenyl diisocyanate as the curing agent. The effect of polyamine bonding agents on the capsule formation was tested by adding 0.5 or 2 % of Tepan or Tepanol, whose efficacy to bond to ADN was confirmed by detecting ammonia release through infrared spectroscopy. The capsule membrane was examined by optical and scanning electron microscopy. The dissolution time and rate were the parameters adopted to quantify permeability in a straight dissolution test in water, which demonstrated that 0.5 % Tepanol can provide the most effective protection. The infrared spectroscopy indicated that 60 °C temperature for prolonged periods, normally experienced by propellants, does not chemically affect the capsules’ membrane but can turn it lumpy. In conclusion, these polyamine bonding agents can assist the capsule formation over ADN particles using the simple coacervation method, however, their functionality on mechanical properties of propellants needs to be substantiated in forthcoming works as well as the effect of the concentration of bonding agents on propellant formulations.