Purpose: The aim of the present study was to compare and investigate morphometric characteristics of limbal vasculature within the superior and inferior limbal regions using ultra-high resolution optical coherence tomography. Method: Cross-sectional images of the human corneo-scleral limbus were acquired with a research grade ultra-high resolution optical coherence tomographer (UHR-OCT) from 14 healthy subjects after manual retraction of the upper and lower eyelid. The UHR-OCT provides an axial and lateral resolution in biological tissue of ~3μm and ~18μm, respectively. 3D stacks of OCT images (1000 x 1024 x 256) were acquired of the transition from cornea to bulbar conjunctiva at the superior and inferior limbal region. All visible vessels within the limbal region were measured using an Image J circle or ellipse tool. Vessel depth and size measurements were repeated for the same vessel and the concordance correlation coefficient was computed. Quantitative differences in vessel size and depth in the limbal region were analyzed using repeated measured ANOVA. R and SPSS were used for all data analysis procedures. Results: The average vessel size for superior and inferior limbus were 29.28µm ± 17.649 µm (SD) and 23.68µm ± 18.118µm (SD) respectively. The average vessel depth for superior and inferior limbus were 176.76µm ± 108.698µm (SD) and 205.62µm ± 131.991µm (SD) respectively. The concordance correlation coefficient for superior and inferior limbal vessel size were 0.95 (95% CI, 0.935 to 0.964) and 0.994 (95% CI, 0.991 to 0.995) respectively, while that of vessel depth were 0.998 (95% CI, 0.997 to 0.999) and 0.998 (95% CI, 0.997 to 0.998) respectively. The vessels within the superior limbus were larger than the vessels found in the inferior limbus (RM-ANOVA POS p = 0.004), and the vessels within the inferior limbus were on average deeper than the vessels found within the superior limbus (RM-ANOVA POS p = 0.042). There was a positive linear relationship between limbal vessel depth and size within the superior and inferior limbus with a Pearson correlation coefficient of 0.803 and 0.754, respectively. There were on average 9 vessels per subject within the superior limbal region as compared to 13 vessels per subject with the inferior limbal region. Conclusion: This study provided evidence that the UHR-OCT was capable of imaging (and therefore measuring) morphometric characteristics such as the size and depth of vessels within the limbus in a repeatable manner. A positive linear association between vessel depth and size was identified in the superior and inferior limbal regions. The results of this study suggest a definite difference in the size and depth of vessels across different positions of the limbus, and this may be indicative of adaptations to chronic hypoxia caused by the constant covering of the superior limbus by the upper eyelid.

Increased demand for rare earth elements (REEs) for applications in modern technologies has led to an increase in REE exploration. Several deposits are expected to begin mining within a decade, but few studies have examined the possible environmental effects created by these mines. Metal toxicity is thought to be greater in aqueous environments when metals occur as free ions rather than complexes, and the speciation can also impact the treatment technologies utilized to reduce metal concentrations. This research investigates the mineralogical source of REEs and the mechanism of REE mobility in low-temperature waters that have interacted with pilot plant tailings from the Nechalacho deposit, Northwest Territories. The Nechalacho deposit is owned by Avalon Rare Metals Inc. and located approximately 100 km east of Yellowknife. The deposit is hosted within a hydrothermally altered layered nepheline-sodalite syenite in the peralkaline Blatchford Lake complex. The main REE ore minerals are zircon, fergusonite, allanite, monazite, bastnäsite, and synchisite-parasite. Characterization of the tailings using mineral liberation analyzer (MLA) show that the ore minerals are fine grained and well liberated. Bastnäsite and synchisite-parasite are the only potentially soluble ore minerals at low temperature and near-neutral pH. Shake flask experiments were designed to simulate the interaction of tailings with three different leach waters to identify soluble phases and mobile elements. Decanted solutions from the shake flasks were filtered to 0.45µm and 0.01µm. Speciation modelling of the 0.01µm filtrate suggests that carbonate ligands will form the dominant complexes with the REEs, and <2% occur as free metal ions. Higher proportions of LREEs (1-6%) occur as free metal ions than HREEs (<1%) and LREEs occur in higher concentrations (2 to 8 times greater) than the HREE. REEs were found in the colloidal fraction ([REEcolloid] = [REE0.45µm] – [REE0.01µm]). Ionic strength is the dominant control on distribution of REEs between colloidal and dissolved fraction. Colloids captured on filters from ultrafiltration analyzed using scanning electron microscopy and synchrotron microanalysis show REEs are hosted in colloidal rare earth minerals (e.g. zircon) and also show colloidal humic acid, Fe-oxides and Mn-oxides. Speciation modeling shows that REE sorption to these phases is probable. / Thesis (Master, Geological Sciences & Geological Engineering) -- Queen's University, 2014-05-28 11:06:41.351

Percutaneous delivery of drugs promises many advantages over oral or intravenous administration, such as a better control of blood levels, a reduced incidence of systemic toxicity, an absence of hepatic first-pass metabolism, better patient compliance, etc. However, the dermal drug transport is limited by the unsuitable physicochemical properties of most drugs and the efficient barrier function of the skin. Thus, numerous attempts have been reported to improve topical absorption of drugs, concentrating mainly on the barrier function of the stratum corneum by use of penetration enhancers and/or skin warming. An alternative and interesting possibility for improved dermal permeability is the synthesis of derivatives or analogues with the aim of changing the physicochemical properties in favour of skin permeation, efficacy and therapeutic value. Cyclizine (I) is an anti-emetic drug primarily indicated for the prophylaxis and treatment of nausea and vomiting associated with motion sickness, post operation and Meniere's disease. It acts both on the emetic trigger zone and by damping the labyrinthine sensitivity. Pharmacologically it has anti-histaminic, antiserotonergic, local anaesthetic and vagolytic actions. It is widely used and also suitable for children from six year of age. Percutaneous absorption of (I) can, among others, avoid the "first-pass" effect and the discomfort of injection. The main objective of this study was to explore the feasibility of percutaneous absorption of (I) and its alkyl analogues via physicochemical characterization and assessment of their permeation parameters. The intent was also to establish a correlation between the physicochemical properties of these compounds and their percutaneous rate of absorption. To achieve these objectives, the study was undertaken by synthesizing the alkyl analogues and determining the physicochemical parameters relevant to skin transport. Identification and level of purity for the prepared analogues were confirmed by mass spectrometry (MS), nuclear magnetic resonance (NMR) spectrometry and infrared (IR) spectrometry. Experimental aqueous solubility (25 °c & 32 °C) and partition coefficient for each compound were determined. In vitro permeation studies were performed at pH 7.4, using Franz diffusion cells with human epidermal membranes. Diffusion experiments were conducted over a period of 24 hours maintaining a constant temperature (37 DC) by means of water bath. All samples were analysed by high pressure liquid chromatography (HPLC). Cyclizine (I) has a methyl group at N-4. Increasing the alkyl chain length on N-4 of the piperazine ring resulted' in compounds with lower melting points and higher water solubility than (I). (II) exhibited 3-fold increase in water solubility, followed by (IV) with about 2.5 fold increase. The water solubility of (III) was almost the same as that of (I). Log partition coefficients increased linearly with increasing alkyl chain length. The analogues therefore, possessed more favourable physicochemical properties to be delivered percutaneously. Indeed, the in vitro skin permeation data proved that these analogues could be delivered more easily than (I) itself. The flux of (I) was 0.132 ug/cm2/h in a saturated aqueous solution. Compound (II) resulted in a 53-fold (6.952 ug/cm2/h) increase in permeation compared to (I). (III) and (IV) resulted in a 2- and 5fold enhancement of permeation respectively. Based on the results of the study, it seems that increased aqueous solubility and low level of crystallinity play a vital role in optimizing percutaneous absorption of (I) and its alkyl analogues. But the importance of the effect of increased lipophilicity cannot be ignored. The low percutaneous• absorption of (I) might be attributed to its low aqueous solubility and increased crystallinity, as is evident from the higher melting point than the analogues. From all the permeability data using aqueous solutions, it is clear that compound (II) is the best permeant of this series and in addition it is known that this compound antagonizes the effects of histamine. / Thesis (M.Sc. (Pharm.))--North-West University, Potchefstroom Campus, 2004.

The research projects presented in this thesis are mainly focused toward green chemistry and engineering: developing innovative strategies to minimize waste, improve process efficiency and reduce energy consumption. Specifically, the work was centered on the design and applications of green solvents and processes for the sustainable production of pharmaceuticals. The first project was focused on the use of CO₂ to enhance Suzuki coupling reactions of substrates containing unprotected primary amines. This work established that exceptionally challenging substrates like halogenated amino pyridines (i.e. 4-amino-2-bromopyridine and 4-amino-2-chloropyridine) are suitable substrates for Suzuki coupling reactions under standard conditions using CO₂ pressures, without the need for protection/deprotection steps which are traditionally considered to be necessary for these reactions to proceed cleanly. The second project explored the use of water at elevated temperatures (WET) for the sustainable and selective removal of protecting groups. The favorable changes that occur in the physiochemical properties (i.e. density, dielectric constant and ionization constant) of water at elevated temperatures and pressures make it an attractive solvent for the development of sustainable, environmentally green processes for the removal of protecting groups. The water-mediated selective removal of protecting groups such as N-Boc, N-Acetyl and O-Acetyl from a range of organic model compounds was successfully achieved by tuning the temperature (125 to 275°C) or properties of water. The third project investigated the use of Organic-Aqueous Tunable Solvents (OATS) for the rhodium catalyzed hydroformylation of p-methylstyrene. This enables the reactions to be carried out efficiently under homogeneous conditions, followed by a carbon dioxide (CO₂) induced heterogeneous separation. Modest pressures of CO₂ induced the aqueous-rich phase (containing the catalyst) to separate from the organic-rich phase (containing the reactant), thus enabled an easy separation and recycling of catalyst. The use of Al(OtBu)₃ as a potent catalyst toward continuous Meerwein-Ponndorf-Verley (MPV) reductions was established in the fourth project. The MPV reduction of model compounds like benzaldehyde and acetophenone to their corresponding alcohols was investigated in continuous mode as a function of temperature and catalyst loading. These results established a roadmap for the pharmaceutical industry to document the implementation of continuous flow processes in their manufacturing operations.

Neaustinė medžiaga gali būti nauja vaisto forma, todėl yra svarbu rasti biofarmacinį tyrimą, kuris būtų tinkamas įvertinti vaistinių medžiagų atsipalaidavimą iš neaustinės medžiagos. Tyrimo tikslas buvo atlikti tirpimo testo modifikacijas siekiant jį pritaikyti nustatant vaistinių medžiagų atpalaidavimą iš neaustinės medžiagos. / Nonwoven fabric can be a new drug form, it is important to find a biopharmaceutical assay, which would be suitable to assess the drug release from nonwoven fabric. Main aim was to carry out the modifications of the dissolution test in order to adapt it to the process of medicinal substance release from nonwoven fabric.

Pea seeds were tempered at moisture contents of 12.0&amp / #61617 / 0.1, 13.0&amp / #61617 / 0.1, 14.0&amp / #61617 / 0.1 and 15.0&amp / #61617 / 0.3%. The seeds with different moisture contents were then milled and fractioned according to the particle size of 53, 106, 212, 425 and 850 &amp / #956 / m. Tempering the pea seeds (12.0&amp / #61617 / 0.1, 13.0&amp / #61617 / 0.1, 14.0&amp / #61617 / 0.1 and 15.0&amp / #61617 / 0.3%) did not significantly affect the mass and protein fraction in comparison with the pea seeds that are not tempered (11.45&amp / #61617 / 0.05%). For the production of pea protein isolate, aqueous-solvent extraction method was used. The protein was extracted with an alkali solution from the ground pea-seeds and precipitated from the extract by bringing the pH down to isoelectric point (pH=4.5). The precipitated protein was separated from the supernatant by centrifugation. The effects of extraction parameters on the yield of extraction such as pH, particle size, temperature, solvent to solid ratio, and salt were studied. The maximum yields were obtained at these conditions / pH: 12.0 for the alkalinity of the extraction medium, 53 &amp / #956 / m for the particle size, 40&amp / #61616 / C for the extraction temperature, 5.0 for the solvent to solid ratio and 0.0 M for the saline concentration. At these extraction conditions, the maximum protein recovery was 72.75% resulting in a product containing 93.29% protein on a dry basis.

Electrochemical behavior of electrolytic manganese dioxide (EMD), chemically prepared battery grade manganese dioxide (BGM), titanium dioxide (TiO2), lithium iron phosphate (LiFePO4) and lithium manganese phosphate (LiMnPO4) in aqueous lithium hydroxide electrolyte has been investigated. These materials are commonly used as cathodes in non-aqueous electrolyte lithium batteries. The main aim of the work was to determine how the electroreduction/oxidation behavior of these materials in aqueous LiOH compares with that reported in the literature in non-aqueous electrolytes in connection with lithium batteries. An objective was to establish whether these materials could also be used to develop other battery systems using aqueous LiOH as electrolyte. The electrochemical characteristics of the above materials were investigated by subjecting them to slow scan cyclic voltammetry and determining the charge/discharge characteristics of Zn/cathode material-aqueous LiOH batteries. The products of electroreduction/oxidation were characterized by physical techniques using X-ray diffraction (XRD), scanning electron micrography (SEM), X-ray photoelectron spectroscopy (XPS), secondary ion mass spectrometry (SIMS), Thermogravimetric analysis (TG) and infra-red spectrometry (IR). The reduction of ã-MnO2 (EMD) in aqueous lithium hydroxide electrolyte is found to result in intercalation of Li+ into the host structure of ã-MnO2. The process was found to be reversible for many cycles. This is similar to what is known to occur for ã-MnO2 in non-aqueous electrolytes. The mechanism, however, differs from that for reduction/oxidation of ã-MnO2 in aqueous potassium hydroxide electrolyte. KOH electrolyte is used in the state-of-art aqueous alkaline Zn/MnO2 batteries. Alkaline batteries based on aqueous KOH as the electrolyte rely upon a mechanism other than K+ intercalation into MnO2. This mechanism is not reversible. This is explained in terms of the relative ionic sizes of Li+ and K+. The lithium-intercalated MnO2 lattice is stable because Li+ and Mn4+ are of approximately the same size and hence Li+ is accommodated nicely into the host lattice of MnO2. The K+ ion which has almost double the size of Li+ cannot be appropriately accommodated into the host structure and hence the K+ -intercalated MnO2 phase is not stable. Chemically prepared battery grade MnO2 (BGM) is found to undergo electroreduction/oxidation in aqueous LiOH via the same Li+ intercalation mechanism as for the EMD. While the Zn/BGM- aqueous LiOH cell discharges at a voltage higher than that for the Zn/EMD- aqueous LiOH cell under similar conditions, the rechargeability and the material utilization of the BGM cell is poorer. The cathodic behavior of TiO2 (anatase phase) in the presence of aqueous LiOH is not reversible. In addition to LiTiO2, Ti2O3 is also formed. The discharge voltage of the Zn/TiO2- aqueous LiOH cell and material utilization of the TiO2 as cathode are very low. Hence TiO2 is not suitable for use in any aqueous LiOH electrolyte battery. LiFePO4 (olivine-type structure) as a cathode undergoes electrooxidation in aqueous LiOH forming FePO4. However the subsequent reduction forms not only the original LiFePO4 but also Fe3O4. Thus the process is not completely reversible and hence LiFePO4 is not a suitable material for use as a cathode in aqueous battery systems. LiMnPO4 (olivine-type structure) undergoes reversible electrooxidation in aqueous LiOH forming MnPO4. The charge/discharge voltage profile of the Zn/MnPO4-aqueous LiOH cell, its coulombic efficiency and rechargeability are comparable to that of the cell using ã-MnO2. EMD and LiMnPO4 both have the potential for use in rechargeable batteries using aqueous LiOH as the electrolyte. Recommendations for further developmental work for such batteries are made.

Στόχος της μεταπτυχιακής διατριβής αποτέλεσε η πειραματική μελέτη φαινομένων μεταφοράς μάζας από υγρά μη υδατικής φάσης (NAPLs) σε δισδιάστατα πορώδη δοκίμια. Τα υγρά μη υδατικής φάσης αποτελούνται από υδρογονάνθρακες οι οποίοι διαλύονται μερικώς στο νερό. Αποτελούν τη συχνότερα εμφανιζόμενη πηγή μόλυνσης των υπόγειων υδροφορέων και είναι ιδιαίτερα επιβλαβή για τον άνθρωπο. Ο κύριος διαχωρισμός των NAPLs σε κατηγορίες γίνεται με βάση την πυκνότητά τους σε σύγκριση με αυτή του νερού. Έτσι, υπάρχουν τα Light NAPLs (LNAPLs), τα οποία είναι ελαφρύτερα από το νερό με αποτέλεσμα να επιπλέουν στην επιφάνειά του και τα Dense NAPLs (DNAPLs), τα οποία είναι βαρύτερα από το νερό και διαπερνούν τη μάζα του μέχρι να συναντήσουν κάποιο αδιαπέραστο στρώμα. Η πειραματική διάταξη που χρησιμοποιήθηκε αποτελούνταν από γυάλινα δισδιάστατα πορώδη δοκίμια που είχαν κατασκευαστεί με τη λιθογραφική μέθοδο. Με τη βοήθεια αντλίας τα δοκίμια τροφοδοτούνταν με σταθερή παροχή και σε κατάλληλη χρονική στιγμή γινόταν η εισαγωγή του ρύπου στο δοκίμιο. Στη συνέχεια με τη βοήθεια φωτογραφικής μηχανής λαμβάνονταν στιγμιότυπα σε καθορισμένες χρονικές στιγμές και με γραφικές μεθόδους υπολογιζόταν η μεταφορά μάζας. Στο πρώτο κεφάλαιο, περιέχονται εισαγωγικά στοιχεία για τη δομή και τη φύση των υγρών μη υδατικής φάσης καθώς και οι επιπτώσεις τους στο περιβάλλον. Επίσης, γίνεται μια σύντομη αναφορά στο φαινόμενο της διαχύσεως και στο πρώτο πείραμα που παρατηρήθηκε η διάχυση από τον Dalton και περιγράφεται με συντομία το πείραμα που διεξήχθη. Στο δεύτερο κεφάλαιο, γίνεται εκτενής περιγραφή όλων των στοιχείων των υγρών μη υδατικής φάσης και αναλύεται η κίνηση των υγρών αυτών σε όλα τα είδη εδάφους. Επίσης, εξηγείται η διαφορετική συμπεριφορά που αυτά εμφανίζουν στα διάφορα μέσα με βάση τις φυσικές τους ιδιότητες και επίσης παρουσιάζονται οι πρώτες μαθηματικές σχέσεις που δικαιολογούν την κίνησή τους αυτή. Στο τέλος του κεφαλαίο αναφέρονται και χημικές διεργασίες που συμβαίνουν στο υπέδαφος και επηρεάζουν την κίνηση των NAPLs. Στο τρίτο κεφάλαιο περιγράφεται το φαινόμενο μεταφοράς μάζας στο νερό αλλά και σε πορώδη μέσα. Αναφέρονται και περιγράφονται οι σημαντικότεροι και απαραίτητοι τύποι που περιγράφουν τη μεταφορά μάζας και αναλύονται όλοι οι όροι που παίρνουν μέρος στη σύνταξη των τύπων αυτών. Τέλος, αναφέρονται κάποια πειράματα στα οποία χρησιμοποιήθηκαν οι τύποι που περιέχονται στη θεωρία. Στο τέταρτο κεφάλαιο, περιγράφεται η προετοιμασία της πειραματικής διαδικασίας και αναφέρεται ο τεχνικός εξοπλισμός που χρησιμοποιήθηκε για τη διεξαγωγή της. Περιγράφονται όλα τα στάδια του πειράματος με λεπτομέρειες στις διάφορες μεθόδους που χρησιμοποιήθηκαν για τη κατασκευή και τον υπολογισμό των ιδιότητων των δοκιμίων. Επίσης, γίνεται περιγραφή της λειτουργίας του προγράμματος Comsol που χρησιμοποιήθηκε κατά το σχεδιασμό των δοκιμίων. Στο πέμπτο κεφάλαιο, παρουσιάζονται τα αποτελέσματα της πειραματικής διαδικασίας σε μορφή πινάκων και διαγραμμάτων. Τα αποτελέσματα αναλύονται και περιγράφονται με λεπτομέρεια προβλήματα που προέκυψαν κατά τη διεξαγωγή των πειραμάτων. Τέλος εξάγονται συμπεράσματα και γίνονται υποδείξεις για την περαιτέρω διερεύνηση του φαινομένου. / The aim of this Master thesis was the experimental study of mass transfer phenomena of non-aqueous phase liquids (NAPLs) in two-dimensional porous specimens. The liquid non-aqueous phase consisting of hydrocarbons which partially dissolve in the water. Are the most frequently occurring source of contamination of aquifers and is particularly harmful to humans. The main distinction of NAPLs into categories is based on the density compared to that of water. Thus, there are the Light NAPLs (LNAPLs), which is lighter than water so that float on the surface and Dense NAPLs (DNAPLs), which are heavier than water and penetrate the mass of up to meet a impermeable layer . The experimental setup used consisted of two-dimensional porous glass specimens were manufactured with lithographic method. With the pump cores fed with a constant flow and at an appropriate time was the introduction of the pollutant in the essay. Then with the help of camera footage taken at fixed times and graphical methods estimated the mass transfer. In the first chapter, contained introduction to the structure and nature of the non-aqueous phase liquids and their impact on the environment. Also, there is a brief reference to the effect of diffusion in the first experiment observed the diffusion of the Dalton and briefly describes the experiment conducted. The second chapter is a detailed description of all elements of non-aqueous phase liquids and analyzed the movement of fluids across all kinds of terrain. It also explains the different behavior they show in various media based on physical properties and also presents the first mathematical relationships that justify this movement. At the end of the chapter lists and chemical processes occurring in the soil and affect the movement of NAPLs. The third chapter describes the phenomenon of mass transfer in water and in porous media. Listed and described the most important and necessary formulas describing mass transfer and analyze all terms that take part in the preparation of these types. Finally, some experiments indicated that used types contained in the theory. The fourth chapter describes the preparation of the experimental procedure and specifying the equipment used to conduct it. Describes all stages of the experiment in detail the various methods used to construct and calculate the properties of the samples. Also, there is a description of the operation of the program Comsol used in the design of essays. The fifth chapter presents the results of the experimental procedure in the form of tables and diagrams. The results are analyzed and described in detail problems encountered in conducting the experiments. Finally conclusions are drawn and suggestions are made for further investigation of the phenomenon.

Made available in DSpace on 2014-06-11T19:23:33Z (GMT). No. of bitstreams: 0 Previous issue date: 2010-05-13Bitstream added on 2014-06-13T19:50:24Z : No. of bitstreams: 1 botaro_ja_me_arafcf.pdf: 1079828 bytes, checksum: e3d6aa320e7262e913df25c024a8740c (MD5) / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) / Recentemente, a indústria de alimentos está preocupada em desenvolver novos produtos, usando ingredientes inovadores, que promovam benefícios à saúde. O uso de proteínas de leguminosas como uma alternativa para a proteína animal tem sido estudada. O tremoço branco (Lupinus albus L.) apresenta elevada concentração de proteína e óleo, principalmente ácidos graxos insaturados e poliinsaturados, fibra alimentar, açúcares e vitaminas B1 e B2. Por outro lado, o tremoço não pode ser consumido diretamente porque possui alcaloides, que além de serem tóxicos, atribuem gosto amargo ao grão. Como a maioria dos alcaloides é solúvel em água, a quantidade de alcaloide do grão pode ser diminuída através de água corrente, fervente ou salmoura. Sucos de frutas são bastante consumidos no Brasil, especialmente no verão, não somente pelo sabor, mas como fonte de hidratação e por serem ricos em nutrientes. Os sucos de frutas tropicais conquistam cada vez mais o mercado consumidor, sendo o Brasil, um dos principais produtores. A pitanga, fruto da pitangueira (Eugenia uniflora L.) é uma planta frutífera nativa do Brasil (das regiões Sul e Sudeste e que tem se adaptado favoravelmente às condições climáticas e edáficas da região Nordeste), da Argentina e do Uruguai. A pitanga é uma fruta cuja polpa apresenta excelentes condições para industrialização, devido ao seu alto rendimento, aroma agradável e sabor exótico. O objetivo do presente estudo foi o de verificar, através da metodologia de superfície de resposta, as melhores condições para a utilização simultânea de extrato aquoso de tremoço branco e de suco tropical de pitanga, no desenvolvimento de uma bebida. Para tanto, as variáveis independentes foram representadas pelo volume de extrato aquoso de tremoço (mL) e pelo volume de suco de pitanga... / Recently, the food industry is concerned about developing new products, using innovative ingredients that promote health benefits. The use of vegetable protein as an alternative to animal protein is being studied. The white lupine (Lupinus albus L.) has high concentrations of protein and oil, especially non saturated fatty acids and polynonsaturated fats, dietary fiber, sugars and vitamins B1 and B2. On the other hand, the lupine bean can’t be consumed straight because it has alkaloids which besides being toxic, add a bitter taste to the bean. As most alkaloids are water soluble, the amount of alkaloid in the beans can be reduced by running water, boiling or brine. Fruit juices are widely consumed in Brazil, especially in the summer, not only for their flavor, but as a source of hydration and because they are rich in nutrients. The tropical fruit juices are conquering the market more and more, with Brazil being one of the main producers in the world. The Pitanga (Eugenia uniflora L.) is the fruit of the Pitangueira, a native plant of southern Brazil (which has adapted positively to weather and soil conditions in the country’s Northeast), Argentina and Uruguay. Pitanga is a fruit which pulp presents excellent conditions for industrialization, due to its high yield, pleasant aroma and exotic flavor. The aim of the present study was to verify, through the response surface methodology, the optimum conditions for the combined use of aqueous extract of white lupine and tropical pitanga juice in the development of a drink. Therefore, the independent variables were represented by the volume of aqueous extract of lupine (mL) and by the volume of pitanga juice (mL). The dependent variables (responses) were obtained through sensory test of acceptance (appearance, aroma, taste and overall acceptability). The combined... (Complete abstract click electronic access below)

Primary open angle glaucoma (POAG) is a leading cause of blindness worldwide. Elevated intraocular pressure (IOP), resulting from increased aqueous humor outflow resistance, is a major risk factor for the development and progression of POAG. Outflow resistance in the trabecular outflow pathway is mainly (50-75%) generated in the juxtacanalicular connective tissue (JCT), and partially (25-50%) in the portion distal to the inner wall of Schlemm’s canal. The details of how aqueous humor flows through these tissues and how resistance in these tissues is regulated are not fully understood in normal and POAG eyes. Aqueous humor outflow was shown to be “segmental”, with discontinuous active regions of aqueous humor filtration along the trabecular outflow pathway that can be labeled with perfused fluorescent tracers and measured as effective filtration area (EFA). In this study, we investigated the relationship between changes in EFA along the trabecular outflow pathway and outflow facility/IOP under two experimental conditions. The first experiment was designed to increase outflow facility by using netarsudil, a recently approved Rho kinase inhibitor class glaucoma medication, in normal human donor eyes. The second experiment was designed to increase IOP with topical steroid treatment for 5 weeks in mice. The purpose of this study is to verify whether EFA can be modulated by netarsudil or steroid treatment and to demonstrate the morphological changes that may be responsible for the changes of EFA. We analyzed EFA along the trabecular outflow pathway and found that elevated/reduced EFA correlated with increased outflow facility/IOP. Guided by EFA, we performed detailed morphological comparison between the active and inactive portions of aqueous humor filtration tissue to evaluate possible structural changes involved in EFA regulation. We found that increased EFA was associated with a loosened JCT structure and dilated episclearal veins, while decreased EFA was associated with a compacted JCT structure, increased deposition of curly collagen and/or fibrillary structure in the trabecular meshwork, and increased basement membrane continuity. Our data suggest that the netarsudil/steroid-induced morphological changes in the trabecular outflow pathway can result in either an increase or decrease in EFA, which in turn contributes to the regulation of outflow facility/IOP. / 2020-10-24T00:00:00Z