984 resultados para Balanced Crystalloid
Resumo:
A class of three-sided markets (and games) is considered, where value is generated by pairs or triplets of agents belonging to different sectors, as well as by individuals. For these markets we analyze the situation that arises when some agents leave the market with some payoff To this end, we introduce the derived market (and game) and relate it to the Davis and Maschler (1965) reduced game. Consistency with respect to the derived market, together with singleness best and individual anti-monotonicity axiomatically characterize the core for these generalized three-sided assignment markets. These markets may have an empty core, but we define a balanced subclass, where the worth of each triplet is defined as the addition of the worths of the pairs it contains. Keywords: Multi-sided assignment market, Consistency, Core, Nucleolus. JEL Classification: C71, C78
Resumo:
Adopting the perspective of human health risk assessment, an interdisciplinary research group has been investigating since 1998 the quality of mussels and oysters cultivated in coastal zones of Santa Catarina State. Evaluation of physico-chemical parameters considered relevant in measuring the degree of eutrophication showed values compatible with the dynamics of well balanced environmental systems. Concentrations of metallic and semi-metallic elements in seawater and bivalves were found to be similar to or lower than those found in Chile, Greenland and the USA. Further investigations focusing upon sediments will provide new and useful data for the management of sustainable mariculture strategies in Brazil.
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Tässä diplomityössä tarkastellaan teollisuusyrityksen suorituskykyä asiakkaiden näkökulmasta. Työn tavoitteena on rakentaa kohdeyritykselle yrityksen suorituskykyä asiakkaan näkökulmasta kuvaava mittaristo. Työn kirjallisuustutkimuksen perusteella tunnistetaan olennaiset menetelmät asiakaspalvelutarpeiden mittaamiseen ja analysointiin. Lisäksi työssä esitellään suorituskyvyn mittariston rakentamisen mallit ja periaatteet, sekä mittariston implementointiin vaikuttavat tekijät. Empiirisessä osassa toteutetaan avainasiakkaiden palvelutarpeiden ja yrityksen suoritustason kartoitus ja analysointi. Kohdeyritykselle rakennetaan mittariston asiakaspalvelutarpeiden perusteella, soveltuen yrityksen toimintaympäristöön ja strategisiin päämääriin. Mittaristo rakennetaa Balanced Scorecardin asiakasnäkökulman asiakaslupausmittareiden pohjalle. Työn tuloksena kohdeyritys saa kuvan palvelutasostaan. Työssä esitetyn asiakaslupausmittariston avulla kohdeyritys voi seurata ja kehittää suorituskykyään. Lisäksi työssä tuodaan ilmi tärkeitä tekijöitä, jotka vaikuttavat mittariston implementointiin ja esitetään suositusten muodossa toimintaperiaatteita implementointiprosessissa.
Resumo:
Tässä kandidaatintyössä tarkastellaan erilaisia johdon laskentatoimessa käytettyjä menetelmiä, jotka liittyvät asiakkaisiin. Työ on teoriapainotteinen ja se perustuu pitkälti aiheesta kirjoitettuihin artikkeleihin, mutta joukossa on myös muutama käytännön esimerkki. Työn tavoitteena on muodostaa laaja-alainen kirjallisuuskatsaus johdon laskentatoimessa käytettäviin asiakaslaskentamenetelmiin sekä niiden hyötyihin ja ongelmiin. Kiristyvän kilpailun ja globalisaation myötä asiakkaan huomioonottaminen on muodostunut yhä tärkeämmäksi seikaksi yritysmaailmassa. Asiakaslähtöisyydestä on tullut muoti-ilmiö, johon kaikki haluavat panostaa. Tämä lisää johdon tietotarpeita ja asettaa näin uusia vaatimuksia johdon laskentatoimelle. Siirtyminen uusiin laskentamenetelmiin ja toimintatapoihin aiheuttaa jatkuvasti uusia haasteita, sillä muitakaan yrityksen sidosryhmiä ei voi unohtaa asiakaslähtöisyyttä parannettaessa. Yksi eniten huomiota saanut asiakaslaskentamenetelmä on asiakaskannattavuus. Sen tarkoituksena on tutkia, mitkä asiakkaat tai asiakasryhmät ovat kannattavia ja mitkä eivät. Muita esiteltäviä asiakaslaskentamenetelmiä ovat muun muassa asiakkaiden arvottaminen, tavoitekustannuslaskenta, arvoperusteinen hinnoittelu sekä suorituskykymittaristojen asiakasnäkökulmat. Osa asiakaslaskentamenetelmistä on jo nykyisin laajassa käytössä yrityksissä, mutta tulevaisuudessa niiden käyttö lisääntynee entisestään, kun menetelmiä kehitetään helppokäyttöisemmiksi ja luotettavimmiksi.
Resumo:
Optimization of an essentially inactive 3,4-dihydro-2H-pyrano[3,2-c]quinoline carboxylic ester derivative as acetylcholinesterase (AChE) peripheral anionic site (PAS)-binding motif by double O → NH bioisosteric replacement, combined with molecular hybridization with the AChE catalytic anionic site (CAS) inhibitor 6-chlorotacrine and molecular dynamics-driven optimization of the length of the linker has resulted in the development of the trimethylene-linked 1,2,3,4-tetrahydrobenzo[h][1,6]naphthyridine6-chlorotacrine hybrid 5a as a picomolar inhibitor of human AChE (hAChE). The tetra-, penta-, and octamethylene-linked homologues 5bd have been also synthesized for comparison purposes, and found to retain the nanomolar hAChE inhibitory potency of the parent 6-chlorotacrine. Further biological profiling of hybrids 5ad has shown that they are also potent inhibitors of human butyrylcholinesterase and moderately potent Aβ42 and tau anti-aggregating agents, with IC50 values in the submicromolar and low micromolar range, respectively. Also, in vitro studies using an artificial membrane model have predicted a good brain permeability for hybrids 5ad, and hence, their ability to reach their targets in the central nervous system. The multitarget profile of the novel hybrids makes them promising leads for developing anti-Alzheimer drug candidates with more balanced biological activities.
Resumo:
Optimization of an essentially inactive 3,4-dihydro-2H-pyrano[3,2-c]quinoline carboxylic ester derivative as acetylcholinesterase (AChE) peripheral anionic site (PAS)-binding motif by double O → NH bioisosteric replacement, combined with molecular hybridization with the AChE catalytic anionic site (CAS) inhibitor 6-chlorotacrine and molecular dynamics-driven optimization of the length of the linker has resulted in the development of the trimethylene-linked 1,2,3,4-tetrahydrobenzo[h][1,6]naphthyridine6-chlorotacrine hybrid 5a as a picomolar inhibitor of human AChE (hAChE). The tetra-, penta-, and octamethylene-linked homologues 5bd have been also synthesized for comparison purposes, and found to retain the nanomolar hAChE inhibitory potency of the parent 6-chlorotacrine. Further biological profiling of hybrids 5ad has shown that they are also potent inhibitors of human butyrylcholinesterase and moderately potent Aβ42 and tau anti-aggregating agents, with IC50 values in the submicromolar and low micromolar range, respectively. Also, in vitro studies using an artificial membrane model have predicted a good brain permeability for hybrids 5ad, and hence, their ability to reach their targets in the central nervous system. The multitarget profile of the novel hybrids makes them promising leads for developing anti-Alzheimer drug candidates with more balanced biological activities.
Resumo:
Optimization of an essentially inactive 3,4-dihydro-2H-pyrano[3,2-c]quinoline carboxylic ester derivative as acetylcholinesterase (AChE) peripheral anionic site (PAS)-binding motif by double O → NH bioisosteric replacement, combined with molecular hybridization with the AChE catalytic anionic site (CAS) inhibitor 6-chlorotacrine and molecular dynamics-driven optimization of the length of the linker has resulted in the development of the trimethylene-linked 1,2,3,4-tetrahydrobenzo[h][1,6]naphthyridine6-chlorotacrine hybrid 5a as a picomolar inhibitor of human AChE (hAChE). The tetra-, penta-, and octamethylene-linked homologues 5bd have been also synthesized for comparison purposes, and found to retain the nanomolar hAChE inhibitory potency of the parent 6-chlorotacrine. Further biological profiling of hybrids 5ad has shown that they are also potent inhibitors of human butyrylcholinesterase and moderately potent Aβ42 and tau anti-aggregating agents, with IC50 values in the submicromolar and low micromolar range, respectively. Also, in vitro studies using an artificial membrane model have predicted a good brain permeability for hybrids 5ad, and hence, their ability to reach their targets in the central nervous system. The multitarget profile of the novel hybrids makes them promising leads for developing anti-Alzheimer drug candidates with more balanced biological activities.
Resumo:
Optimization of an essentially inactive 3,4-dihydro-2H-pyrano[3,2-c]quinoline carboxylic ester derivative as acetylcholinesterase (AChE) peripheral anionic site (PAS)-binding motif by double O → NH bioisosteric replacement, combined with molecular hybridization with the AChE catalytic anionic site (CAS) inhibitor 6-chlorotacrine and molecular dynamics-driven optimization of the length of the linker has resulted in the development of the trimethylene-linked 1,2,3,4-tetrahydrobenzo[h][1,6]naphthyridine6-chlorotacrine hybrid 5a as a picomolar inhibitor of human AChE (hAChE). The tetra-, penta-, and octamethylene-linked homologues 5bd have been also synthesized for comparison purposes, and found to retain the nanomolar hAChE inhibitory potency of the parent 6-chlorotacrine. Further biological profiling of hybrids 5ad has shown that they are also potent inhibitors of human butyrylcholinesterase and moderately potent Aβ42 and tau anti-aggregating agents, with IC50 values in the submicromolar and low micromolar range, respectively. Also, in vitro studies using an artificial membrane model have predicted a good brain permeability for hybrids 5ad, and hence, their ability to reach their targets in the central nervous system. The multitarget profile of the novel hybrids makes them promising leads for developing anti-Alzheimer drug candidates with more balanced biological activities.
Resumo:
The amphiphilic nature of metal extractants causes the formation of micelles and other microscopic aggregates when in contact with water and an organic diluent. These phenomena and their effects on metal extraction were studied using carboxylic acid (Versatic 10) and organophosphorus acid (Cyanex 272) based extractants. Special emphasis was laid on the study of phase behaviour in a pre neutralisation stage when the extractant is transformed to a sodium or ammonium salt form. The pre neutralised extractants were used to extract nickel and to separate cobalt and nickel. Phase diagrams corresponding to the pre neutralisation stage in a metal extraction process were determined. The maximal solubilisation of the components in the system water(NH3)/extractant/isooctane takes place when the molar ratio between the ammonia salt form and the free form of the extractant is 0.5 for the carboxylic acid and 1 for the organophosphorus acid extractant. These values correspond to the complex stoichiometry of NH4A•HA and NIi4A, respectively. When such a solution is contacted with water a microemulsion is formed. If the aqueous phase contains also metal ions (e.g. Ni²+), complexation will take place on the microscopic interface of the micellar aggregates. Experimental evidence showing that the initial stage of nickel extraction with pre neutralised Versatic 10 is a fast pseudohomogeneous reaction was obtained. About 90% of the metal were extracted in the first 15 s after the initial contact. For nickel extraction with pre neutralised Versatic 10 it was found that the highest metal loading and the lowest residual ammonia and water contents in the organic phase are achieved when the feeds are balanced so that the stoichiometry is 2NH4+(org) = Nit2+(aq). In the case of Co/Ni separation using pre neutralised Cyanex 272 the highest separation is achieved when the Co/extractant molar ratio in the feeds is 1 : 4 and at the same time the optimal degree of neutralisation of the Cyanex 272 is about 50%. The adsorption of the extractants on solid surfaces may cause accumulation of solid fine particles at the interface between the aqueous and organic phases in metal extraction processes. Copper extraction processes are known to suffer of this problem. Experiments were carried out using model silica and mica particles. It was found that high copper loading, aromacity of the diluent, modification agents and the presence of aqueous phase decrease the adsorption of the hydroxyoxime on silica surfaces.
Resumo:
Tämän kandidaatintyön aiheena on laadun hallinta makeisteollisuudessa, joka rajautuu tarkemmin käsittelemään asiakkaan kokemaa laatua ja sen seurantaa. Työssä tutkitaan, mistä eri osa-alueista asiakkaan kokema laatu muodostuu ja millä mittareilla näitä tekijöitä voidaan mitata. Työn tarkoituksena on luoda kattava mittaristo asiakkaan kokeman laadun seurannan työkaluksi. Tarkoituksena ei siis ole luoda uusia mittareita, vaan koota olemassa olevista mittareista mittaristo, joka tarjoaa yritykselle hyvän lähtökohdan alkaa kehittää toimintaa asiakaslähtöisemmäksi. Asiakkaan kokema laatu jaetaan tuotteen, toiminnan ja palvelun laatuun. Tärkeimpien laatutekijöiden ollessa selvillä, tutkitaan mittaamisen ja mittareiden valinnan teoriaa. Näiden teorioiden pohjalta luodaan mittaristo, joka sisältää mittarit valituille laatutekijöille. Tällä mittaristolla yritys pystyy löytämään asiakkaan kokemaan laatuun vaikuttavat ongelmakohdat. Laadunhallinta on osa laatujohtamista. Laatujohtaminen taas vaatii tietynlaisia ja työkaluja, jotta sen avulla voidaan kehittää laatua. Tässä työssä esitelty laadun mittaamisen ja seurannan työkalu on hyvä laadun hallinnan apuväline. Tehokas laadunhallinta edellyttää oikein valittujen tunnussuureiden asianmukaista mittaamista. On siis tiedettävä, mitä ja miten mitataan, sekä miten saatuja mittaustuloksia hyödynnetään. Erityisesti tuleekin kiinnittää huomiota mittaamisen kohteiden ja tavoitteiden asetantaan sekä laatumittareiden ja näiden raja-arvojen valintaan. Mittareiden valitaan alalle yleisiä käytäntöjä ja teoriamalleja hyväksikäyttäen. Näiden mallien perusteella valitaan mittarit laatutekijöille ja kootaan mittaristo laadun seurannan työkaluksi. Työkalun avulla voidaan havaita asiakkaan kokemaan laatuun mahdollisesti negatiivisesti vaikuttavat asiat, jonka jälkeen niitä voidaan parantaa. Työkalu on hyvin käytettävissä työn toimintaympäristön valmistavissa yrityksissä. Kuitenkin työn rajaukset ja haasteet tulee huomioida.
Resumo:
Background: None of the HIV T-cell vaccine candidates that have reached advanced clinical testing have been able to induce protective T cell immunity. A major reason for these failures may have been suboptimal T cell immunogen designs. Methods: To overcome this problem, we used a novel immunogen design approach that is based on functional T cell response data from more than 1,000 HIV-1 clade B and C infected individuals and which aims to direct the T cell response to the most vulnerable sites of HIV-1. Results: Our approach identified 16 regions in Gag, Pol, Vif and Nef that were relatively conserved and predominantly targeted by individuals with reduced viral loads. These regions formed the basis of the HIVACAT T-cell Immunogen (HTI) sequence which is 529 amino acids in length, includes more than 50 optimally defined CD4+ and CD8+ T-cell epitopes restricted by a wide range of HLA class I and II molecules and covers viral sites where mutations led to a dramatic reduction in viral replicative fitness. In both, C57BL/6 mice and Indian rhesus macaques immunized with an HTI-expressing DNA plasmid (DNA.HTI) induced broad and balanced T-cell responses to several segments within Gag, Pol, and Vif. DNA.HTI induced robust CD4+ and CD8+ T cell responses that were increased by a booster vaccination using modified virus Ankara (MVA.HTI), expanding the DNA.HTI induced response to up to 3.2% IFN-γ T-cells in macaques. HTI-specific T cells showed a central and effector memory phenotype with a significant fraction of the IFN-γ+ CD8+ T cells being Granzyme B+ and able to degranulate (CD107a+). Conclusions: These data demonstrate the immunogenicity of a novel HIV-1 T cell vaccine concept that induced broadly balanced responses to vulnerable sites of HIV-1 while avoiding the induction of responses to potential decoy targets that may divert effective T-cell responses towards variable and less protective viral determinants.
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Many researchers and professionals have reported nonsubstance addiction to online entertainments in adolescents. However, very few scales have been designed to assess problem Internet use in this population, in spite of their high exposure and obvious vulnerability. The aim of this study was to review the currently available scales for assessing problematic Internet use and to validate a new scale of this kind for use, specifically in this age group, the Problematic Internet Entertainment Use Scale for Adolescents. The research was carried out in Spain in a gender-balanced sample of 1131 high school students aged between 12 and 18 years. Psychometric analyses showed the scale to be unidimensional, with excellent internal consistency (Cronbach"s alpha of 0.92), good construct validity, and positive associations with alternative measures of maladaptive Internet use. This selfadministered scale can rapidly measure the presence of symptoms of behavioral addiction to online videogames and social networking sites, as well as their degree of severity. The results estimate the prevalence of this problematic behavior in Spanish adolescents to be around 5 percent.
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Glucose-oxidase (GOD), suffers conformational change during freeze-drying. In order to determine the protection level granted by amorphous matrices (AM) of saccharose, maltose, trehalose and their combinations, the thermal inactivation constants (K D) of GOD trapped in these systems were determined. For its evaluation, GOD samples were balanced at different water activities and heated up to 30, 50 and 70 ºC. The best AM found for GOD stability was saccharose-trehalose (5/10% p/v). The K D values (K D.10-4) at a w = 0.0 were 3 at 30 ºC and 6 at 70 ºC. For non-protected GOD under the same conditions these values were 48 at 30 ºC and 257 at 70 ºC.
Resumo:
Un transmissor d’AM (modulació per amplitud), utilitza una de les moltes tècniques de modulació existents avui en dia. És molta la importància que té la modulació de senyals i aquests en són alguns exemples: -Facilita la propagació del senyal per cable o per aire. -Ordena l’espectre, distribuint Canals a les diferents informacions. -Disminueix la dimensió de les antenes. -Optimitza l’ample de banda de cada canal. -Evita interferències entre Canals. -Protegeix la informació de les degradacions per soroll. -Defineix la qualitat de la informació transmesa. L’objectiu principal d’aquest treball, serà realitzar un transmissor d’AM utilitzant components electrònics disponibles al mercat. Això es realitzarà mitjançant diversos procediments de disseny. Es realitzarà un procediment de disseny teòric, tot utilitzant els “datasheets” dels diferents components. Es realitzarà un procediment de disseny mitjançant la simulació, gràcies al qual es podrà provar el disseny del dispositiu i realitzar-ne algunes parts impossibles a reproduir teòricament. I finalment es realitzarà el dispositiu a la pràctica. Entre les conclusions més rellevants obtingudes en aquest treball, voldríem destacar la importància de la simulació per poder dissenyar circuits de radiofreqüència. En aquest treball s’ha demostrat que gràcies a una bona simulació, el primer prototip de dispositiu creat ens ha funcionat a la perfecció. D’altre banda, també comentar la importància d’un disseny adequat d’antena per poder aprofitar al màxim el rendiment del nostre dispositiu. Per concloure, la realització d’un aparell transmissor aporta unes nocions equilibrades d’electrònica i telecomunicacions importants per al disseny de dispositius de comunicació.
Resumo:
The analytical method developed to evaluate tamoxifen in dog plasma samples was precise, accurate, robust and linear in the range of 5-200 ng/mL. The limits of detection and quantification were 0.981 ng/mL and 2.97 ng/mL, respectively. Besides, the intra-day precision and accuracy variations were 8.78 and 10.16%, respectively. Tamoxifen concentrations were analyzed by combined reversed phase liquid chromatography and UV detection (lambda=280 nm). The study was conducted using an open randomized 2-period crossover balanced design with a 1-week washout period between the doses. This simple, rapid and selective method is suitable for pharmacokinetic, bioavailability and bioequivalence studies.