168 research outputs found

    Validations of the names of seven Podocarpaceae macrofossils

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    Seven names of macrofossil taxa belonging to Podocarpaceae are here validated; they were all previously published but not validly so under the International Code of Botanical Nomenclature. The names apply to species in the genera Acmopyle Pilg. [A. setiger (Townrow) R. S. Hill & R. J. Carp. ex R. R. Mill & R. S. Hill], Dacrycarpus (Endl.) de Laub. [D. praecupressinus (Ettingsh.) D. R. Greenw. ex R. R. Mill & R. S. Hill], Falcatifolium de Laub. [F. eocenicum (D. R. Greenw.) R. S. Hill & L. J. Scriven ex R. R. Mill & R. S. Hill], Prumnopitys Phil. [P. tasmanica (Townrow) D. R. Greenw. ex R. R. Mill & R. S. Hill], Sigmaphyllum R. S. Hill & L. J. Scriven [S. australe (D. R. Greenw.) R. S. Hill & L. J. Scriven ex R. R. Mill & R. S. Hill], Smithtonia R. S. Hill & M. Pole [S. lanceolata (D. R. Greenw.) R. S. Hill & M. Pole ex R. R. Mill & R. S. Hill] and Willungia R. S. Hill & M. Pole [W. maslinensis (D. T. Blackburn) R. S. Hill & M. Pole ex R. R. Mill & R. S. Hill]. All these combinations were originally published without exact basionym references; instead, the authors cited the complete pagination of the paper in which the intended basionym was made.Robert R. Mill and Robert S. Hil

    The development of direct extrusion-injection moulded zein matrices as novel oral controlled drug delivery systems

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    Purpose: To evaluate the potential of zein as a sole excipient for controlled release formulations prepared by hot melt extrusion. Methods: Physical mixtures of zein, water and crystalline paracetamol were hot melt extruded (HME) at 80°C and injection moulded (IM) into caplet forms. HME-IM Caplets were characterised using differential scanning calorimetry, ATR-FTIR spectroscopy, scanning electron microscopy and powder X-ray diffraction. Hydration and drug release kinetics of the caplets were investigated and fitted to a diffusion model. Results: For the formulations with lower drug loadings, the drug was found to be in the non-crystalline state, while for the ones with higher drug loadings paracetamol is mostly crystalline. Release was found to be largely independent of drug loading but strongly dependent upon device dimensions, and predominately governed by a Fickian diffusion mechanism, while the hydration kinetics shows the features of Case II diffusion. Conclusions: In this study a prototype controlled release caplet formulation using zein as the sole excipient was successfully prepared using direct HME-IM processing. The results demonstrated the unique advantage of the hot melt extruded zein formulations on the tuneability of drug release rate by alternating the device dimensions

    Diagnostic Testing of Pediatric Fevers: Meta-Analysis of 13 National Surveys Assessing Influences of Malaria Endemicity and Source of Care on Test Uptake for Febrile Children under Five Years.

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    In 2010, the World Health Organization revised guidelines to recommend diagnosis of all suspected malaria cases prior to treatment. There has been no systematic assessment of malaria test uptake for pediatric fevers at the population level as countries start implementing guidelines. We examined test use for pediatric fevers in relation to malaria endemicity and treatment-seeking behavior in multiple sub-Saharan African countries in initial years of implementation. We compiled data from national population-based surveys reporting fever prevalence, care-seeking and diagnostic use for children under five years in 13 sub-Saharan African countries in 2009-2011/12 (n = 105,791). Mixed-effects logistic regression models quantified the influence of source of care and malaria endemicity on test use after adjusting for socioeconomic covariates. Results were stratified by malaria endemicity categories: low (PfPR2-10<5%), moderate (PfPR2-10 5-40%), high (PfPR2-10>40%). Among febrile under-fives surveyed, 16.9% (95% CI: 11.8%-21.9%) were tested. Compared to hospitals, febrile children attending non-hospital sources (OR: 0.62, 95% CI: 0.56-0.69) and community health workers (OR: 0.31, 95% CI: 0.23-0.43) were less often tested. Febrile children in high-risk areas had reduced odds of testing compared to low-risk settings (OR: 0.51, 95% CI: 0.42-0.62). Febrile children in least poor households were more often tested than in poorest (OR: 1.63, 95% CI: 1.39-1.91), as were children with better-educated mothers compared to least educated (OR: 1.33, 95% CI: 1.16-1.54). Diagnostic testing of pediatric fevers was low and inequitable at the outset of new guidelines. Greater testing is needed at lower or less formal sources where pediatric fevers are commonly managed, particularly to reach the poorest. Lower test uptake in high-risk settings merits further investigation given potential implications for diagnostic scale-up in these areas. Findings could inform continued implementation of new guidelines to improve access to and equity in point-of-care diagnostics use for pediatric fevers

    Epidermal conditions, lesions and malformations in cetaceans of the Strait of Gibraltar

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