RESUMO
Aphanolaimus strilliae n. sp. and Makatinus africanus n. sp. are described from freshwater sources in the Telperion Nature Reserve, Mpumalanga, South Africa. Aphanolaimus strilliae n. sp. is characterised by a body length of 1240-1613 µm, more than 800 body annules, lateral field originating between the first and second lateral body pore at the 34th-46th annule, first lateral body pore located at the 25th-35th annule, vagina V-shaped and bent anteriorly, 142-195 µm long uterus and 165-207 µm long tail with spinneret offset. This species is ovoviviparous and no males were found. Makatinus africanus n. sp. is characterised by a large, thick body (3228-4128 µm long, a = 30-39 wide), slightly set off lip region with amalgamated lips; 31-34 µm long odontostyle; long tongue-shaped cardia, and stout, short tail (30-43 µm long) with a small peg / digitate extension and male absent. Populations of three known species, Chronogaster africana, Eutobrilus annetteae and Neotobrilus ampiei, from fresh water at the Telperion Nature Reserve are described and scanning electron microscope graphs of these species published for the first time.
Assuntos
Helmintos , Nematoides , Animais , Cromadoria , Feminino , Água Doce , Masculino , África do SulRESUMO
This study reports the laboratory optimization for the preparation of sustained release amoxicillin (AMX) ethylcellulose microcapsules by an emulsion solvent evaporation process by adjusting the viscosity and concentration of ethylcellulose, ratio of amoxicillin to ethylcellulose, and concentration of emulsifier and pore inducer. When ethylcellulose with a viscosity of 45 mPa.s was used, almost no material stuck to the inside wall of the beaker and uniform microcapsules were prepared. The average diameter of microcapsules increased and yield and release rate decreased as the concentration of ethylcellulose increased from 1% to 8%. The release of amoxicillin from microcapsules was influenced by the ratio of the weight of drug to that of ethylcellulose and ratios of 2:1 and 4:1 were most suited for optimum amoxicillin release. The average diameter of microcapsules decreased and the release rate increased as the concentration of the emulsifier increased from 1.5% to 6.0%, however, the size distribution became significantly wider with the increase in the concentration of sorbitan monooleate. Addition of small amounts of a water-soluble agent sucrose improved the release of active ingredient from the microcapsule matrix without influencing the morphology and particulate properties of the microcapsules.