{"id":120419,"date":"2023-04-15T11:05:51","date_gmt":"2023-04-15T11:05:51","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/sin-categoria\/farmacotecnia-de-formas-orales-solidas-y-su-evaluacion-biofarmaceutica-mediante-datos-de-excrecion-renal\/"},"modified":"2023-04-15T11:05:51","modified_gmt":"2023-04-15T11:05:51","slug":"farmacotecnia-de-formas-orales-solidas-y-su-evaluacion-biofarmaceutica-mediante-datos-de-excrecion-renal","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/ciencias-medicas\/farmacotecnia-de-formas-orales-solidas-y-su-evaluacion-biofarmaceutica-mediante-datos-de-excrecion-renal\/","title":{"rendered":"Farmacotecnia de formas orales solidas y su evaluacion biofarmaceutica mediante datos de excrecion renal."},"content":{"rendered":"<h2>Tesis doctoral de <strong> Mar\u00eda De La Paloma Ballesteros Papantonakis <\/strong><\/h2>\n<p>Se estudia la biodisponibilidad de tres formas farmaceuticas que contienen como principio activo el sulfametoxazol. Las formas de dosificacion son:  comprimidos normales  comprimidos recubiertos y comprimidos de microcapsulas  sobre los que se realizan todos los ensayos galenicos habituales  destacando los de velocidad de disolucion. La biodisponibilidad se estudia en tres grupos de voluntarios sanos mediante datos de excrecion renal. Finalmente se realiza el tratamiento de los datos experimentales en el que se utiliza la ecuacion de weibul con muy buenos resultados  obteniendose correlacion entre el tiempo de disolucion in vitro y el tiempo de excrecion.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Farmacotecnia de formas orales solidas y su evaluacion biofarmaceutica mediante datos de excrecion renal.<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Farmacotecnia de formas orales solidas y su evaluacion biofarmaceutica mediante datos de excrecion renal. <\/li>\n<li><strong>Autor:<\/strong>\u00a0 Mar\u00eda De La Paloma Ballesteros Papantonakis <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Complutense de Madrid<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 01\/01\/1986<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<h3>Direcci\u00f3n y tribunal<\/h3>\n<ul>\n<li><strong>Director de la tesis<\/strong>\n<ul>\n<li>Rafael Cadorniga Carro<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: Fermin Vazquez Lopez <\/li>\n<li>Jos\u00e9 Cemeli Pons (vocal)<\/li>\n<li>Eugenio Sell\u00e9s Flores (vocal)<\/li>\n<li>Manuel Cordoba Borrego (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Mar\u00eda De La Paloma Ballesteros Papantonakis Se estudia la biodisponibilidad de tres formas farmaceuticas que contienen como [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center 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