http://rdf.ncbi.nlm.nih.gov/pubchem/patent/BR-112015026298-A2

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filingDate 2014-04-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7dcc887ca070356a387d9a26beacef7b
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publicationDate 2017-07-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber BR-112015026298-A2
titleOfInvention dispensing vehicle, methods for providing an individual's plasma aromatase inhibitor, for synchronizing ovulation, for inducing superovulation, for improving fertility, for inducing double ovulation, and for enhancing twin formation in a mammal, use of a dispensing vehicle, a luteolytic dose of a prostaglandin, and an ovulatory dose, and kit for providing a mammalian plasma aromatase inhibitor
abstract 1/2 summary “Dispensing vehicle, methods to provide an individual's plasma aromatase inhibitor, to synchronize ovulation, to induce superovulation, to improve fertility, to induce double ovulation and to improve twin formation in a mammal, use of a dispensing vehicle, a luteological dose of a prostaglandin, and an ovulatory dose A kit for providing an aromatase inhibitor in a mammalian plasma is described herein as an intravaginal device that provides biologically active circulating concentrations of an aromatase inhibitor for at least about 4 days. Three estradiol inhibitory compounds (letrozole, anastrozole and fenbendazole) were tested in vitro using bovine granular cell culture. Letrozole has been found to be the most efficient and potent inhibitor. Liposome-based and one wax-based formulations were used to evaluate the diffusion of letrozole through the bovine vaginal mucosa in a diffusion chamber study. The samples were collected within 24 hours. The wax-based vehicle was selected for further development of an intravaginal letrozole device based on its fixed dispensing rate. In an in vivo study in cattle, 3 different intravaginal devices containing 3 g of letrozole were tested: wax (with 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine, dope) + gel coating (n = 2), wax + gel coating (n = 4) and wax (n = 4). Blood samples were collected serially from time 0 to 120 hours, and daily thereafter to measure circulating concentrations of letrozole by lc / ms / ms. Addition of a letrozole-containing gel coating improved initial absorption and accelerated increase in plasma concentrations of the active ingredient, while the letrozole-containing 2/2 wax-based vehicle maintained prolonged release from the intravaginal device.
priorityDate 2013-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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