Caracterização do insumo ibuprofeno e a correlação com propriedades de dissolução e de fluxo / Characterization of ibuprofen raw material and correlation with dissolution and flow properties

Ibuprofen is a moderately active non-steroidal anti-inflammatorydrug, derived from β-phenylpropionic acid. Its analgesic action, which is related to its anti-inflammatoryproperties, is due to a decrease in the production of enzymes cyclo-oxygenase-1 (COX-1) and cyclo-oxygenase-2 (COX-2). Ibuprofen exhibits distinct morphologies when crystallized under different conditions. In this study, the characteristics of the ibuprofen raw material and their impact on drug dissolution and processing properties were analyzed. Samples of raw ibuprofen from 3 different manufacturers were characterized by a variety of techniques. The analysis confirmed that all 3 samples exhibited the same crystalline form; thus, polymorphism could be discarded as one of the causes of any variation in performance of the drug. The results showed that the physical characteristics of each sample influenced its flow and dissolution properties. In fact, there was a detectable variation in the physical characteristics of the drug among the 3 different manufacturers. This demonstrates the importance of testing the characteristics of the drug raw material in order to correlate them with its performance in processing and eventual use, enabling pharmacotechnical improvement and development...

O ibuprofeno é um agente anti-inflamatório não esteróide, derivado do ácido fenilpropiônico que possui atividade anti-inflamatória de ação moderada. Sua ação analgésica está relacionada às propriedades anti-inflamatórias devido à redução da produção da ciclooxigenase-1 (COX-1) e da ciclooxigenase-2 (COX-2). O ibuprofeno exibe diferentes morfologias quando cristalizado em diferentes solventes. Neste estudo, se avaliaram as características de matérias-primas do ibuprofeno e o impacto destas nas propriedades de dissolução e processamento. Foram avaliadas três matérias-primas do ibuprofeno de três diferentes fabricantes, utilizando variadas técnicas de caracterização. As análises confirmaram que todas apresentavam a mesma forma cristalina do ibuprofeno; assim, o polimorfismo foi descartado como uma das causas de influência na dissolução e no fluxo do fármaco. Os resultados mostraram que características físicas da matéria-prima ibuprofeno tiveram impacto nas propriedades de fluxo e dissolução e que existe uma variabilidade das características físicas do fármaco entre diferentes fabricantes. Isto mostra a importância da avaliação de características da matéria-prima para correlacioná-las com propriedades de desempenho, possibilitando o desenvolvimento e melhoramento farmacotécnico...

Simultaneous determination of some pharmaceuticals in hospital effluents Using HPLC with UV and fluorescence detectors

The development and validation of an HPLC/UV/Fluorescence [FL] detection method is described, which enables the measurement of the most consumed pharmaceuticals [methotrexate, caffeine, diclofenac, glimepiride and ibuprofen] in Jordanian hospital effluents. Separation was done on a RP-C8 column at a flow rate of 1 ml/min using 1:1 H2O/acetonitrile with 0.1% trifluoroacetic acid. The samples [200 ml each] were extracted and cleaned-up on C18 cartridges. Correlation coefficients of the pharmaceuticals calibration were higher than 0.997 using a UV detector and 0.996 using a fluorescence detector for methotrexate. Recoveries were ranged from 87% to 108.3%

Desarrollo de la formulación de la suspensión oral de ibuprofeno 100 mg/5 mL para uso pediátrico / Development of formulation for oral suspension Ibuprofen 100 mg/5mL for pediatric use

Se empleó el método de prueba y error para el desarrollo de la formulación de la suspensión oral de ibuprofeno 100 mg/5 mL para uso pediátrico; se estudió su estabilidad químico-física por el método acelerado y de vida de estante; se envasó en frasco de vidrio Ambar por 120 mL y se almacenó a temperatura ambiente. Se realizó el estudio reológico y la determinación de la viscosidad aparente, además, se efectuó el estudio microbiológico a través de la prueba de efectividad de preservativo antimicrobiano y el conteo microbiano; se comprobó la seguridad del producto mediante el estudio toxicológico. Todos los resultados cumplieron con los límites de calidad establecidos en la literatura científica, USP 30, para este tipo de forma farmacéutica. Se concluye que el medicamento desarrollado está correctamente formulado, desde el punto de vista galénico con un tiempo de vida útil de 24 meses bajo las condiciones estudiadas.

Authors used the test and error method to develop the formulation of Ibuprofen oral suspension (100 mg/5 mL) for pediatric use. Its chemical-physic stability was studied through accelerated method and shelf life. It was bottled in amber glass small bottles by 120 mL, and it was stored at room temperature. A rheology study and assessment of apparent viscosity was made as well as a microbiologic one by test of effectiveness of antimicrobial preservative and the microbial count. Product safe was verified by toxicology study. All results fulfilled quality limits established in scientific literature, USP 30, for this type of pharmaceutical method. We conclude that drug developed is correctly formulated, from the doctoral point of view with a time of useful life of 24 months under study conditions.

Studying the effect of surfactant on eudragit RS100 microspheres prepared by solvent evaporation technique

Solvent evaporation technique was used to prepare Eudragit RS100 microspheres containing ibuprofen as an example for acidic drugs. The aqueous phase was 0.1 N HCl containing different concentrations of either cetrimide or dioctyl sodium sulfosuccinate [DOSS] as an antiaggregating agent. It was found that the percent of drug content was equal to theoretical drug content on using 0.25, 0.5 or 1% cetrimide. This may be due to that, cetrimide acts as a good transport barrier for dichloromethane, but not for the drug. At the same time the percent of drug content was markedly decreased on using 1.5% cetrimide. That is may be due to the cetrimide micelle formation. The effect of different concentrations of DOSS on the percent of drug content was also studied

In-vitro evaluation of sustained release ibuprofen microspheres

Microspheres for oral use have been employed to target and to sustain the release of the drug. The objective of this study was to use the melt dispersion technique and aqueous vehicle to entrap ibuprofen into wax carrier (carnauba wax) with the aid of surfactant (Pluronic L-62). The effects of different levels of Pluronic L-62, stirring speed, and ibuprofen levels, as well as the in-vitro release rate of ibuprofen were evaluated. The in-vitro dissolution of ibuprofen in phosphate buffer pH 7.2 showed that microspheres prepared with low amount of drug (1.5 g) released 58.1 percent of ibuprofen after 6 hours, while microspheres prepared with high amount of drug (6.0 g) released only 38.9 percent of ibuprofen. Microsphere formulations prepared by using aqueous vehicle were spherical and of smooth surface. In general the melt dispersion technique was a successful method for preparing sustained release ibuprofen microspheres

Solubilization of certain Analgesics by cetomacrogol 1000

Solubilization of certain nonsteroidal anti-inflammatory drugs, viz., phenacetin, ibuprofen and indomethacin by Cetomacrogol 1000 [Cetomacrogol] has been investigated. The values of the ratio of mole drug solubilized per mole micellar Cetomacrogol revealed that the solubilizing power of Cetomacrogol towards ibuprofen is higher than that for phenacetin or indomethacin. One Cetomacrogol micelle solubilizes 38, 17 and 6 molecules of ibuprofen, phenacetin and indomethacin, respectively. Spectrophotometry as well as solubility measurements in different solvents have been used to provide evidence on the environment of the solubilizate molecule in the micelle. On the basis of the results obtained, it was concluded that these drugs are solubilized as follows: Phenacetin and ibuprofen are solubilized in the hydrocarbon core and in the polyoxyethylene region adjacent to the hydrocarbon core. Indomethacin is wholly solubilized in the polyoxyethylene layer adjacent to the hydrocarbon core. The ability of the surfactants to accelerate the dissolution rate of the drug was also investigated. The dissolution profiles of these drugs in Cetomacrogol revealed marked enhancement of dissolution and there is a good correlation between the dissolution efficiency of the three drugs and their solubility in Cetomacrogol at the same temperature