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1.
J Microencapsul ; 34(6): 560-570, 2017 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-28805476

RESUMO

The aim of this work was to obtain microencapsulated stable Aspergillus niger peptidases by post fermentation spray drying. The enzymatic extract was evaluated before and after spray drying microencapsulation to verify the effects of five different process parameters on the extract enzymatic activity, i.e. air flow, extract feed rate, drying temperature, homogenising time and weight ratio of extract to encapsulation material. The optimal conditions were determined by desirability functions and experimentally confirmed. Additionally, the stability of the microparticles was assessed during 60 days at 4 °C, 25 °C and 40 °C. The results revealed that the microparticles stored at 4 °C retained approximately 100% of their proteolytic activity at nine days of storage. Considering the industrial adaptation of the bioprocess and the prospect of commercial application of the proteases, the evaluation of different parameters for drying enzymes is required as a valuable alternative to obtain biotechnological products with high added value.


Assuntos
Aspergillus niger/enzimologia , Fibras na Dieta/metabolismo , Fermentação , Resíduos Industriais , Peptídeo Hidrolases/química , Composição de Medicamentos , Estabilidade Enzimática
2.
AAPS PharmSciTech ; 17(2): 252-61, 2016 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-26040724

RESUMO

This work aimed at improving the solubility of curcumin by the preparation of spray-dried ternary solid dispersions containing Gelucire®50/13-Aerosil® and quantifying the resulting in vivo oral bioavailability and anti-inflammatory activity. The solid dispersion containing 40% of curcumin was characterised by calorimetry, infrared spectroscopy and X-ray powder diffraction. The solubility and dissolution rate of curcumin in aqueous HCl or phosphate buffer improved up to 3600- and 7.3-fold, respectively. Accelerated stability test demonstrated that the solid dispersion was stable for 9 months. The pharmacokinetic study showed a 5.5-fold increase in curcumin in rat blood plasma when compared to unprocessed curcumin. The solid dispersion also provided enhanced anti-inflammatory activity in rat paw oedema. Finally, the solid dispersion proposed here is a promising way to enhance curcumin bioavailability at an industrial pharmaceutical perspective, since its preparation applies the spray drying, which is an easy to scale up technique. The findings herein stimulate further in vivo evaluations and clinical tests as a cancer and Alzheimer chemoprevention agent.


Assuntos
Anti-Inflamatórios/química , Anti-Inflamatórios/farmacocinética , Curcumina/química , Curcumina/farmacocinética , Estabilidade de Medicamentos , Animais , Anti-Inflamatórios/farmacologia , Disponibilidade Biológica , Química Farmacêutica/métodos , Curcumina/farmacologia , Gorduras/química , Gorduras/farmacocinética , Gorduras/farmacologia , Masculino , Óleos/química , Óleos/farmacocinética , Óleos/farmacologia , Ratos , Ratos Wistar , Dióxido de Silício/química , Dióxido de Silício/farmacocinética , Dióxido de Silício/farmacologia , Solubilidade , Tecnologia Farmacêutica/métodos , Difração de Raios X/métodos
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