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1.
Eur J Pharm Biopharm ; 156: 20-39, 2020 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-32871196

RESUMO

The research presented here shows QbD implementation for the optimisation of the key process parameters in electrohydrodynamic atomisation (EHDA). Here, the electrosprayed nanoparticles and electrospun fibers consisting of a polymeric matrix and dye. Eight formulations were assessed consisting of 5% w/v of polycaprolactone (PCL) in dichloromethane (DCM) and 5% w/v polyvinylpyrrolidone (PVP) in ethanol. A full factorial DOE was used to assess the various parameters (applied voltage, deposition distance, flow rate). Further particle and fiber analysis using Scanning Electron Microscopy (SEM), Differential Scanning Calorimetry (DSC), Thermogravimetric Analysis (TGA), Fourier Transform Infrared Spectroscopy (FTIR), particle/fiber size distribution. In addition to this in vitro release studied were carried out using fluorescein and Rhodamine B as model dyes and in vitro permeation studies were applied. The results show a significant difference in the morphology of resultant structures as well as a more rapid release profile for the PVP particles and fibers in comparison to the sustained release profiles found with PCL. In vitro drug release studies showed 100% drug release after 7 days for PCL particles and showed 100% drug release within 120 min for PVP particles. The release kinetics and the permeation study showed that the MN successfully pierced the membrane and the electrospun MN coating released a large amount of the loaded drug within 6 h. This study has demonstrated the capability of these robust MNs to encapsulate a diverse range drugs within a polymeric matrix giving rise to the potential of developed personalised medical devices.


Assuntos
Microinjeções/instrumentação , Agulhas , Polímeros/química , Pesquisa Qualitativa , Tecnologia Farmacêutica/instrumentação , Liberação Controlada de Fármacos , Microinjeções/normas , Agulhas/normas , Poliésteres/química , Poliésteres/normas , Polímeros/normas , Povidona/química , Povidona/normas , Espectroscopia de Infravermelho com Transformada de Fourier/métodos , Tecnologia Farmacêutica/normas
2.
Drug Discov Today ; 25(8): 1513-1520, 2020 08.
Artigo em Inglês | MEDLINE | ID: mdl-32561300

RESUMO

Recently, remarkable efforts have focused on research towards enhancing and delivering efficacious and advanced therapeutic agents. Even though this involves significant challenges, innovative techniques and materials have been explored to overcome these. The advantageous properties of mesoporous silica nanoparticles (MSNs), such as unique morphologies and geometries, makes then favorable for use for various drug delivery targeting purposes, particularly in cancer therapy. As we discuss here, MSNs have been utilized over the past few decades to improve the efficiency of anticancer drugs by enhancing their solubility to render them suitable for application, reducing adverse effects, and improving their anticancer cytotoxic efficiency.


Assuntos
Antineoplásicos/administração & dosagem , Portadores de Fármacos/administração & dosagem , Dióxido de Silício/administração & dosagem , Animais , Humanos , Porosidade
3.
J Drug Target ; 23(4): 305-10, 2015 May.
Artigo em Inglês | MEDLINE | ID: mdl-25582133

RESUMO

A scalable platform to prepare multi-functional ocular lenses is demonstrated. Using rapidly dissolving polyvinylpyrrolidone (PVP) as the active stabilizing matrix, both sides of ocular lenses were coated using a modified scaled-up masking electrohydrodynamic atomization (EHDA) technique (flow rates variable between 5 and 10 µL/min, applied voltage 4-11 kV). Each side was coated (using a specially designed flip-able well) selectively with a pre-determined morphology and model drug substance. PVP nanoparticles (inner side, to be in contact with the cornea, mean size

Assuntos
Cloranfenicol/administração & dosagem , Sistemas de Liberação de Medicamentos , Lentes Intraoculares , Nanopartículas , Antibacterianos/administração & dosagem , Antibacterianos/farmacologia , Química Farmacêutica/métodos , Cloranfenicol/farmacologia , Excipientes/química , Tamanho da Partícula , Polímeros/química , Povidona/química , Staphylococcus aureus/efeitos dos fármacos , Temperatura
4.
J Agric Food Chem ; 59(13): 7346-52, 2011 Jul 13.
Artigo em Inglês | MEDLINE | ID: mdl-21557618

RESUMO

The importance of the linkage between nutrition and health is a hot issue. Like other food-related sectors, the meat industry is undergoing foremost transformations, driven among other things by changes in consumer requirements. The present study was designed to evaluate the lipid stability and antioxidative potential of leg and breast microsomal fraction of broiler meat fed on ALA and ATA. For the first 3 weeks of growth, broilers were fed on feed supplemented with ATA (200 mg/kg of feed) and during the last 3 weeks broilers were fed on feed supplemented with ALA (25, 75, 150 mg/kg of feed) and a constant level of ATA (200 mg/kg of feed). The body weight of the carcass was measured after every week of growth until 6 weeks. Positive correlation between the antioxidant activity and the TPC was observed. Higher values of TBARS were detected in leg muscles than in breast muscles. HPLC data revealed ALA and ATA contents were higher in T(4) (leg, 5.55 ± 0.19 and 3.87 ± 0.15 µg/mg of protein; breast, 5.63 ± 0.20 and 2.03 ± 0.10 µg/mg of protein, respectively) and lowest in T(5) (ALA, leg, 1.40 ± 0.06 µg/mg of protein; breast, 1.54 ± 0.05 µg/mg of protein; ATA, leg, 1.25 ± 0.06 µg/mg of protein; breast, 0.63 ± 0.008 µg/mg of protein), in which the only oxidized oil was used. Oxidized oil in feed reduced weight gain and increased TBARS, whereas TPC, DPPH, ALA, and ATA values decreased in both leg and breast meat.


Assuntos
Antioxidantes/análise , Lipídeos/análise , Carne/análise , Microssomos/química , Ácido Tióctico/administração & dosagem , alfa-Tocoferol/administração & dosagem , Animais , Galinhas , Dieta , Estabilidade de Medicamentos , Músculo Esquelético/química , Músculo Esquelético/ultraestrutura , Substâncias Reativas com Ácido Tiobarbitúrico/análise
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