Search results for " Supercritical"
showing 3 items of 33 documents
Modification of PVDF nanoparticles by controlled free radical graft copolymerization in supercritical carbon dioxide
2014
PVDF (polyvinylidenefluoride) membranes are widely used in microfiltration (MF) and ultrafiltration (UF) due to their excellent processability, chemical resistance, well-controlled porosity, and good thermal properties [1]. Moreover this polymer is also frequently adopted in bio-medical devices owing to its good biocompatibility [2]. On the other hand, the use of PVDF membranes in biomedical applications is limited to some extent by the hydrophobicity of their exposed area, which mainly arises from the nature of the pore surface. Prompted by these considerations in the present work we have studied the modification of PVDF nanoparticles with hydroxyethylmethacrylate (HEMA) thus obtaining a m…
Impact of the Extraction Method on the Chemical Composition and Antioxidant Potency of Rosmarinus officinalis L. Extracts
2023
Rosmarinus officinalis L. is a dietary source that produces polyphenols as secondary metabolites. These natural compounds with potent antioxidant abilities are increasingly recommended as a supplement to inhibit oxidative stress. In the current work, we evaluated the impact of the extraction method on the chemical composition of R. officinalis extract, especially on the content of carnosic (CA) and rosmarinic (RA) acids using UPLC-MS-DAD as well as on their antioxidant potency. Four extracts of Tunisian rosemary were obtained from non-conventional extraction techniques:ultrasound-assisted extraction (UAE),supercritical extraction (SFE) and UAE and SFE combined ((UAE-SFE(I), UAE-SFE(II)). Th…
Sterilization of three-dimensional tissue engineering scaffolds by supercritical carbon dioxide
2014
Medical devices, implants or patient-care equipment that will come into intimate contact with a patient must be effectively decontaminated to prevent infection or disease transmission. Non-sterile devices have significant ramifications for patient morbidity and mortality and two processes must be undertaken in order to make an item acceptable for use or implantation: cleaning and disinfection (or sterilization) [1]. Sterilization is the destruction of living organisms, and must be done without damaging the material surface and without compromising the bulk material strength or biocompatibility of implantable device. Common sterilization processes include steam autoclaving, gamma irradiation…