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1.
Recent Pat Drug Deliv Formul ; 13(1): 46-61, 2019.
Article in English | MEDLINE | ID: mdl-30836929

ABSTRACT

BACKGROUND: The Jojoba Simmondsia Chinensis oil is used as one of the main ingredients which has an antioxidant, moisturizing and stabilizing activity. Likewise, grape seed (Vitis vinifera) oil is also used in this preparation which also has some remarkable medicinal properties such as antioxidant, astringent and is also used as a moisturizer. The Valacyclovir Solid Lipid Nanoparticles (SLN) are prepared in combination. OBJECTIVE: The prime objective of the study was to prepare a nanodispersion with good stability indicating zeta potential. The formulations were prepared by varying concentrations of jojoba oil and grape seed oil which form the hybrid nanoparticles with the drug. METHODS: The high-pressure hot-homogenization technique was used to prepare the nanoparticles. The prepared nanoparticles were subjected to characterization analysis such as Mean particle size, Zaverage, and Zeta potential by using Dynamic Light Scattering (DLS) and Photon Correlation Spectroscopy (PCS). The best formulation was subjected to Transmission Electron Microscopy (TEM) technique for surface morphology and other characterizations. The crystalline pattern of the drug alone, drug-loaded nanoparticles and nanoparticles without the drug was studied by XRD. The drug excipients compatibility studies were performed by using Fourier-Transform Infrared Spectroscopy (FTIR) Differential Scanning Calorimetry and (DSC). The other factors such as in vitro drug release, and % drug entrapment efficiency were studied by using suitable methods. RESULTS: The results demonstrated that the particles are in nano range with good stability with appreciable Zeta potential (-48.2±mV). The selected formulations were analyzed for MPS which demonstrated the value of 306.7±183.4 and 416.5±289.3. The best formulation VNP5 demonstrated the Bellshaped curve and confirmed the uniform distribution. CONCLUSION: Based on the patents, it was demonstrated that valacyclovir is widely used in the treatment and prophylaxis of viral infections in human, particularly infections caused by the herpes group of viruses. Valacyclovir is an effective drug for the treatment of cold sores.


Subject(s)
Lipids/chemical synthesis , Nanoparticles/chemistry , Patents as Topic , Plant Oils/chemical synthesis , Valacyclovir/chemical synthesis , Animals , Antiviral Agents/administration & dosage , Antiviral Agents/chemical synthesis , Chemistry, Pharmaceutical/methods , Drug Delivery Systems/methods , Grape Seed Extract/administration & dosage , Grape Seed Extract/chemical synthesis , Lipids/administration & dosage , Plant Oils/administration & dosage , Rats , Rats, Wistar , Skin Absorption/drug effects , Skin Absorption/physiology , Valacyclovir/administration & dosage , X-Ray Diffraction/methods
2.
J Agric Food Chem ; 63(8): 2233-40, 2015 Mar 04.
Article in English | MEDLINE | ID: mdl-25671729

ABSTRACT

Grape seed polyphenolic extract (GSPE) rich in the flavan-3-ols (+)-catechin and (-)-epicatechin beneficially modulates Alzheimer's Disease phenotypes in animal models. The parent molecules in the extract are converted to a series of methylated and glucuronidated derivatives. To fully characterize these metabolites and establish a robust quantitative assay of their levels in biological fluids, we have implemented a partial synthetic approach utilizing chemical methylation followed by enzymatic glucuronidation. Liquid chromatography/time-of-flight mass spectrometry (LC-TOF-MS) and nuclear magnetic resonance (NMR) spectroscopy were used to assign unequivocal structures to the compounds. An analytical method using solid-phase extraction and LC-MS/MS in selective reaction monitoring mode (SRM) was validated for their quantitation in plasma. These studies provide a basis for improvements in future work on the bioavailability, metabolism, and mechanism of action of metabolites derived from dietary flavan-3-ols in a range of interventions.


Subject(s)
Catechin/chemical synthesis , Grape Seed Extract/chemical synthesis , Animals , Catechin/blood , Catechin/metabolism , Grape Seed Extract/blood , Grape Seed Extract/metabolism , Rats
3.
J Oral Rehabil ; 38(7): 541-6, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21058972

ABSTRACT

The effect of biomodification of dentin matrices using collagen cross-linkers, glutaraldehyde (GD) and grape seed extract (GSE), on the reduced modulus of elasticity (Er) and nanohardness (H) of the hybrid layer and underlying dentin was investigated at the dentin-resin bonded interface. The coronal dentin of nine molars were exposed and divided into groups: 5% GD, 6·5% GSE and control. Control samples were etched, bonded with Adper Single Bond Plus and Premise composite. GD and GSE were applied for 1 h prior to bonding procedures. After 24 h, samples were sectioned, and resin-dentin beams were either kept in distilled water or exposed to collagenase treatment for 24 h. Nano-indentations were performed at the hybrid layer and underlying dentin. GD and GSE treatment increased the Er and H of resin-dentin interface structures when compared to the control group (P<0·05), particularly the hybrid layer, and may be a promising novel approach to strengthen the dentin-resin bonded interface structures when using these adhesive system and resin-based composite.


Subject(s)
Composite Resins/chemical synthesis , Dental Bonding/methods , Dentin-Bonding Agents/chemistry , Glutaral/chemical synthesis , Grape Seed Extract/chemical synthesis , Adhesiveness , Dentin , Elasticity , Humans , Materials Testing , Nanotechnology/methods , Surface Properties
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