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1.
Int J Biol Macromol ; 89: 689-99, 2016 Aug.
Article in English | MEDLINE | ID: mdl-27026342

ABSTRACT

Acyclovir a BCS class III drug exhibits poor bioavailability due to limited permeability. The intention of this research work was to formulate and characterize thiolated xyloglucan polysaccharide nanoparticles (TH-NPs) of acyclovir with the purpose of increasing its oral bioavailability. Acyclovir-loaded TH-NPs were prepared using a cross-linking agent. Interactions of formulation excipients were reconnoitered using Fourier transform infrared spectroscopy (FT-IR). The formulated nanoparticles were lyophilised by the addition of a cryoprotectant and characterized for its particle size, morphology and stability and optimized using Box Behnken Design.The optimized TH-NP formulation exhibited particle size of 474.4±2.01 and an entrapment efficiency of 81.57%. A marked enhancement in the mucoadhesion was also observed. In-vivo study in a rat model proved that relative bioavailability of acyclovir TH-NPs is ∼2.575 fold greater than that of the marketed acyclovir drug suspension.


Subject(s)
Acyclovir/chemistry , Biological Availability , Glucans/chemistry , Nanoparticles/chemistry , Xylans/chemistry , Acyclovir/therapeutic use , Administration, Oral , Animals , Antiviral Agents/chemistry , Antiviral Agents/therapeutic use , Drug Carriers/chemistry , Drug Carriers/therapeutic use , Glucans/therapeutic use , Humans , Nanoparticles/therapeutic use , Particle Size , Rats , Xylans/therapeutic use
2.
Carbohydr Polym ; 135: 356-62, 2016 Jan 01.
Article in English | MEDLINE | ID: mdl-26453888

ABSTRACT

A novel polymer in the form of a thiolated derivative of natural tamarind seed polysaccharide or xyloglucan was synthesized and its chacteristics as a mucoadhesive polymer were studied as a part of the study undertaken herein. The synthetic route followed involves a two-step reaction mechanism of firstly oxidizing xyloglucan and then further conjugating it with l-cysteine to form thiolated xyloglucan or thiomer via imine linkage. The thiomer thus formed was characterized using various analytical techniques as differential scanning calorimetry (DSC), X-ray diffraction analysis (XRD), and nuclear magnetic resonance (NMR). Ellman's method was used to determine the numbers of thiol groups/g of thiolated xyloglucan. Zeta potential measurements were carried out for thiolated xyloglucan. Viscosities of the formulated xyloglucan and thiolated xyloglucan gels were comparatively evaluated along with the evaluation of mucoadhesive properties of the gels using ex vivo bioadhesion study employing freshly excised sheep intestinal mucosa.


Subject(s)
Cysteine/chemistry , Glucans/chemistry , Xylans/chemistry , Adhesiveness , Animals , Calorimetry, Differential Scanning , Gels , Intestinal Mucosa/chemistry , Magnetic Resonance Spectroscopy , Powder Diffraction , Sheep , Spectroscopy, Fourier Transform Infrared , Viscosity , X-Ray Diffraction
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