preparation and characterization of thermoresponsive in-situ forming poloxamer hydrogel for controlled release of nile red-loaded solid lipid nanoparticles

Authors

golnar dorraj

department of pharmaceutics and nanotechnology, school of pharmacy, shahid beheshti university of medical sciences, po box: 14155-6153, tehran, iran. hamid r. moghimi

department of pharmaceutics and nanotechnology, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran. pharmaceutical sciences research center, shahid beheshti university of medical sciences, tehran, iran.

abstract

preparation and characterization of thermoresponsive in-situ forming poloxamer hydrogel for controlled release of nile red-loaded solid lipid nanoparticles. nanoparticles (nps) are cleared rapidly from systemic circulation and do not provide sustained action in most cases. to solve this problem, this investigation introduces an erodible in-situ forming gel system as potential vehicles for prolonged release of nps. in this study, nile red-containing slns were prepared by solidification of an oil-in-water microemulsion using stearic acid, surfactants and co-surfactants. sln particles were then loaded in a poloxamerthermoresponsive sol-gel matrix. dialysis membrane and membrane-less diffusion method were used to study release of the fluorescent probe. erosion test were carried out by gravimetric method and the medium was checked for zeta potential to investigate existence of intact slns. sol-gel transition temperature was determined by stirring method. release results showed high entrapment of nile red in lipid matrix of sln. therefore, nile red content in erosion medium was attributed to sln particles. zeta potential of slns remained unchanged after sol-gel loading (p>0.05). the correlated released amount of nile red to dissolved gel weight implied erosion could be major mechanism of sln release. results also showed that sln increase erosion rate of poloxamer gel and its sol-gel transition temperature. the present study show that thermoresponsivepoloxamer gel can be used to control the release of nps and those intact nps are released from this system. the prepared formulation can be used for further investigations in vivo.

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

Preparation and Characterization of Thermoresponsive In-situ Forming Poloxamer Hydrogel for Controlled Release of Nile red-loaded Solid Lipid Nanoparticles

Preparation and characterization of thermoresponsive in-situ forming poloxamer hydrogel for controlled release of Nile red-loaded solid lipid nanoparticles. Nanoparticles (NPs) are cleared rapidly from systemic circulation and do not provide sustained action in most cases. To solve this problem, this investigation introduces an erodible in-situ forming gel system as potential vehicles for prolo...

full text

Preparation and characterization of solid lipid nanoparticles loaded with doxorubicin.

Solid lipid nanoparticles (SLN) loaded with doxorubicin were prepared by solvent emulsification-diffusion method. Glyceryl caprate (Capmul)MCM C10) was used as lipid core, and curdlan as the shell material. Dimethyl sulfoxide (DMSO) was used to dissolve both lipid and drug. Polyethylene glycol 660 hydroxystearate (Solutol)HS15) was employed as surfactant. Major formulation parameters were optim...

full text

Preparation, characterization, and optimization of primaquine-loaded solid lipid nanoparticles

Primaquine (PQ) is one of the most widely used antimalarial drugs and is the only available drug that combats the relapsing form of malaria. PQ use in higher doses is limited by severe tissue toxicity including hematological- and gastrointestinal-related side effects. Nanoformulation of drugs in an appropriate drug carrier system has been extensively studied and shown to have the potential to i...

full text

Preparation, Characterization and In-vitro release of Piroxicam-loaded Solid Lipid Nanoparticles

Solid lipid nanoparticles (SLNs) of piroxicam where produced by solvent emulsification diffusion method in a solvent saturated system. The SLNs where composed of tripamitin lipid, polyvinyl alcohol (PVAL) stabilizer, and solvent ethyl acetate. All the formulation were subjected to particle size analysis, zeta potential, drug entrapment efficiency, percent drug loading determination and in-vitro...

full text

Preparation, characterization and evaluation of Ginkgo biloba solid lipid nanoparticles

Objective(s): In this work, Ginkgo biloba extract (GBE) loaded solid lipid nanoparticles (SLNs) were synthesized via high pressure homogenization method and their physicochemical properties, as well as cytotoxicity and antibacterial activities were evaluated.Methods: Ginkgo biloba extract SLNs (GBE-SLNs) were prepared using high pressure homogenization method. The morphology and size of S...

full text

Sustained release Curcumin loaded Solid Lipid Nanoparticles.

PURPOSE curcumin is poorly water soluble drug with low bioavailability. Use of lipid systems in lipophilic substances increases solubility and bioavailability of poorly soluble drugs. The aim of this study was to prepare curcumin loaded Solid Lipid Nanoparticles (SLNs) with high loading efficiency, small particle size and prolonged release profile with enhanced antibacterial efficacy. METHODS...

full text

My Resources

Save resource for easier access later


Journal title:
iranian journal of pharmaceutical sciences

جلد ۹، شماره ۴، صفحات ۳۹-۵۰

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023