superoxide dismutase-loaded solid lipid nanoparticles prepared by cold homogenization method: characterization and permeation study through burned rat skin

نویسندگان

masoud ali karami school of pharmacy, ahvaz jundishapur university of medical sciences, ahvaz, ir iran

behzad sharif makhmal zadeh school of pharmacy, ahvaz jundishapur university of medical sciences, ahvaz, ir iran; nanotechnology research center, ahvaz jundishapur university of medical sciences, ahvaz, ir iran; school of pharmacy, ahvaz jundishapur university of medical sciences, ahvaz, ir iran

maryam koochak school of pharmacy, ahvaz jundishapur university of medical sciences, ahvaz, ir iran

eskandar moghimipur school of pharmacy, ahvaz jundishapur university of medical sciences, ahvaz, ir iran

چکیده

conclusions the results indicated that sod-loaded in sln was delivered into deep burned skin layer and induced high enzyme activity through the skin. low particle size, application of lecithin as surfactant and low crystallinity index (ci) percentage were important factors for increasing sod penetration through the burned rat skin. percentage of activity by sln dispersions through rat skin was 13 folds more than the control. objectives we developed solid lipid nanoparticles (sln) dispersions for enhancing superoxide dismutase penetration across burned rat skin and enzyme protection against environmental degradation. methods solid lipid nanoparticles were prepared with cold homogenization method because sod is a thermo sensitive compound. the characteristics of slns such as particle size, entrapment efficiency and enzyme release pattern and permeability through burned rat skin were evaluated. background superoxide dismutase (sod), which inhibits lipid peroxidation and scavengers oxygen radicals, is an effective enzyme for treatment of skin ulcer lesion especially due to burns. superoxide dismutase is a hydrophilic compound with high molecular weight and low affinity for partitioning into skin. moreover, another important limitation for its use in medicine is thermal denaturation and inactivation. results solid lipid nanoparticles showed more than 90% entrapment efficiency and particle size lower than 102 nm. in vitro release study demonstrated sod burst and sustained release characters in this manner with maximum of 65% of enzyme released after 48 hours. the sod activity was measured and results indicated that sln could protect activity of the enzyme. differential scanning calorimetry of slns showed low crystalinity index percentage that is a reason for high entrapment efficiency and burst release character.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Cellular uptake of β-carotene from protein stabilized solid lipid nanoparticles prepared by homogenization-evaporation method.

With a homogenization-evaporation method, β-carotene (BC) loaded nanoparticles were prepared with different ratios of food-grade sodium caseinate (SC), whey protein isolate (WPI), or soy protein isolate (SPI) to BC and evaluated for their physiochemical stability, in vitro cytotoxicity, and cellular uptake by Caco-2 cells. The particle diameters of the BC loaded nanoparticles with 0.75% SC or 1...

متن کامل

Fabrication, appraisal, and transdermal permeation of sildenafil citrate-loaded nanostructured lipid carriers versus solid lipid nanoparticles

Although sildenafil citrate (SC) is used extensively for erectile dysfunction, oral delivery of SC encounters many obstacles. Furthermore, the physicochemical characteristics of this amphoteric drug are challenging for delivery system formulation and transdermal permeation. This article concerns the assessment of the potential of nanomedicine for improving SC delivery and transdermal permeation...

متن کامل

Formulation and Physicochemical Characterization of Lycopene-Loaded Solid Lipid Nanoparticles.

PURPOSE Lycopene belongs to the carotenoids that shows good pharmacological properties including antioxidant, anti-inflammatory and anticancer. However, as a result of very low aqueous solubility, it has a limited systemic absorption, following oral administration. METHODS Here, we prepared a stable lycopene-loaded solid lipid nanoparticles using Precirol® ATO5, Compritol 888 ATO and myristic...

متن کامل

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...

متن کامل

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...

متن کامل

Tamoxifen Drug Loading Solid Lipid Nanoparticles Prepared by Hot High Pressure Homogenization Techniques

As drug delivery systems Nanoparticulate widely investigated because of many advantages such as smaller size, controlled drug release potential, targeting ability, enhancement of therapeutic efficacy and reduction of toxicity. So, Solid Lipid Nanoparticles have recently received considerable attention as alternative drug delivery carrier. In this study Solid Lipid Nanoparticles (SLNs) containin...

متن کامل

منابع من

با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید


عنوان ژورنال:
jundishapur journal of natural pharmaceutical products

جلد ۱۱، شماره ۴، صفحات ۰-۰

میزبانی شده توسط پلتفرم ابری doprax.com

copyright © 2015-2023