کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5819487 1557353 2014 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Formulation and in vitro characterization of novel sildenafil citrate-loaded polyvinyl alcohol-polyethylene glycol graft copolymer-based orally dissolving films
ترجمه فارسی عنوان
فرمولاسیون و بررسی درون سلولی سیلدنافیل سیترات لید شده پی وی سی پی وی سی پلی اتیلن گلیکول پروپان تلومر مبتنی بر حلال های خوراکی
کلمات کلیدی
فیلم در حال پخش در فیلم، پلی وینیل الکل پلی اتیلن گلیکول کوپلیمر پیوند، سیلدنافیل سیترات، فرمولاسیون، مشخصات آزمایشگاهی،
موضوعات مرتبط
علوم پزشکی و سلامت داروسازی، سم شناسی و علوم دارویی علوم دارویی
چکیده انگلیسی

This work was aimed to develop novel sildenafil citrate (SC)-loaded polyvinyl alcohol (PVA)-polyethylene glycol (PEG) graft copolymer (Kollicoat® IR)-based orally dissolving films (ODFs) using a solvent casting method. Formulation factors such as plasticizers and disintegrants were optimized on the basis of characteristics of blank ODFs. The SC-loaded ODF with a loading capacity up to 6.25 mg in an area of 6 cm2 was prepared and evaluated in terms of mechanical properties, disintegration time and dissolution rate. The physicochemical properties of drug-loaded ODF were also investigated using the scanning electron microscope (SEM), X-ray diffraction (XRD), differential scanning calorimetry (DSC) and Fourier transform infrared spectroscopy (FT-IR). The blank ODF composed of Kollicoat® IR, sodium alginate (ALG-Na) and glycerol (10:2:1.5, w/w) had a remarkably short disintegration time of about 20 s. The SC-loaded ODF showed a delayed disintegration time (about 25 s), but exhibited improved mechanical properties when compared to the blank ODF. SC was homogenously dispersed throughout the ODF and the crystalline form of drug had been partly changed, existing strong hydrogen bonding between the drug and carriers. The Kollicoat® IR/ALG-Na based ODFs containing SC might be an alternative to conventional tablet for the treatment of male erectile dysfunction.

199

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: International Journal of Pharmaceutics - Volume 473, Issues 1–2, 1 October 2014, Pages 398-406
نویسندگان
, , , , , , ,