Synthesis of novel superdisintegrants for pharmaceutical tableting based on functionalized nanocellulose hydrogels

Synthesis of novel superdisintegrants for pharmaceutical tableting based on functionalized nanocellulose hydrogels


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دانشگاه علوم پزشکی تبریز
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نویسندگان: مرجان قربانی , خسرو ادیب کیا , حامد همیشه کار

کلمات کلیدی: Nanocrystalline cellulose Superdisintegrant Hydrogel Tablet Nanoparticle

نشریه: 15044 , 0 , 167 , 2021

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نویسنده ثبت کننده مقاله حامد همیشه کار
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه مرکز تحقیقات علوم تغذیه
کد مقاله 75265
عنوان فارسی مقاله Synthesis of novel superdisintegrants for pharmaceutical tableting based on functionalized nanocellulose hydrogels
عنوان لاتین مقاله Synthesis of novel superdisintegrants for pharmaceutical tableting based on functionalized nanocellulose hydrogels
ناشر 5
آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ بلی
عنوان نشریه (خارج از لیست فوق)
نوع مقاله Original Article
نحوه ایندکس شدن مقاله ایندکس شده سطح یک – ISI - Web of Science
آدرس لینک مقاله/ همایش در شبکه اینترنت

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Superdisintegrants have an important function in Fast dissolving tablets (FDT). It's believed that an increase in surface to the mass (size reduction) can enhance their performance. Due to the obligation of pharmaceutical excipients being in GRAS (generally recognized as safe) list, we've devoted our research to modify one of the routinely used and important natural polymer, cellulose, as superdisintegrant. Nanocrystalline cellulose (NCC) was extracted from microcrystalline cellulose (MCC) via the sulfuric acid hydrolysis process. NCC derivatives have been synthesized by Itaconic acid/Hydroxyethyl methacrylate (IA/HEMA) via maleic anhydride (MA) to acquire unique swellability properties in to achieve superabsorbent cellulose-based nano hydrogel with the cross-linking system. The disintegration performance of prepared tablets was compared with tablets composed of sodium starch glycolate (SSG) and MCC as positive and negative controls. The results show that the disintegration time of tablets formulated with synthesized modified NCC (m-NCC) decreased dramatically compared to other disintegrants. The dissolution analysis showed suitable condition for complete drug release in a shorter time. The in vitro cytotoxic experiments proved the biocompatibility of newly synthesized superdisintegrant. The dissolution Analysis findings suggest that our developed novel superdisintegrant paves the way for the formulation of fast dissolving tablets containing rapidly acting medicines such as zolpidem

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نویسنده نفر چندم مقاله
مرجان قربانیسوم
خسرو ادیب کیاچهارم
حامد همیشه کارپنجم

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نام فایل تاریخ درج فایل اندازه فایل دانلود
Ghorbani,2020,72.pdf1399/12/082690296دانلود