Synthesis of novel superdisintegrants for pharmaceutical tableting based on functionalized nanocellulose hydrogels
Synthesis of novel superdisintegrants for pharmaceutical tableting based on functionalized nanocellulose hydrogels
نویسندگان: مرجان قربانی , خسرو ادیب کیا , حامد همیشه کار
کلمات کلیدی: Nanocrystalline cellulose
Superdisintegrant
Hydrogel
Tablet
Nanoparticle
نشریه: 15044 , 0 , 167 , 2021
| 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) |
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| نوع مقاله |
Original Article |
| نحوه ایندکس شدن مقاله |
ایندکس شده سطح یک – ISI - Web of Science |
| آدرس لینک مقاله/ همایش در شبکه اینترنت |
|
| 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 |
| نام فایل |
تاریخ درج فایل |
اندازه فایل |
دانلود |
| Ghorbani,2020,72.pdf | 1399/12/08 | 2690296 | دانلود |