نتایج جستجو برای: extended release tablets

تعداد نتایج: 437298  

R Aboofazeli SA Mortazavi

In this study, attempts were made to evaluate the effect of various acrylic acid based Carbopols on the release profile of a beta-adrenoreceptor blocking drug, propranolol HCl, from matrix-type tablets invitro. For this purpose, tablets containing 160 mg of propranolol HCl along with various amounts of Carbopols 934 (C934), 971 (C971), 974 (C974) and Pemulen (Pem) were prepared using the wet gr...

2016
Ghulam Razaque Gul M. Khan Muhammad Z. Danish Shafi Muhammad Nisar A. Shahwani Kamran A. Khan Nayab B. Rizvi Muhammad Younis

In present study, directly compressed controlled released matrix tablets of Diltiazem Hydrochloride were formulated at drug-to-polymer ratios (D: P) of 10:1, 10:2, 10:3 using polymers Ethocel 45 Premium, K100 LV Methocel, K15M EP Premium Methocel as rate controlling agents. In some formulations of Diltiazem hydrochloride and Ethocel 45 Premium matrices, 30% of filler was replaced by Co-excipien...

Journal: :pharmaceutical and biomedical research 0
deepak singh rajiv academy for pharmacy, delhi mathura road, p.o. chhatikara, mathura-281001, india vijay sharma department of pharmaceutics, sri sai college of pharmacy, dalhousie road, badhani, pathankot – 145001, punjab, india kamla pathak department of pharmaceutics, pharmacy college saifai, uprims & r, saifai, etawah -206130, uttar pradesh, india

the objective of research was to explore the suitability of lipids like compritol 888 ato and stearic acid as release retardant to develop sustained release (sr) tablets. the sr micromatrices of lipid (s) and glipizide were prepared (lm1- lm6) as intermediate product by fusion method and assessed for various pharmacotechnical properties. micromatrices were formulated as sr tablets (f1-f6) by di...

Background and purpose: The dissolution of a drug has a major role on its bioavailability. Any change in physico-chemical properties can result in changes in drug release, and furthermore in its bioavailability. Evidence suggest that physicochemical properties of medicinal solids depend on the presence of heat and humidity. In order to overcome such changes, it is necessary to determine the sto...

اکبری, جعفر , سعیدی, مجید , شفیعی, وجیهه , عنایتی فرد, رضا ,

Abstract Background and purpose: The dissolution of a drug has an important role in its bioavailability. Any change in the physico-chemical properties can result in changes in the drug release, and furthermore in its bioavailability. In order to overcome such changes, it is necessary to determine the storage conditions required for obtaining a desired drug release. Materials and methods: Di...

Journal: :Chemical & pharmaceutical bulletin 2016
Meiqiong Tang Ping Hu Shigui Huang Qiang Zheng Hao Yu Yun He

The primary objective of the present study was to develop extended-release matrix formulations of apremilast for the oral delivery and to study their in vitro and in vivo correlation. Five extended-release formulations containing hydroxypropylmethylcellulose (HPMC) as the retarding excipient with different release rate of apremilast were prepared. Dissolution tests of all the formulated tablets...

Journal: :iranian journal of pharmaceutical research 0
r jacky dias s shamling sakhare k krishnat mali

the purpose of this study was to design and optimize an oral controlled release acyclovir mucoadhesive tablet, in term of its drug release and mucoadhesive strength. a 32 full factorial design was employed to study the effect of independent variables like carbopol-934p and hydroxypropyl methylcellulose k100m, which significantly influence characteristics like swelling index, ex-vivo mucoadhesiv...

Journal: :iranian journal of pharmaceutical sciences 0
harun-or- rashid department of pharmaceutical technology, university of dhaka, dhaka, bangladesh abul kalam lutful kabir department of pharmacy, stamford university bangladesh, dhaka - 1217 md. zakir hossaina department of pharmaceutical technology, university of dhaka, dhaka, bangladesh abu shara shamsur rouf department of pharmaceutical technology, university of dhaka, dhaka, bangladesh

the purpose of this work was to develop once daily sustained release (sr) matrix tablets of naproxen, an anti-inflammatory agent. the tablets were prepared by wet granulation method along with hydrophilic matrix materials like methocel k 15m cr and methocel k 100m cr. the granules were evaluated for bulk density, angle of repose, compressibility index, total porosity and drug content. the table...

Drug delivery via buccal mucosa by means of buccoadhesive formulations offer distinct advantages over peroral administration. Recently, plant gums and exudates have been screened for their use as pharmaceutical adjuvants. The aim of this study is to evaluate matrix tablets containing Plantago psyllium seed mucilage in addition to carbopol as a mucoadhesive agent, and propranolol hydrochloride a...

Journal: :research in pharmaceutical sciences 0
j k patel n v patel s h shah

a controlled release matrix formulation for mesalamine was designed and developed to achieve a 24 h release profile. using compritol 888 ato (glyceryl behenate) as an inert matrix-forming agent to control the release of mesalamine, formulation granules containing the solid dispersions were investigated. pectin, a polysaccharide, was used as bacterial dependent polymer for colon targeting. the m...

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