نتایج جستجو برای: hydroxy propyl methyl cellulose k4m

تعداد نتایج: 167315  

2010
Bendgude Namdeo Tukaram Iyer Vidaya Rajagopalan Poddar Sushi Ikumar Shartchandra

This paper reviews the use of texture analysis in studying the performance of hydrophilic matrices of highly soluble drugs and different types of excipients (i.e. water-soluble, water-insoluble and swellable, and water insoluble and non-swellable). Tablets were prepared by direct compression, and their swelling and erosion in presence of these different excipients were assessed with the help of...

2013
Jatin Sood Varinder kaur Pravin Pawar

Article history: Received on: 15/12/2012 Revised on: 24/02/2013 Accepted on: 11/03/2013 Available online: 30/03/2013 Verapamil Hydrochloride is a calcium channel blocking anti-anginal agent. Extensive first pass metabolism, low bioavailability (~20%) and short biological half life (4.8 hrs) altogether makes it an ideal candidate for transdermal drug delivery. The objectives of this study were t...

Journal: :Acta Crystallographica Section E Structure Reports Online 2009

2013
Carlos Alemán Alberto Bianco Fernando Formaggio Alessandro Moretto Marco Crisma Claudio Toniolo

Aib α-Aminoisobutyric acid or Cα-methylalanine (αMe)Phe Cα-methylphenylalanine (αMe)Val Cα-methylvaline BOP (Benzotriazol-1-yloxy)tris(dimethylamino)phosphonium CIP 2-Chloro-1,3-dimethylimidazolidium phosphate Db z g Cα,α-dibenzylglycine Deg Cα,α-diethylglycine Dφg Cα,α-diphenylglycine Dp n g Cα,α-di-n-propylglycine EDC 1-(3-Dimethylamino)propyl-3-ethylcarbodiimide HATU 2-(1H-7-aza-1,2,3-benzot...

2010
M. M. Rohman M. D. Hossain Masayuki Fujita

The dominant onion bulb glutathione S-transferases (GSTs) (named as GSTc, GSTd and GSTe) were separated by DEAE cellulose column chromatography, and the inhibitory interactions of glutathione (GSH) derivatives (S-methyl GSH, S-propyl GSH, S-butyl GSH, and S-hexyl GSH), four coumarins (coumarin, 7-hydroxy coumarin, esculetin and scopoletin) were tested with theses GSTs. The activities of GSTs we...

2010
Burkhon Zh Elmuradov Kambarali Turgunov Bakhodir Tashkhodjaev Khusniddin M. Shakhidoyatov

The title compound, C(15)H(16)N(2)O(2)·H(2)O, was synthesized via the alkyl-ation of 3-hydroxy-methyl-idene-2,3-dihydro-1H-pyrrolo[2,1-b]quinazolin-9-one with n-propyl iodide in the presence of sodium hydroxide. The organic mol-ecule and the water mol-ecule both lie on a crystallographic mirror plane. In the crystal structure, inter-molecular O-H⋯O and O-H⋯N hydrogen bonds link the components i...

2015
María-Pilar Sánchez-Sánchez Araceli Martín-Illana Roberto Ruiz-Caro Paulina Bermejo María-José Abad Rubén Carro Luis-Miguel Bedoya Aitana Tamayo Juan Rubio Anxo Fernández-Ferreiro Francisco Otero-Espinar María-Dolores Veiga Hitoshi Sashiwa

Vaginal formulations for the prevention of sexually transmitted infections are currently gaining importance in drug development. Polysaccharides, such as chitosan and carrageenan, which have good binding capacity with mucosal tissues, are now included in vaginal delivery systems. Marine polymer-based vaginal mucoadhesive solid formulations have been developed for the controlled release of acycl...

2017
Aveary R Menze Jefferson P Sinnott Alexander Y Nazarenko

Naltrexone [systematic name: 17-(cyclo-propyl-meth-yl)-3,14-di-hydroxy-4,5α-epoxymorphinan-6-one] is an opioid receptor competitive antagonist that has been widely used to prevent relapse in opioid- and alcohol-dependent subjects. Its chloride salt forms non-isomorphic solvates with ethanol (C20H24NO4+·Cl-·C2H5OH) (I), propan-2-ol (C20H24NO4+·Cl-·C3H7OH) (II), and 2-methyl-propan-2-ol (C20H24NO...

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