Functions
Starch 1500®, Partially Pregelatinized Maize Starch, Used as a Binder Disintegrant in High Shear Wet Granulation Comparison to Povidone and Croscarmellose SodiumThis study compares the high shear granulation and tablet properties of two formulations. One is based on a polymer granulation binder, PVP, in combination with a super disintegrant, croscarmellose sodium (CCS). This formulation was developed external to Colorcon. The other formulation utilized partially pregelatinized maize starch, Starch 1500, as both the binder and the disintegrant.
Starch 1500® Product Information Sheet
Application of Ethylcellulose in Preparation of Extended Release Theophylline Inert Matrix Tablets by Wet GranulationThe outcome of this study illustrates that an aqueous ethylcellulose dispersion (Surelease™) was successfully utilized to formulate and manufacture extended release theophyllin inert matrices. The influence of varying polymer concentration, filler choice and compression force on drug release profiles were studied as well.
A Comparison of Delayed Release Film Coating Systems for Pharmaceutical Dosage FormsThis ADS was adapted from the CRS 2010 poster to evaluate and compare the dispersion properties, film properties and enteric performance at varying pH conditions, of four commercially available aqueous,delayed release film coating systems.
Formulation and Process Considerations for Delayed Release Multi-Particulates of Esomeprazole Magnesium This ADS was adapted from the 2008 AAPS poster. The objective of this study was to investigate and establish an application process for an enteric coating system, Acryl-EZE®, aqueous acrylic enteric system, on an esomeprazole magnesium trihydrate (40 mg) multi-particulate system.
Acryl-EZE® 93A Product InformationFeatures and benefits of the Acryl-EZE 93A series of aqueous, acrylic enteric delayed release coating systems.
Acryl-EZE® MP Product InformationFeatures and benefits of the Acryl-EZE MP series of aqueous, acrylic enteric delayed release coating systems.
Evaluation of the Enteric Performance of Lansoprazole Mini-Tabs Coated in a Perforated PanThe focus of this study was to investigate the potential of successful manufacture and enteric coating of lansoprazole mini-tabs using methacrylic acid co-polymers in a perforated pan. Along with other findings, this study will show that the mechanical strength of the mini-tabs significantly improved upon application of a seal-coat.
Investigation of Enteric Coating of Min-tabs Using a Perforated Pan or a Fluid-bed MachineIn this study the feasibility of using a perforated coating pan was evaluated and compared to a fluid-bed machine. Differences between the two processes, in terms of coated tablet appearance, physical properties and enteric protection were studied.
Investigation of Venlafaxine HCl Release from Extruded and Spheronized Beads Coated with Ethylcellulose using Organic or Aqueous Coating SystemsThe objective of this study was to investigate the overall performance of an extruded and spheronized formulation containing venlafaxine HCl, a highly water soluble drug (572 mg/mL)(3), coated with ethylcellulose from organic or aqueous systems.
The Influence of Solvent Type on Extended Release Coating with Ethylcellulose Barrier MembranesThe objective of this work was to investigate the influence of four acceptable solvent combinations on EC solution viscosity and consequent drug release from coated beads.
Evaluation of a Continuous Coating Process for the Application of a Regulatory Compliant Nutritional Enteric Coating on Soft Gelatin CapsulesThis ADS was adapted from the Supply Side West poster presented in October 2008. The purpose of the study was to evaluate a continuous coating process for the application of a delayed release coating system onto soft gelatin capsules.
New Enteric Coating System (Nutrateric®) for Nutritional SupplementsThis ADS was adapted from the CRS poster presented in June 2005, summarizing the performance of Nutrateric when applied to tablets or soft gelatin capsules.
Nutrateric® II Enteric Coating System for Nutritional SupplementsA case study to introduce Nutrateric II, a new generation of enteric film coating designed for nutritional, food and dietary supplements. The system delivers productivity improvements, of greater than 40%, in both coating dispersion preparation and process time without any compromise in enteric protection. This study compares the preparation and productivity to the first generation Nutrateric product.
Performance Comparison of Two Delayed Release Coating Systems for Dietary SupplementsThis ADS was adapted from the CRS 2010 poster comparing the DR performance of an aqueous ethylcellulose and pH dependent pore-former based coating, with a shellac-based coating on garlic tablets.
The Influence of Pore Former Concentration and Coating Weight Gain on Drug Release from Multi-Particulates Coated with Nutrateric®This ADS was adapted from the AAPS poster presented in November 2008. The outcome of this study successfully illustrates the combination of a pH dependent pore former and an aqueous ethylcellulose dispersion resulted in the desired delayed drug release profiles from multi-particulate systems. Coating level and port former concentrations were tailored to alter the duration of the delay in drug release followed by rapid release in higher pH media.
AAPS 2011 - Pilot and Production Scale Evaluation of an Improved High Productivity Delayed Release Coating for Dietary SupplementsUsing a Design of Experiment (DOE) approach, this study evaluated the optimum ratio of Surelease to NS Enteric to provide protection in simulated gastric fluid (SGF) while allowing acceptable disintegration performance in simulated intestinal fluid (SIF). The effects of coating dispersion solids concentration and coating weight gain were also investigated.
Opadry® amb - Moisture Vapor TransmissionEvaluation of Opadry amb compared with alternative coating formulations and their effect on moisture uptake.
Development of USP Delayed Release Aspirin Tablets using Opadry® Enteric, Acrylic-Based Coating System The objective of this study was to develop aspirin delayed release tablets that comply with USP requirements.
Drug Release From Acrylic-Based Opadry® Enteric (94 Series) Coated TabletsOpadry® Enteric (94 Series), enteric coating system, is a fully formulated, delayed release coating system for solid oral dosage forms that is based on MAC, specifically the poly [methacrylic acid, methyl methacrylate (1:1), type A].
Opadry® Enteric 91, 94, 95 seriesOpadry Enteric is a family of fully formulated, delayed release coating systems for solid oral dosage forms, which are applied by organic or hydro-alcoholic processing techniques.
Opadry® Enteric Product InformationFeatures and benefits of the Opadry Enteric platform of PVAP (Phthalavin®) based, delayed release coating systems.
Film Coating Process Considerations for the Application of High Productivity, High Solids Concentration Film Coating FormulationsUsing a Design of Experiments (DOE) approach, this study examines the effect of solids concentration on color uniformity and coating weight variation (CWV) in a batch coating process.
Opadry® II - Product Information BrochureImproved efficiency PVA and HPMC coating formulations reduce coating processing time by 25-30% compared with conventional systems. For use in Nutritional and Pharmacuetical applications.
Opadry® tm - Taste Mask ComparisonProduct technology summary including stability profile, film properties, color effects and regulatory guidelines.
欧巴代中药包衣参数欧巴代中药的使用
Opadry® fx™ PropertiesProduct technology summary including stability profile, film properties, color effects and regulatory guidelines.
Opaglos® 2 Sales BrochureProduct features and benefits.
Opalux® Tablet Sealant CoatingProduct Overivew.
The Influence of Hydrophilic Pore-Formers on Metoprolol Succinate Release from Mini-tabs Coated with Aqueous Ethylcellulose DispersionThis ADS was adapted from the CRS 2010 poster to investigate the influence of incorporating different levels of pore-former into aqueous EC system (Surelease) on the release of a freely water-soluble drug metoprolol succinate, from coated mini-tabs.
Surelease® E-7-19020 Product InformationFeatures and benefits of the Surelease E-7-19020, aqueous ethylcellulose coating system.
Surelease® E-7-19050 Product InformationFeatures and benefits of the Surelease E-7-19050, aqueous ethylcellulose coating system.
The Influence of Post Coating Thermal Treatment on Film Properties and Drug Release from Ethylcellulose Barrier Membrane Coating SystemsThe results of this study demonstrate that post coating treatment can affect both physico-mechanical properties of EC films and drug release from EC-coated multi-particulates.
Sureteric® YAE-6-18107 Product InformationFeatures and benefits of Sureteric YAE-6-18107 PVAP (Phthalavin®) based delayed release coating systems.
Starch 1500® Brochure
Technical Evaluation of SureSpheres™ 20/25 Mesh (850-710 micron) as Drug Layering Substrates (Starter Seeds)SureSpheres Application Data - Technical Evaluation - 20/25 Mesh
The Influence of Plasticizer Type and Level on Drug Release from Ethylcellulose Barrier Membrane MultiparticulatesADS adapted from 2009 CRS poster, The Influence of Plasticizer Type and Level on Drug Release from Ethylcellulose Barrier Membrane Multiparticulates
SureSpheres Product Information BrochureSureSpheres features & benefits
Investigation of Ethylcellulose in the Preparation of Theophylline Extended Release Inert Matrix TabletsThis research illustrates the influence of EC particle size and molecular weight on drug release from inert matrices containing a sparingly water soluble drug. The influence of varying the polymer concentration, filler choice and compression force on drug release was also evaluated.
Investigation of Moisture-Activated Granulation of Hydrophilic Polymer Blends in Verapamil HCl Extended Release MatricesADS adapted from 2009 CRS poster, Investigation of Moisture-Activated Granulation of Hydrophilic Polymer Blends in Verapamil HCl Extended Release Matrices
The Influence of Hydrodynamic Conditions on Verapamil Hydrochloride Release from Hydrophilic Matrices Using Ionic and Non-Ionic PolyersThis ADS was adapted from the 2008 AAPS poster. The purpose of this study was to investigate the effects of hydrodynamic conditions on drug release rates from a matrix tablet with a soluble active ingredient, using different combinations of HPMC. The study will show that the combination of HPMC with ionic polymers in ER matrices provides robust formulations which are insensitive to hydrodynamic conditions.
Use of Roller Compaction in the Preparation of Verapamil Hydrochloride Extended Release Matrix Tablets Containing Hydrophilic PolymersThis ADS was adapted from the 2008 CRS poster evaluating the effects of roller compaction on the flow and compressibility of blends of HPMC, polyvinyl acetate phthalate(PVAP) and carbomer [cross-linked poly (acrylicacid)]. Drug release of an ER verapamil HCl matrix formulation containing this blend was also evaluated.
An Introduction to METHOCEL™ Cellulose EthersA description of the METHOCEL line of premium cellulose ethers.
The Influence of In Vitro Dissolution Method on the Release of a Highly Water Soluble Drug from Polyethylene Oxide and Hypromellose Hydrophilic Extended Release MatricesThis ADS was adapted from the 2008 AAPS poster. The objective of this study was to investigate the influence of different dissolution methods on the release of a high solubility drug from an ER matrix formulation containing either HPMC or PEO as the rate-controlling polymer.
