Relaxation tests for the time dependent behavior of pharmaceutical tablets: A revised interpretation
Relaxation tests are often used in the pharmaceutical field to assess the strain rate sensitivity of pharmaceutical powders and tablets. These tests involve applying a constant strain to the powder in the die and then monitoring the stress evolution over time. Interpreting these tests is complicated because different physical phenomena, mainly…
Development and characterization of new functionalized polyurethanes for sustained and site-specific…
23. January 2017 Abstract The main objective of the present paper has been the development and study of two new biodegradable polyurethanes, PU(dithiodiethanol-DTDI) and…
THE BIOPROCESSING SUMMIT – Overcoming Formulation Challenges for Biopharmaceuticals…
23. January 2017 THE BIOPROCESSING SUMMIT - Overcoming Formulation Challenges for Biopharmaceuticals Development August 21-22, 2017 | Westin Copley Place…
Inkjet Printing of Proteins: an Experimental Approach
22. January 2017 Abstract Peptides and proteins represent a promissory group of molecules used by the pharmaceutical industry for drug therapy with great potential for…
Increased dissolution rates of tranilast solid dispersions extruded with inorganic excipients
22. January 2017
Abstract
The purpose of this study was to evaluate the performance of Neusilin® (NEU) a synthetic magnesium aluminometasilicate as inorganic drug carrier co-processed with the hydrophilic surfactants…
Amorphous solid dispersion of cyclosporine A prepared with fine droplet drying process:…
21. January 2017 Abstract The present study aimed to develop an amorphous solid dispersion (ASD) of cyclosporine A (CsA) by a fine droplet drying (FDD) process for…
How to tailor medication formulations for patients with dysphagia
21. January 2017
An overview of dysphagia and how to ensure patients are receiving the safest and most efficacious oral formulations.
Dysphagia is the term used to describe a swallowing disorder usually resulting…
Surface modified zeolite-based granulates for the sustained release ofdiclofenac sodium
21. January 2017 Surface modified zeolite-based granulates for the sustained release ofdiclofenac sodium In this study, a granulate for the oral controlled delivery of…
The biopharmaceutical classification system of excipients
21. January 2017 The increasing number of new chemical entities is bringing new challenges to the field of drug delivery. These drugs present bioavailability issues that are…
Natural Polymers for Drug Delivery – Book
20. January 2017
Main Description
Natural polymers have been utilized extensively in food, pharmaceuticals, cosmetics, textiles, oil drilling and paint industries. Their non-toxic and inexpensive attributes readily enhance…
Applications of glycopolymer libraries as protein aggregation modulators and drug delivery systems
20. January 2017
Abstract
The biopharmaceutical market has been on the rise for the past two decades and is expected to continue to excel, currently presenting a growing rate of more than double than conventional pharma.…
Formulation and evaluation of Raloxifene hydrochloride tablets with improved dissolution profile
20. January 2017
Abstract
The objective of this research activity was to formulate and evaluate Raloxifene Hydrochloride (RLX HCl) tablets (BCS class II drug) with enhanced aqueous solubility thereby achieving a…
BIODEGRADABLE FIBERS – Enabling Controlled Pharmaceutical & Biologic Delivery for…
20. January 2017
BIODEGRADABLE FIBERS - Enabling Controlled Pharmaceutical & Biologic Delivery for Next-Generation Medical Applications
INTRODUCTION
Incorporating a broad range of pharmaceutical- or…
Fractal aspects of the flow and shear behaviour of free-flowable particle size fractions of…
19. January 2017
Abstract
Flowability of powder excipients is directly influenced by their size and shape although the granulometric influence of the flow and shear behaviour of particulate matter is not studied frequently.…
Mucoadhesive amorphous solid dispersions for sustained release of poorly water soluble drugs
19. January 2017
Abstract
The oral delivery of mucoadhesive patches has been shown to enhance the absorption of large molecules such as peptides. We hypothesized that this mechanism could have utility for poorly soluble…
An update on electrostatic powder coating for pharmaceuticals
19. January 2017 Abstract Derived from dry powder coating of metals, electrostatic powder coating for pharmaceuticals is a technology for coating drug solid dosage forms.…
ORALLY DISINTEGRATING TABLETS – Patient-Centric Dose Design, Developments in Orally…
18. January 2017
INTRODUCTION
The orally disintegrating tablet, or ODT, offers an easy-to-take alternative form to consumers of over-the-counter (OTC) treatments who perhaps do not have access to water, and…
DEUTSCHER EUDRAGIT® WORKSHOP
18. January 2017
Wednesday, 2017-03-08 - Thursday, 2017-03-09
Darmstadt
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EUDRAGIT® COMPACT COURSE
18. January 2017
Thursday, 2017-03-09 - Thursday, 2017-03-09
Piscataway, NJ 08854
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Effects of Pharmaceutical Excipients on the in Vitro Release Rate of Sodium Salicylate from Oily…
18. January 2017 Abstract Objectives: The work objective was to study the possible effects of different pharmaceutical excipients on the release of sodium salicylate from…
What does Process Validation mean in the world of Pharmaceutical Excipients?
18. January 2017
What is Process Validation?
Validation for ExcipientsThe concept of validating pharmaceutical processes or, in FDA’s definition, “the establishment of scientific evidence that a process is capable of…
IPEC-Americas 2016 Accomplishments
18. January 2017
During the December 7, 2016 Board of Trustees meeting that took place in Arlington, VA, Priscilla Zawislak, IPEC-Americas Chair, presented an overview of the organizations accomplishments over the past…
Evidence of acceptability of oral paediatric medicines: a review
17. January 2017 Objectives The aim of this review was to map the currently available evidence on acceptability of oral paediatric medicines to aid in the selection of…
Investigation of Drug–Polymer Compatibility Using Chemometric-Assisted UV-Spectrophotometry
17. January 2017 Abstract A simple chemometric-assisted UV-spectrophotometric method was used to study the compatibility of clindamycin hydrochloride (HC1) with two…
Excipient Selection In Parenteral Formulation Development
17. January 2017 Excipient Selection In Parenteral Formulation Development Excipients are the integral part of pharmaceutical products development to achieve desired…
Excipients Use in Parenteral and Lyophilized Formulation Development
17. January 2017 Excipients Use in Parenteral and Lyophilized Formulation Development Abstract Excipients are the integral part of pharmaceutical product development…
Filing DMFs in eCTD Format – IPEC Webinar Feb 15 & 16
17. January 2017
Filing DMFs in eCTD Format - IPEC Webinar Feb 15 & 16
Feb 15 &16 2017
Learn the Standards, Groundwork, Expertise and Technology Required to Submit Compliant DMF/ASMF Submissions.
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Excipients & Nanotechnology – IPEC Webinar March 15
17. January 2017 Excipients & Nanotechnology - IPEC Webinar March 15 March 15, 2017 An overview of nanotechnology - what is it, why is it…
SEMINAR ON FUNCTIONAL INGREDIENTS FOR FOOD SUPPLEMENTS
17. January 2017
Wednesday, 2017-03-15 - Wednesday, 2017-03-15
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Do you like pharma-excipients?
16. January 2017 Then we gladly invite you to support us growing the community by - sharing the information on the pharma excipients linkedin group with your…
3RD INTERNATIONAL SYMPOSIUM ON SOLUBILITY ENHANCEMENT – ACADEMIA SPECIAL
16. January 2017
Wednesday, 2017-02-01 - Thursday, 2017-02-02
Evonik site in Darmstadt
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EUDRAGIT® BASIC SEMINAR
16. January 2017
EUDRAGIT® BASIC SEMINAR
Thursday, 2017-02-23 - Thursday, 2017-02-23
Khartoum, Soudan
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AGE RELATED BIORELEVANT DISSOLUTION TESTING FOR PAEDIATRIC FORMULATIONS
16. January 2017
INTRODUCTION
Dissolution of oral dosage forms depends on the GI tract physiological conditions, and definition of the dissolution profile in conditions that reflect the in vivo GI environment can lead…
An evaluation of tools via patient-reported outcome measures to assess the acceptability of existing…
16. January 2017
Introduction
Palatability of liquid medicines is a recognised challenge within the paediatric population
Acceptability: “The overall ability of the patient and its caregiver to use the medicine as…
Elemental Impurities: Implications for Manufacturers of Drug Products, APIs & Excipients
15. January 2017
Elemental Impurities: Implications for Manufacturers of Drug Products, APIs & Excipients
Introduction
The International Conference on Harmonization (ICH) finalized the ICH Q3D Guideline…