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Paediatric
Application of 3D printing technology and quality by design approach for development of…
Pediatric population is a sensitive sector of the healthcare and pharmaceutical field with additional needs compared to the adult population. Extemporaneous formulations for children are generally prepared by manipulating adult formulations, but medication errors can result in suboptimal efficacy…
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Pediatric Oral Formulations: An Updated Review of Commercially Available Pediatric Oral Formulations…
Oral pediatric formulations are either ready-to-use or require manipulation, and multi-use or single-use. Strong encouragement for preservative-free pediatric formulations has resulted in fewer multi-use solutions or suspensions in favor of single-use solid oral dosage forms. This updated review…
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Safe excipient exposure in neonates and small children – protocol for the SEEN project.
07. February 2017
INTRODUCTION: The pharmacokinetics of excipients in neonates differs from that of older children. In a recent pan--European survey, two thirds of neonates received at least one potentially harmful excipient, such as ethanol and benzoates. The content of sweeteners…
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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 intended”
Patient needs must be met when medicines are…
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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 to accurate prediction of the in vivo performance (1).…
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Efavirenz dissolution enhancement III: Colloid milling, pharmacokinetics and electronic tongue…
03. January 2017
Abstract
Efavirenz (EFV), a non-nucleoside reverse transcriptase inhibitor (NNRTI), is part of first-line therapy for the treatment of human immunodeficiency virus type 1 infection (HIV-1/AIDS). This drug shows relatively low oral absorption and bioavailability, as…
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Pediatric Medicines Are Not Child’s Play! AAPS Blog
24. August 2016
Pediatric Medicines Are Not Child’s Play! AAPS Blog
Jennifer Walsh
Since the introduction of pediatric regulations in the USA (Pediatric Research Equity Act and Best Pharmaceuticals for Children Act) and Europe, there has been a huge increase in the number of…
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Taste acceptance of Captopril and Furosemide Extemporaneous Oral Pediatric Formulations among…
11. August 2016
Many pediatric patients require medications that are not available in age appropriate formulations, especially those with cardiovascular diseases. The use of a suitable vehicle is critical for the preparation of extemporaneous formulations with the expected effect.…
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STEP Database Updated – 40 Excipients now!
25. February 2016
The STEP stands for Safety and Toxicity of Excipients for Paediatrics. It is a user-designed resource developed by European Paediatric Formulation Initiative (EuPFI) and United States Paediatric Formulation Initiative (USPFI) in collaboration for storage and…
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STEP database – Safety and Toxicity of Excipients for Paediatrics
10. February 2016
The STEP stands for Safety and Toxicity of Excipients for Paediatrics. The STEP database is a user-designed free resource that compiles the safety and toxicity information of excipients that is manually extracted from selected information sources. Three tier…
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