Paediatric Formulation: Design and Development
Antonio Lopalco1, Nunzio Denora1
1Department of Pharmacy-Pharmaceutical Sciences, University of Bari Aldo Moro, 70125 Bari, Italy.
Insights
Developing pediatric medicines requires careful consideration of unique patient needs, including dose flexibility and tolerability. This special issue updates on state-of-the-art methods and challenges in creating effective pediatric formulations.
Area of Science:
- Pharmaceutical Sciences
- Pediatric Drug Development
- Formulation Science
Background:
- Pediatric medicine development faces unique challenges due to distinct patient population needs.
- Key considerations include patient variability, dose flexibility, administration routes, compliance, and drug/excipient tolerability.
Discussion:
- This special issue addresses state-of-the-art methodologies and operational challenges in pediatric formulation design and development.
- It focuses on advancing age-appropriate treatments for pediatric diseases.
- Key areas include formulation development, drug delivery design, and the efficacy, safety, and tolerability of drugs and excipients.
Key Insights:
- Re-evaluation of current practices is needed for significant progress in pediatric drug formulation.
- Addressing specific pediatric needs is crucial for effective and safe treatments.
- The collection highlights advancements in formulation development and drug delivery for children.
Outlook:
- Future efforts should prioritize innovative approaches to pediatric formulation.
- Continued research is essential to overcome existing challenges in pediatric drug development.
- Enhancing the efficacy, safety, and tolerability profile of pediatric medicines remains a critical goal.
Abstract:
The development of medicines designed for children can be challenging since this distinct patient population requires specific needs. A formulation designed for paediatric patients must consider the following aspects: patient population variability; dose flexibility; route of administration; patient compliance; drug and excipient tolerability. The purpose of this Special Issue entitled "Paediatric Formulation: Design and Development" is to provide an update on both state-of-the-art methodology and operational challenges in the design and development of paediatric formulations. It aims at re-evaluating what is needed for more progress in the design and development of age-appropriate treatments for paediatric diseases, focusing on: formulation development; drug delivery design; efficacy, safety, and tolerability of drugs and excipients. This editorial, briefly, summarizes the objects of nine original research and review papers published in this Special Issue.
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