Rational Design of Topical Semi-Solid Dosage Forms-How Far Are We?

Specific aspects of semi-solid dosage forms for topical application include the nature of the barrier to be overcome, aspects of susceptibility to physical and chemical instability, and a greater influence of sensory perception. Advances in understanding the driving forces of skin penetration as wel...

Full description

Saved in:
Bibliographic Details
Main Authors: Michael E. Herbig (Author), Dirk-Heinrich Evers (Author), Sascha Gorissen (Author), Melanie Köllmer (Author)
Format: Book
Published: MDPI AG, 2023-06-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

MARC

LEADER 00000 am a22000003u 4500
001 doaj_c6864d0e220e44d8a0cc7a72111ce1bc
042 |a dc 
100 1 0 |a Michael E. Herbig  |e author 
700 1 0 |a Dirk-Heinrich Evers  |e author 
700 1 0 |a Sascha Gorissen  |e author 
700 1 0 |a Melanie Köllmer  |e author 
245 0 0 |a Rational Design of Topical Semi-Solid Dosage Forms-How Far Are We? 
260 |b MDPI AG,   |c 2023-06-01T00:00:00Z. 
500 |a 10.3390/pharmaceutics15071822 
500 |a 1999-4923 
520 |a Specific aspects of semi-solid dosage forms for topical application include the nature of the barrier to be overcome, aspects of susceptibility to physical and chemical instability, and a greater influence of sensory perception. Advances in understanding the driving forces of skin penetration as well as the design principles and inner structure of formulations, provide a good basis for the more rational design of such dosage forms, which still often follow more traditional design approaches. This review analyses the opportunities and constraints of rational formulation design approaches in the industrial development of new topical drugs. As the selection of drug candidates with favorable physicochemical properties increases the speed and probability of success, models for drug selection based on theoretical and experimental approaches are discussed. This paper reviews how progress in the scientific understanding of mechanisms and vehicle-influence of skin penetration can be used for rational formulation design. The characterization of semi-solid formulations is discussed with a special focus on modern rheological approaches and analytical methods for investigating and optimizing the chemical stability of active ingredients in consideration of applicable guidelines. In conclusion, the combination of a good understanding of scientific principles combined with early consideration of regulatory requirements for product quality are enablers for the successful development of innovative and robust semi-solid formulations for topical application. 
546 |a EN 
690 |a semi-solid formulation 
690 |a topical delivery 
690 |a pre-formulation 
690 |a solubility 
690 |a saturation 
690 |a skin penetration 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceutics, Vol 15, Iss 7, p 1822 (2023) 
787 0 |n https://www.mdpi.com/1999-4923/15/7/1822 
787 0 |n https://doaj.org/toc/1999-4923 
856 4 1 |u https://doaj.org/article/c6864d0e220e44d8a0cc7a72111ce1bc  |z Connect to this object online.