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Semisolid Dosage



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Autore: Daniels Rolf Visualizza persona
Titolo: Semisolid Dosage Visualizza cluster
Pubblicazione: Basel, Switzerland, : MDPI - Multidisciplinary Digital Publishing Institute, 2020
Descrizione fisica: 1 electronic resource (182 p.)
Soggetto topico: Medicine
Soggetto non controllato: dermal drug delivery
diffusion cell
Franz diffusion
Skin-PAMPA
Strat-M® membrane
nanocarrier
nonivamide
methyl cellulose
skin penetration
substantivity
thermogel
tacrolimus formulation
nanogels
drug delivery
human excised skin
Jurkat cells
in situ hydrogel-forming powder
nitric oxide-releasing formulation
S-nitrosoglutathione (GSNO)
antibacterial
wound dressing
wound healing
dermal delivery
porcine skin
in vitro permeation
methadone
pain
in vitro
permeation
niacinamide
solvent
PAMPA
skin
curcumin
deformable liposomes
liposome surface charge
hydrogel
chitosan
wound therapy
IVRT
metronidazole
topical cream
semisolid dosage forms
sameness
FDA's SUPAC-SS guidance
acceptance criteria
positive and negative controls
discriminatory ability
Amphotericin B
Sepigel 305®
Leishmania infantum
cutaneous leishmaniasis
topical treatment
birch bark extract
oleogels
hydrogen bonding
triterpene
rheology
gel strength
eosinophilic esophagitis
budesonide
xanthan gum
guar gum
mucoadhesion
esophagus permeability
rheological characterization
pediatric medicine
compounded preparation
non-ionic emulsifiers
intercellular lipids
confocal Raman spectroscopy (CRS)
polyethylene glycol alkyl ethers
polyethylene glycol sorbitan fatty acid esters
Persona (resp. second.): LunterDominique
DanielsRolf
Sommario/riassunto: Even in ancient times, semi-solid preparations for cutaneous application, popularly known as ointments, played an important role in human society. An advanced scientific investigation of “ointments” as dosage forms was initiated in the 1950s. It was only from then on that the intensive physico-chemical characterization of ointments as well as the inclusion of dermatological aspects led to a comprehensive understanding of the various interactions between the vehicle, the active ingredient and the skin. From then on, many researchers were involved in optimizing semi-solid formulations with respect to continuously changing therapeutic and patient needs. Aspects that have been dealt with were the optimization of dermato-biopharmaceutical properties and many different issues related to patient compliance, such as skin tolerance, applicability, and cosmetic appeal. Moreover, processing technology has been improved and analytical techniques were developed and refined in order to enable the improved characterization of the formulation itself as well as its interaction with the skin. This Special Issue serves to highlight and capture the contemporary progress and current research on semi-solid formulations as dermal drug delivery systems. We invite articles on all aspects of semi-solid formulations, highlighting the research currently undertaken to improve and better understand these complex drug delivery systems with respect to their formulation, processing and characterization issues.
Titolo autorizzato: Semisolid Dosage  Visualizza cluster
Formato: Materiale a stampa
Livello bibliografico Monografia
Lingua di pubblicazione: Inglese
Record Nr.: 9910557436403321
Lo trovi qui: Univ. Federico II
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