Topical delivery of niacinamide: Influence of neat solvents.


Journal

International journal of pharmaceutics
ISSN: 1873-3476
Titre abrégé: Int J Pharm
Pays: Netherlands
ID NLM: 7804127

Informations de publication

Date de publication:
15 Apr 2020
Historique:
received: 31 12 2019
revised: 08 02 2020
accepted: 10 02 2020
pubmed: 15 2 2020
medline: 29 12 2020
entrez: 15 2 2020
Statut: ppublish

Résumé

Niacinamide (NIA) has been widely used in cosmetic and personal care formulations for several skin conditions. Permeation of topical NIA has been confirmed in a number of studies under infinite dose conditions. However, there is limited information in the literature regarding permeation of NIA following application of topical formulations in amounts that reflect the real-life use of such products by consumers. The aim of the present work was therefore to investigate skin delivery of NIA from single solvent systems in porcine skin under finite dose conditions. A secondary aim was to probe the processes underlying the previously reported low recovery of NIA following in vitro permeation and mass balance studies. The solubility and stability of NIA in various single solvent systems was examined. The solvents investigated included Transcutol® P (TC), propylene glycol (PG), 1-2 hexanediol (HEX), 1-2 pentanediol (1-2P), 1-5 pentanediol (1-5P), 1-3 butanediol (1-3B), glycerol (GLY) and dimethyl isosorbide (DMI). Skin permeation and deposition of the molecule was investigated in full thickness porcine skin in vitro finite dose Franz-type diffusion experiments followed by mass balance studies. Stability of NIA for 72 h in the solvents was confirmed. The solubility of NIA in the solvents ranged from 82.9 ± 0.8 to 311.9 ± 4.5 mg/mL. TC delivered the highest percentage permeation of NIA at 24 h, 32.6 ± 12.1% of the applied dose. Low total recovery of NIA after mass balance studies was observed for some vehicles, with values ranging from 55.2 ± 12.8% to 106.3 ± 2.3%. This reflected the formation of a number of NIA degradation by-products in the receptor phase during the permeation studies. Identification of other vehicles for synergistic enhancement of NIA skin delivery will be the subject of future work.

Identifiants

pubmed: 32057889
pii: S0378-5173(20)30121-6
doi: 10.1016/j.ijpharm.2020.119137
pii:
doi:

Substances chimiques

Cosmetics 0
Solvents 0
Vitamin B Complex 12001-76-2
Niacinamide 25X51I8RD4

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

119137

Informations de copyright

Copyright © 2020 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Fotis Iliopoulos (F)

UCL School of Pharmacy, 29-39 Brunswick Square, London WC1N 1AX, UK.

Bruno C Sil (BC)

London Metropolitan University, 166-220 Holloway Road, London N7 8DB, UK.

A S M Monjur Al Hossain (ASM)

UCL School of Pharmacy, 29-39 Brunswick Square, London WC1N 1AX, UK.

David J Moore (DJ)

GlaxoSmithKline Consumer Healthcare, St George's Avenue, Weybridge, Surrey KT13 0DE, UK.

Robert A Lucas (RA)

GlaxoSmithKline Consumer Healthcare, St George's Avenue, Weybridge, Surrey KT13 0DE, UK.

Majella E Lane (ME)

UCL School of Pharmacy, 29-39 Brunswick Square, London WC1N 1AX, UK. Electronic address: m.lane@ucl.ac.uk.

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Classifications MeSH