Chitosan/Pomegranate Seed Oil Emulgel Composition as a New Strategy for Dermal Delivery of Hydrocortisone.

anti-inflammatory activity chitosan emulgel hydrocortisone multifunctional drug carrier penetration enhancer pomegranate seed oil

Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
28 Mar 2024
Historique:
received: 28 02 2024
revised: 19 03 2024
accepted: 26 03 2024
medline: 13 4 2024
pubmed: 13 4 2024
entrez: 13 4 2024
Statut: epublish

Résumé

Multifunctional delivery systems capable of modulating drug release and exerting adjunctive pharmacological activity have attracted particular attention. Chitosan (CS) and pomegranate seed oil (PO) appear to be attractive bioactive components framing the strategy of complex therapy and multifunctional drug carriers. This research is aimed at evaluating the potential of CS in combination with PO in studies on topical emulgels containing hydrocortisone as a model anti-inflammatory agent. Its particular goal was to distinguish alterations in anti-inflammatory action followed with drug dissolution or penetrative behavior between the designed formulations that differ in CS/PO weight ratio. All formulations favored hydrocortisone release with up to a two-fold increase in the drug dissolution rate within first 5 h as compared to conventional topical preparations. The clear effect of CS/PO on the emulgel biological performance was observed, and CS was found to be prerequisite for the modulation of hydrocortisone absorption and accumulation. In turn, a greater amount of PO played the predominant role in the inhibition of hyaluronidase activity and enhanced the anti-inflammatory effect of preparation E-3. Emulgels showed a negligible reduction in mouse fibroblasts' L929 cell viability, confirming their non-irritancy with skin cells. Overall, the designed formulation with a CS/PO ratio of 6:4 appeared to be the most promising topical carrier for the effective treatment of inflammatory skin diseases among the tested subjects.

Identifiants

pubmed: 38612575
pii: ijms25073765
doi: 10.3390/ijms25073765
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Medical University of Bialystok
ID : B.SUB.24.351/01.S

Auteurs

Zofia Helena Bagińska (ZH)

Student Scientific Group, Department of Pharmaceutical Technology, Medical University of Bialystok, Mickiewicza 2c, 15-222 Białystok, Poland.

Magdalena Paczkowska-Walendowska (M)

Department of Pharmacognosy and Biomaterials, Poznan University of Medical Sciences, Rokietnicka 3 Str., 60-806 Poznań, Poland.

Anna Basa (A)

Faculty of Chemistry, University of Bialystok, Ciołkowskiego 1K, 15-245 Białystok, Poland.

Michał Rachalewski (M)

Dr Irena Eris, Centre for Science and Research, Armii Krajowej 12, 05-500 Piaseczno, Poland.

Karolina Lendzion (K)

Dr Irena Eris, Centre for Science and Research, Armii Krajowej 12, 05-500 Piaseczno, Poland.

Judyta Cielecka-Piontek (J)

Department of Pharmacognosy and Biomaterials, Poznan University of Medical Sciences, Rokietnicka 3 Str., 60-806 Poznań, Poland.

Emilia Szymańska (E)

Department of Pharmaceutical Technology, Medical University of Bialystok, Mickiewicza 2c, 15-222 Białystok, Poland.

Classifications MeSH