Atorvastatin Entrapped Noisome (Atrosome): Green Preparation Approach for Wound Healing.


Journal

AAPS PharmSciTech
ISSN: 1530-9932
Titre abrégé: AAPS PharmSciTech
Pays: United States
ID NLM: 100960111

Informations de publication

Date de publication:
09 Mar 2022
Historique:
received: 20 12 2021
accepted: 04 02 2022
entrez: 10 3 2022
pubmed: 11 3 2022
medline: 12 3 2022
Statut: epublish

Résumé

The present study aimed to formulate atorvastatin niosome (Atrosome) through an ultrasonic technique and to determine its contribution to the extent of wound healing in an animal model. The optimized Atrosome formulation (Atrosome-2) was stable at 4 °C for 3 months. Differential scanning calorimetry (DSC), ATR-Fourier transform infrared spectroscopy (ATR-FTIR), and powder X-ray diffraction (PXRD) analysis revealed that atorvastatin (ATR) was well encapsulated within the niosomes either in a stabilized amorphous form or a molecularly dispersed state. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), and atomic force microscope (AFM) confirmed the spherical nature of the Atrosomes. The optimized formulation showed polydispersity index, particle size, drug encapsulation efficiency (EE%), and zeta potential of 0.457 ± 0.05, 196.33 ± 6.45 nm, 86.15 ± 0.58 %, and - 20.73 ± 0.98 mV, respectively. ATR release from the Atrosome gel followed the first-order kinetic model and showed no cytotoxicity in the in vitro cytotoxicity test. Cell viability (human foreskin fibroblast cell line) was nearly 99%. An excision wound model was also applied in male Wistar rats to examine the in vivo efficacy of the optimized formulation, followed by investigating malondialdehyde (MDA, an end-product of lipid peroxidation), superoxide dismutase (SOD, an endogenous antioxidant), hydroxyproline levels, and glutathione peroxidase (GPx) in skin tissue samples. MDA significantly decreased in the Atrosome gel group after 21 days, while GPx, SOD, and hydroxyproline levels demonstrated an increase. According to histological results, rats receiving Atrosomes were treated effectively faster when compared to the other formulation used.

Identifiants

pubmed: 35266075
doi: 10.1208/s12249-022-02231-x
pii: 10.1208/s12249-022-02231-x
doi:

Substances chimiques

Liposomes 0
Atorvastatin A0JWA85V8F

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

81

Informations de copyright

© 2022. The Author(s).

Références

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Auteurs

Shidrokh Abootorabi (S)

Department of Pharmaceutics, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran.

Jafar Akbari (J)

Department of Pharmaceutics, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran. jakbari@mazums.ac.ir.

Majid Saeedi (M)

Department of Pharmaceutics, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran.
Pharmaceutical Sciences Research Center, Haemoglobinopathy Institute, Mazandaran University of Medical Sciences, Sari, Iran.

Mohammad Seyedabadi (M)

Department of Toxicology and Pharmacology, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran.
Pharmaceutical Sciences Research Center7, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran.

Mohammad Ranaee (M)

Clinical Research Development Unite of Rouhani Hospital, Babol University of Medical Sciences, Babol, Iran.
Cancer Research Center, Health Research Institute, Babol University of Medical Sciences, Babol, Iran.

Kofi Asare-Addo (K)

Department of Pharmacy, University of Huddersfield, Huddersfield, HD1 3DH, UK.

Ali Nokhodchi (A)

Pharmaceutics Research Laboratory, School of Life Sciences, University of Sussex, Brighton, BN1 9QJ, UK. a.nokhodchi@sussex.ac.uk.

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