Bile acid-based advanced drug delivery systems, bilosomes and micelles as novel carriers for therapeutics.


Journal

Cell biochemistry and function
ISSN: 1099-0844
Titre abrégé: Cell Biochem Funct
Pays: England
ID NLM: 8305874

Informations de publication

Date de publication:
Aug 2022
Historique:
revised: 07 06 2022
received: 31 12 2021
accepted: 11 06 2022
pubmed: 14 7 2022
medline: 23 8 2022
entrez: 13 7 2022
Statut: ppublish

Résumé

Diabetes mellitus affects almost half a billion patients worldwide and results from either destruction of β-cells responsible for insulin secretion or increased tissue resistance to insulin stimulation and the reduction of glycemic control. Novel drug delivery systems can improve treatment efficacy in diabetic patients. The low aqueous solubility of most oral antidiabetic drugs decreases drug bioavailability; therefore, there is a demand for the use of novel methods to overcome this issue. The application of bile acids mixed micelles and bilosomes can provide an enhancement in drug efficacy. Bile acids are amphiphilic steroidal molecules that contain a saturated tetracyclic hydrocarbon cyclopentanoperhydrophenanthrene ring, and consist of three 6-membered rings and a 5-membered ring, a short aliphatic side chain, and a tough steroid nucleus. This review offers a comprehensive and informative data focusing on the great potential of bile acid, their salts, and their derivatives for the development of new antidiabetic drug delivery system.

Identifiants

pubmed: 35830577
doi: 10.1002/cbf.3732
doi:

Substances chimiques

Bile Acids and Salts 0
Drug Carriers 0
Micelles 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

623-635

Informations de copyright

© 2022 John Wiley & Sons Ltd.

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Auteurs

Mohadeseh Nemati (M)

Department of Biochemistry, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran.

Anahita Fathi-Azarbayjani (A)

Experimental and Applied Pharmaceutical Research Center, Urmia University of Medical Sciences, Urmia, Iran.

Hani Al-Salami (H)

Biotechnology and Drug Development Research Laboratory, Curtin Medical School, Curtin Health Innovation Research Institute, Curtin University, Perth, WA, Australia.

Elmira Roshani Asl (E)

Department of Biochemistry, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran.

Yousef Rasmi (Y)

Department of Biochemistry, School of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
Cellular and Molecular Research Center, Cellular and Molecular Medicine Institute, Urmia University of Medical Sciences, Urmia, Iran.

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