Highly Efficient Oral Iguratimod/Polyvinyl Alcohol Nanodrugs Fabricated by High-Gravity Nanoprecipitation Technique for Treatment of Rheumatoid Arthritis.

high-gravity nanoprecipitation technique (HGNPT) iguratimod (IGUR) nanodrugs oral drug delivery rheumatoid arthritis (RA)

Journal

Small (Weinheim an der Bergstrasse, Germany)
ISSN: 1613-6829
Titre abrégé: Small
Pays: Germany
ID NLM: 101235338

Informations de publication

Date de publication:
14 Nov 2023
Historique:
revised: 22 10 2023
received: 17 05 2023
medline: 15 11 2023
pubmed: 15 11 2023
entrez: 15 11 2023
Statut: aheadofprint

Résumé

Rheumatoid arthritis (RA), a systemic autoimmune disease, poses a significant human health threat. Iguratimod (IGUR), a novel disease-modifying antirheumatic drug (DMARD), has attracted great attention for RA treatment. Due to IGUR's hydrophobic nature, there's a pressing need for effective pharmaceutical formulations to enhance bioavailability and therapeutic efficacy. The high-gravity nanoprecipitation technique (HGNPT) emerges as a promising approach for formulating poorly water-soluble drugs. In this study, IGUR nanodrugs (NanoIGUR) are synthesized using HGNPT, with a focus on optimizing various operational parameters. The outcomes revealed that HGNPT enabled the continuous production of NanoIGUR with smaller sizes (ranging from 300 to 1000 nm), more uniform shapes, and reduced crystallinity. In vitro drug release tests demonstrated improved dissolution rates with decreasing particle size and crystallinity. Notably, in vitro and in vivo investigations showcased NanoIGUR's efficacy in inhibiting synovial fibroblast proliferation, migration, and invasion, as well as reducing inflammation in collagen-induced arthritis. This study introduces a promising strategy to enhance and broaden the application of poorly water-soluble drugs.

Identifiants

pubmed: 37964398
doi: 10.1002/smll.202304150
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e2304150

Subventions

Organisme : National Natural Science Foundation of China
ID : 52072023
Organisme : National Natural Science Foundation of China
ID : 21622601
Organisme : National Natural Science Foundation of China
ID : 51972339
Organisme : National Natural Science Foundation of China
ID : 81571573

Informations de copyright

© 2023 Wiley-VCH GmbH.

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Auteurs

Cheng Tao (C)

College of Chemical Engineering, Beijing University of Chemical Technology, Beijing, 100029, P. R. China.

Feifei Li (F)

Beijing Advanced Innovation Center for Soft Matter Science and Engineering, Beijing University of Chemical Technology, Beijing, 100029, P. R. China.

Zhenzhen Ma (Z)

Department of Rheumatology and Immunology, Peking University Third Hospital, Beijing, 100191, P. R. China.

Xiaoming Li (X)

College of Chemical Engineering, Beijing University of Chemical Technology, Beijing, 100029, P. R. China.
Beijing Advanced Innovation Center for Soft Matter Science and Engineering, Beijing University of Chemical Technology, Beijing, 100029, P. R. China.

Yali Zhang (Y)

College of Chemical Engineering, Beijing University of Chemical Technology, Beijing, 100029, P. R. China.

Yuan Le (Y)

College of Chemical Engineering, Beijing University of Chemical Technology, Beijing, 100029, P. R. China.

Jiexin Wang (J)

College of Chemical Engineering, Beijing University of Chemical Technology, Beijing, 100029, P. R. China.

Jinxia Zhao (J)

Department of Rheumatology and Immunology, Peking University Third Hospital, Beijing, 100191, P. R. China.

Chaoyong Liu (C)

Beijing Advanced Innovation Center for Soft Matter Science and Engineering, Beijing University of Chemical Technology, Beijing, 100029, P. R. China.
College of Life Science and Technology, Beijing University of Chemical Technology, Beijing, 100029, P. R. China.

Jianjun Zhang (J)

College of Chemical Engineering, Beijing University of Chemical Technology, Beijing, 100029, P. R. China.

Classifications MeSH