Development and evaluation of a novel biodegradable implants with excellent inflammatory response suppression effect by hot-melt extrusion.

Biocompatibility Dexamethasone Hot-melt extrusion Implantable drug delivery system Inflammation

Journal

European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences
ISSN: 1879-0720
Titre abrégé: Eur J Pharm Sci
Pays: Netherlands
ID NLM: 9317982

Informations de publication

Date de publication:
01 Nov 2021
Historique:
received: 18 11 2020
revised: 03 08 2021
accepted: 20 08 2021
pubmed: 25 8 2021
medline: 16 9 2021
entrez: 24 8 2021
Statut: ppublish

Résumé

Dexamethasone (Dex) is a widely used drug for the treatment of inflammatory and autoimmune conditions, however, long-term systemic use of Dex is associated with serious adverse effects. The objective of the present study was to develop an implantable device to avoid side effects and realize a controlled release of Dex at the implant site. Hydrophobic Dex was incorporated into biodegradable polyesters derived from PCL and Pluronic® L64 (PCL-Pluronic L64-PCL, PCLC) by hot-melt extrusion (HME) method to prepare Dex/PCLC implantable devices. Drug loading and encapsulation efficiency, a series of physicochemical properties, and in vivo features of the implants were studied. The maximum value of the drug loading and encapsulation efficiency for the Dex/PCLC implants were up to 47% and 94%, respectively. Incorporation of Dex resulted in accelerated crystallization of PCLC, decreased the wettability, increased contact angles and viscosity, and accelerated Dex release rate and degradation rate from the implants in vivo. Moreover, Dex/PCLC implants showed excellent biocompatibility. Furthermore, the inflammatory response to the Dex/PCLC implants was less severe than that to the positive control group. All these results suggested that Dex/PCLC implants might be a safe and controlled local drug delivery system with excellent inflammatory response suppression effect.

Identifiants

pubmed: 34428483
pii: S0928-0987(21)00284-0
doi: 10.1016/j.ejps.2021.105981
pii:
doi:

Substances chimiques

Drug Implants 0
Polyesters 0
Dexamethasone 7S5I7G3JQL

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

105981

Informations de copyright

Copyright © 2021 Elsevier B.V. All rights reserved.

Auteurs

Rangrang Fan (R)

State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, and Collaborative Innovation Center for Biotherapy, No. 17, Renminnan Road, Chengdu, 610041, PR China; Department of Neurosurgery, West China Hospital, Sichuan University, Chengdu 610041, PR China.

Di Chuan (D)

State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, and Collaborative Innovation Center for Biotherapy, No. 17, Renminnan Road, Chengdu, 610041, PR China.

Huan Hou (H)

State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, and Collaborative Innovation Center for Biotherapy, No. 17, Renminnan Road, Chengdu, 610041, PR China.

Haifeng Chen (H)

Department of Neurosurgery, West China Hospital, Sichuan University, Chengdu 610041, PR China.

Jianguo Xu (J)

Department of Neurosurgery, West China Hospital, Sichuan University, Chengdu 610041, PR China.

Gang Guo (G)

State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, and Collaborative Innovation Center for Biotherapy, No. 17, Renminnan Road, Chengdu, 610041, PR China. Electronic address: guogang@scu.edu.cn.

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Classifications MeSH