Formulation and Evaluation of Fenbendazole Extended-Release Extrudes Processed by Hot-Melt Extrusion.
extended-release
fenbendazole
hot-melt extrusion
Journal
Polymers
ISSN: 2073-4360
Titre abrégé: Polymers (Basel)
Pays: Switzerland
ID NLM: 101545357
Informations de publication
Date de publication:
06 Oct 2022
06 Oct 2022
Historique:
received:
09
09
2022
revised:
03
10
2022
accepted:
04
10
2022
entrez:
14
10
2022
pubmed:
15
10
2022
medline:
15
10
2022
Statut:
epublish
Résumé
This study aimed to demonstrate the feasibility of hot-melt extrusion in the development of extended-release formulations of Fenbendazole (Fen) dispersed in PEO/PCL blend-based matrices. Their thermal, physical, chemical and viscosity properties were assessed by differential scanning calorimetry, thermogravimetric analysis/derivative thermogravimetry, Fourier transform infrared spectroscopy, X-ray diffraction spectroscopy, and melt flow index. Drug dispersion was analyzed by scanning electron microscopy with electron dispersive X-ray spectroscopy, and drug release was evaluated by ultraviolet-visible spectroscopy. A thermal analysis indicated the conversion of the drug to its amorphous state. FTIR analysis endorsed the thermal studies pointing to a decrease in the drug's crystallinity with the establishment of intermolecular interactions. XRD analysis confirmed the amorphous nature of Fen. MFI test revealed that PCL acts as a plasticizer when melt-processed with PEO. SEM images displayed irregular surfaces with voids and pores, while EDX spectra demonstrated a homogeneous drug distribution throughout the polymeric carrier. Dissolution testing revealed that PCL retards the drug release proportionally to the content of such polymer incorporated. These melt-extruded matrices showed that the drug release rate in a PEO/PCL blend can easily be tailored by altering the ratio of PCL to address the issues related to the multiple-dosing regimen of Fen in ruminants.
Identifiants
pubmed: 36236135
pii: polym14194188
doi: 10.3390/polym14194188
pmc: PMC9573241
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : Irish Research Council
ID : GOIPG/2022/1734
Organisme : Athlone Institute of Technology
ID : PA01007
Références
Biomaterials. 1993;14(2):83-90
pubmed: 8435462
ACS Appl Mater Interfaces. 2012 Aug;4(8):4331-7
pubmed: 22839659
Adv Drug Deliv Rev. 1997 Dec 8;28(3):303-322
pubmed: 10837572
Pharmaceutics. 2020 Mar 01;12(3):
pubmed: 32121578
Expert Opin Drug Deliv. 2020 Sep;17(9):1289-1304
pubmed: 32619149
Polymers (Basel). 2017 Jul 19;9(7):
pubmed: 30970963
Drug Metab Rev. 1993;25(3):235-79
pubmed: 8404459
Adv Drug Deliv Rev. 2004 Jun 23;56(10):1415-36
pubmed: 15191790
Molecules. 2019 May 27;24(10):
pubmed: 31137865
Biomaterials. 2002 Nov;23(21):4241-8
pubmed: 12194527
Adv Pharm Bull. 2017 Jun;7(2):329-334
pubmed: 28761836
Pharm Dev Technol. 2004 Aug;9(3):321-8
pubmed: 15458237
Drug Dev Ind Pharm. 2006 Sep;32(8):991-1002
pubmed: 16954112
Drug Dev Ind Pharm. 2014 Jul;40(7):845-51
pubmed: 24001212
J Microencapsul. 2013;30(2):151-60
pubmed: 22852775
Drug Discov Today. 2002 Aug 1;7(15):823-9
pubmed: 12546970
J Pharm Pharmacol. 2014 Feb;66(2):148-66
pubmed: 24325738
Drug Dev Ind Pharm. 2011 Feb;37(2):149-59
pubmed: 20615154
Colloids Surf B Biointerfaces. 2005 Jul 10;43(3-4):238-44
pubmed: 15979289
Mater Sci Eng C Mater Biol Appl. 2019 Jan 1;94:694-702
pubmed: 30423756
Int J Pharm. 2008 Mar 3;351(1-2):201-8
pubmed: 18036753
Int J Pharm. 2020 Feb 25;576:118989
pubmed: 31931076
Vet Q. 1993 Dec;15(4):157-9
pubmed: 8122352
AAPS PharmSciTech. 2019 Jan 28;20(3):92
pubmed: 30690659
Vet Res Commun. 1993;17(2):137-42
pubmed: 8212523