Phase behavior of pharmaceutically relevant polymer/solvent mixtures.
Amorphous solid dispersion
HPMCAS
Liquid-liquid phase separation
Miscibility gap
PC-SAFT
PVP
PVPVA64
Solvent selection
Journal
International journal of pharmaceutics
ISSN: 1873-3476
Titre abrégé: Int J Pharm
Pays: Netherlands
ID NLM: 7804127
Informations de publication
Date de publication:
15 Mar 2020
15 Mar 2020
Historique:
received:
07
11
2019
revised:
16
01
2020
accepted:
17
01
2020
pubmed:
29
1
2020
medline:
26
11
2020
entrez:
29
1
2020
Statut:
ppublish
Résumé
In the pharmaceutical industry, polymers are used as excipients for formulating poorly water-soluble active pharmaceutical ingredients (APIs) in so-called "amorphous solid dispersions" (ASDs). ASDs can be produced via solvent-based processes, where API and polymer are both dissolved in a solvent, followed by a solvent evaporation step (e.g. spray drying). Aiming at a homogeneous API/polymer formulation, phase separation of the components (API, polymer, solvent) during solvent evaporation must be avoided. The latter is often determined by the phase behavior of polymer/solvent mixtures used for ASD processing. Therefore, this work investigates the polymer-solvent interactions in these mixtures. Suitable polymer/solvent combinations investigated in this work comprise the pharmaceutically relevant polymers poly(vinylpyrrolidone) (PVP), poly(vinylpyrrolidone-co-vinyl acetate) (PVPVA64), and hydroxyppropyl methylcellulose acetate succinate 126G (HPMCAS) as well as the solvents acetone, dichloromethane (DCM), ethanol, ethyl acetate, methanol, and water. Based on vapor-sorption experiments demixing of solvents and polymers were predicted using the Perturbed-Chain Statistical Associating Fluid Theory (PC-SAFT). These were found to be correct for all investigated solvent/polymer mixtures. Acetone, DCM, ethanol, methanol, and water were found to be completely miscible with PVPVA64. DCM, ethanol, methanol, and water were found to be completely miscible with PVP K90, while none of the investigated solvents was appropriate for avoiding immiscibility with HPMCAS. In addition, the impact of temperature, polymer molecular weight, and solvent-mixture composition on miscibility was successfully predicted using PC-SAFT. Thus, the proposed methodology allows identifying suitable solvents or solvent mixtures relevant for solvent-based preparations of pharmaceutical ASD formulations with low experimental effort.
Identifiants
pubmed: 31988034
pii: S0378-5173(20)30049-1
doi: 10.1016/j.ijpharm.2020.119065
pii:
doi:
Substances chimiques
Excipients
0
Polymers
0
Pyrrolidines
0
Solvents
0
Vinyl Compounds
0
poly(vinylpyrrolidone-co-vinyl-acetate)
0
hydroxypropylmethylcellulose acetate succinate
71138-97-1
Methylcellulose
9004-67-5
Povidone
FZ989GH94E
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
119065Informations de copyright
Copyright © 2020 Elsevier B.V. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.