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Functionality-type and chemical-composition separation of poly(lactide-co-glycolide) using gradient elution normal-phase liquid chromatography with basic and acidic additives.
Serizawa, Masashi; Reekers, Jeroen; van Delft, Pieter; van Bruijnsvoort, Michel; Schoenmakers, Peter J; Gargano, Andrea F G.
Affiliation
  • Serizawa M; Van't Hoff Institute for Molecular Sciences, University of Amsterdam, Science Park 904, 1098 XH Amsterdam, the Netherlands; Centre for Analytical Sciences Amsterdam, Science Park 904, 1098 XH Amsterdam, the Netherlands; Material Characterization laboratory, Mitsubishi Chemical Corporation, 1000 Kamo
  • Reekers J; Van't Hoff Institute for Molecular Sciences, University of Amsterdam, Science Park 904, 1098 XH Amsterdam, the Netherlands; Centre for Analytical Sciences Amsterdam, Science Park 904, 1098 XH Amsterdam, the Netherlands.
  • van Delft P; Corbion, 4200 AA Gorinchem, the Netherlands.
  • van Bruijnsvoort M; Corbion, 4200 AA Gorinchem, the Netherlands.
  • Schoenmakers PJ; Van't Hoff Institute for Molecular Sciences, University of Amsterdam, Science Park 904, 1098 XH Amsterdam, the Netherlands; Centre for Analytical Sciences Amsterdam, Science Park 904, 1098 XH Amsterdam, the Netherlands.
  • Gargano AFG; Van't Hoff Institute for Molecular Sciences, University of Amsterdam, Science Park 904, 1098 XH Amsterdam, the Netherlands; Centre for Analytical Sciences Amsterdam, Science Park 904, 1098 XH Amsterdam, the Netherlands. Electronic address: a.gargano@uva.nl.
J Chromatogr A ; 1730: 465137, 2024 Aug 16.
Article de En | MEDLINE | ID: mdl-38996514
ABSTRACT
End groups of poly(Lactide-co-glycolide) (PLGA) play an important role in determining the properties of polymers for use in drug delivery systems. For instance, it has been reported that the encapsulation efficiency in PLGA microspheres varies significantly between ester-terminated and acid-terminated PLGA. More importantly, the in-vivo degradation time of such polymer excipients is influenced by the functional end-group of the copolymer used. The end group distribution in PLGA polymers has been studied using electrospray and matrix-assisted laser-desorption/ionization - high-resolution mass spectrometry. In both cases, the application of these methods is typically limited to PLGA having a molecular weight of up to 4 kDa. 13Carbon-nuclear-magnetic-resonance has also been reported as a method to differentiate and quantify PLGA end groups with a molecular weight up to 136 kDa. However, reported NMR methods take over 12 h per sample, limiting throughput.Cryoprobe NMR can reduce the time required for the process, however such NMR equipment is costly, which makes it unsuitable for the quality control of PLGA. Here, we present a normal-phase liquid chromatography method capable of resolving functionality type distribution (FTD) and, partially, chemical composition distribution (CCD) in commercial PLGA polymers obtained from ring opening polymerization. This method can separate PLGA polymers with a molecular weight of up to 183.0 kDa while also enabling the simultaneous separation of the difference of Lactic acid (LA)/Glycolic acid (GA) ratios. To achieve this, a cross-linked diol column was used with a ternary gradient from HEX to 0.1 % v/v TEA in EA to 0.1 % v/v FA in THF to allow first for the elution of mono-ester terminated PLGA, followed by the di-acid terminated. In addition, a separation of ester-terminated PLGA in the difference of the LA/GA ratio was achieved. This method is expected to aid in understanding the correlation between PLGA's FTD, CCD, and physical properties, facilitating product development and quality control.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Acide polyglycolique / Copolymère d'acide poly(lactique-co-glycolique) Langue: En Journal: J Chromatogr A Année: 2024 Type de document: Article

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Acide polyglycolique / Copolymère d'acide poly(lactique-co-glycolique) Langue: En Journal: J Chromatogr A Année: 2024 Type de document: Article