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Characterization of commercial PLGAs by NMR spectroscopy.
- Source :
-
Drug delivery and translational research [Drug Deliv Transl Res] 2022 Mar; Vol. 12 (3), pp. 720-729. Date of Electronic Publication: 2021 Aug 20. - Publication Year :
- 2022
-
Abstract
- Poly(lactic-co-glycolic acid) (PLGA) is among the most common of biodegradable polymers studied in various biomedical applications such as drug delivery and tissue engineering. To facilitate the understanding of the often overlooked impact of PLGA microstructure on important factors affecting PLGA performance, we measured four key parameters of 17 commonly used commercial PLGA polymers (Expansorb®, Resomer®, Purasorb®, Lactel®, and Wako®) by NMR spectroscopy. <superscript>1</superscript> HNMR and <superscript>13</superscript> CNMR spectra were used to determine lactic to glycolic ratio (L/G ratio), polymer end-capping, glycolic blockiness (Rc), and average glycolic and lactic block lengths (L <subscript>G</subscript> and L <subscript>L</subscript> ). In PLGAs with a labeled L/G ratio of 50/50 and acid end-capping, the actual lactic content slightly decreased as molecular weight increased in both Expansorb® and Resomer®. Whether or not acid- or ester-, termination of these PLGAs was confirmed to be consistent with their brand labels. Moreover, in the ester end-capped 75/25 L/G ratio group, the blockiness value (Rc) of Resomer® RG 756S (Rc: 1.7) was highest in its group; whereas for the 50/50 acid end-capped group, Expansorb® DLG 50-2A (Rc: 1.9) displayed notably higher values than their counterparts. Expansorb® 50-2E (L <subscript>L</subscript> : 2.5, L <subscript>G</subscript> : 2.6) and Resomer® RG 502 (L <subscript>L</subscript> : 2.6, L <subscript>G</subscript> : 2.5) showed the lowest block lengths, suggesting they may undergo a steadier hydrolytic process compared to random, heterogeneously distributed PLGA.<br /> (© 2021. Controlled Release Society.)
Details
- Language :
- English
- ISSN :
- 2190-3948
- Volume :
- 12
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Drug delivery and translational research
- Publication Type :
- Academic Journal
- Accession number :
- 34415565
- Full Text :
- https://doi.org/10.1007/s13346-021-01023-3