Development of a fast and precise method for simultaneous quantification of the PLGA monomers lactic and glycolic acid by HPLC
- Author:
Pourasghar MARCEL
1
;
Koenneke ALJOSCHA
;
Meiers PETER
;
Schneider MARC
Author Information
1. Department of Pharmacy
- Keywords:
Poly(lactide-co-glycolide acid) (PLGA);
Alkaline hydrolysis;
Quantification;
Drug delivery system;
RP-HPLC
- From:
Journal of Pharmaceutical Analysis
2019;9(2):100-107
- CountryChina
- Language:Chinese
-
Abstract:
Poly(lactide-co-glycolide acid) (PLGA) is an extraordinary well-described polymer and has excellent pharmaceutical properties like high biocompatibility and good biodegradability. Hence, it is one of the most used materials for drug delivery and biomedical systems, also being present in several US Food and Drug Administration-approved carrier systems and therapeutic devices. For both applications, the quantification of the polymer is inalienable. During the development of a production process, parameters like yield or loading efficacy are essential to be determined. Although PLGA is a well-defined biomaterial, it still lacks a sensitive and convenient quantification approach for PLGA-based systems. Thus, we present a novel method for the fast and precise quantification of PLGA by RP-HPLC. The polymer is hydrolyzed into its monomers, glycolic acid and lactic acid. Afterwards, the monomers are derivatized with the absorption-enhancing molecule 2,4′-dibromoacetophenone. Furthermore, the wavelength of the deri-vatized monomers is shifted to higher wavelengths, where the used solvents show a lower absorption, increasing the sensitivity and detectability. The developed method has a detection limit of 0.1 μg/mL, enabling the quantification of low amounts of PLGA. By quantifying both monomers separately, in-formation about the PLGA monomer ratio can be also directly obtained, being relevant for degradation behavior. Compared to existing approaches, like gravimetric or nuclear magnetic resonance measure-ments, which are tedious or expensive, the developed method is fast, ideal for routine screening, and it is selective since no stabilizer or excipient is interfering. Due to the high sensitivity and rapidity of the method, it is suitable for both laboratory and industrial uses.
