Determination of water-soluble acid distribution in poly(lactide-co-glycolide)

被引:50
作者
Ding, AG [1 ]
Schwendeman, SP [1 ]
机构
[1] Univ Michigan, Coll Pharm, Dept Pharmaceut Sci, Ann Arbor, MI 48109 USA
关键词
poly(lactic/glycolic acid) (PLGA); polymer chemical degradation; distribution;
D O I
10.1002/jps.10524
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Determination of the kinetics of water-soluble degradation products inside poly(lactide-co-glycolide) (PLGA) delivery systems during polymer degradation is important to evaluate the polymer microclimate conditions, particularly microclimate pH changes for optimization of encapsulated drug stability. A pre-derivatization high-performance liquid chromatography (HPLC) method was developed for separation and quantification of water-soluble acid impurities and degradation products in PLGA. Thin PLGA films (similar to200 mum) were incubated in PBS/0.02% Tween 80, pH 7.4, for 6 weeks. Water-soluble monomers and oligomers were obtained from polymer films after repeated CHCl3/H2O extraction and then derivatized into bromophenacyl esters. With the common chromophore, the esters were separated and quantified by HPLC with increased ultraviolet (UV) sensitivity at 254 nm. The total amount of water-soluble acids in the extract was validated by potentiometric titration with tetrabutyl ammonium hydroxide. During the first 3 weeks of incubation of PLGA 50:50 (inherent viscosity = 0.63 dL/g), the principal water-soluble acids in the polymer were glycolic, lactic, and lactoyllactic acids, and an unknown oligomer. After 4 weeks of incubation, a large fraction of higher molecular weight oligomers was observed. Pre-derivatization HPLC can be used to accurately measure water-soluble acid distribution, and may be invaluable to examine the degradation behavior of PLGAs, including the underlying mechanism of polymer microclimate pH development (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:322 / 331
页数:10
相关论文
共 35 条
[1]  
Andriano KP, 1999, J BIOMED MATER RES, V48, P602, DOI 10.1002/(SICI)1097-4636(1999)48:5<602::AID-JBM3>3.0.CO
[2]  
2-6
[3]   A theoretical model of erosion and macromolecular drug release from biodegrading microspheres [J].
Batycky, RP ;
Hanes, J ;
Langer, R ;
Edwards, DA .
JOURNAL OF PHARMACEUTICAL SCIENCES, 1997, 86 (12) :1464-1477
[4]   Tetracycline-HCl-loaded poly(DL-lactide-co-glycolide) microspheres prepared by a spray drying technique:: influence of γ-irradiation on radical formation and polymer degradation [J].
Bittner, B ;
Mäder, K ;
Kroll, C ;
Borchert, HH ;
Kissel, T .
JOURNAL OF CONTROLLED RELEASE, 1999, 59 (01) :23-32
[5]  
Carino GP, 1999, DRUGS PHARM SCI, V98, P459
[6]   Protein stability in controlled-release systems [J].
Fu, K ;
Klibanov, AM ;
Langer, R .
NATURE BIOTECHNOLOGY, 2000, 18 (01) :24-25
[7]   In vitro degradation study of polyester microspheres by a new HPLC method for monomer release determination [J].
Giunchedi, P ;
Conti, B ;
Scalia, S ;
Conte, U .
JOURNAL OF CONTROLLED RELEASE, 1998, 56 (1-3) :53-62
[8]   HYDROLYTIC DEGRADATION OF DEVICES BASED ON POLY(DL-LACTIC ACID) SIZE-DEPENDENCE [J].
GRIZZI, I ;
GARREAU, H ;
LI, S ;
VERT, M .
BIOMATERIALS, 1995, 16 (04) :305-311
[10]   Stabilization of a model formalinized protein antigen encapsulated in poly(lactide-co-glycolide)-based microspheres [J].
Jiang, WL ;
Schwendeman, SP .
JOURNAL OF PHARMACEUTICAL SCIENCES, 2001, 90 (10) :1558-1569