Release of Hydrophilic Drug from Biodegradable Polymer Blends

被引:7
作者
Tan, L. P. [1 ]
Hidayat, A. [1 ]
Lao, L. L. [1 ]
Quah, L. F. [1 ]
机构
[1] Nanyang Technol Univ, Sch Mat Sci & Engn, Singapore 639798, Singapore
关键词
Drug; lidocaine-HCl release; polymer blending; biodegradable; PHASE-SEPARATION; DELIVERY-SYSTEM; MICROSPHERES; STENTS; DEGRADATION; MATRICES; BEHAVIOR; PROTEIN; ACID);
D O I
10.1163/092050609X12457418874260
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
This paper reports on the release behavior of the drug lidocaine-HCl from a immiscible polymeric blend. Biodegradable polymer blends of poly(L-lactic acid)/poly(lactic-co-glycolic acid) (PLLA/PLGA) were loaded with lidocaine-HCl, and the release of lidocaine-HCl from these blends was monitored. It was found that the release profiles were significantly affected by the affinity and subsequent partitioning of the drug into one of the two phases in the blends. It was hypothesized that the hydrophilic lidocaine-HCl seems to have a tendency to reside in the PLGA component of the PLLA/PLGA blend. This resulted in a release very much controlled by the degradation of PLGA, even when PLLA is the major phase of the blend. A mathematical model was further employed to quantify the partitioning, as well as model the lidocaine-HCl release profiles of different blend compositions. (C) Koninklijke Brill NV, Leiden, 2009
引用
收藏
页码:1381 / 1392
页数:12
相关论文
共 18 条
[1]   Microspheres from poly(D,L-lactide)/poly(1,5-dioxepan-2-one) miscible blends for controlled drug delivery [J].
Edlund, U ;
Albertsson, AC .
JOURNAL OF BIOACTIVE AND COMPATIBLE POLYMERS, 2000, 15 (03) :214-229
[2]  
Edlund U, 1999, J APPL POLYM SCI, V72, P227, DOI 10.1002/(SICI)1097-4628(19990411)72:2<227::AID-APP8>3.3.CO
[3]  
2-Q
[4]   Release of tetracycline hydrochloride from electrospun poly(ethylene-co-vinylacetate), poly(lactic acid), and a blend [J].
Kenawy, ER ;
Bowlin, GL ;
Mansfield, K ;
Layman, J ;
Simpson, DG ;
Sanders, EH ;
Wnek, GE .
JOURNAL OF CONTROLLED RELEASE, 2002, 81 (1-2) :57-64
[5]   Modeling of drug release from biodegradable polymer blends [J].
Lao, Luciana Lisa ;
Venkatraman, Subbu S. ;
Peppas, Nicholas A. .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2008, 70 (03) :796-803
[6]   Self-expandable chitosan stent: design and preparation [J].
Lauto, A ;
Ohebshalom, M ;
Esposito, M ;
Mingin, J ;
Li, PS ;
Felsen, D ;
Goldstein, M ;
Poppas, DP .
BIOMATERIALS, 2001, 22 (13) :1869-1874
[7]   Blends of enteric and GIT-insoluble polymers used for film coating: physicochemical characterization and drug release patterns [J].
Lecomte, F ;
Siepmann, J ;
Walther, M ;
MacRae, RJ ;
Bodmeier, R .
JOURNAL OF CONTROLLED RELEASE, 2003, 89 (03) :457-471
[8]  
LEEK R, 1997, J CONTROL RELEASE, V48, P259
[9]   Adjusting drug diffusivity using miscible polymer blends [J].
Lyu, SP ;
Sparer, R ;
Hobot, C ;
Dang, K .
JOURNAL OF CONTROLLED RELEASE, 2005, 102 (03) :679-687
[10]   Chitin/PLGA blend microspheres as a biodegradable drug delivery system: a new delivery system for protein [J].
Mi, FL ;
Shyu, SS ;
Lin, YM ;
Wu, YB ;
Peng, CK ;
Tsai, YH .
BIOMATERIALS, 2003, 24 (27) :5023-5036