Controlled release of growth hormone from thermosensitive triblock copolymer systems:: In vitro and in vivo evaluation

被引:58
作者
Chen, Sibao [1 ]
Singh, Jagdish [1 ]
机构
[1] N Dakota State Univ, Coll Pharm Nursing & Allied Sci, Dept Pharmaceut Sci, Fargo, ND 58105 USA
关键词
controlled release; protein; thermosensitive polymer; biocompatible; growth hormone; subcutaneous;
D O I
10.1016/j.ijpharm.2007.10.016
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The purpose of this study was to design injectable controlled release polymer formulations for growth hormone using triblock copolymer PLGA-PEG-PLGA (MW 1400-1000-1400). Porcine growth hormone (pGH) formulations were prepared by adding pGH into 30% (w/v) aqueous solution of triblock copolymer. pGH concentrations in the released samples were determined using a standard MicroBCA method. In vitro release studies demonstrated that there were no initial burst of pGH from both formulations containing a low dose (0.12%, w/v) and a high dose (0.42%, w/v) of pGH. In vivo absorption study of pGH in rabbits showed that constant serum levels of exogenous pGH (3-7 ng/mL from high dose and 2-4 ng/mL from low dose) were detected for nearly 4 weeks from delivery systems upon single subcutaneous injection. The absolute bioavailability of pGH enhanced from the thermosensitive polymer-based systems, which was similar to 5-15-fold those of subcutaneous aqueous solution. MTT assay and light microscopy were used to investigate the in vitro and in vivo biocompatibility of thermosensitive polymer delivery systems, respectively. Both in vitro and in vivo results support the biocompatible nature of these polymer delivery systems. Thus, the triblock copolymer used in this study was able to control the release of incorporated pGH in vitro and in vivo for longer duration and the delivery system was biocompatible. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:58 / 65
页数:8
相关论文
共 52 条
[1]   Biodegradation and biocompatibility of PLA and PLGA microspheres [J].
Anderson, JM ;
Shive, MS .
ADVANCED DRUG DELIVERY REVIEWS, 1997, 28 (01) :5-24
[2]   Sterilization, toxicity, biocompatibility and clinical applications of polylactic acid polyglycolic acid copolymers [J].
Athanasiou, KA ;
Niederauer, GG ;
Agrawal, CM .
BIOMATERIALS, 1996, 17 (02) :93-102
[3]   Sustained release of human growth hormone from PLGA solution depots [J].
Brodbeck, KJ ;
Pushpala, S ;
McHugh, AJ .
PHARMACEUTICAL RESEARCH, 1999, 16 (12) :1825-1829
[4]  
CAPAN Y, 2003, AAPS PHARMSCITECH, V4, P1
[5]   POLYETHER POLYESTER BLOCK COPOLYMERS BY NON-CATALYZED POLYMERIZATION OF EPSILON-CAPROLACTONE WITH POLY(ETHYLENE GLYCOL) [J].
CERRAI, P ;
TRICOLI, M ;
ANDRUZZI, F ;
PACI, M ;
PACI, M .
POLYMER, 1989, 30 (02) :338-343
[6]   In vitro release of levonorgestrel from phase sensitive and thermosensitive smart polymer delivery systems [J].
Chen, SB ;
Singh, J .
PHARMACEUTICAL DEVELOPMENT AND TECHNOLOGY, 2005, 10 (02) :319-325
[7]   Controlled delivery of testosterone from smart polymer solution based systems: In vitro evaluation [J].
Chen, SB ;
Singh, J .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2005, 295 (1-2) :183-190
[8]   Triblock copolymers: synthesis, characterization, and delivery of a model protein [J].
Chen, SB ;
Pieper, R ;
Webster, DC ;
Singh, J .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2005, 288 (02) :207-218
[9]   Recombinant human growth hormone poly(lactic-co-glycolic acid) (PLGA) microspheres provide a long lasting effect [J].
Cleland, JL ;
Duenas, E ;
Daugherty, A ;
Marian, M ;
Yang, J ;
Wilson, M ;
Celniker, AC ;
Shahzamani, A ;
Quarmby, V ;
Chu, H ;
Mukku, V ;
Mac, A ;
Roussakis, M ;
Gillette, N ;
Boyd, B ;
Yeung, D ;
Brooks, D ;
Maa, YF ;
Hsu, C ;
Jones, AJS .
JOURNAL OF CONTROLLED RELEASE, 1997, 49 (2-3) :193-205
[10]   The stability of recombinant human growth hormone in poly(lactic-co-glycolic acid) (PLGA) microspheres [J].
Cleland, JL ;
Mac, A ;
Boyd, B ;
Yang, J ;
Duenas, ET ;
Yeung, D ;
Brooks, D ;
Hsu, C ;
Chu, H ;
Mukku, V ;
Jones, AJS .
PHARMACEUTICAL RESEARCH, 1997, 14 (04) :420-425