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生长激素从热敏性三嵌段共聚物系统中的控释:体外和体内评价。

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

作者信息

Chen Sibao, Singh Jagdish

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy, Nursing, and Allied Sciences, North Dakota State University, Fargo, ND 58105, USA.

出版信息

Int J Pharm. 2008 Mar 20;352(1-2):58-65. doi: 10.1016/j.ijpharm.2007.10.016. Epub 2007 Oct 22.

DOI:10.1016/j.ijpharm.2007.10.016
PMID:18036752
Abstract

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 approximately 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.

摘要

本研究的目的是使用三嵌段共聚物PLGA-PEG-PLGA(分子量1400-1000-1400)设计用于生长激素的可注射控释聚合物制剂。通过将猪生长激素(pGH)添加到三嵌段共聚物的30%(w/v)水溶液中来制备pGH制剂。使用标准的微量BCA法测定释放样品中的pGH浓度。体外释放研究表明,含有低剂量(0.12%,w/v)和高剂量(0.42%,w/v)pGH的两种制剂均未出现pGH的初始突释。对兔体内pGH的吸收研究表明,单次皮下注射给药后,从给药系统中可在近4周内检测到外源性pGH的恒定血清水平(高剂量为3-7 ng/mL,低剂量为2-4 ng/mL)。基于热敏聚合物的系统提高了pGH的绝对生物利用度,约为皮下水溶液的5-15倍。分别使用MTT法和光学显微镜研究热敏聚合物给药系统的体外和体内生物相容性。体外和体内结果均支持这些聚合物给药系统的生物相容性。因此,本研究中使用的三嵌段共聚物能够在体外和体内较长时间地控制掺入的pGH的释放,并且该给药系统具有生物相容性。

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