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生长激素经肝素稳定化处理。

Stabilization of somatropin by heparin.

作者信息

Zamiri Camellia, Groves Michael J

机构信息

Department of Biopharmaceutical Sciences, College of Pharmacy, University of Illinois at Chicago, Chicago, IL 60612, USA.

出版信息

J Pharm Pharmacol. 2005 May;57(5):555-64. doi: 10.1211/0022357055975.

Abstract

Somatropin, human growth hormone (hGH), is an unstable protein, posing challenging problems for its formulation and long-term stability. Since hGH formed insoluble adducts with heparin our aim was to evaluate heparin as a stabilizing agent for the drug. These adducts were characterized by particle diameter, tertiary structure variations and release studies. Studies were also carried out to determine the stability of hGH in the presence and absence of heparin by an interfacial denaturation method and real-time stability studies by measuring hGH activity and particle diameter. Moreover, biological activity of hGH and hGH/UH (unfractionated heparin) adducts was identified by daily subcutaneous injections to hypophysectomized rats. There was a decrease in mean hydrodynamic particle diameter of hGH/UH adducts with increased pH (54.4 to 12.2 nm from pH 3 to pH 7) indicating that the adducts were either dissociating or dissolving at high pH. Furthermore, second-derivative spectroscopy indicated that complexation of hGH with heparin did not cause a major disruption in the tertiary structure of hGH but decreased the hydrophilic environment around the tyrosine residues. Release of hGH from hGH/UH adducts was pH and ionic strength dependent with the highest release at pH 8 (93%) and lowest release at pH 3 (0%) over the first hour. Interfacial denaturation methods indicated that vortex agitation over 120 s resulted in no change in the optical density of hGH/UH adducts compared with a substantial increase for hGH alone at pH 6.8. Real-time stability studies over 93 days demonstrated that hGH/UH adducts at both pH 3 and 7 with an excess of heparin produced the highest percent of active hGH remaining in the solution at 4 degrees C and 37 degrees C. The higher stability of hGH/UH adducts with excess heparin compared with the stoichiometric ratio was also confirmed by particle size measurements during storage. The biological activity of these adducts was comparable with hGH alone by weight-gain studies in hypophysectomized rats. The findings suggest the value of using hGH/heparin adducts to stabilize the protein.

摘要

生长激素,即人生长激素(hGH),是一种不稳定的蛋白质,这给其制剂和长期稳定性带来了具有挑战性的问题。由于hGH会与肝素形成不溶性加合物,我们的目的是评估肝素作为该药物的稳定剂。这些加合物通过粒径、三级结构变化和释放研究进行表征。还通过界面变性方法以及通过测量hGH活性和粒径的实时稳定性研究,来确定hGH在有肝素和无肝素存在时的稳定性。此外,通过对垂体切除大鼠每日皮下注射,鉴定了hGH和hGH/未分级肝素(UH)加合物的生物活性。随着pH值升高,hGH/UH加合物的平均流体动力学粒径减小(从pH 3时的54.4纳米降至pH 7时的12.2纳米),这表明加合物在高pH值下要么解离要么溶解。此外,二阶导数光谱表明,hGH与肝素的络合不会导致hGH三级结构的重大破坏,但会减少酪氨酸残基周围的亲水环境。hGH从hGH/UH加合物中的释放在第一小时内取决于pH值和离子强度,在pH 8时释放最高(93%),在pH 3时释放最低(0%)。界面变性方法表明,与在pH 6.8时单独的hGH光密度大幅增加相比,超过120秒的涡旋搅拌导致hGH/UH加合物的光密度没有变化。超过93天的实时稳定性研究表明,在pH 3和7时,含有过量肝素的hGH/UH加合物在4℃和37℃下在溶液中剩余的活性hGH百分比最高。在储存期间通过粒径测量也证实了与化学计量比相比,含有过量肝素的hGH/UH加合物具有更高的稳定性。通过对垂体切除大鼠的体重增加研究,这些加合物的生物活性与单独的hGH相当。这些发现表明使用hGH/肝素加合物来稳定蛋白质的价值。

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