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首页> 外文期刊>Journal of biomedical materials research. Part B, Applied biomaterials. >Release of bioactive human growth hormone from a biodegradable material: poly(epsilon-caprolactone).
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Release of bioactive human growth hormone from a biodegradable material: poly(epsilon-caprolactone).

机译:从可生物降解的物质:聚(ε-己内酯)中释放生物活性的人类生长激素。

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摘要

We have characterized the biodegradable material poly(epsilon-caprolactone) (PCL) as a delivery system for recombinant human growth hormone (hGH). Two contrasting methods for the manufacture of the biomaterial were investigated: namely, solvent casting and solvent casting particulate leaching; the latter yielded porous PCL discs. The degree of porosity, which was assessed by scanning electron microscopy, could be controlled by incorporating selected concentrations of particulate sodium chloride during the manufacturing process. Bioactive hGH released from the PCL preparations was quantified with a highly sensitive and precise bioassay which was based upon hGH activation of rat lymphoma Nb2 cells. Eluates obtained from control discs of PCL which had not been loaded with hGH proved to be nontoxic when tested on these cells. The release of bioactive hGH from hormone-loaded nonporous discs of PCL was found to be a direct function of the initial hormone loading dose. Increased porosity of the discs manufactured by solvent casting particulate leaching increased the delivery of hGH from discs which had been immersion loaded. However, hGH release after surface loading was independent of porosity. Hormone concentrations were also assessed by immunoassay so that the ratios of bio- to immunoactivity (B:I ratio) of the hormone release could be determined. We found that the B:I ratio of the hormone after release from unstored discs was identical to that of the hormone prior to its incorporation into the PCL, demonstrating that the mild incorporation procedures utilized had not adversely affected the structural integrity of the hormone. However, if the hormone-loaded discs were stored at 37 degrees C prior to elution, the B:I ratios of the hGH released decreased indicating that this compromised the bioactive site.
机译:我们已经表征了可生物降解的材料聚(ε-己内酯)(PCL)作为重组人生长激素(hGH)的传递系统。研究了两种用于制造生物材料的对比方法:溶剂浇铸和溶剂浇铸微粒浸出;后者产生了多孔PCL圆盘。通过扫描电子显微镜评估的孔隙度可以通过在制造过程中掺入选定浓度的氯化钠颗粒来控制。从PCL制剂中释放的生物活性hGH通过高度灵敏,精确的生物测定进行定量,该测定基于大鼠淋巴瘤Nb2细胞的hGH活化。当在这些细胞上测试时,从PCL对照盘上未装载hGH的洗脱液证明是无毒的。已发现从荷尔蒙负载的PCL无孔椎间盘释放生物活性hGH是初始荷尔蒙负载剂量的直接函数。通过溶剂浇铸微粒浸出法制造的圆盘的孔隙率增加,从而增加了hGH从浸入式圆盘的输送。但是,表面加载后hGH的释放与孔隙率无关。还通过免疫测定法评估激素浓度,从而可以确定激素释放的生物活性与免疫活性之比(B:I比)。我们发现,从未保存的椎间盘释放后,荷尔蒙的B:I比率与掺入PCL之前的荷尔蒙的B:I比率相同,这表明所采用的温和掺入程序并未对荷尔蒙的结构完整性产生不利影响。但是,如果在洗脱之前将荷尔蒙载剂的碟片存储在37摄氏度下,则释放的hGH的B:I比值会降低,表明这损害了生物活性位点。

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