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使用透明质酸钠的人生长激素缓释制剂的表征及体内研究

Characterization and in vivo study of sustained-release formulation of human growth hormone using sodium hyaluronate.

作者信息

Hahn Sei Kwang, Kim Sun Jin, Kim Myung Jin, Kim Duk Hee

机构信息

Biotech Group, LG Life Sciences Co, Yusong-gu, Taejon, 305-380, Korea.

出版信息

Pharm Res. 2004 Aug;21(8):1374-81. doi: 10.1023/b:pham.0000036910.41224.de.

Abstract

PURPOSE

Aiming at once-a-week injection, a novel sustained release formulation of recombinant human growth hormone (SR-hGH) using sodium hyaluronate was developed for the treatment of children who have growth failure due to the lack of adequate secretion of endogenous growth hormone.

METHODS

SR-hGH was produced in the form of solid microparticle using a Niro spray dryer and characterized by Malvern particle size analysis, scanning electron microscopy (SEM), size exclusion chromatography (SEC), reverse phase-high-performance chromatography (RP-HPLC), and sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE). After in vitro release test, pharmacokinetic and pharmacodynamic studies were carried out in beagle dogs. SR-hGH was dispersed in medium-chain triglyceride (MCT) and administered at a dose of 1.0 mg hGH/kg subcutaneously.

RESULTS

SR-hGH microparticles were successfully produced with a mean particle size of 5.6+/-1.0 microm. Physicochemical analysis with SEC, RP-HPLC, and SDS-PAGE showed that hGH extracted from SR-hGH was intact and comparable to that of hGH bulk standard indicating no structural change in hGH during the formulation processes. Monomeric content of hGH recovered from SR-hGH was 97.4% by SEC analysis, and its purity was 96% by RP-HPLC analysis. In vitro release test showed the sustained-release characteristics of SR-hGH up to 48 h with the complete release of hGH loaded. The continuous and monotonous release profile observed in in vitro release test was supported by pharmacokinetic study in beagle dogs. Delayed absorption of hGH was observed with Cmax of 69.5+/-8.0 ng/ml and Tmax between 10 and 12 h. The administration of SR-hGH induced elevation of serum insulin-like growth factor-I (IGF-I) level for 6 days with a maximum value higher than the predose level by ca. 350 ng/ml. After 6 days, IGF-I level returned to the initial baseline level.

CONCLUSIONS

Sustained-release formulation of hGH for once-a-week injection was successfully developed using high-molecular-weight sodium hyaluronate. No adverse effect was observed during and after the in vivo test using beagle dogs.

摘要

目的

为满足每周一次注射的需求,研发了一种使用透明质酸钠的重组人生长激素新型缓释制剂(SR-hGH),用于治疗因内源性生长激素分泌不足而导致生长发育迟缓的儿童。

方法

采用尼鲁喷雾干燥器制备固体微粒形式的SR-hGH,并通过马尔文粒度分析、扫描电子显微镜(SEM)、尺寸排阻色谱(SEC)、反相高效液相色谱(RP-HPLC)和十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)对其进行表征。体外释放试验后,在比格犬身上进行了药代动力学和药效学研究。将SR-hGH分散在中链甘油三酯(MCT)中,以1.0 mg hGH/kg的剂量皮下给药。

结果

成功制备出平均粒径为5.6±1.0微米的SR-hGH微粒。通过SEC、RP-HPLC和SDS-PAGE进行的理化分析表明,从SR-hGH中提取的hGH完整无损,与hGH原料药标准品相当,表明在制剂过程中hGH的结构没有变化。通过SEC分析,从SR-hGH中回收的hGH单体含量为97.4%,通过RP-HPLC分析,其纯度为96%。体外释放试验表明,SR-hGH具有长达48小时的缓释特性,负载的hGH完全释放。比格犬的药代动力学研究支持了体外释放试验中观察到的持续且单调的释放曲线。观察到hGH吸收延迟,Cmax为69.5±8.0 ng/ml,Tmax在10至12小时之间。给予SR-hGH可使血清胰岛素样生长因子-I(IGF-I)水平升高6天,最大值比给药前水平高约350 ng/ml。6天后,IGF-I水平恢复到初始基线水平。

结论

使用高分子量透明质酸钠成功研发出每周一次注射的hGH缓释制剂。在使用比格犬进行的体内试验期间及之后未观察到不良反应。

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