Kim Sun Jin, Hahn Sei Kwang, Kim Myung Jin, Kim Duk Hee, Lee Young Phil
Biotech Group, LG Life Sciences Co., 104-1, Moonji-dong, Yusong-gu, Daejeon, 305-380, South Korea.
J Control Release. 2005 May 18;104(2):323-35. doi: 10.1016/j.jconrel.2005.02.012. Epub 2005 Apr 7.
A novel sustained release formulation of recombinant human growth hormone (SR-rhGH) was developed as a once-a-week injection formulation using sodium hyaluronate. SR-rhGH was produced in the form of solid microparticles by spray drying technology. A single administration of a prototype formulation of SR-rhGH with a ratio of hGH:HA=1:1 to cynomolgus monkeys through a fine 26-gauge needle induced continuous elevation of serum IGF-I level for 6 days demonstrating the bioactivity of hGH released from the prototype formulation. For expanded pre-clinical and clinical developments, a pilot-scale process under aseptic condition was established and used for the preparation of the optimized formulation of SR-rhGH with a ratio of hGH:HA=1:3. When the ratio of hGH to HA changed from 1:1 to 1:3, hGH released more slowly in vitro from SR-rhGH with almost complete release of hGH loaded. According to pharmacokinetic and pharmacodynamic studies in beagle dogs, sustained release of hGH from the optimized formulation of SR-rhGH continued for a more extended period longer than 72 h with a lower C(max) than those of prototype formulations. The single administration resulted in an elevation of serum insulin-like growth factor-I (IGF-I) level for 6 days with a maximum value higher than the baseline level by ca. 350 ng/mL, which supported the possibility of SR-rhGH as a once-a-week injection formulation of hGH. The bioavailability of both formulations was comparable to that of hGH daily injection formulation. Finally, toxicity studies revealed no evidence of adverse effect in both cynomolgus monkeys and beagle dogs.
一种新型的重组人生长激素缓释制剂(SR-rhGH)被开发出来,它是一种使用透明质酸钠的每周一次注射制剂。SR-rhGH通过喷雾干燥技术制成固体微粒形式。通过一根26号细针给食蟹猴单次注射hGH:HA比例为1:1的SR-rhGH原型制剂,可使血清IGF-I水平持续升高6天,证明了从原型制剂中释放的hGH具有生物活性。为了进行扩大的临床前和临床开发,建立了无菌条件下的中试规模工艺,并用于制备hGH:HA比例为1:3的SR-rhGH优化制剂。当hGH与HA的比例从1:1变为1:3时,hGH在体外从SR-rhGH中释放得更慢,且负载的hGH几乎完全释放。根据对比格犬的药代动力学和药效学研究,SR-rhGH优化制剂中hGH的持续释放时间超过72小时,且C(max)低于原型制剂。单次给药可使血清胰岛素样生长因子-I(IGF-I)水平升高6天,最大值比基线水平高约350 ng/mL,这支持了SR-rhGH作为hGH每周一次注射制剂的可能性。两种制剂的生物利用度与hGH每日注射制剂相当。最后,毒性研究表明在食蟹猴和比格犬中均未发现不良反应的证据。