{"title":"人生长激素长效制剂的发展前景。","authors":"Andreas Jostel, Stephen M Shalet","doi":"10.2165/00024677-200605030-00002","DOIUrl":null,"url":null,"abstract":"<p><p>In healthy humans, growth hormone (GH) is secreted in distinct pulses with an underlying nyctohemeral pattern. Current forms of somatropin replacement are unable to closely mimic such a release pattern, but are still able to exert the beneficial action of GH. A limited number of short-term studies in rodents and humans suggest that longitudinal growth may be superior when somatropin is given with a pulsatile mode of administration, whereas hepatic insulin-like growth factor-I generation and beneficial changes in body composition appear to be equal or even enhanced with continuous somatropin administration.Recent developments in drug delivery technology have allowed the use of slow-release preparations of somatropin in humans. The most successful technology so far has been the encapsulation of somatropin molecules in poly(D,L-lactic-co-glycolic acid) biodegradable microspheres. Pharmacokinetic and pharmacodynamic data have been published on two such preparations; Nutropin Depot((R)) and hGH-Biosphere((R)). The latter has a superior release profile, but outcomes data from multicenter trials in both children and adults have been presented for the former: catch-up growth was observed in children, although to a lesser degree than historic comparative data obtained with the use of daily somatropin injections and the effects on metabolic derangements in GH-deficient patients appeared similar to those observed with daily injections. Improved sustained-release somatropin preparations will need further study of their long-term efficacy, but, if successful, will be highly attractive in terms of patient compliance and convenience.</p>","PeriodicalId":23310,"journal":{"name":"Treatments in Endocrinology","volume":"5 3","pages":"139-45"},"PeriodicalIF":0.0000,"publicationDate":"2006-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2165/00024677-200605030-00002","citationCount":"2","resultStr":"{\"title\":\"Prospects for the development of long-acting formulations of human somatropin.\",\"authors\":\"Andreas Jostel, Stephen M Shalet\",\"doi\":\"10.2165/00024677-200605030-00002\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>In healthy humans, growth hormone (GH) is secreted in distinct pulses with an underlying nyctohemeral pattern. Current forms of somatropin replacement are unable to closely mimic such a release pattern, but are still able to exert the beneficial action of GH. A limited number of short-term studies in rodents and humans suggest that longitudinal growth may be superior when somatropin is given with a pulsatile mode of administration, whereas hepatic insulin-like growth factor-I generation and beneficial changes in body composition appear to be equal or even enhanced with continuous somatropin administration.Recent developments in drug delivery technology have allowed the use of slow-release preparations of somatropin in humans. The most successful technology so far has been the encapsulation of somatropin molecules in poly(D,L-lactic-co-glycolic acid) biodegradable microspheres. Pharmacokinetic and pharmacodynamic data have been published on two such preparations; Nutropin Depot((R)) and hGH-Biosphere((R)). The latter has a superior release profile, but outcomes data from multicenter trials in both children and adults have been presented for the former: catch-up growth was observed in children, although to a lesser degree than historic comparative data obtained with the use of daily somatropin injections and the effects on metabolic derangements in GH-deficient patients appeared similar to those observed with daily injections. Improved sustained-release somatropin preparations will need further study of their long-term efficacy, but, if successful, will be highly attractive in terms of patient compliance and convenience.</p>\",\"PeriodicalId\":23310,\"journal\":{\"name\":\"Treatments in Endocrinology\",\"volume\":\"5 3\",\"pages\":\"139-45\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2006-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.2165/00024677-200605030-00002\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Treatments in Endocrinology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2165/00024677-200605030-00002\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Treatments in Endocrinology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2165/00024677-200605030-00002","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2
摘要
在健康的人类中,生长激素(GH)以不同的脉冲分泌,具有潜在的昼夜循环模式。目前形式的生长激素替代不能密切模仿这样的释放模式,但仍然能够发挥生长激素的有益作用。对啮齿动物和人类进行的有限数量的短期研究表明,当以脉动方式给予生长激素时,纵向生长可能更优越,而肝脏胰岛素样生长因子- 1的产生和身体成分的有益变化似乎与持续使用生长激素相等甚至增强。药物输送技术的最新发展已经允许在人体中使用生长激素的缓释制剂。迄今为止,最成功的技术是将生长激素分子封装在聚(D, l -乳酸-羟基乙酸)可生物降解的微球中。两种此类制剂的药代动力学和药效学数据已发表;Nutropin Depot(右)和hGH-Biosphere(右)。后者具有更好的释放特性,但是来自儿童和成人的多中心试验的结果数据显示,前者在儿童中观察到追赶生长,尽管与使用每日注射生长激素获得的历史比较数据相比程度较低,并且对gh缺乏患者代谢紊乱的影响似乎与每日注射相似。改进的生长激素缓释制剂需要进一步研究其长期疗效,但如果成功,将在患者依从性和便利性方面具有很高的吸引力。
Prospects for the development of long-acting formulations of human somatropin.
In healthy humans, growth hormone (GH) is secreted in distinct pulses with an underlying nyctohemeral pattern. Current forms of somatropin replacement are unable to closely mimic such a release pattern, but are still able to exert the beneficial action of GH. A limited number of short-term studies in rodents and humans suggest that longitudinal growth may be superior when somatropin is given with a pulsatile mode of administration, whereas hepatic insulin-like growth factor-I generation and beneficial changes in body composition appear to be equal or even enhanced with continuous somatropin administration.Recent developments in drug delivery technology have allowed the use of slow-release preparations of somatropin in humans. The most successful technology so far has been the encapsulation of somatropin molecules in poly(D,L-lactic-co-glycolic acid) biodegradable microspheres. Pharmacokinetic and pharmacodynamic data have been published on two such preparations; Nutropin Depot((R)) and hGH-Biosphere((R)). The latter has a superior release profile, but outcomes data from multicenter trials in both children and adults have been presented for the former: catch-up growth was observed in children, although to a lesser degree than historic comparative data obtained with the use of daily somatropin injections and the effects on metabolic derangements in GH-deficient patients appeared similar to those observed with daily injections. Improved sustained-release somatropin preparations will need further study of their long-term efficacy, but, if successful, will be highly attractive in terms of patient compliance and convenience.