Bartus Raymond T, Emerich Dwaine F, Hotz Joyce, Blaustein Marc, Dean Reginald L, Perdomo Brigido, Basile Anthony S
Alkermes, Inc, Cambridge, MA, USA.
Neuropsychopharmacology. 2003 Nov;28(11):1973-82. doi: 10.1038/sj.npp.1300274.
While oral naltrexone is effective in treating alcohol and opiate dependencies, poor patient adherence and widely fluctuating plasma levels limit its efficacy. To overcome these problems, an extended-release formulation of naltrexone (Vivitrex) was developed by encapsulating naltrexone into injectable, biodegradable polymer microspheres. Pharmacokinetic studies in rats demonstrated that this formulation produced stable, pharmacologically relevant plasma levels of naltrexone for approximately 1 month following either subcutaneous or intramuscular injections. While rats receiving placebo microspheres demonstrated a pronounced analgesic response to morphine in the hot-plate test, morphine analgesia was completely blocked in rats treated with extended-release naltrexone. This antagonism began on day 1 following administration and lasted for 28 days. Rats reinjected with extended-release naltrexone 34 days after the initial dose and tested for another 35 days showed consistent suppression of morphine analgesia for an additional 28 days. mu-Opioid receptor density, as measured by [(3)H]DAMGO autoradiography, increased up to two-fold following a single injection of extended-release naltrexone. Saturation binding assays using [(3)H]DAMGO showed changes in the midbrain and striatum at 1 week after extended-release naltrexone administration, and after 1 month in the neocortex. These receptor increases persisted for 2-4 weeks after dissipation of the morphine antagonist actions of naltrexone. These data suggest that therapeutically relevant plasma levels of naltrexone can be maintained using monthly injections of an extended-release microsphere formulation, and that changes in mu-opioid receptor density do not impact its efficacy in suppressing morphine-induced analgesia in the rat. Clinical trials of extended release naltrexone for treating alcohol and opiate dependency are currently ongoing.
虽然口服纳曲酮对治疗酒精和阿片类药物依赖有效,但患者依从性差以及血浆水平波动较大限制了其疗效。为克服这些问题,通过将纳曲酮封装到可注射的、可生物降解的聚合物微球中,开发出了一种长效释放制剂(Vivitrex)。在大鼠身上进行的药代动力学研究表明,皮下或肌肉注射该制剂后,可在约1个月内产生稳定的、具有药理学相关性的纳曲酮血浆水平。在热板试验中,接受安慰剂微球的大鼠对吗啡表现出明显的镇痛反应,而接受长效释放纳曲酮治疗的大鼠的吗啡镇痛作用则被完全阻断。这种拮抗作用在给药后第1天开始,持续28天。在初始剂量34天后再次注射长效释放纳曲酮并再测试35天的大鼠,其吗啡镇痛作用持续被抑制达28天。通过[(3)H]DAMGO放射自显影法测定,单次注射长效释放纳曲酮后,μ-阿片受体密度增加了两倍。使用[(3)H]DAMGO进行的饱和结合试验显示,在长效释放纳曲酮给药1周后,中脑和纹状体出现变化,1个月后新皮层出现变化。在纳曲酮的吗啡拮抗作用消失后,这些受体增加持续2 - 4周。这些数据表明,每月注射长效释放微球制剂可维持治疗相关的纳曲酮血浆水平,且μ-阿片受体密度的变化不影响其在大鼠中抑制吗啡诱导的镇痛作用的疗效。目前正在进行长效释放纳曲酮治疗酒精和阿片类药物依赖的临床试验。