AstraZeneca Pharmaceuticals LP, Wilmington, DE 19850-5437, USA.
Curr Med Res Opin. 2013 Jul;29(7):813-25. doi: 10.1185/03007995.2013.794774. Epub 2013 Apr 30.
A series of studies were conducted to guide the development and characterise the pharmacokinetics of extended-release quetiapine fumarate (quetiapine XR), a once-daily formulation to control the release of the drug.
Data from these studies are described and discussed herein.
Once-daily quetiapine XR produced a similar area under the plasma concentration-time curve (AUC), minimum plasma concentration (Cmin) and a slightly lower maximum plasma concentration (Cmax) than the equivalent dose of immediate-release quetiapine (quetiapine IR) given twice daily. In a crossover, head-to-head study, total daily exposure, measured by AUC at steady state, was less variable with quetiapine XR versus quetiapine IR (percent coefficient of variation 39.2% versus 51.2%, respectively). Compared with fasting, a high-fat meal increased the AUC and Cmax for quetiapine XR, whereas a light meal had no significant effect on these parameters. Quetiapine XR exhibits a less pronounced D2 receptor occupancy peak and receptor occupancy levels remain higher for longer compared with quetiapine IR. Quetiapine XR was generally well tolerated with a safety profile similar to quetiapine IR, although the intensity of sedation in the first hours of treatment was significantly lower (p < 0.01) with quetiapine XR versus IR.
At steady state, quetiapine XR provided a similar AUC and Cmin and a slightly lower Cmax relative to an equivalent dose of quetiapine IR administered twice daily. Quetiapine XR exhibited linear pharmacokinetics in the dose range tested and no food effect was observed with a light meal. Once-daily dosing and simpler dose titration makes using quetiapine XR convenient for clinicians and patients. Quetiapine XR has predictable pharmacokinetics and was generally well tolerated, with significantly lower intensity of sedation after the first hours of administration compared with quetiapine IR. With once-daily quetiapine XR, the impact of daytime sedation may be mitigated by evening dosing.
进行了一系列研究,以指导富马酸喹硫平(quetiapine XR)的开发并对其药代动力学特征进行描述,这是一种每日一次的制剂,用于控制药物释放。
本文描述和讨论了这些研究的数据。
与每日两次服用的等效剂量的即时释放喹硫平(quetiapine IR)相比,每日一次的 quetiapine XR 产生了相似的血浆浓度-时间曲线下面积(AUC)、最小血浆浓度(Cmin)和略低的最大血浆浓度(Cmax)。在一项交叉、头对头研究中,稳态时通过 AUC 测量的每日总暴露量,quetiapine XR 比 quetiapine IR 更具变异性(分别为 39.2%和 51.2%)。与空腹相比,高脂肪餐增加了 quetiapine XR 的 AUC 和 Cmax,而低热量餐对这些参数没有显著影响。与 quetiapine IR 相比,quetiapine XR 表现出不太明显的 D2 受体占有率峰值,并且受体占有率水平保持更高的时间更长。与 quetiapine IR 相比,quetiapine XR 通常具有良好的耐受性,安全性特征相似,尽管在治疗的最初几个小时镇静强度显著降低(p < 0.01)。
在稳态时,quetiapine XR 与每日两次服用的等效剂量的 quetiapine IR 相比,提供了相似的 AUC 和 Cmin,以及略低的 Cmax。quetiapine XR 在测试剂量范围内表现出线性药代动力学,并且与低热量餐相比,没有观察到食物效应。每日一次给药和更简单的剂量滴定使临床医生和患者使用 quetiapine XR 更加方便。quetiapine XR 具有可预测的药代动力学特性,通常具有良好的耐受性,与 quetiapine IR 相比,在首次给药后的几个小时内镇静强度显著降低。与每日一次的 quetiapine XR 相比,通过晚上给药可能减轻白天镇静的影响。