Olugemo Kemi, Solorio Daniel, Sheridan Claire, Young Clarence L
PAREXEL International Corporation , Baltimore MD , USA.
Postgrad Med. 2015 Mar;127(2):223-31. doi: 10.1080/00325481.2015.1000231. Epub 2015 Jan 31.
Indomethacin is a potent analgesic that, similar to other nonsteroidal anti-inflammatory drugs, is associated with serious dose-related adverse events. There is a need for newer nonsteroidal anti-inflammatory drug products with improved tolerability. Low-dose submicron indomethacin was developed using SoluMatrix Fine Particle Technology™ to enable treatment at lower doses than commercially available indomethacin drug products. This study evaluated the pharmacokinetics and safety of submicron indomethacin 20 and 40 mg compared with indomethacin 50-mg capsules.
This was a phase 1, randomized, open-label, 4-period, 4-sequence, single-dose crossover study. Forty healthy volunteers received low-dose submicron indomethacin 20- or 40-mg capsules, or indomethacin 50-mg capsules under fasting or fed conditions. Pharmacokinetic parameters and safety were assessed.
Comparable fasting peak plasma levels (mean ± standard deviation) were demonstrated for submicron indomethacin 40 mg (2368.79 ± 631.38 ng/ml) and indomethacin 50 mg (2369.40 ± 969.06 ng/ml). The overall systemic exposure (geometric least squares mean; 95% CI) was > 21% lower for submicron indomethacin 40 mg (6007.71 ng·h/mL; 5585.73-6461.58) compared with indomethacin 50 mg (7646.23 ng·h/ml; 7110.44-8222.40) under fasting conditions. Food delayed the rate but did not affect the extent of indomethacin absorption from submicron indomethacin 40 mg. Submicron indomethacin 40 mg administration resulted in earlier time to peak plasma levels (median 1.67; min-max 0.5-3.5 hours) under fasting conditions compared with indomethacin 50 mg (2.02; 0.5-5.0 hours). Submicron indomethacin 20 and 40 mg were dose proportional and generally well tolerated.
Compared with indomethacin 50 mg, submicron indomethacin 40 mg achieved similar peak plasma concentrations, lower systemic exposure, and a faster time to peak plasma concentration, indicating rapid absorption. The current formulation of low-dose submicron indomethacin has recently demonstrated efficacy in 2 phase 3 studies in patients with acute pain following bunionectomy and represents a new, low-dose treatment option for patients with acute pain.
吲哚美辛是一种强效镇痛药,与其他非甾体抗炎药类似,会引发严重的剂量相关不良事件。因此,需要研发耐受性更好的新型非甾体抗炎药产品。低剂量亚微米级吲哚美辛采用SoluMatrix微粒技术™开发,能够以低于市售吲哚美辛药品的剂量进行治疗。本研究评估了20毫克和40毫克亚微米级吲哚美辛与50毫克吲哚美辛胶囊相比的药代动力学和安全性。
这是一项1期随机、开放标签、4周期、4序列、单剂量交叉研究。40名健康志愿者在空腹或进食条件下接受20毫克或40毫克低剂量亚微米级吲哚美辛胶囊,或50毫克吲哚美辛胶囊。评估药代动力学参数和安全性。
40毫克亚微米级吲哚美辛(2368.79±631.38纳克/毫升)和50毫克吲哚美辛(2369.40±969.06纳克/毫升)的空腹血浆峰值水平相当。在空腹条件下,40毫克亚微米级吲哚美辛的总体全身暴露量(几何最小二乘均值;95%置信区间)比50毫克吲哚美辛(7646.23纳克·小时/毫升;7110.44 - 8222.40)低>21%(6007.71纳克·小时/毫升;5585.73 - 6461.58)。食物会延迟40毫克亚微米级吲哚美辛中吲哚美辛的吸收速率,但不影响吸收程度。与50毫克吲哚美辛(2.02;0.5 - 5.0小时)相比,空腹条件下服用40毫克亚微米级吲哚美辛达到血浆峰值水平的时间更早(中位数1.67;最小值 - 最大值0.5 - 3.5小时)。20毫克和40毫克亚微米级吲哚美辛剂量成比例,且总体耐受性良好。
与50毫克吲哚美辛相比,40毫克亚微米级吲哚美辛达到了相似的血浆峰值浓度、更低的全身暴露量以及更快的血浆峰值浓度达峰时间,表明吸收迅速。目前低剂量亚微米级吲哚美辛制剂最近在两项3期研究中已证明对拇囊炎切除术后急性疼痛患者有效,代表了一种针对急性疼痛患者的新型低剂量治疗选择。