Nyman-Pantelidis M, Nilsson A, Wagner Z G, Borgå O
Clinical Research & Development, Astra Draco AB, Lund, Sweden.
Aliment Pharmacol Ther. 1994 Dec;8(6):617-22. doi: 10.1111/j.1365-2036.1994.tb00339.x.
The retrograde spread of two budesonide enema formulations with different viscosities was investigated. The study design was open, randomized and two-period crossover. Three female and two male patients (age range: 35-45 years) with distal ulcerative colitis or proctitis participated. Both enema formulations contained a dose of 2 mg budesonide/100 mL. An unabsorbable radioactive marker (99mTc-labelled human serum albumin microcolloid) was added to the enema just before administration. All doses were given in the evening with the patients lying in a supine position during the whole investigation. The intestinal spread was followed for 8 h using scintigraphic imaging. Plasma samples for budesonide assay were taken during the 12 h after administration of the low viscosity enema.
Budesonide plasma levels were measurable for up to 4-6 h. Cmax was 2.5 nmol/L (range: 0.9-4.5 nmol/L) and was attained in 1.5 h (range 1-3 h). The patients had no difficulty in retaining the enemas. There was a statistically significant difference in spread between the low and high viscosity enema. The low viscosity enema spread over an area situated between the rectum and the splenic flexure. The spread occurred mainly in the first 15 min after administration. In contrast, the high viscosity enema, in most cases, spread only over a minor part of this area and the rate and extent of spreading was also more variable with this formulation.
The spread of a low viscosity enema appears to be well suited for the treatment of proctitis and distal colitis.
研究了两种不同粘度的布地奈德灌肠剂的逆向扩散情况。研究设计为开放性、随机、两期交叉试验。三名女性和两名男性患者(年龄范围:35 - 45岁)参与,他们患有远端溃疡性结肠炎或直肠炎。两种灌肠剂均含有2 mg布地奈德/100 mL的剂量。在给药前,向灌肠剂中加入一种不可吸收的放射性标记物(99mTc标记的人血清白蛋白微胶体)。所有剂量均在晚上给予,在整个研究过程中患者保持仰卧位。使用闪烁成像跟踪肠道扩散8小时。在给予低粘度灌肠剂后的12小时内采集血浆样本用于布地奈德测定。
布地奈德血浆水平在长达4 - 6小时内可测量。Cmax为2.5 nmol/L(范围:0.9 - 4.5 nmol/L),在1.5小时(范围1 - 3小时)达到。患者保留灌肠剂没有困难。低粘度和高粘度灌肠剂在扩散方面存在统计学上的显著差异。低粘度灌肠剂扩散到直肠和脾曲之间的区域。扩散主要发生在给药后的前15分钟。相比之下,高粘度灌肠剂在大多数情况下仅扩散到该区域的一小部分,并且这种制剂的扩散速率和程度也更具可变性。
低粘度灌肠剂的扩散似乎非常适合治疗直肠炎和远端结肠炎。