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每日一次的茶碱产品因食物诱导出现“剂量倾泻”,导致茶碱中毒。

Food-induced "dose-dumping" from a once-a-day theophylline product as a cause of theophylline toxicity.

作者信息

Hendeles L, Weinberger M, Milavetz G, Hill M, Vaughan L

出版信息

Chest. 1985 Jun;87(6):758-65. doi: 10.1378/chest.87.6.758.

Abstract

Three slow-release preparations of theophylline have received approval from the U.S. Food and Drug Administration (FDA) for "once-daily" dosing indications, amid controversy regarding the appropriateness of this decision. Because of specific concerns regarding data submitted to the FDA in support of the first of these products to be approved, Theo-24, we examined the absorption characteristics of this newly marketed formulation. Eight healthy volunteers received, in a crossover manner, single doses of a theophylline reference solution and Theo-24, taken both fasting and after a breakfast of bacon and eggs. The concentrations of theophylline were measured up to 60 hours after the dose. Absorption of Theo-24 after an overnight fast was very slow, with only 71 +/- 6 percent (mean +/- SE) of the dose ultimately absorbed. In contrast, food caused precipitous "dose-dumping," resulting in dose-normalized peak levels in the serum that averaged 2.3 times higher than after a fasting dose. About half of the dose was absorbed in a four-hour period, generally beginning six to eight hours after the postprandial dose, and complete absorption was then attained within 24 hours (p less than 0.001). Toxic effects of theophylline occurred in four subjects when they took the dose with food whereas no toxic effects occurred during the fasting regimen. Consequently, doses of Theo-24 that would have attained a predicted peak concentration of 15 micrograms/ml after multiple dosing taken without food would, if taken with food, have resulted in larger fluctuations and in peak concentrations in the potentially toxic range for six of the eight subjects.

摘要

三种茶碱缓释制剂已获得美国食品药品监督管理局(FDA)批准用于“每日一次”给药适应症,但这一决定的合理性存在争议。由于对提交给FDA以支持首批获批产品之一Theo-24的数据存在特定担忧,我们研究了这种新上市制剂的吸收特性。八名健康志愿者采用交叉方式,分别单次服用茶碱参比溶液和Theo-24,服药时间分别为空腹和早餐食用培根和鸡蛋之后。在给药后长达60小时内测定茶碱浓度。空腹过夜后Theo-24的吸收非常缓慢,最终只有71±6%(均值±标准误)的剂量被吸收。相比之下,食物导致急剧的“剂量倾泻”,使血清中剂量标准化的峰值水平平均比空腹给药后高2.3倍。约一半的剂量在4小时内被吸收,通常在餐后剂量后6至8小时开始,然后在24小时内完全吸收(p<0.001)。四名受试者在与食物同服剂量时出现了茶碱的毒性作用,而在空腹给药方案期间未出现毒性作用。因此,在空腹多次给药后预计峰值浓度能达到15微克/毫升的Theo-24剂量,如果与食物同服,八名受试者中有六人的血药浓度波动会更大,且峰值浓度会处于潜在中毒范围内。

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