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普通剂型和肠溶衣剂型泼尼松龙在人体中的血浆水平。

Plasma prednisolone levels in man following administration in plain and enteric-coated forms.

作者信息

Wilson C G, May C S, Paterson J W

出版信息

Br J Clin Pharmacol. 1977 Jun;4(3):351-5. doi: 10.1111/j.1365-2125.1977.tb00723.x.

Abstract

1 Prednisolone plasma levels were measured in seven patients by a competitive protein binding method after administration of prednisolone (20 mg) by mouth as plain or enteric-coated tablets. 2 The mean peak plasma prednisolone concentration after the enteric-coated preparation, 199 ng ml-1, was significantly lower than after the plain tablet, 268 ng ml-1, and occurred later, at 4.69 h compared with 1.72 h. The bioavailability of the two preparations was similar. 3 It is concluded that, although the plasma concentration versus time profiles are different, the absorption of prednisolone from plain and enteric-coated preparations is equal.

摘要
  1. 通过竞争性蛋白结合法测定了7例患者口服普通片或肠溶片形式的泼尼松龙(20mg)后的血浆泼尼松龙水平。2. 肠溶片制剂后血浆泼尼松龙的平均峰值浓度为199ng/ml,明显低于普通片的268ng/ml,且出现时间较晚,分别为4.69小时和1.72小时。两种制剂的生物利用度相似。3. 结论是,尽管血浆浓度-时间曲线不同,但普通片和肠溶片制剂中泼尼松龙的吸收是相同的。

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Absorption of enteric and non-enteric coated prednisolone tablets.肠溶和非肠溶包衣泼尼松龙片的吸收情况。
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Clinical pharmacokinetics of prednisone and prednisolone.泼尼松和泼尼松龙的临床药代动力学
Clin Pharmacokinet. 1990 Aug;19(2):126-46. doi: 10.2165/00003088-199019020-00003.

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