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前体药物磷酸依托泊苷在胃液和胆汁中转化为依托泊苷。

Conversion of the prodrug etoposide phosphate to etoposide in gastric juice and bile.

作者信息

de Jong R S, Slijfer E A, Uges D R, Mulder N H, de Vries E G

机构信息

Department of Internal Medicine, University Hospital Groningen, The Netherlands.

出版信息

Br J Cancer. 1997;76(11):1480-3. doi: 10.1038/bjc.1997.581.

Abstract

Etoposide phosphate is a water-soluble prodrug of etoposide. It was expected that this prodrug could be used to overcome the solubility limitations and erratic bioavailability of oral etoposide. To investigate the possibility of prodrug conversion to etoposide within the gastrointestinal lumen, etoposide phosphate was dissolved in water and incubated with human gastric juice or human bile in vitro. Samples were collected during 150 min and analysed for etoposide concentration with high-performance liquid chromatography. Conversion of prodrug to etoposide during incubation with gastric juice was negligible. There was significant conversion during incubation with bile at pH 7-8. The percentage of prodrug converted to etoposide at pH 8 after 60 min was 78 +/- 18% (mean +/- S.D.) for a 0.1 mg ml-1 prodrug solution and 36 +/- 26% for 0.5 mg ml-1. At pH 7, after 60 min 22% of prodrug was converted to etoposide when incubated at 0.1 mg ml-1 and 10% at 0.5 mg ml-1. No conversion was found after inactivation of alkaline phosphate (AP) by overnight heating of bile at 65 degrees C or by the addition of disodium edetate to the bile. In conclusion, because of AP in bile, variable conversion of etoposide phosphate to etoposide can be expected within the intestinal lumen after oral administration. This could have important pharmacokinetic consequences.

摘要

磷酸依托泊苷是依托泊苷的水溶性前体药物。预期这种前体药物可用于克服口服依托泊苷的溶解度限制和不稳定的生物利用度。为了研究前体药物在胃肠道腔内转化为依托泊苷的可能性,将磷酸依托泊苷溶解于水中,并在体外与人胃液或人胆汁一起孵育。在150分钟内收集样品,并用高效液相色谱法分析依托泊苷浓度。在与胃液孵育期间,前体药物向依托泊苷的转化可忽略不计。在pH 7 - 8的胆汁孵育期间有显著转化。对于0.1 mg/ml的前体药物溶液,在pH 8下孵育60分钟后,转化为依托泊苷的前体药物百分比为78±18%(平均值±标准差),对于0.5 mg/ml为36±26%。在pH 7下,在0.1 mg/ml孵育60分钟后,22%的前体药物转化为依托泊苷,在0.5 mg/ml时为10%。通过在65℃下将胆汁过夜加热或向胆汁中加入依地酸二钠使碱性磷酸酶(AP)失活后,未发现转化。总之,由于胆汁中的AP,口服给药后在肠腔内磷酸依托泊苷向依托泊苷的转化可能会有所不同。这可能会产生重要的药代动力学后果。

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Bioavailability of low-dose oral etoposide.低剂量口服依托泊苷的生物利用度。
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