Kuhlmann J, Woodcock B, Wilke J, Welling H, Rietbrock N
J Cardiovasc Pharmacol. 1985 Sep-Oct;7(5):1003-6. doi: 10.1097/00005344-198509000-00030.
Cytostatic drugs reduce the rate and extent of beta-acetyldigoxin absorption attributable to reversible damage of the gastrointestinal mucosa. As beta-acetyldigoxin verapamil is an agent rapidly absorbed in the proximal small bowel, plasma concentrations and apparent absorption of verapamil administered orally (160 mg) have been determined in nine patients with nongastrointestinal cancer before and 24 h after cytostatic treatment. The cytostatic therapy reduced the area under the plasma verapamil concentration-time curve in eight of the patients, with a mean reduction of 35% (p less than 0.05). It is concluded that, as previously found for digoxin, the absorption of verapamil is diminished owing to impairment of the absorptive capacity of the mucosa of the upper small intestine.
细胞抑制药物会降低β-乙酰地高辛的吸收速率和程度,这归因于胃肠道黏膜的可逆性损伤。由于β-乙酰地高辛维拉帕米是一种在近端小肠快速吸收的药物,因此对9例非胃肠道癌症患者在进行细胞抑制治疗前及治疗后24小时测定了口服(160毫克)维拉帕米后的血浆浓度和表观吸收情况。细胞抑制治疗使8例患者的血浆维拉帕米浓度-时间曲线下面积减小,平均减小35%(P<0.05)。结论是,正如之前对地高辛的研究发现,维拉帕米的吸收因上段小肠黏膜吸收能力受损而减少。