Chen Kaifeng, Luo Ping, Zhu Shaihong, Lin Yaqi, Yang Nan, Huang Shuqi, Ding Qin, Zhu Liyong, Pei Qi
Department of Pharmacy, The Third Xiangya Hospital, Central South University, Changsha 410013, China.
Department of General Surgery, The Third Xiangya Hospital, Central South University, Changsha 410013, China.
Pharmaceutics. 2022 Sep 20;14(10):1986. doi: 10.3390/pharmaceutics14101986.
Omeprazole is commonly prescribed to obese patients and patients after laparoscopic sleeve gastrectomy (LSG). The pharmacokinetics of oral omeprazole after LSG are still unknown. Therefore, the aim of this study was to investigate the pharmacokinetics of oral omeprazole in obese patients before and after LSG. A total of 331 blood samples were collected from 62 obese patients preoperatively (visit 1) followed by 41 patients 7 days post-LSG (visit 2) and 20 patients 1 month post-LSG (visit 3). Population pharmacokinetic analysis was performed using NONMEM to characterize the effect of LSG on omeprazole absorption and disposition. A one-compartment model with 12 transit absorption compartments and linear elimination successfully described the data. Compared with pre-surgery, the oral omeprazole time to maximum plasma concentration (T) was reduced and maximum plasma concentration (C) was higher, but the apparent clearance (CL/F) and area under the plasma concentration-time curve (AUC) were unchanged 7 days and 1 month after surgery. In addition, the CYP2C19 genotype and liver function exhibited a significant influence on omeprazole CL/F. LSG increased the rate of omeprazole absorption but did not affect omeprazole exposure. A dose of 20 mg omeprazole once daily may be adequate for relieving gastrointestinal tract discomfort at short-term follow-up post-LSG.
奥美拉唑常用于肥胖患者及腹腔镜袖状胃切除术(LSG)后的患者。LSG后口服奥美拉唑的药代动力学仍不清楚。因此,本研究的目的是调查肥胖患者在LSG前后口服奥美拉唑的药代动力学。共从62例肥胖患者术前(访视1)采集了331份血样,随后在LSG后7天对41例患者(访视2)和LSG后1个月对20例患者(访视3)进行了血样采集。使用NONMEM进行群体药代动力学分析,以表征LSG对奥美拉唑吸收和处置的影响。一个具有12个转运吸收室和线性消除的单室模型成功地描述了数据。与手术前相比,口服奥美拉唑的达峰时间(T)缩短,血药峰浓度(C)升高,但术后7天和1个月时的表观清除率(CL/F)和血药浓度-时间曲线下面积(AUC)未发生变化。此外,CYP2C19基因型和肝功能对奥美拉唑的CL/F有显著影响。LSG提高了奥美拉唑的吸收速率,但不影响奥美拉唑的暴露量。每日一次20 mg的奥美拉唑剂量可能足以缓解LSG后短期随访中的胃肠道不适。