Change in Vancomycin Absorption after Intraperitoneal Injection and Correlation between Intraperitoneal Vancomycin Absorption and Peritoneal Equilibration Test Score in Mice with Peritoneal Injuries.

IF 1.7 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Akihiro Moritsuka, Hirotaka Miyamoto, Yukina Takahashi, Haruna Hirata, Yuki Kawauchi, Shintaro Fumoto, Koyo Nishida
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Abstract

Peritonitis is a serious complication in peritoneal dialysis patients and requires antibiotic administration. Intraperitoneal vancomycin is an empiric therapy for peritonitis caused by Gram-positive cocci; however, there is no way to predict vancomycin absorption after intraperitoneal administration. Therefore, we aimed to evaluate the changes in vancomycin absorption after intraperitoneal injection into mice with chlorhexidine gluconate (CG) induced peritoneal injuries. Additionally, we examined the correlation between intraperitoneal vancomycin absorption and peritoneal equilibration test (PET) score. PET score was determined using glucose concentration in the peritoneal dialysis fluid at each dwell time (Dt) and D2 (2 h of dwell time)/D0 (0 h of dwell time) glucose ratio. Vancomycin was injected into the peritoneal cavity of mice, blood was collected after 1-8 h, and peritoneal fluid was recovered. The residual ratio of intraperitoneal vancomycin was significantly decreased in the CG group at all time points compared to that in the vehicle group. CG group significantly exhibited higher serum vancomycin concentrations than the vehicle group, and the maximum serum concentration increased depending on CG concentration, with 0.05 and 0.1% CG groups showing 3.9- and 6.1-times higher vancomycin concentrations, respectively, than the vehicle group. A significant correlation was observed between the Dt/D0 glucose ratios and residual vancomycin ratios in the peritoneal fluid 2 or 6 h after intraperitoneal injection. A good correlation was observed between the D2/D0 glucose and residual vancomycin ratios 6 h after intraperitoneal vancomycin injection. Thus, PET score can predict residual intraperitoneal vancomycin, aiding in dosing decisions.

腹膜损伤小鼠腹腔注射万古霉素吸收变化及腹腔注射万古霉素吸收与腹膜平衡测试评分的关系
腹膜炎是腹膜透析患者的严重并发症,需要抗生素治疗。腹膜注射万古霉素是治疗革兰氏阳性球菌所致腹膜炎的经验性治疗方法;然而,没有办法预测万古霉素腹腔内给药后的吸收。因此,我们旨在评估葡萄糖酸氯己定(CG)腹腔注射万古霉素对小鼠腹膜损伤后的吸收变化。此外,我们检查了腹膜万古霉素吸收与腹膜平衡试验(PET)评分之间的相关性。PET评分采用各静置时间腹膜透析液葡萄糖浓度(Dt)和D2(静置时间2 h)/D0(静置时间0 h)葡萄糖比。小鼠腹腔注射万古霉素,1 ~ 8 h后采血,回收腹膜液。与载药组相比,CG组各时间点腹腔万古霉素残留率均显著降低。CG组万古霉素血清浓度显著高于对照组,且血清最大浓度随CG浓度的升高而升高,其中0.05和0.1% CG组万古霉素浓度分别比对照组高3.9倍和6.1倍。腹腔注射后2 h或6 h腹膜液中Dt/D0葡萄糖比值与残留万古霉素比值显著相关。腹腔注射万古霉素6 h后,D2/D0葡萄糖与残留万古霉素比值呈良好的相关性。因此,PET评分可以预测腹腔内残留万古霉素,有助于决定剂量。
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来源期刊
CiteScore
3.50
自引率
5.00%
发文量
247
审稿时长
2 months
期刊介绍: Biological and Pharmaceutical Bulletin (Biol. Pharm. Bull.) began publication in 1978 as the Journal of Pharmacobio-Dynamics. It covers various biological topics in the pharmaceutical and health sciences. A fourth Society journal, the Journal of Health Science, was merged with Biol. Pharm. Bull. in 2012. The main aim of the Society’s journals is to advance the pharmaceutical sciences with research reports, information exchange, and high-quality discussion. The average review time for articles submitted to the journals is around one month for first decision. The complete texts of all of the Society’s journals can be freely accessed through J-STAGE. The Society’s editorial committee hopes that the content of its journals will be useful to your research, and also invites you to submit your own work to the journals.
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