Černá Petra, Wittenburg Luke, Hawley Jennifer, Willis McKenna, Siegenthaler Britta, Lappin Michael R
Department of Clinical Sciences, Colorado State University, Fort Collins, CO 80523, USA.
Department of Surgical and Radiological Sciences, School of Veterinary Medicine, University of California-Davis, Davis, CA 95616, USA.
Pathogens. 2025 Jul 7;14(7):666. doi: 10.3390/pathogens14070666.
Antiviral drugs like EIDD-2801 (molnupiravir; MPV) have been successfully used in the treatment of feline infectious peritonitis (FIP). The previous study of the pharmacokinetics of MPV in healthy cats showed promise for its use and safety. The objective was to determine the pharmacokinetics of molnupiravir in cats with naturally occurring FIP by measuring MPV and EIDD-193 (β-D-N4-hydroxycytidine; NHC) serum levels. Blood was collected from seven cats diagnosed with naturally occurring FIP treated at 1, 2, 4, 6 and 12 h post oral MPV administration and at 12 h post pill administration 7 days later. Serum concentrations of MPV and NHC were determined using a previously published high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method. The mean dose of MPV was 15.44 mg/kg (SD ± 1.82). The mean peak serum concentration of MPV (C) after a single PO dose of MPV was 38 ng/mL (SD ± 5). The mean peak serum concentration of NHC (C) after a single PO dose of MVP was 1551 ng/mL (SD ± 720). the time to reach NHC C (T) was 2.6 h (SD ± 1.4), and the NHC elimination half-life was 1.6 h (SD ± 1.1). Minimal drug accumulation was seen in trough concentrations following twice-daily dosing for 7 days. The low MPV levels may be explained by fast conversion to its active metabolite NHC. The mean NHC concentrations at all time points were at least 4 times the reported in vitro IC for feline coronavirus strains and twice-daily dosing for seven days did not lead to drug accumulation within the serum. The results support the use of MPV in the treatment of FIP, and if therapeutic drug monitoring is to be performed, NHC should be measured.
像EIDD - 2801(莫努匹拉韦;MPV)这样的抗病毒药物已成功用于治疗猫传染性腹膜炎(FIP)。先前对MPV在健康猫体内的药代动力学研究显示了其应用前景和安全性。目的是通过测量MPV和EIDD - 193(β - D - N4 - 羟基胞苷;NHC)的血清水平来确定莫努匹拉韦在自然感染FIP的猫体内的药代动力学。在口服MPV后1、2、4、6和12小时以及7天后口服药丸后12小时,从7只被诊断为自然感染FIP并接受治疗的猫身上采集血液。使用先前发表的高效液相色谱 - 串联质谱(HPLC - MS/MS)方法测定MPV和NHC的血清浓度。MPV的平均剂量为15.44 mg/kg(标准差±1.82)。单次口服MPV后,MPV的平均血清峰值浓度(C)为38 ng/mL(标准差±5)。单次口服MVP后,NHC的平均血清峰值浓度(C)为1551 ng/mL(标准差±720)。达到NHC C的时间(T)为2.6小时(标准差±1.4),NHC消除半衰期为1.6小时(标准差±1.1)。每日两次给药7天后,谷浓度中未见明显药物蓄积。MPV水平较低可能是由于其快速转化为活性代谢物NHC所致。所有时间点的平均NHC浓度至少是报道的猫冠状病毒株体外IC的4倍,每日两次给药7天未导致血清内药物蓄积。这些结果支持将MPV用于治疗FIP,并且如果要进行治疗药物监测,应测量NHC。