Sasabe Hiroyuki, Shimokawa Yoshihiko, Shibata Masakazu, Hashizume Kenta, Hamasako Yusuke, Ohzone Yoshihiro, Kashiyama Eiji, Umehara Ken
Tokushima Research Institute, Otsuka Pharmaceutical Co., Ltd., Tokushima, Japan
Tokushima Research Institute, Otsuka Pharmaceutical Co., Ltd., Tokushima, Japan.
Antimicrob Agents Chemother. 2016 May 23;60(6):3497-508. doi: 10.1128/AAC.03049-15. Print 2016 Jun.
Delamanid (Deltyba, OPC-67683) is the first approved drug in a novel class of nitro-dihydro-imidazooxazoles developed for the treatment of multidrug-resistant tuberculosis. Patients with tuberculosis require treatment with multiple drugs, several of which have known drug-drug interactions. Transporters regulate drug absorption, distribution, and excretion; therefore, the inhibition of transport by one agent may alter the pharmacokinetics of another, leading to unexpected adverse events. Therefore, it is important to understand how delamanid affects transport activity. In the present study, the potencies of delamanid and its main metabolites as the substrates and inhibitors of various transporters were evaluated in vitro Delamanid was not transported by the efflux ATP-binding cassette (ABC) transporters P-glycoprotein (P-gp; MDR1/ABCB1) and breast cancer resistance protein (BCRP/ABCG2), solute carrier (SLC) transporters, organic anion-transporting polypeptides, or organic cation transporter 1. Similarly, metabolite 1 (M1) was not a substrate for any of these transporters except P-gp. Delamanid showed no inhibitory effect on ABC transporters MDR1, BCRP, and bile salt export pump (BSEP; ABCB11), SLC transporters, or organic anion transporters. M1 and M2 inhibited P-gp- and BCRP-mediated transport but did so only at the 50% inhibitory concentrations (M1, 4.65 and 5.71 μmol/liter, respectively; M2, 7.80 and 6.02 μmol/liter, respectively), well above the corresponding maximum concentration in plasma values observed following the administration of multiple doses in clinical trials. M3 and M4 did not affect the activities of any of the transporters tested. These in vitro data suggest that delamanid is unlikely to have clinically relevant interactions with drugs for which absorption and disposition are mediated by this group of transporters.
地拉米定(Deltyba,OPC-67683)是新型硝基二氢咪唑并恶唑类中首个获批用于治疗耐多药结核病的药物。结核病患者需要多种药物联合治疗,其中几种药物存在已知的药物相互作用。转运体调节药物的吸收、分布和排泄;因此,一种药物对转运的抑制可能会改变另一种药物的药代动力学,导致意外的不良事件。所以,了解地拉米定如何影响转运活性很重要。在本研究中,体外评估了地拉米定及其主要代谢产物作为各种转运体底物和抑制剂的效力。地拉米定不被外排ATP结合盒(ABC)转运体P-糖蛋白(P-gp;MDR1/ABCB1)、乳腺癌耐药蛋白(BCRP/ABCG2)、溶质载体(SLC)转运体、有机阴离子转运多肽或有机阳离子转运体1转运。同样,代谢产物1(M1)除了P-gp外,不是这些转运体中任何一种的底物。地拉米定对ABC转运体MDR1、BCRP和胆盐输出泵(BSEP;ABCB11)、SLC转运体或有机阴离子转运体没有抑制作用。M1和M2抑制P-gp和BCRP介导的转运,但仅在50%抑制浓度时(M1分别为4.65和5.71 μmol/升;M2分别为7.80和6.02 μmol/升)才会如此,远高于临床试验中多次给药后观察到的相应血浆最大浓度值。M3和M4不影响所测试的任何转运体的活性。这些体外数据表明,地拉米定不太可能与由这组转运体介导吸收和处置的药物发生具有临床相关性的相互作用。