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利托那韦。临床药代动力学及与其他抗HIV药物的相互作用。

Ritonavir. Clinical pharmacokinetics and interactions with other anti-HIV agents.

作者信息

Hsu A, Granneman G R, Bertz R J

机构信息

Abbott Laboratories, Abbott Park, Illinois, USA.

出版信息

Clin Pharmacokinet. 1998 Oct;35(4):275-91. doi: 10.2165/00003088-199835040-00002.

Abstract

Ritonavir is 1 of the 4 potent synthetic HIV protease inhibitors, approved by the US Food and Drug Administration (FDA) between 1995 and 1997, that have revolutionised HIV therapy. The extent of oral absorption is high and is not affected by food. Within the clinical concentration range, ritonavir is approximately 98 to 99% bound to plasma proteins, including albumin and alpha 1-acid glycoprotein. Cerebrospinal fluid (CSF) drug concentrations are low in relation to total plasma concentration. However, parallel decreases in the viral burden have been observed in the plasma, CSF and other tissues. Ritonavir is primarily metabolised by cytochrome P450 (CYP) 3A isozymes and, to a lesser extent, by CYP2D6. Four major oxidative metabolites have been identified in humans, but are unlikely to contribute to the antiviral effect. About 34% and 3.5% of a 600 mg dose is excreted as unchanged drug in the faeces and urine, respectively. The clinically relevant t1/2 beta is about 3 to 5 hours. Because of autoinduction, plasma concentrations generally reach steady state 2 weeks after the start of administration. The pharmacokinetics of ritonavir are relatively linear after multiple doses, with apparent oral clearance averaging 7 to 9 L/h. In vitro, ritonavir is a potent inhibitor of CYP3A. In vivo, ritonavir significantly increases the AUC of drugs primarily eliminated by CYP3A metabolism (e.g. clarithromycin, ketoconazole, rifabutin, and other HIV protease inhibitors, including indinavir, saquinavir and nelfinavir) with effects ranging from an increase of 77% to 20-fold in humans. It also inhibits CYP2D6-mediated metabolism, but to a significantly lesser extent (145% increase in desipramine AUC). Since ritonavir is also an inducer of several metabolising enzymes [CYP1A4, glucuronosyl transferase (GT), and possibly CYP2C9 and CYP2C19], the magnitude of drug interactions is difficult to predict, particularly for drugs that are metabolised by multiple enzymes or have low intrinsic clearance by CYP3A. For example, the AUC of CYP3A substrate methadone was slightly decreased and alprazolam was unaffected. Ritonavir is minimally affected by other CYP3A inhibitors, including ketoconazole. Rifampicin (rifampin), a potent CYP3A inducer, decreased the AUC of ritonavir by only 35%. The degree and duration of suppression of HIV replication is significantly correlated with the plasma concentrations. Thus, the large increase in the plasma concentrations of other protease inhibitors when coadministered with ritonavir forms the basis of rational dual protease inhibitor regimens, providing patients with 2 potent drugs at significantly reduced doses and less frequent dosage intervals. Combination treatment of ritonavir with saquinavir and indinavir results in potent and sustained clinical activity. Other important factors with combination regimens include reduced interpatient variability for high clearance agents, and elimination of the food effect on the bioavailibility of indinavir.

摘要

利托那韦是4种强效合成HIV蛋白酶抑制剂之一,于1995年至1997年间获得美国食品药品监督管理局(FDA)批准,彻底改变了HIV治疗方式。其口服吸收程度高,不受食物影响。在临床浓度范围内,利托那韦约98%至99%与血浆蛋白结合,包括白蛋白和α1 - 酸性糖蛋白。脑脊液(CSF)药物浓度相对于总血浆浓度较低。然而,在血浆、脑脊液和其他组织中均观察到病毒载量平行下降。利托那韦主要由细胞色素P450(CYP)3A同工酶代谢,在较小程度上由CYP2D6代谢。在人体内已鉴定出4种主要氧化代谢物,但它们不太可能产生抗病毒作用。600mg剂量的利托那韦约34%和3.5%分别以原形药物经粪便和尿液排出。临床相关的t1/2β约为3至5小时。由于自身诱导作用,血浆浓度一般在给药开始后2周达到稳态。多次给药后,利托那韦的药代动力学相对呈线性,表观口服清除率平均为7至9L/h。在体外,利托那韦是CYP3A的强效抑制剂。在体内,利托那韦显著增加主要经CYP3A代谢消除的药物的AUC(例如克拉霉素、酮康唑、利福布汀以及其他HIV蛋白酶抑制剂,包括茚地那韦、沙奎那韦和奈非那韦),在人体内增加幅度从77%至20倍不等。它也抑制CYP2D6介导的代谢,但程度明显较小(地昔帕明AUC增加145%)。由于利托那韦也是几种代谢酶[CYP1A4、葡萄糖醛酸转移酶(GT),可能还有CYP2C9和CYP2C19]的诱导剂,药物相互作用的程度难以预测,尤其是对于那些由多种酶代谢或经CYP3A固有清除率低的药物。例如,CYP3A底物美沙酮的AUC略有下降,而阿普唑仑未受影响。利托那韦受其他CYP3A抑制剂(包括酮康唑)的影响极小。利福平是一种强效CYP3A诱导剂,仅使利托那韦的AUC降低35%。HIV复制的抑制程度和持续时间与血浆浓度显著相关。因此,与利托那韦合用时其他蛋白酶抑制剂血浆浓度的大幅增加构成了合理的双重蛋白酶抑制剂治疗方案的基础,使患者能够以显著降低的剂量和更不频繁的给药间隔使用两种强效药物。利托那韦与沙奎那韦和茚地那韦联合治疗可产生强效且持续的临床活性。联合治疗方案的其他重要因素包括降低高清除率药物患者间的变异性,以及消除食物对茚地那韦生物利用度的影响。

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