Center of Excellence in Pharmacology and Molecular Biology of Malaria and Cholangiocarcinoma, Chulabhorn International College, Thailand.
Drug Discovery and Development Center, Office of Advanced Science and Technology, Thammasat University (Rangsit Campus), Klongneung, Pathumthani 12121, Thailand.
Am J Chin Med. 2022;50(7):1719-1737. doi: 10.1142/S0192415X22500732. Epub 2022 Aug 27.
Andrographolide (APE) has been used for COVID-19 treatment in various clinical settings in South-East Asia due to its benefits on reduction of viral clearance and prevention of disease progression. However, the limitation of APE clinical use is the high incidence of adverse events. The objective of this study was to find the optimal dosage regimens of APE for COVID-19 treatment. The whole-body physiologically-based pharmacokinetic (PBPK) models were constructed using data from the published articles and validated against clinical observations. The inhibitory effect of APE was determined for the potency of drug efficacy. For prevention of pneumonia, multiple oral doses such as 120[Formula: see text]mg for three doses, followed by 60[Formula: see text]mg three times daily for 4 consecutive days, or 200[Formula: see text]mg intravenous infusion at the rate of 20 mg/h once daily is advised in patients with mild COVID-19. For prevention of pneumonia and reduction of viral clearance time, the recommended dosage regimen is 500[Formula: see text]mg intravenous infusion at the rate of 25[Formula: see text]mg/h once daily in patients with mild-to-moderate COVID-19. One hundred virtual populations (50 males and 50 females) were simulated for oral and intravenous infusion formulations of APE. The eligible PBPK/PD models successfully predicted optimal dosage regimens and formulations of APE for prevention of disease progression and/or reduction of viral clearance time. Additionally, APE should be co-administered with other antiviral drugs to enhance therapeutic efficacy for COVID-19 treatment.
穿心莲内酯(APE)因其可降低病毒清除率和预防疾病进展而在东南亚的各种临床环境中用于 COVID-19 治疗。然而,APE 临床应用的局限性在于不良反应发生率高。本研究的目的是寻找 COVID-19 治疗中 APE 的最佳剂量方案。使用来自已发表文章的数据构建了全身生理基于药代动力学(PBPK)模型,并通过临床观察进行了验证。APE 的抑制作用取决于药物功效的效力来确定。对于预防肺炎,建议在轻度 COVID-19 患者中口服多次剂量,如三剂 120[Formula: see text]mg,然后连续 4 天每日 3 次 60[Formula: see text]mg,或每天一次以 20mg/h 的速度静脉输注 200[Formula: see text]mg。对于预防肺炎和减少病毒清除时间,建议在轻度至中度 COVID-19 患者中以 25[Formula: see text]mg/h 的速度每天静脉输注一次 500[Formula: see text]mg。模拟了 100 个虚拟人群(50 名男性和 50 名女性)用于口服和静脉输注 APE 制剂。合格的 PBPK/PD 模型成功预测了 APE 预防疾病进展和/或减少病毒清除时间的最佳剂量方案和制剂。此外,APE 应与其他抗病毒药物联合使用,以提高 COVID-19 治疗的疗效。