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一种替代草药在冠状病毒病联合治疗中的口服给药处置动力学和剂量的综合综述。

A comprehensive review on disposition kinetics and dosage of oral administration of , an alternative herbal medicine, in co-treatment of coronavirus disease.

作者信息

Songvut Phanit, Suriyo Tawit, Panomvana Duangchit, Rangkadilok Nuchanart, Satayavivad Jutamaad

机构信息

Laboratory of Pharmacology, Chulabhorn Research Institute, Bangkok, Thailand.

Center of Excellence on Environmental Health and Toxicology (EHT), OPS, MHESI, Bangkok, Thailand.

出版信息

Front Pharmacol. 2022 Aug 19;13:952660. doi: 10.3389/fphar.2022.952660. eCollection 2022.

Abstract

Coronavirus disease 2019 (COVID-19) is a present global health crisis that is driving the investigation of alternative phytomedicines for antiviral purposes. The evidence suggests that crude or extract is a promising candidate for treating symptoms of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). This review aims to consolidate the available reports on the disposition kinetics of andrographolide, a main active component of . The second objective of this review is to summarize the available reports on an appropriate oral dosage for the use of andrographolide in upper respiratory tract infections (URTIs) and other viral infectious diseases. The data were collected from the literature on absorption, distribution, biotransformation, and excretion of andrographolide, and information was also obtained from scientific databases about the use of . The finding of this review on pharmacokinetics indicates that andrographolide is slightly absorbed into the blood circulation and exhibits poor oral bioavailability, whereas its distribution process is unrestricted. In the termination phase, andrographolide preferentially undergoes biotransformation partly through phase I hydroxylation and phase II conjugation, and it is then eliminated via the renal excretion and hepatobiliary system. The key summary of the recommended dosage for andrographolide in uncomplicated URTI treatment is 30 mg/day for children and 60 mg/day for adults. The dose for adult patients with pharyngotonsillitis could be increased to 180 mg/day, but not exceed 360 mg/day. Co-treatment with in concert with the standard supportive care for influenza reduced the severity of symptoms, shortened treatment duration, and decreased the risk of developing post-influenza complications. The recommended starting dose for use in patients with mild COVID-19 is 180 mg/day of andrographolide, based on the dose used in patients experiencing a URTI with inflammation. This review is not only applicable for evaluating the appropriate doses of andrographolide for antiviral treatments but also encourages future research evaluating the effectiveness of these recommended dosages during the COVID-19 pandemic.

摘要

2019冠状病毒病(COVID-19)是当前的全球健康危机,这推动了对用于抗病毒目的的替代植物药的研究。有证据表明,[此处原文缺失相关植物药名称]的 crude 或提取物是治疗严重急性呼吸综合征冠状病毒2(SARS-CoV-2)症状的一个有前景的候选药物。本综述旨在整合关于穿心莲内酯([此处原文缺失相关植物药名称]的主要活性成分)处置动力学的现有报告。本综述的第二个目标是总结关于穿心莲内酯在上呼吸道感染(URTIs)和其他病毒感染性疾病中使用的合适口服剂量的现有报告。数据从关于穿心莲内酯吸收、分布、生物转化和排泄的文献中收集,并且也从科学数据库中获取了关于[此处原文缺失相关植物药名称]使用的信息。本综述关于药代动力学的发现表明,穿心莲内酯少量吸收进入血液循环,口服生物利用度较差,而其分布过程不受限制。在消除阶段,穿心莲内酯部分通过I相羟基化和II相结合优先进行生物转化,然后通过肾脏排泄和肝胆系统消除。穿心莲内酯在单纯性URTI治疗中推荐剂量的关键总结是儿童30毫克/天,成人60毫克/天。患有咽扁桃体炎的成年患者剂量可增加至180毫克/天,但不超过360毫克/天。与[此处原文缺失相关药物名称]联合治疗并配合流感的标准支持性护理可减轻症状严重程度、缩短治疗持续时间并降低发生流感后并发症的风险。基于患有炎症的URTI患者使用的剂量,轻度COVID-19患者使用穿心莲内酯的推荐起始剂量为180毫克/天。本综述不仅适用于评估穿心莲内酯用于抗病毒治疗的合适剂量,还鼓励未来开展研究评估这些推荐剂量在COVID-19大流行期间的有效性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ff/9437296/f2c1cc62ba9b/fphar-13-952660-g001.jpg

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