[Evaluation for druggability of traditional Chinese medicine preparations in medical institutions based on human use experience].

药方 可药性 医学 中医药 替代医学 传统医学 高三尖杉酯碱 药理学 病理 生物化学 化学 髓系白血病 免疫学 基因
作者
Jingxian Zhuo,Zhenwen Qiu,Jie Zhou,Yanmei Wu,Maolin Yang,Zhong-Qi Yang
出处
期刊:PubMed 卷期号:47 (15): 4256-4260 被引量:2
标识
DOI:10.19540/j.cnki.cjcmm.202204012.601
摘要

Traditional Chinese medicine(TCM) preparations in medical institutions are an important source of research and development(R&D) of TCM new drug. With years of usage in therapy, these preparations' safety and effectiveness have generally been validated in clinic. However, there are still a few disadvantages in TCM new medicine development, such as similar prescriptions, excessive prescription ingredients, too broad clinical orientation, lack of solid clinical data, issue in pharmaceutical quality control, and intellectual property disputes. Nowadays, the Three-Combined Evaluation System has strengthened policy support for the new TCM R&D. In order to improve the success rate of TCM R&D, due to the difficulties within, this paper proposes the process of transforming TCM preparations in medical institutions into new TCM and advocates the evaluation for druggability based on Human Use Experience(HUE). The potencial preparations ought to follow traditional Chinese Medical theory, sufficient HUE data in indication, syndrome type of TCM, target population, usage, dosage, and course of treatment are required. Particular attention should be paid to the source, evolution, and improvement process of prescription, and evaluate the dosage, ingredients, and herb resources of prescription. To assess the feasibility of mass production, it is necessary to determine whether the pharmaceutical process is mostly consistent with the new drug and whether the dosage form is reasonable. By summarizing the clinical application of the preparations, the whole picture of its clinical application would be reveal as much as possible. It is beneficial to evaluate its clinical value and R&D prospect. In consideration of the lack of clinical safety data of preparations, safety profile needs to be collected according to the prescription. The quality of clinical data needs to be evaluated by focusing on the integrity and accuracy of data to reduce bias and confusion. Significant care should be paid to intellectual property protection to avoid legal disputes.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
Willa完成签到,获得积分10
3秒前
3秒前
4秒前
sdl发布了新的文献求助10
5秒前
5秒前
小王发布了新的文献求助10
6秒前
7秒前
我是老大应助依依采纳,获得10
7秒前
8秒前
lishi完成签到,获得积分10
8秒前
9秒前
SCINEXUS发布了新的文献求助50
9秒前
务实紫雪发布了新的文献求助10
9秒前
廉晓健发布了新的文献求助10
10秒前
田様应助小趴菜采纳,获得10
11秒前
11秒前
11秒前
11秒前
谦让谷菱完成签到,获得积分10
11秒前
sandy发布了新的文献求助10
12秒前
ChilinHo完成签到,获得积分20
12秒前
大气映冬发布了新的文献求助10
13秒前
刚子发布了新的文献求助10
15秒前
李建芳完成签到,获得积分20
15秒前
ChilinHo发布了新的文献求助10
15秒前
Chasing完成签到 ,获得积分10
16秒前
16秒前
我是老大应助科研通管家采纳,获得10
16秒前
所所应助科研通管家采纳,获得10
16秒前
科研通AI5应助科研通管家采纳,获得10
16秒前
充电宝应助科研通管家采纳,获得10
17秒前
爆米花应助科研通管家采纳,获得10
17秒前
Ava应助科研通管家采纳,获得10
17秒前
小马甲应助科研通管家采纳,获得10
17秒前
17秒前
17秒前
17秒前
科研通AI5应助科研通管家采纳,获得10
17秒前
17秒前
高分求助中
【此为提示信息,请勿应助】请按要求发布求助,避免被关 20000
ISCN 2024 – An International System for Human Cytogenomic Nomenclature (2024) 3000
Continuum Thermodynamics and Material Modelling 2000
Encyclopedia of Geology (2nd Edition) 2000
105th Edition CRC Handbook of Chemistry and Physics 1600
Izeltabart tapatansine - AdisInsight 800
Maneuvering of a Damaged Navy Combatant 650
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3774527
求助须知:如何正确求助?哪些是违规求助? 3320249
关于积分的说明 10199220
捐赠科研通 3034929
什么是DOI,文献DOI怎么找? 1665282
邀请新用户注册赠送积分活动 796771
科研通“疑难数据库(出版商)”最低求助积分说明 757570