相关实验视频
Updated: Apr 30, 2026

07:34
Manual Therapy for a Chronic Non-Specific Low Back Pain Rat Model
Published on: August 11, 2023
663
开发和验证传统中医药的方法模型的良好实践建议:一个探索性的顺序混合方法研究研究
Su Li1,2,3, Luan Zhang4, Yangyang Wang2,3
1Guangzhou University of Chinese Medicine, Guangzhou, Guangdong, China.
Frontiers in pharmacology
|February 17, 2025
概括
这项研究开发了一种标准化方法模型,用于传统中医药 (TCM) 的良好实践建议 (GPR). 该模型确保了TCM GPRs的科学和合理的制定,定义和报告.
科学领域:
- 综合医学是一个整体的医学.
- 基于证据的实践.
- 开发方法论 开发方法论
背景情况:
- 传统中医 (TCM) 缺乏制定良好实践建议 (GPR) 的标准化方法.
- 在TCM的临床经验需要一个结构化的方法来制定可靠的指导方针.
- 现有的TCM指导方针在质量和一致性方面可能有所不同.
研究的目的:
- 开发一个合理和标准化的方法模型,用于创建TCM良好实践建议 (GPR).
- 根据临床经验和最佳实践指导TCM GPR的制定.
- 建立一个定义,制定和报告TCM GPRs的框架.
主要方法:
- 采用了一种探索性的顺序混合方法方法.
- 使用最适合框架合成方法论和TCM指导方针的文献系统编码.
- 使用现实数据,和测试和可区分性测试验证开发的方法模型的有效性.
主要成果:
- 成功开发了一个TCM GPR方法模型,包括3个主题和10个子主题.
- 该模型显示数据和,表明该主题的全面覆盖.
- 验证证实了良好的合适性,在不同的指南特征中进行区分,以及结构合理性.
结论:
- 开发的TCM GPR方法模型标准化了TCM GPRs的制定,定义和报告.
- 该模型促进了TCM GPRs的科学和理性的形成.
- 为创建强大的TCM GPRs提供理论和方法指南.
相关概念视频
Preclinical Development: Overview
4.8K
Preclinical development consists of a series of tests that ensure the safety and efficacy of a new therapeutic compound before it is tested in humans. There are four main phases to this process. First, safety pharmacology tests are conducted to ensure the drug does not produce any acutely harmful effects. These tests examine parameters such as bronchoconstriction, cardiac dysrhythmias, blood pressure changes, and ataxia. Next, preliminary toxicological testing is performed to determine the...
4.8K
Drug Administration and Therapy Phases: Overview
1.9K
Drugs, the chemical agents used in diagnosing, treating, or preventing diseases, undergo a four-phase process of development: pharmaceutic, pharmacokinetics, pharmacodynamics, and therapeutic.
The pharmaceutical phase focuses on leveraging the physicochemical properties of the drug to design and manufacture an effective product. Variants include orally administered tablets or capsules, topical creams or ointments, and parenteral-delivery solutions or emulsions.
The pharmacokinetic phase...
The pharmaceutical phase focuses on leveraging the physicochemical properties of the drug to design and manufacture an effective product. Variants include orally administered tablets or capsules, topical creams or ointments, and parenteral-delivery solutions or emulsions.
The pharmacokinetic phase...
1.9K
In Vitro Drug Dissolution: Compendial Testing Models I
560
Compendial dissolution methods are standardized procedures defined by pharmacopeias to evaluate the rate at which a drug dissolves in a specific medium. These methods ensure batch-to-batch consistency, enable quality control, and support the prediction of drug bioavailability. They are critical for both immediate and modified-release drug products.The apparatuses used for dissolution testing differ in their design and mechanical function, but all aim to simulate the physiological environment of...
560
In Vitro Drug Dissolution: Alternative Methods
380
Alternative drug dissolution methods include the rotating bottle, intrinsic dissolution test, peristalsis, and the Franz diffusion cell method. The rotating bottle method involves meticulously rotating tightly capped controlled-release beads in a temperature-controlled bath. Periodic decanting of samples allows for residue assay, followed by refilling with fresh medium and testing at various pH levels to emulate the gastrointestinal tract conditions.In contrast, the intrinsic dissolution test...
380

