聚光灯下的黄类药物:弥合物理化学性质和配方策略之间的差距
Marta Berga1, Konstantins Logviss1, Liga Lauberte1
1Laboratory of Finished Dosage Forms, Faculty of Pharmacy, Riga Stradiņš University, LV-1007 Riga, Latvia.
Pharmaceuticals (Basel, Switzerland)
|October 28, 2023
概括
黄类生物可用性至关重要,但经常被忽视. 这项研究回顾了可溶性和点等物理化学性质,突出了提高这些有益植物化合物的吸收的配方策略.
科学领域:
- 药理学和植物化学
- 营养科学 营养科学
- 材料科学 材料科学 材料科学
背景情况:
- 黄类,丰富的植物多,提供健康益处,但它们的生物利用性往往是有限的.
- 溶解性和吸收性差,阻碍了许多基于黄类的食补充剂和草药产品的有效性.
研究的目的:
- 审查与生物可用性相关的黄类化合物的物理化学性质.
- 确定与难溶性黄酸相关的挑战,并讨论提高吸收的配方策略.
主要方法:
- 对关键物理化学性质 (pKa,log P,可溶性,透性,化温度) 的实验和计算数据的编制和分析.
- 对各种黄类子类的综述,包括糖和糖化物.
- 讨论改善生物可用性的配方方法.
主要成果:
- 在各类黄类子类之间存在物理化学性质的显著差异.
- 许多黄类化合物,特别是酸甘,具有较低的溶解度和高点 ("粉").
- 黄类甘油酸通常比它们的酸盐对应物更具有水友性.
结论:
- 溶解度差对于黄类生物可用性来说是一个很大的挑战.
- 诸如减小尺寸,固体分散,载体和基于脂质的系统等配方策略对于改善黄类吸收和治疗潜力至关重要.
相关概念视频
Factors Influencing Drug Absorption: Physicochemical Parameters
303
The physicochemical characteristics of drugs play a crucial role in formulating stable and bioavailable drug products. The solubility of a drug, governed by the varying pH along the GI tract and its dissociation constant (pKa), is pivotal in determining its ionization state and absorption rate. Notably, weak acids and bases remain unionized and are absorbed more rapidly.
Enhanced drug absorption can be achieved by reducing particle sizes and increasing surface areas, thereby facilitating...
Enhanced drug absorption can be achieved by reducing particle sizes and increasing surface areas, thereby facilitating...
303
Factors Affecting Dissolution: Drug Permeability, Stability and Stereochemistry
209
Orally administered drugs primarily enter the systemic circulation via passive diffusion through the intestinal membranes. The drug's absorption is influenced by drug stability in the gastrointestinal GI tract, membrane permeability, the surface area available for absorption, luminal drug concentration, and residence time in the lumen. Drug permeability can be enhanced by adjusting the lipophilicity, polarity, or molecular size of the drug, promoting its passive transport across intestinal...
209
Factors Influencing Drug Absorption: Pharmaceutical Parameters
136
Solid dosage forms such as tablets and capsules undergo rigorous manufacturing processes to ensure stability and effectiveness. Their dissolution and absorption properties are influenced significantly by the choice of excipients (inactive ingredients that serve various roles in the formulation), and the methodology applied during production. The manufacturing parameters, such as compression force and granulation techniques, significantly affect dissolution rates. Elevated compression forces...
136
Factors Affecting Drug Biotransformation: Physicochemical and Chemical Properties of Drugs
256
A drug's physicochemical properties fundamentally influence its metabolism. For instance, a drug's molecular size and shape critically determine its interaction with enzymes and transporters — larger drugs may face difficulty reaching enzyme active sites, altering their metabolic pathways. The pKa of a drug, which establishes its ionization state, can impact its solubility and absorption, thereby influencing metabolism.
The drug's acidity or basicity is essential in...
The drug's acidity or basicity is essential in...
256
Biopharmaceutics and Pharmacokinetics: Overview
2.1K
Understanding drugs, drug products, and their performance in pharmaceutical science is pivotal. Drugs, whether simple molecules or complex compounds, are designed to interact with the body's biological systems to diagnose, treat, or prevent diseases. Drug products include various delivery systems such as tablets, capsules, injections, and inhalers. The performance of these drug products is gauged by their ability to deliver the active ingredient to the desired site of action at the...
2.1K
Factors Influencing Bioavailability: First-Pass Elimination
6.4K
When a drug is taken orally, it undergoes a journey starting from the gastrointestinal (GI) tract, passing through the portal vein, reaching the liver, and finally entering the systemic circulation. This process involves the absorption of the drug across the GI tract. The liver is the primary site for metabolizing the drug, with some metabolism also occurring in the gut wall. This journey significantly reduces the quantity of the drug that reaches the systemic circulation, a phenomenon known as...
6.4K


