德斯弗兰在小猪中吸收和处置的药理动力学
Chih-Cherng Lu1,2, Shung-Tai Ho1,3, Oliver Yao-Pu Hu4
1Department of Anesthesiology, Tri-Service General Hospital, National Defense Medical Center, Taipei, Taiwan.
Frontiers in pharmacology
|April 17, 2024
概括
起初,小猪对德斯兰的吸收遵循了零阶动力学,第一阶动力学和两模型最好地描述了排放. 大多数desflurane在2小时后仍然存在体内.
科学领域:
- 麻醉学和药理学 麻醉学和药理学
- 药理动力学和药理动力学
背景情况:
- 有限的数据存在于动脉血液中desflurane的药理动力学.
- 呼吸道和动脉血液度对于理解麻醉行为至关重要.
研究的目的:
- 为了研究小猪中德斯弗兰的药理学参数.
- 为了比较呼吸道和动脉/静脉血液中的德斯兰度.
主要方法:
- 七只小猪2小时吸入6%的脱氨酸,然后进行2小时的处置阶段.
- 度测量在吸入/潮尾空气,大腿动脉和肺动脉血液中.
- 使用血液度和心脏输出率来计算吸收和排放率.
主要成果:
- 德斯兰的吸收率最初很高,然后下降. 洗显示了类似的模式.
- 度-时间曲线符合零级输入和第一级配置动力学.
- 动脉和静脉度最适合于两部分模型;21.9%在2小时后被消除.
结论:
- 在固定的吸入度下,小猪对德斯兰的吸收遵循零级动力学.
- 排列遵循第一阶动力学,并符合两模型.
- 经过2小时的清除阶段,体内仍然存在大量的德斯弗.
相关概念视频
Methods for Studying Drug Absorption: In situ
231
In situ experiments, such as the Doluisio method and Single-Pass Perfusion technique, provide critical insights into drug uptake by simulating in vivo conditions for drug absorption.
The Doluisio method involves perfusing a prepared segment of a rat's small intestine with a solution of radiolabeled drug and a non-absorbable marker. This helps to differentiate between absorbed and non-absorbed drug concentrations. The intestinal segment is connected at both ends using tubing and syringes,...
The Doluisio method involves perfusing a prepared segment of a rat's small intestine with a solution of radiolabeled drug and a non-absorbable marker. This helps to differentiate between absorbed and non-absorbed drug concentrations. The intestinal segment is connected at both ends using tubing and syringes,...
231
Nonlinear Pharmacokinetics: Dependence of Elimination Half-Life and Dose Clearance
134
The elimination half-life and drug clearance of drugs following nonlinear kinetics can vary with dosage. The Michaelis-Menten parameters and drug concentration influence these factors. As the dose increases, the elimination half-life tends to lengthen, resulting in a reduction in clearance and a disproportionately larger area under the curve. The total clearance can be derived from the Michaelis-Menten equation for drugs following a one-compartment model.
A study on guinea pigs examined the...
A study on guinea pigs examined the...
134
Drug Excretion: Pulmonary and Glandular Routes
108
Gaseous substances like general anesthetics are absorbed and excreted through the lungs via simple diffusion. This process depends on factors such as pulmonary blood flow, respiration rate, and the substance's solubility. Gaseous anesthetics like nitrous oxide with low blood solubility are excreted rapidly, while compounds like alcohol, with high blood and tissue solubility, are excreted slowly.
Drugs can also be excreted in breast milk, which is crucial for breastfeeding infants. The...
Drugs can also be excreted in breast milk, which is crucial for breastfeeding infants. The...
108
Factors Affecting Drug Distribution: Organ Perfusion Rate
125
Drug distribution within the body is a complex process influenced by several factors, including perfusion rate, the rate at which the bloodstream transports drugs to tissue. This limitation becomes particularly significant when dealing with highly lipophilic drugs. In such cases, the rate at which the drug can move across membranes is crucial, and if the membrane is highly permeable to the drug, distribution becomes rate-limited by perfusion.
Perfusion rate-limited distribution relies on the...
Perfusion rate-limited distribution relies on the...
125
Inhalational Anesthetics: Overview
274
Inhalation anesthetics are drugs that induce general anesthesia upon inhalation. They work by increasing the sensitivity of GABAA receptors or inhibiting NMDA receptors, leading to a decrease in central nervous system activity. The depth of anesthesia can be rapidly adjusted by changing the concentration of the inhaled gas. Some common examples of inhalational anesthetics include volatile liquids like isoflurane, desflurane, sevoflurane and gases like xenon and nitrous oxide. Isoflurane, a...
274


