芬太尼及其衍生物:止痛药还是杀人药?
Jiri Patocka1, Wenda Wu1,2, Patrik Oleksak1
1Department of Chemistry, Faculty of Science, University of Hradec Kralove, 50003 Hradec Kralove, Czech Republic.
Heliyon
|April 22, 2024
概括
芬太尼是一种强大的合成阿片类药物,正在推动美国阿片类药物流行,是年轻人死亡的主要原因. 它的衍生品很容易合成,这引发了人们对其被滥用为化学武器的担忧.
科学领域:
- 药理学 药理学是指药理学的学科.
- 毒理学 毒理学 毒理学
- 公共卫生 公共卫生
背景情况:
- 芬太尼是一种强大的合成阿片类止痛药.
- 它的高强度 (100倍吗啡) 和快速作用使其有效治疗严重的疼痛.
- 在过去的二十年中,全球滥用芬太尼及其衍生品的数量急剧增加.
研究的目的:
- 审查芬太尼及其衍生物的特性和药理学.
- 检查与芬太尼及其类型相关的过量服用病例.
- 讨论美国目前的阿片类药物流行以及潜在的化学武器滥用.
主要方法:
- 科学文章和专利的文献评论.
- 报告过量服用死亡病例的分析.
- 讨论药理性质和合成可访问性.
主要成果:
- 芬太尼是目前美国阿片类药物流行的主要驱动因素.
- 它是美国18-45岁成年人死亡的主要原因.
- 已经记录了1400多种芬太尼衍生物,突出了合成的容易性和滥用潜力.
结论:
- 芬太尼及其衍生品由于广泛滥用和高死亡率,造成了严重的公共卫生危机.
- 这些化合物的可访问性和效力引发了对其作为化学武器的潜在使用的严重担忧.
- 迫切需要注意解决芬太尼及其类型所带来的多方面的威胁.
相关概念视频
Opioid Analgesics: Synthetic and Semisynthetic Opioids
287
Synthetic and semisynthetic opioids are pivotal in pain management and tackling opioid addiction. Semisynthetic opioids, including morphinans (morphine derivatives), oxycodone, oxymorphone, hydrocodone, and hydromorphone, have improved pharmacokinetic profiles compared to morphine. Additionally, heroin and 6-MAM (6-Monoacetylmorphine) show better CNS penetration than morphine due to heightened lipid solubility. Hydromorphone, a potent opioid, undergoes hepatic metabolism to form the active...
287
Opioid Analgesics: Morphine and Other Natural Cogeners
243
Opioids are a class of drugs that mimic endogenous opioid peptides and act on opioid receptors, and help in pain relief. These compounds are classified as natural, synthetic, or semi-synthetic. Natural opioids, like morphine, codeine, and thebaine, are derived from the opium poppy plant (Papaver somniferum or Papaver album) and are termed opiates. Synthetic opioids are artificial, while semi-synthetic opioids combine natural and synthetic compounds. Morphine, a prototypical opioid, possesses a...
243
Analgesia and Pain Management
614
Pain is critical to various clinical pathologies, provoking an urgent need for effective management. Pain, whether acute or chronic, is a complex neurochemical process. Its alleviation depends on the type, with nonopioid analgesics effective for mild to moderate pain, such as musculoskeletal or inflammatory pain, while neuropathic pain responds best to anticonvulsants, tricyclic antidepressants, or serotonin/norepinephrine reuptake inhibitors. For severe acute or chronic pain, opioids may be...
614
Opioid Receptors: Overview
764
Opioid receptors, including the mu (μ, MOR), delta (δ, DOR), and kappa (κ, KOR) types, belong to the rhodopsin family of G protein-coupled receptors. These receptors are located throughout the central and peripheral nervous systems and in non-neuronal tissues such as macrophages and astrocytes. Opioid receptor ligands can be categorized into agonists or antagonists. Highly selective agonists include [d-Ala2, MePhe4, Gly(ol)5]-enkephalin or DAMGO for MOR, [D-Pen2,...
764
Parenteral Anesthetics: Overview
119
Intravenous anesthetics are drugs administered parenterally to induce anesthesia or sedation. Propofol is a widely used agent formulated as a 1% emulsion in soybean oil, glycerol, and egg phosphatide. It induces rapid anesthesia primarily due to its rapid distribution from the bloodstream to target tissues and is metabolized in the liver. However, it can cause significant pain on injection and hypertriglyceridemia. Fospropofol, a water-based prodrug of propofol, lacks these adverse effects.
119
Drug Classes and Categories
2.0K
Drugs can be classified according to their chemical composition or their intended therapeutic application. For instance, anti-infective agents that possess the ability to eliminate pathogens or suppress their growth and reproduction can be grouped based on the organisms they target or their chemical structure. Furthermore, drugs can be divided into prescription, nonprescription, or controlled substances. Prescription medications, such as antibiotics, require oversight from a licensed healthcare...
2.0K


