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Opioid Analgesics: Synthetic and Semisynthetic Opioids01:15

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
Analgesia and Pain Management01:25

Analgesia and Pain Management

585
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...
585
Opioid Receptors: Overview01:22

Opioid Receptors: Overview

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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,...
761
Drug Abuse and Addiction: Pharmacological Phenomena01:15

Drug Abuse and Addiction: Pharmacological Phenomena

467
Drug dependence, abuse, and addiction are complex phenomena that can precipitate various abnormal states. Physical dependence refers to a state of pharmacological adaptation to a drug. This adaptation often results in tolerance—a reduced response to the drug after repeated administrations. When the drug use is abruptly stopped, withdrawal symptoms occur due to the body's need to readjust from the pharmacologically induced imbalance. However, tolerance and withdrawal symptoms do not...
467
Opioid Analgesics: Morphine and Other Natural Cogeners01:20

Opioid Analgesics: Morphine and Other Natural Cogeners

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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...
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Updated: Jun 27, 2025

Formulation of Diblock Polymeric Nanoparticles through Nanoprecipitation Technique
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多维阿片类药物滥用威使用纳米粒子-聚合物混合配方.

Sheryhan F Gad1, Anastasiia Vasiukhina2, Joseph S Keller3

  • 1Department of Industrial and Molecular Pharmaceutics, Purdue University, 575 West Stadium Avenue, West Lafayette, IN 47907, USA; Department of Pharmaceutics, Faculty of Pharmacy, Assiut University, Assiut, Egypt.

Journal of controlled release : official journal of the Controlled Release Society
|April 30, 2024
PubMed
概括

新的滥用威配方 (ADF) 使用酸纳米颗粒来阻止阿片类药物提取和热改. 这种混合药片可以阻止滥用,同时保持口服治疗效果.

关键词:
滥用威剂的配方可以阻止滥用.滥用药物滥用药物滥用药物滥用药物滥用药物滥用药物凝型聚合物形成的聚合物纳米颗粒 纳米颗粒这是一种阿片类药物.

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相关实验视频

Last Updated: Jun 27, 2025

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06:47

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Published on: September 20, 2011

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科学领域:

  • 制药科学 制药科学
  • 材料科学 材料科学 材料科学
  • 药物运输 药物运输 药物运输

背景情况:

  • 处方阿片类药物滥用是一个重大的公共卫生危机,导致过量死亡.
  • 现有的滥用威配方 (ADF) 旨在防止改,但可以通过先进的提取方法来规避.
  • 制定全面的战略对于打击阿片类药物滥用和转移至关重要.

研究的目的:

  • 开发和评估一种使用酸纳米粒子 (NP) 来增强阿片类药物保护的新型混合滥用抑止药片 (NP-Tab).
  • 评估NP-Tab对常见滥用方法的抗性,包括溶剂提取,注射和热改 ().
  • 为了确认NP-Tab在按规定口服后的治疗效果.

主要方法:

  • 制造铁交联的酸NP封装thebaine (一种模型阿片类药物).
  • 配制的NP-Tab片含有NP,香草和奇托.
  • 在模拟滥用条件下的NP-Tab性能评估:粉碎,悬浮在溶剂中,针穿透和加热.
  • 在模拟胃液中对药物释放的评估.

主要成果:

  • 粉碎的NP-Tab在水溶剂中形成瞬时凝,阻碍了针的提取.
  • 酸NP有效地阻止了通过有机溶剂提取阿片类药物.
  • NP促进了阿片类药物的热降解,减少了的奖励.
  • NP-Tab在模拟的胃液中显示了thebaine的快速释放,从而保持了口服治疗潜力.

结论:

  • 开发的NP-Tab提供了对提取,注入和热操纵的全面滥用威.
  • 这种混合配方有效地补充了现有的ADF技术.
  • 在预期的口服中,NP-Tab保留了治疗疗效,解决了阿片类药物滥用预防的关键需求.