阻断滥用制剂综述:制剂技术和审批过程中的监管立场。

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pharmaceutical Development and Technology Pub Date : 2024-10-01 Epub Date: 2024-09-03 DOI:10.1080/10837450.2024.2398526
Jaydip Bhola, Chetan Borkhataria
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引用次数: 0

摘要

在过去几年里,药物滥用已成为一个全球性的健康问题。随着用于止痛的阿片类处方的增加,阿片类药物的滥用也在增加。许多其他类别的药物也被滥用和误用,如抗抑郁药、兴奋剂、致幻剂、抗精神病药和抗胆碱能药。其中一个主要原因是,被误诊为抑郁症、焦虑症和严重疼痛的患者被开具了这些药物,而这些药物很可能会成瘾。在这篇综述中,我们介绍了阻断滥用技术的工作原理、阻断滥用制剂中使用的关键成分、已上市的具有阻断滥用特性的阿片类药物产品简介以及监管机构在阿片类药物产品审批过程中的立场。最后,报告总结了制药业和食品及药物管理局为减少药物滥用所做的努力,鼓励开发具有抑制滥用特性的制剂。现有的大多数具有抑制滥用功能的药物产品都含有聚氧化乙烯,这种物质会在高温下降解。这就需要研究人员注意寻找替代成分或工艺来克服上述问题。从监管角度来看,只有少数几个监管机构发布了有关 ADF 的指导意见。传达其他监管机构对 ADF 的看法也很重要。
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A review on abuse-deterrent formulations: formulation technology and regulatory stands in approval process.

Drug abuse has become a global health problem over the past few years. Opioid abuse increased with an increase in the prescription of opioids for pain management. Many other classes of drugs are also abused and misused like anti-depressants, stimulants, hallucinogens, anti-psychotic, and anticholinergic drugs. One of the major reasons is that patients falsely diagnosed with depression, anxiety, and severe pain are prescribed these drugs, which are likely to be addictive. Abuse-deterrent formulations are one means to control drug abuse and overdose of prescription opioids. In this review, we explained how abuse-deterrent technology works, key ingredients used in abuse-deterrent formulations, a brief about marketed opioid drug products with abuse-deterrent properties, and the stand of regulatory agencies in the approval process of opioid drug products. In the end, it summarized that pharmaceutical industries and the FDA put their efforts into reducing drug abuse by encouraging the development of ADFs. Most available drug product having abuse-deterrent features contains Polyethylene oxide, which degrades at high temperatures. It requires the attention of the researcher to find an alternate ingredient or process to overcome said problem. From a regulatory point of view, only a few regulatory agencies have published their guidance on ADFs. It is important to convey other regulatory organizations' perspectives on ADFs as well.

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来源期刊
CiteScore
5.90
自引率
2.90%
发文量
82
审稿时长
1 months
期刊介绍: Pharmaceutical Development & Technology publishes research on the design, development, manufacture, and evaluation of conventional and novel drug delivery systems, emphasizing practical solutions and applications to theoretical and research-based problems. The journal aims to publish significant, innovative and original research to advance the frontiers of pharmaceutical development and technology. Through original articles, reviews (where prior discussion with the EIC is encouraged), short reports, book reviews and technical notes, Pharmaceutical Development & Technology covers aspects such as: -Preformulation and pharmaceutical formulation studies -Pharmaceutical materials selection and characterization -Pharmaceutical process development, engineering, scale-up and industrialisation, and process validation -QbD in the form a risk assessment and DoE driven approaches -Design of dosage forms and drug delivery systems -Emerging pharmaceutical formulation and drug delivery technologies with a focus on personalised therapies -Drug delivery systems research and quality improvement -Pharmaceutical regulatory affairs This journal will not consider for publication manuscripts focusing purely on clinical evaluations, botanicals, or animal models.
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