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Strengths, weaknesses, opportunities and challenges for long acting injectable therapies: Insights for applications in HIV therapy

机译:长效注射疗法的优势,劣势,机遇和挑战:在艾滋病治疗中的应用见解

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Advances in solid drug nanoparticle technologies have resulted in a number of long-acting (LA) formulations with the potential for once monthly or longer administration. Such formulations offer great utility for chronic diseases, particularly when a lack of medication compliance may be detrimental to treatment response. Two such formulations are in clinical development for HIV but the concept of LA delivery has its origins in indications such as schizophrenia and contraception. Many terms have been utilised to describe the LA approach and standardisation would be beneficial. Ultimately, definitions will depend upon specific indications and routes of delivery, but for HIV we propose benchmarks that reflect perceived clinical benefits and available data on patient attitudes. Specifically, we propose dosing intervals of >= 1 week, >= 1 month or >= 6 months, for oral, injectable or implantable strategies, respectively. This review focuses upon the critical importance of potency in achieving the LA outcome for injectable formulations and explores established and emerging technologies that have been employed across indications. Key technological challenges such as the need for consistency and ease of administration for drug combinations, are also discussed. Finally, the review explores the gaps in knowledge regarding the pharmacology of drug release from particulate-based LA injectable suspensions. A number of hypotheses are discussed based upon available data relating to local drug metabolism, active transport systems, the lymphatics, macrophages and patient-specific factors. Greater knowledge of the mechanisms that underpin drug release and protracted exposure will help facilitate further development of this strategy to achieve the promising clinical benefits. (C) 2016 Elsevier B.V. All rights reserved.
机译:固体药物纳米颗粒技术的进步已经导致了许多长效(LA)制剂,它们有可能每月一次或更长时间给药。这样的制剂为慢性疾病提供了很大的实用性,特别是当缺乏药物依从性可能不利于治疗反应时。两种这样的制剂正在针对HIV的临床开发中,但是LA递送的概念起源于诸如精神分裂症和避孕等适应症。已经使用了许多术语来描述LA方法,标准化将是有益的。最终,定义将取决于具体的适应症和分娩途径,但是对于HIV,我们提出了可反映可感知的临床益处和有关患者态度的可用数据的基准。具体来说,我们建议口服,可注射或可植入策略的给药间隔分别为≥1周,≥1个月或≥6个月。这篇综述着重于在可注射制剂中达到LA结果的效力的至关重要性,并探讨了已在各种适应症中采用的成熟技术和新兴技术。还讨论了关键技术挑战,例如对药物组合的一致性和易于管理的需求。最后,该综述探讨了有关从基于颗粒的LA注射剂悬浮液释放药物的药理学知识的空白。基于与局部药物代谢,主动转运系统,淋巴管,巨噬细胞和患者特异性因素有关的可用数据,讨论了许多假设。对支持药物释放和长期暴露的机制的更多了解将有助于促进该策略的进一步发展,以实现有希望的临床益处。 (C)2016 Elsevier B.V.保留所有权利。

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