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塞来昔布再利用的挑战与机遇。

Challenges and Opportunities for Celecoxib Repurposing.

机构信息

Department of Pharmaceutical Technology and Biopharmaceutics, Faculty of Pharmacy, Jagiellonian University Medical College, 9 Medyczna Street, 30-688, Cracow, Poland.

出版信息

Pharm Res. 2023 Oct;40(10):2329-2345. doi: 10.1007/s11095-023-03571-4. Epub 2023 Aug 8.

DOI:10.1007/s11095-023-03571-4
PMID:37552383
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10661717/
Abstract

Drug repositioning, also known as drug repurposing, reprofiling, or rediscovery, is considered to be one of the most promising strategies to accelerate the development of new original drug products. Multiple examples of successful rediscovery or therapeutic switching of old molecules that did not show clinical benefits or safety in initial trials encourage the following of the discovery of new therapeutic pathways for them. This review summarizes the efforts that have been made, mostly over the last decade, to identify new therapeutic targets for celecoxib. To achieve this goal, records gathered in MEDLINE PubMed and Scopus databases along with the registry of clinical trials by the US National Library of Medicine at the U.S. National Institutes of Health were explored. Since celecoxib is a non-steroidal anti-inflammatory drug that represents the class of selective COX-2 inhibitors (coxibs), its clinical potential in metronomic cancer therapy, the treatment of mental disorders, or infectious diseases has been discussed. In the end, the perspective of a formulator, facing various challenges related to unfavorable physicochemical properties of celecoxib upon the development of new oral dosage forms, long-acting injectables, and topical formulations, including the latest trends in the pharmaceutical technology, such as the application of mesoporous carriers, biodegradable microparticles, lipid-based nanosystems, or spanlastics, was presented.

摘要

药物重定位,也称为药物重新定位、重新定位或重新发现,被认为是加速新原创药物产品开发的最有前途的策略之一。多个成功重新发现或改变旧分子治疗用途的例子,这些分子在最初的试验中没有显示出临床益处或安全性,这鼓励了为它们发现新的治疗途径。这篇综述总结了过去十年中为塞来昔布确定新治疗靶点所做的努力。为了实现这一目标,探索了 MEDLINE PubMed 和 Scopus 数据库中的记录,以及美国国立卫生研究院美国国家医学图书馆的临床试验注册处。由于塞来昔布是非甾体抗炎药,代表选择性 COX-2 抑制剂(昔布类)的一类,因此讨论了其在肿瘤节律治疗、精神障碍或传染病治疗中的临床潜力。最后,面对在开发新的口服剂型、长效注射剂和局部制剂时塞来昔布的不良理化性质所带来的各种挑战,制剂师的观点,包括药物技术的最新趋势,如介孔载体、可生物降解的微球、基于脂质的纳米系统或spanlastics 的应用,被提出。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37d9/10661717/41a6a101bfce/11095_2023_3571_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37d9/10661717/b9c6ade7bda3/11095_2023_3571_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37d9/10661717/41a6a101bfce/11095_2023_3571_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37d9/10661717/b9c6ade7bda3/11095_2023_3571_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37d9/10661717/41a6a101bfce/11095_2023_3571_Fig2_HTML.jpg

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Naunyn Schmiedebergs Arch Pharmacol. 2023 Jul;396(7):1571-1581. doi: 10.1007/s00210-022-02339-8. Epub 2022 Nov 24.
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Stabilizer-induced different in vivo behaviors for intramuscularly long-acting celecoxib nanocrystals.载体制剂诱导的体内长效塞来昔布纳米晶行为差异。
Int J Pharm. 2022 Nov 25;628:122298. doi: 10.1016/j.ijpharm.2022.122298. Epub 2022 Oct 17.
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Effect of celecoxib on improving depression: A systematic review and meta-analysis.
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Biomedicines. 2025 Mar 13;13(3):706. doi: 10.3390/biomedicines13030706.
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Potential Benefits of Adding Alendronate, Celecoxib, Itraconazole, Ramelteon, and Simvastatin to Endometrial Cancer Treatment: The EC5 Regimen.在子宫内膜癌治疗中添加阿仑膦酸钠、塞来昔布、伊曲康唑、雷美替胺和辛伐他汀的潜在益处:EC5方案
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