Recent advances, challenges and updates on the development of therapeutics for malaria.

IF 3.8 3区 生物学 Q1 BIOLOGY EXCLI Journal Pub Date : 2024-05-06 eCollection Date: 2024-01-01 DOI:10.17179/excli2023-6856
Rimmy Nandal, Davinder Kumar, Navidha Aggarwal, Virender Kumar, Balasubramanian Narasimhan, Rakesh Kumar Marwaha, Prabodh Chander Sharma, Surender Kumar, Nitin Bansal, Hitesh Chopra, Aakash Deep
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Abstract

Malaria has developed as a serious worldwide health issue as a result of the introduction of resistant Plasmodium species strains. Because of the common chemo resistance to most of the existing drugs on the market, it poses a severe health problem and significant obstacles in drug research. Malaria treatment has evolved during the last two decades in response to Plasmodium falciparum drug sensitivity and a return of the disease in tropical areas. Plasmodium falciparum is now highly resistant to the majority of antimalarial drugs. The parasite resistance drew focus to developing novel antimalarials to combat parasite resistance. The requirement for many novel antimalarial drugs in the future year necessitates adopting various drug development methodologies. Different innovative strategies for discovering antimalarial drugs are now being examined here. This review is primarily concerned with the description of newly synthesized antimalarial compounds, i.e. Tafenoquine, Cipargamin, Ferroquine, Artefenomel, DSM265, MMV390048 designed to improve the activity of pure antimalarial enantiomers. In this review, we selected the representative malarial drugs in clinical trials, classified them with detailed targets according to their action, discussed the relationship within the human trials, and generated a summative discussion with prospective expectations.

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疟疾治疗药物开发的最新进展、挑战和更新。
由于抗药性疟原虫菌株的出现,疟疾已成为一个严重的世界性健康问题。由于疟原虫对市场上现有的大多数药物普遍具有抗药性,因此疟疾已成为一个严重的健康问题,并给药物研究带来了巨大障碍。在过去的二十年里,疟疾治疗不断发展,以应对恶性疟原虫对药物的敏感性和热带地区疟疾的复发。目前,恶性疟原虫对大多数抗疟药物具有高度抗药性。寄生虫的抗药性促使人们关注开发新型抗疟药物,以消除寄生虫的抗药性。由于未来一年需要许多新型抗疟药物,因此有必要采用各种药物开发方法。本文将对发现抗疟药物的不同创新策略进行研究。本综述主要介绍新合成的抗疟化合物,即他非诺喹、西帕加明、铁喹、Artefenomel、DSM265、MMV390048,旨在提高纯抗疟对映体的活性。在这篇综述中,我们选择了临床试验中具有代表性的抗疟药物,根据其作用的详细靶点对它们进行了分类,讨论了它们在人体试验中的关系,并进行了具有前瞻性期望的总结性讨论。
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来源期刊
EXCLI Journal
EXCLI Journal BIOLOGY-
CiteScore
8.00
自引率
2.20%
发文量
65
审稿时长
6-12 weeks
期刊介绍: EXCLI Journal publishes original research reports, authoritative reviews and case reports of experimental and clinical sciences. The journal is particularly keen to keep a broad view of science and technology, and therefore welcomes papers which bridge disciplines and may not suit the narrow specialism of other journals. Although the general emphasis is on biological sciences, studies from the following fields are explicitly encouraged (alphabetical order): aging research, behavioral sciences, biochemistry, cell biology, chemistry including analytical chemistry, clinical and preclinical studies, drug development, environmental health, ergonomics, forensic medicine, genetics, hepatology and gastroenterology, immunology, neurosciences, occupational medicine, oncology and cancer research, pharmacology, proteomics, psychiatric research, psychology, systems biology, toxicology
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