आईएसएसएन: 2278-0238

फार्मेसी और जीवन विज्ञान में अनुसंधान और विकास के अंतर्राष्ट्रीय जर्नल

खुला एक्सेस

हमारा समूह 1000 से अधिक वैज्ञानिक सोसायटी के सहयोग से हर साल संयुक्त राज्य अमेरिका, यूरोप और एशिया में 3000+ वैश्विक सम्मेलन श्रृंखला कार्यक्रम आयोजित करता है और 700+ ओपन एक्सेस जर्नल प्रकाशित करता है जिसमें 50000 से अधिक प्रतिष्ठित व्यक्तित्व, प्रतिष्ठित वैज्ञानिक संपादकीय बोर्ड के सदस्यों के रूप में शामिल होते हैं।

ओपन एक्सेस जर्नल्स को अधिक पाठक और उद्धरण मिल रहे हैं
700 जर्नल और 15,000,000 पाठक प्रत्येक जर्नल को 25,000+ पाठक मिल रहे हैं

में अनुक्रमित
  • RefSeek
  • हमदर्द विश्वविद्यालय
  • ईबीएससीओ एज़
  • पबलोन्स
  • आईसीएमजेई
इस पृष्ठ को साझा करें

अमूर्त

Antimalarial drug discovery and development: Issues and prospects

Dipak Chetia

There was no significant progress in the reduction of malaria cases globally during the period 2015-2017 as per the latest epidemiological report (WHO, Malaria Report 2018). The malaria affected countries mainly rely on Artemisinin-based Combination Therapy (ACT) as no new drug has been discovered during the last couple of years. Therefore, the discovery of new antimalarial drugs to target the parasite at various stages of its life cycle is an urgent necessity to address the current stagnant therapeutic situation as well as to fight against the rapidly emerging resistant strains of the malaria parasites. The objective of the presentation is to highlight the achievements and shortcomings, possibilities of working on new areas for development of potent antimalarial drugs, problems and issues in the screening of antimalarial compounds, necessity for development of easy, affordable and fast screening method. Salient points related to current status and possible newer research targets to be taken into consideration for antimalarial drug discovery and development shall be systematically discussed and deliberated (Figure 1). The prime target of currently used antimalarial drugs is the erythrocytic stage of the parasite and except few, others show very less therapeutic efficacy individually. Additionally, most of these drugs are not effective against resistant malaria. Potent antimalarial drug candidates based on novel targets need to be developed not only for erythrocytic stage but also to target the parasite at other stages which may work by different mechanism of action against the parasites. There is a need for developing easier, affordable and fast screening method to enable more medicinal chemists to involve in the new antimalarial drug discovery and development programmes. The development of most effective and long acting chemicals/ drugs for malaria intervention is equally important in the control of malaria.