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在苏丹瓦德迈达尼地区进行的一项体外研究,评估恶性疟原虫对氯喹、周效磺胺/乙胺嘧啶、奎宁和甲氟喹的反应。

In vitro study assessing the response of plasmodium falciparum malaria to chloroquine, sulfadoxine/pyrimethamine, quinine and mefloquine in Wad Medani District, Sudan.

作者信息

Nour Bakri Y, Faragalla Ibrahim A, Saeed Osman K, Mohamadani A Abd Allah

机构信息

Faculty of Medicine, Blue Nile Research and Training Institute, University of Gezira, PO Box 101, Wad Medani, Sudan.

出版信息

Saudi Med J. 2006 Jun;27(6):808-12.

Abstract

OBJECTIVE

To assess the in vitro response of Plasmodium falciparum malaria to chloroquine (CQ), sulfadoxine/pyrimethamine (SDX/PYR), Quinine (QU) and Mefloquine (MQ) and monitoring their resistance.

METHODS

In 1999 to 2000, an in vitro study was carried out in Wad Medani district in Sudan. The standard protocol of the WHO in vitro micro-test Mark II was used for the selection of the subjects, the collection of blood samples, the culture techniques, the examination of the post-culture blood slides and the interpretation of the results.

RESULTS

In vitro micro-test Mark II were performed on 62 Plasmodium falciparum isolates. Of these isolates, 42 produced successful schizonts growth. The data obtained showed that 29 of 42 isolates (69%) were CQ resistant with an effective concentrations (EC); EC50 = 399.621 nM, EC90 = 2754.145 nM and EC99 = 13284.967 nM to inhibit the schizont maturation, the values of SDX/PYR showed a flat regression line as an indication of in vitro reduced response with an EC50 = 0.262 nM, EC90 = 147.390 nM and EC99 = 25722.296 nM, and the response to the QU indicated only one of the 42 isolates (2.4%) was resistant with an EC50 = 150.085 nM, EC90 = 822.825 nM and EC99 = 3293.667 nM, while all the 42 isolates were sensitive to MQ with an EC50 = 190.763 nM, EC90 = 615.125 nM and EC99 = 1597.504 nM.

CONCLUSION

The results of this study revealed a high degree of in vitro resistance to CQ and reduced in vitro response to SDX/PYR and QU, while MQ was fully sensitive. The effective concentrations to inhibit 50, 90 and 99% of the parasite maturation were determined for antimalarial drugs efficacy monitoring surveillance in Sudan.

摘要

目的

评估恶性疟原虫对氯喹(CQ)、周效磺胺/乙胺嘧啶(SDX/PYR)、奎宁(QU)和甲氟喹(MQ)的体外反应,并监测其耐药性。

方法

1999年至2000年,在苏丹的瓦德迈达尼地区开展了一项体外研究。采用世界卫生组织体外微量试验Mark II的标准方案来选择研究对象、采集血样、进行培养技术操作、检查培养后的血涂片以及解读结果。

结果

对62株恶性疟原虫分离株进行了体外微量试验Mark II。在这些分离株中,42株成功实现了裂殖体生长。所获数据显示,42株分离株中有29株(69%)对氯喹耐药,其抑制裂殖体成熟的有效浓度(EC)为:EC50 = 399.621纳摩尔/升,EC90 = 2754.145纳摩尔/升,EC99 = 13284.967纳摩尔/升;SDX/PYR的值显示为一条平缓的回归线,表明体外反应降低,EC50 = 0.262纳摩尔/升,EC90 = 147.390纳摩尔/升,EC99 = 25722.296纳摩尔/升;对奎宁的反应表明,42株分离株中只有1株(2.4%)耐药,EC50 = 150.085纳摩尔/升,EC90 = 822.825纳摩尔/升,EC99 = 3293.667纳摩尔/升;而所有42株分离株对甲氟喹敏感,EC50 = 190.763纳摩尔/升,EC90 = 615.125纳摩尔/升,EC99 = 1597.504纳摩尔/升。

结论

本研究结果显示恶性疟原虫对氯喹具有高度体外耐药性,对SDX/PYR和奎宁的体外反应降低,而对甲氟喹完全敏感。确定了抑制50%、90%和99%疟原虫成熟的有效浓度,用于苏丹抗疟药物疗效监测。

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