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用于疟疾早期治疗起始的奎宁栓剂配方——一项初步研究。

Formulation of quinine suppository for initiation of early treatment of malaria - a preliminary study.

作者信息

Soremekun Rebecca O, Silva Boladale O, Tayo Fola, Igwilo Cecilia I

机构信息

Department of Clinical Pharmacy and Biopharmacy, Faculty of Pharmacy, University of Lagos, PMB 12003 Lagos, Nigeria.

Department of Pharmaceutics, Faculty of Pharmacy, University of Lagos, PMB 12003 Lagos, Nigeria.

出版信息

Malariaworld J. 2012 Dec 10;3:14. doi: 10.5281/zenodo.10997879. eCollection 2012.

Abstract

BACKGROUND

In the management of malaria, there is the need for early initiation of treatment. An antimalarial drug for home use must be easy to administer, safe, effective and affordable. Parenteral quinine is the gold standard for treatment of severe malaria. A rectal formulation of quinine will therefore serve the purpose of early initiation of care in patients that lack easy access to medical centers. The main objective of this preliminary work was to develop a quinine suppository with adequate release properties that also meets the dual conditions of affordability and ease of administration.

MATERIALS AND METHODS

Cocoa butter and Fattibase™ were used in the preparation of suppositories containing 200 mg quinine bisulphate. The release profiles of formulations with varying concentrations of polysorbate 80 (0 - 5%) were evaluated by in vitro dissolution in pH 8 buffer medium.

RESULTS

The addition of polysorbate 80 improved the release of quinine significantly at 2 and 5%. Cocoa butter suppository with 1% polysorbate 80 released 73.6 mg quinine bisulphate in 1 hr while release from suppositories with 2% and 5% surfactant was higher. Fattibase™ suppositories had better release profiles than cocoa butter formulations. The formulation with 5% polysorbate 80 released 170 mg quinine in 1 hr. Formulations with the two bases released quinine in adequate quantities for the management of malaria.

CONCLUSIONS

The particle size of quinine is an important factor affecting the physical appearance and drug release from the suppository. The Fattibase™ suppositories were more stable but cost five times the price of the cocoa butter formulations. The cocoa butter formulations, however, still released quinine in sufficient quantities for the management of malaria. Cocoa butter formulations will be more affordable in resource-limited malaria-endemic regions of the world.

摘要

背景

在疟疾管理中,需要尽早开始治疗。用于家庭使用的抗疟药物必须易于给药、安全、有效且价格合理。肠胃外注射奎宁是治疗重症疟疾的金标准。因此,奎宁直肠给药制剂将有助于在难以前往医疗中心的患者中尽早开始治疗。这项初步工作的主要目标是开发一种具有适当释放特性且同时满足价格合理和易于给药双重条件的奎宁栓剂。

材料与方法

可可脂和Fattibase™用于制备含有200mg硫酸氢奎宁的栓剂。通过在pH 8缓冲介质中的体外溶出度评估含有不同浓度聚山梨酯80(0 - 5%)的制剂的释放曲线。

结果

添加聚山梨酯80在2%和5%时显著改善了奎宁的释放。含有1%聚山梨酯80的可可脂栓剂在1小时内释放73.6mg硫酸氢奎宁,而含有2%和5%表面活性剂的栓剂释放量更高。Fattibase™栓剂的释放曲线比可可脂制剂更好。含有5%聚山梨酯80的制剂在1小时内释放170mg奎宁。两种基质的制剂释放的奎宁量足以用于疟疾治疗。

结论

奎宁的粒径是影响栓剂外观和药物释放的重要因素。Fattibase™栓剂更稳定,但价格是可可脂制剂的五倍。然而,可可脂制剂仍能释放足够量的奎宁用于疟疾治疗。在世界上资源有限的疟疾流行地区,可可脂制剂将更具价格优势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8244/11153357/b2a24ceed514/MWJ-3-14-f1.jpg

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