磷酸二氢青蒿素-哌喹固体脂基片抗疟疾性能评价。

Chime Salome A, A. A., Onunkwo Godswill C
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引用次数: 0

摘要

以二氢青蒿素-磷酸哌喹为代表的青蒿素为基础的联合疗法(ACTs)是治疗恶性疟原虫疟疾的一线药物之一。然而,对ACTs的耐药性的出现表明有必要开发新的缓释治疗,以确保最大的生物利用度。目的采用固化反胶束溶液(SRMS)制备双氢青蒿素(DHA)-磷酸哌喹(PQ)缓释片。方法采用不同比例的Phospholipon®90H和Softisan®154融合制备SRMS,并对其进行表征。该片剂采用自行制作并经验证的模具制备。测试了配方的重量、硬度、脆性、软化时间、侵蚀时间和体内外溶出率的均匀性。采用改良的小鼠彼得4天抑制试验研究其抗疟作用。结果分析采用单因素方差分析(ANOVA)。结果胶囊光滑,平均质量为1300±0.06 ~ 1312±0.11 mg, DHA含量为61 mg, PQ含量为450 mg。波洛沙姆188 (R2、S2、T2批)配制的片剂硬度为7.1 ~ 9.0 Kgf,软化时间为29.50±1.90 min,侵蚀时间为62.00±2.58 ~ 152.00±1.89 min,显著缩短了软化和侵蚀时间(p < 0.05)。体外释放结果表明,优化后的制剂在12 h释放量最大。第7天,与市售制剂相比,优化后的制剂的寄生虫清除率和体内吸收率显著提高(p < 0.05)。结论基于SRMS的dha - pq片剂比压缩片剂更容易生产,成本相对较低。由于它们的缓释特性和提高的生物利用度,它们还显示出对疟疾的治疗效果特别好,并被推荐给制药公司进行进一步研究。
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Assessment of the anti-malarial properties of dihydroartemisinin-piperaquine phosphate solid lipid-based tablets.
BACKGROUND Artemisinin based combination therapies (ACTs) typified by dihydroartemisinin-piperaquine phosphate is one of the first line drugs used in the treatment of Plasmodium falciparum malaria. However, the emergence of drug resistance to ACTs show the necessity to develop novel sustained release treatment in order to ensure maximum bioavailability. OBJECTIVES To formulate dihydroartemisinin (DHA)-piperaquine phosphate (PQ) sustained release tablets based on solidified reverse micellar solutions (SRMS). METHODS The SRMS was prepared by fusion using varying ratios of Phospholipon® 90H and Softisan® 154 and characterised. The tablets were prepared by using an in-house made and validated mould. The formulations were tested for uniformity of weight, hardness, friability, softening time, erosion time and in vitro-in vivo dissolution rate. Anti malarial properties were studied by modified Peter's 4-days suppressive test in mice. One-way analysis of variance (ANOVA) was used in analysis of results. RESULTS Smooth caplets, with average weight of 1300 ± 0.06 to 1312 ± 0.11 mg, drug content of 61 mg for DHA and t 450 mg for PQ. Tablets hardness ranged from 7.1 to 9.0 Kgf and softening time of 29.50 ± 1.90 min. Erosion time of 62.00 ± 2.58 to 152.00 ± 1.89 min were obtained for tablets formulated with Poloxamer 188 (Batches R2, S2 and T2) which significantly reduced the softening and erosion time (p < 0.05). In vitro release showed that optimized formulation had maximum release at 12 h. Formulations exhibited significantly higher parasitaemia clearance and in vivo absorption compared to marketed formulations at day 7 (p < 0.05). CONCLUSION DHA-PQ tablets based on SRMS is much easier and relatively cheaper to produce than compressed tablets. They also showed exceptionally better treatment of malaria owing to their sustained release properties and improved bioavailability and is recommended to Pharmaceutical companies for further studies.
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