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新型纳米壳聚糖两性霉素 B 制剂对利什曼原虫有显著改善作用。

Novel nano-sized chitosan amphotericin B formulation with considerable improvement against Leishmania major.

机构信息

Department of Clinical Research, Pasteur Institute of Iran, Tehran, Iran.

Department of Radiopharmacy, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Nanomedicine (Lond). 2018 Dec;13(24):3129-3147. doi: 10.2217/nnm-2018-0063. Epub 2018 Nov 22.

DOI:10.2217/nnm-2018-0063
PMID:30463469
Abstract

AIM

Improvement in the treatment of Leishmania major's pathological effects through increasing the dose of amphotericin B loaded into nanochitosan.

MATERIALS & METHODS: The phase separation method was used for nanochitosan synthesis and amphotericin loading. Also a novel solvent was designed and the nanodrug efficacy was evaluated in vitro and in vivo (pathology) environments.

RESULTS

The drug loading efficiency of 90%, along with slow drug-release with cellular uptake of 98.6% was achieved. The novel solvent was composed of 10% acetic acid, and it was succeeded to dissolve AK10 mg/kg. Also, AK10 mg/kg had no side effects in in vitro and in vivo environments. In addition, the complete wound healing and parasite inhibition were achieved by using AK10 mg/kg in terms of improvement the treatment indicators.

CONCLUSION

Increasing the therapeutic dose of AK to 10 mg/kg caused the successful treatment of L. major's pathological effects in in vitro and in vivo environments.

摘要

目的

通过增加纳米壳聚糖负载两性霉素 B 的剂量来改善利什曼原虫病理效应的治疗效果。

材料与方法

采用相分离法合成纳米壳聚糖并负载两性霉素 B。还设计了一种新型溶剂,并在体外和体内(病理学)环境中评估了纳米药物的疗效。

结果

实现了 90%的药物载药量,以及 98.6%的细胞摄取的缓慢药物释放。新型溶剂由 10%的乙酸组成,成功溶解了 AK10mg/kg。此外,AK10mg/kg 在体外和体内环境中均无副作用。此外,通过使用 AK10mg/kg,在改善治疗指标方面,完全实现了伤口愈合和寄生虫抑制,从而成功治疗了 L. major 的病理效应。

结论

将 AK 的治疗剂量增加到 10mg/kg 导致在体外和体内环境中成功治疗 L. major 的病理效应。

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