In Vivo and in Silico Trypanocidal Activity Evaluation of (-)-Cubebin Encapsulated in PLGA Microspheres as Potential Treatment in Acute Phase

被引:7
作者
Neres, Nayara B. R. [1 ]
Montagnini, Daniel [1 ]
Ferreira, Daniele S. [1 ]
Parreira, Renato L. T. [1 ]
Orenha, Renato P. [1 ]
Lima, Thais C. [1 ]
Molina, Eduardo F. [1 ]
Cunha, Wilson R. [1 ]
Silva, Marcio L. A. [1 ]
Esperandim, Viviane R. [1 ]
机构
[1] Univ Franca, Nucleo Pesquisas Ciencias Exatas & Tecnol, BR-14404600 Franca, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Chagas disease; (− )-cubebin; lignans; molecular docking; PLGA; TRYPANOSOMA-CRUZI; CHAGAS-DISEASE; NATURAL-PRODUCTS; NANOPARTICLES; DRUG; PHARMACOKINETICS; DERIVATIVES; HYPOCRELLIN; MECHANISMS; DELIVERY;
D O I
10.1002/cbdv.202100052
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this study, the trypomastigotes of a Y strain of Trypanosoma cruzi were inoculated intraperitoneally into male BALB/c mice weighing approximately 25 g each, which were divided into groups for evaluation of the trypanocidal activity. For the treatment of experimental groups, encapsulated and unencapsulated (-)-cubebin, Benznidazole, and two groups as negative controls were used. The encapsulated (-)-cubebin showed a 68.1 % encapsulation efficiency. The parasitemia peak of substances remained around the 9(th) day after the observed reduction in the number of circulating trypomastigotes. The encapsulated (-)-cubebin and (-)-cubebin unloaded showed a decrease of 61.3 % and 58.5 % in the number of parasites as compared to the negative control, respectively. Moreover, animals treated with encapsulated (-)-cubebin had a higher survival time as compared to the other groups. In conclusion, the results obtained were more promising for encapsulated (-)-cubebin as compared to unloaded particles.
引用
收藏
页数:8
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