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亚麻荠属(Bixaceae)和桂竹香属(L.)Mosyakin & Clemants(苋科)精油纳米脂质体配方治疗 。

L. (Bixaceae) and (L.) Mosyakin & Clemants (Amaranthaceae) Essential Oils Formulated in Nanocochleates against .

机构信息

Department of Pharmacy, Institute of Pharmacy and Food, Havana University, Havana 17100, Cuba.

Department of Physiological Science, Latin American School of Medical Sciences, Havana 11300, Cuba.

出版信息

Molecules. 2019 Nov 20;24(23):4222. doi: 10.3390/molecules24234222.

Abstract

Leishmaniasis is a group of neglected tropical diseases caused by protozoan parasites of the genus. The absence of effective vaccines and the limitations of current treatments make the search for effective therapies a real need. Different plant-derived essential oils (EOs) have shown antileishmanial effects, in particular from L. (EO-Bo) and (L.) Mosyakin & Clemants (EO-Da). In the present study, the EO-Bo and EO-Da, formulated in nanocochleates (EO-Bo-NC and EO-Da-NC, respectively), were evaluated in vitro and in vivo against . The EO-Bo-NC and EO-Da-NC did not increase the in vitro inhibitory activity of the EOs, although the EO-Bo-NC showed reduced cytotoxic effects. In the animal model, both formulations (30 mg/kg/intralesional route/every 4 days/4 times) showed no deaths or weight loss greater than 10%. In the animal (mouse) model, EO-Bo-NC contributed to the control of infection ( < 0.05) in comparison with EO-Bo treatment, while the mice treated with EO-Da-NC exhibited larger lesions ( < 0.05) compared to those treated with EO-Da. The enhanced in vivo activity observed for EO-Bo-NC suggests that lipid-based nanoformulations like nanocochleates should be explored for their potential in the proper delivery of drugs, and in particular, the delivery of hydrophobic materials for effective cutaneous leishmaniasis treatment.

摘要

利什曼病是一组由原生动物寄生虫引起的被忽视的热带病。缺乏有效的疫苗和当前治疗方法的局限性使得寻找有效的治疗方法成为一种真正的需求。不同的植物源性精油(EOs)已显示出抗利什曼原虫的作用,特别是来自 (EO-Bo)和 (L.)Mosyakin & Clemants(EO-Da)。在本研究中,纳米耳蜗(EO-Bo-NC 和 EO-Da-NC,分别)中的 EO-Bo 和 EO-Da 进行了体外和体内评估。EO-Bo-NC 和 EO-Da-NC 并没有增加 EOs 的体外抑制活性,尽管 EO-Bo-NC 显示出降低的细胞毒性作用。在动物模型中,两种制剂(30mg/kg/皮内途径/每 4 天/4 次)均未导致死亡或体重减轻超过 10%。在动物(小鼠)模型中,与 EO-Bo 治疗相比,EO-Bo-NC 有助于控制感染(<0.05),而用 EO-Da-NC 治疗的小鼠表现出更大的病变(<0.05)与用 EO-Da 治疗的小鼠相比。与 EO-Bo 相比,EO-Bo-NC 在体内观察到的增强活性表明,基于脂质的纳米制剂(如纳米耳蜗)应探索其在适当输送药物方面的潜力,特别是输送疏水性材料以有效治疗皮肤利什曼病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e864/6930544/43e22df350d0/molecules-24-04222-g001.jpg

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