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含五环三萜的聚氨酯纳米结构的体外抗增殖和抗菌评估

Anti-proliferative and antibacterial in vitro evaluation of the polyurethane nanostructures incorporating pentacyclic triterpenes.

作者信息

Oprean Camelia, Zambori Csilla, Borcan Florin, Soica Codruta, Zupko Istvan, Minorics Renata, Bojin Florina, Ambrus Rita, Muntean Delia, Danciu Corina, Pinzaru Iulia Andreea, Dehelean Cristina, Paunescu Virgil, Tanasie Gabriela

机构信息

a Faculty of Pharmacy , University of Medicine and Pharmacy "Victor Babeş" , Timişoara , România.

b Faculty of Medicine , University of Medicine and Pharmacy "Victor Babeş" , Timişoara , România.

出版信息

Pharm Biol. 2016 Nov;54(11):2714-2722. doi: 10.1080/13880209.2016.1180538. Epub 2016 May 9.

Abstract

CONTEXT

Oleanolic and ursolic acids are antitumor and antibacterial agents which are extensively studied. Their major disadvantage is the poor water solubility which limits their applications.

OBJECTIVES

Oleanolic and ursolic acid were encapsulated into polyurethane nanostructures that act as drug carriers. In order to evaluate the effectiveness of the particles, anti-microbial and anti-proliferative activity compared to un-encapsulated active compounds was tested.

MATERIALS AND METHODS

Using an interfacial polycondensation technique, combined with spontaneous emulsification, structures with nanoscale dimensions were obtained. Scanning electron microscopy, differential scanning calorimetry and X-ray assays confirmed the encapsulation process. Concentrations of 10 and 30 μM particles and un-encapsulated compounds were tested by MTT viability assay for several breast cancer lines, with an exposure time of 72 h. For the antibacterial studies, the dilution method with MIC determination was used.

RESULTS

Ursolic acid had an excellent inhibitory effect with IC value of 2.47, 1.20, 1.26 and 1.34 μM on MCF7, T47D, MDA-MB-231 and MDA-MB-361, respectively. Oleanolic acid did not show anti-proliferative activity. The pure compounds showed their antibacterial activity only against Bacillus species and Candida albicans, but MIC values were too high to be considered efficient antimicrobial agents (2280 and 4570 μg mL  , respectively). Polyurethane nanoparticles which incorporated the agents did not show any biological activity.

DISCUSSION AND CONCLUSION

Although the active compounds did not fully exert their anti-proliferative activity following encapsulation inside polymeric nanoparticles, in vivo evaluation is needed in order to obtain an exhaustive conclusion, as the active compounds could be released as a result of metabolic activity.

摘要

背景

齐墩果酸和熊果酸是经过广泛研究的抗肿瘤和抗菌剂。它们的主要缺点是水溶性差,这限制了它们的应用。

目的

将齐墩果酸和熊果酸封装到作为药物载体的聚氨酯纳米结构中。为了评估这些颗粒的有效性,测试了与未封装的活性化合物相比的抗菌和抗增殖活性。

材料与方法

采用界面缩聚技术,结合自发乳化,获得了纳米级尺寸的结构。扫描电子显微镜、差示扫描量热法和X射线分析证实了封装过程。通过MTT活力测定法对几种乳腺癌细胞系测试了10和30μM颗粒及未封装化合物的浓度,暴露时间为72小时。对于抗菌研究,使用了测定最低抑菌浓度的稀释法。

结果

熊果酸对MCF7、T47D、MDA-MB-231和MDA-MB-361的IC值分别为2.47、1.20、1.26和1.34μM,具有优异的抑制作用。齐墩果酸未显示抗增殖活性。纯化合物仅对芽孢杆菌属和白色念珠菌显示抗菌活性,但最低抑菌浓度值过高,不能被视为有效的抗菌剂(分别为2280和4570μg/mL)。掺入这些药剂的聚氨酯纳米颗粒未显示任何生物活性。

讨论与结论

尽管活性化合物在封装到聚合物纳米颗粒中后未充分发挥其抗增殖活性,但仍需要进行体内评估以得出详尽的结论,因为活性化合物可能会因代谢活性而释放。

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