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糖基化环糊精纳米载体作为增强抗生素活性的“特洛伊木马”

Sugar-Grafted Cyclodextrin Nanocarrier as a "Trojan Horse" for Potentiating Antibiotic Activity.

作者信息

Li Min, Neoh Koon Gee, Xu Liqun, Yuan Liang, Leong David Tai, Kang En-Tang, Chua Kim Lee, Hsu Li Yang

机构信息

Department of Chemical and Biomolecular Engineering, National University of Singapore, Kent Ridge,, Singapore, 117585, Singapore.

Department of Biochemistry, National University of Singapore, Kent Ridge,, Singapore, 117543, Singapore.

出版信息

Pharm Res. 2016 May;33(5):1161-74. doi: 10.1007/s11095-016-1861-0. Epub 2016 Jan 20.

Abstract

PURPOSE

The use of "Trojan Horse" nanocarriers for antibiotics to enhance the activity of antibiotics against susceptible and resistant bacteria is investigated.

METHODS

Antibiotic carriers (CD-MAN and CD-GLU) are prepared from β-cyclodextrin grafted with sugar molecules (D-mannose and D-glucose, respectively) via azide-alkyne click reaction. The sugar molecules serve as a chemoattractant enticing the bacteria to take in higher amounts of the antibiotic, resulting in rapid killing of the bacteria.

RESULTS

Three types of hydrophobic antibiotics, erythromycin, rifampicin and ciprofloxacin, are used as model drugs and loaded into the carriers. The minimum inhibitory concentration of the antibiotics in the CD-MAN-antibiotic and CD-GLU-antibiotic complexes for Gram-negative Escherichia coli, Pseudomonas aeruginosa and Acinetobacter baumannii strains, and a number of Gram-positive Staphylococcus aureus strains, including the methicillin-resistant strains (MRSA), are reduced by a factor ranging from 3 to >100. The CD-MAN-antibiotic complex is also able to prolong the stability of the loaded antibiotic and inhibit development of intrinsic antibiotic resistance in the bacteria.

CONCLUSIONS

These non-cytotoxic sugar-modfied nanocarriers can potentiate the activity of existing antibiotics, especially against multidrug-resistant bacteria, which is highly advantageous in view of the paucity of new antibiotics in the pipeline.

摘要

目的

研究使用“特洛伊木马”纳米载体来增强抗生素对敏感菌和耐药菌的活性。

方法

通过叠氮-炔烃点击反应,由分别接枝了糖分子(D-甘露糖和D-葡萄糖)的β-环糊精制备抗生素载体(CD-MAN和CD-GLU)。糖分子作为化学引诱剂,诱使细菌摄取更多量的抗生素,从而快速杀灭细菌。

结果

使用三种疏水性抗生素红霉素、利福平和环丙沙星作为模型药物并载入载体。对于革兰氏阴性大肠杆菌、铜绿假单胞菌和鲍曼不动杆菌菌株,以及包括耐甲氧西林菌株(MRSA)在内的多种革兰氏阳性金黄色葡萄球菌菌株,CD-MAN-抗生素和CD-GLU-抗生素复合物中抗生素的最低抑菌浓度降低了3至>100倍。CD-MAN-抗生素复合物还能够延长载入抗生素的稳定性,并抑制细菌内在抗生素耐药性的发展。

结论

这些无细胞毒性的糖修饰纳米载体可以增强现有抗生素的活性,尤其是对多重耐药菌,鉴于正在研发的新抗生素数量稀少,这具有很大优势。

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