Heparin increases the antibiotic efficacy of colistin

G. P. Szekeres, E. Hanozin, Robyn Diehn, Jan Horlebein, Lukasz Polewski, Andreas Zappe, D. Lauster, K. Pagel
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Abstract

The increasing antibiotic resistance in bacteria is an alarming phenomenon all around the world. Certain strains have developed resistance against multiple antimicrobial molecules, in which cases, the final option is to use a last-resort drug. These drugs, however, are last-resort for a reason: they can pose serious risk on vital organ functions in the patient. To mitigate the risk of severe side-effects and to reduce the rate of bacterial mutation, co-administration with other molecules that increase their efficacy seems to be the only suitable option. This leads to a reduced dose while maintaining the same level of antibiotic activity within the body. In this study, the effect of heparin derivatives on the antibiotic activity of colistin and their interactions were studied by ion mobility, mass spectrometry, and bacterium growth assays. The results show that during the association of colistin and heparin, they retain their structure while higher-stoichiometry complexes can form. When long-chain heparin is co-administered, multiple colistin molecules can associate with it, which increases the antibiotic activity by ∼40% relative to the sole administration of colistin.
肝素提高粘菌素的抗生素疗效
细菌中抗生素耐药性的增加是世界各地令人担忧的现象。某些菌株对多种抗菌分子产生了耐药性,在这种情况下,最后的选择是使用最后的药物。然而,这些药物是最后的手段,原因是:它们会对患者的重要器官功能造成严重风险。为了减轻严重副作用的风险并降低细菌突变率,与其他分子联合给药以提高其疗效似乎是唯一合适的选择。这导致剂量减少,同时在体内保持相同水平的抗生素活性。在本研究中,通过离子迁移率、质谱和细菌生长测定研究了肝素衍生物对粘菌素抗生素活性的影响及其相互作用。结果表明,在粘菌素和肝素结合的过程中,它们保持了结构,同时可以形成更高化学计量的复合物。当长链肝素联合给药时,多个粘菌素分子可以与之结合,这使抗生素活性比单独给药粘菌素增加了约40%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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