Stepanova Mariia, Levit Mariia, Egorova Tatiana, Nashchekina Yulia, Sall Tatiana, Demyanova Elena, Guryanov Ivan, Korzhikova-Vlakh Evgenia
Institute of Macromolecular Compounds of Russian Academy of Sciences, 199004 St. Petersburg, Russia.
Institute of Highly Pure Biopreparations, 197110 St. Petersburg, Russia.
Pharmaceutics. 2024 Aug 17;16(8):1080. doi: 10.3390/pharmaceutics16081080.
Growing resistance to traditional antibiotics poses a global threat to public health. In this regard, modification of known antibiotics, but with limited applications due to side effects, is one of the extremely promising approaches at present. In this study, we proposed the synthesis of novel complex polymeric conjugates of the peptide antibiotic colistin (CT). A biocompatible and water-soluble synthetic glycopolymer, namely, poly(2-deoxy-2-methacrylamido--glucose) (PMAG), was used as a polymer carrier. In addition to monoconjugates containing CT linked to PMAG by hydrolyzable and stable bonds, a set of complex conjugates also containing the siderophore deferoxamine (DFOA) and vitamin B12 was developed. The structures of the conjugates were confirmed by H NMR and FTIR-spectroscopy, while the compositions of conjugates were determined by UV-Vis spectrophotometry and HPLC analysis. The buffer media with pH 7.4, corresponding to blood or ileum pH, and 5.2, corresponding to the intestinal pH after ingestion or pH in the focus of inflammation, were used to study the release of CT. The resulting conjugates were examined for cytotoxicity and antimicrobial activity. All conjugates showed less cytotoxicity than free colistin. A Caco-2 cell permeability assay was carried out for complex conjugates to simulate the drug absorption in the intestine. In contrast to free CT, which showed very low permeability through the Caco-2 monolayer, the complex polymeric conjugates of vitamin B12 and CT provided significant transport. The antimicrobial activity of the conjugates depended on the conjugate composition. It was found that conjugates containing CT linked to the polymer by a hydrolyzable bond were found to be more active than conjugates with a non-hydrolyzable bond between CT and PMAG. Conjugates containing DFOA complexed with Fe were characterized by enhanced antimicrobial activity against compared to other conjugates.
对传统抗生素的耐药性不断增加对全球公共卫生构成威胁。在这方面,对已知抗生素进行修饰,但由于副作用其应用有限,是目前极具前景的方法之一。在本研究中,我们提出合成肽抗生素黏菌素(CT)的新型复合聚合物缀合物。一种生物相容性且水溶性的合成糖聚合物,即聚(2-脱氧-2-甲基丙烯酰胺基-α-D-葡萄糖)(PMAG),被用作聚合物载体。除了通过可水解和稳定键与PMAG连接的含CT的单缀合物外,还开发了一组还含有铁载体去铁胺(DFOA)和维生素B12的复合缀合物。通过1H NMR和FTIR光谱确认缀合物的结构,同时通过紫外-可见分光光度法和HPLC分析确定缀合物的组成。使用pH 7.4(对应于血液或回肠pH)和5.2(对应于摄入后肠道pH或炎症部位pH)的缓冲介质来研究CT的释放。对所得缀合物进行细胞毒性和抗菌活性检测。所有缀合物的细胞毒性均低于游离黏菌素。对复合缀合物进行Caco-2细胞通透性测定以模拟药物在肠道中的吸收。与在Caco-2单层中通透性非常低的游离CT相反,维生素B12和CT的复合聚合物缀合物具有显著的转运能力。缀合物的抗菌活性取决于缀合物组成。发现通过可水解键与聚合物连接的含CT的缀合物比CT与PMAG之间具有不可水解键的缀合物更具活性。与其他缀合物相比,含有与铁络合的DFOA的缀合物对……具有增强的抗菌活性。