Pacheco Fabian, Barrera Alejandro, Ciro Yhors, Polo-Cerón Dorian, Salamanca Constain H, Oñate-Garzón José
Grupo de Investigación en Química y Biotecnología (QUIBIO), Facultad de Ciencias Básicas, Universidad Santiago de Cali, Cali 760035, Colombia.
Laboratorio de Investigación en Catálisis y Procesos (LICAP), Departamento de Química, Facultad de Ciencias Naturales y Exactas, Universidad del Valle, Cali 760001, Colombia.
Pharmaceutics. 2024 Aug 24;16(9):1115. doi: 10.3390/pharmaceutics16091115.
The natural evolution of microorganisms, as well as the inappropriate use of medicines, have accelerated the problem of drug resistance to many of the antibiotics employed today. Colistin, a lipopeptide antibiotic used as a last resort against multi-resistant strains, has also begun to present these challenges. Therefore, this study was focused on establishing whether colistin associated with chitosan nanoparticles could improve its antibiotic activity on an extremely resistant clinical isolate of , which is a clinically relevant Gram-negative bacterium. For this aim, nanoparticulate systems based on phytic acid cross-linked chitosan and loaded with colistin were prepared by the ionic gelation method. The characterization included particle size, polydispersity index-PDI, and zeta potential measurements, as well as thermal (DSC) and spectrophotometric (FTIR) analysis. Encapsulation efficiency was assessed by the bicinchoninic acid (BCA) method, while the antimicrobial evaluation was made following the CLSI guidelines. The results showed that colistin-loaded nanoparticles were monodispersed (PDI = 0.196) with a particle size of around 266 nm and a positive zeta potential (+33.5 mV), and were able to associate with around 65.8% of colistin and decrease the minimum inhibitory concentration from 16 μg/mL to 4 μg/mL. These results suggest that the association of antibiotics with nanostructured systems could be an interesting alternative to recover the antimicrobial activity on resistant strains.
微生物的自然进化以及药物的不当使用,加速了如今许多抗生素的耐药性问题。黏菌素作为一种用于对抗多重耐药菌株的脂肽类抗生素,也开始面临这些挑战。因此,本研究聚焦于确定与壳聚糖纳米粒结合的黏菌素是否能提高其对一种具有极强耐药性的临床分离菌株(一种具有临床相关性的革兰氏阴性菌)的抗菌活性。为此,采用离子凝胶法制备了基于植酸交联壳聚糖并负载黏菌素的纳米颗粒系统。表征包括粒径、多分散指数(PDI)、zeta电位测量,以及热分析(DSC)和分光光度分析(FTIR)。通过二辛可宁酸(BCA)法评估包封效率,同时按照CLSI指南进行抗菌评估。结果表明,负载黏菌素的纳米粒呈单分散(PDI = 0.196),粒径约为266 nm,zeta电位为正(+33.5 mV),并且能够结合约65.8%的黏菌素,并将最低抑菌浓度从16 μg/mL降至4 μg/mL。这些结果表明,抗生素与纳米结构系统的结合可能是恢复对耐药菌株抗菌活性的一种有趣的替代方法。
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