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与植酸交联并负载黏菌素的壳聚糖纳米颗粒对广泛耐药细菌的合成、表征及生物学评价

Synthesis, Characterization, and Biological Evaluation of Chitosan Nanoparticles Cross-Linked with Phytic Acid and Loaded with Colistin against Extensively Drug-Resistant Bacteria.

作者信息

Pacheco Fabian, Barrera Alejandro, Ciro Yhors, Polo-Cerón Dorian, Salamanca Constain H, Oñate-Garzón José

机构信息

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.

出版信息

Pharmaceutics. 2024 Aug 24;16(9):1115. doi: 10.3390/pharmaceutics16091115.


DOI:10.3390/pharmaceutics16091115
PMID:39339153
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11435368/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e70/11435368/77a53fee5188/pharmaceutics-16-01115-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e70/11435368/3e23f8a95198/pharmaceutics-16-01115-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e70/11435368/89935ee5a8e1/pharmaceutics-16-01115-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e70/11435368/fb7866cb056a/pharmaceutics-16-01115-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e70/11435368/468fce6df84d/pharmaceutics-16-01115-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e70/11435368/77a53fee5188/pharmaceutics-16-01115-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e70/11435368/3e23f8a95198/pharmaceutics-16-01115-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e70/11435368/89935ee5a8e1/pharmaceutics-16-01115-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e70/11435368/fb7866cb056a/pharmaceutics-16-01115-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e70/11435368/468fce6df84d/pharmaceutics-16-01115-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0e70/11435368/77a53fee5188/pharmaceutics-16-01115-g005.jpg

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Synthesis, Characterization, and Biological Evaluation of Chitosan Nanoparticles Cross-Linked with Phytic Acid and Loaded with Colistin against Extensively Drug-Resistant Bacteria.

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[1]
Advanced therapeutic strategy for managing surgical site infections with natural nanoemulsion-antimicrobial combination.

Front Pharmacol. 2025-7-2

[2]
Development, Characterization, and Antimicrobial Evaluation of Hybrid Nanoparticles (HNPs) Based on Phospholipids, Cholesterol, Colistin, and Chitosan Against Multidrug-Resistant Gram-Negative Bacteria.

Pharmaceutics. 2025-2-1

本文引用的文献

[1]
In Vitro Evaluation of Colistin Conjugated with Chitosan-Capped Gold Nanoparticles as a Possible Formulation Applied in a Metered-Dose Inhaler.

Antibiotics (Basel). 2024-7-6

[2]
The Antimicrobial Effects of Colistin Encapsulated in Chelating Complex Micelles for the Treatment of Multi-Drug-Resistant Gram-Negative Bacteria: A Pharmacokinetic Study.

Antibiotics (Basel). 2023-4-30

[3]
Succinyl Chitosan-Colistin Conjugates as Promising Drug Delivery Systems.

Int J Mol Sci. 2022-12-22

[4]
Silver Nanoparticles Conjugated with Colistin Enhanced the Antimicrobial Activity against Gram-Negative Bacteria.

Molecules. 2022-9-7

[5]
Integrating In Vitro and In Silico Analysis of a Cationic Antimicrobial Peptide Interaction with Model Membranes of Colistin-Resistant Strains.

Pharmaceutics. 2022-6-12

[6]
Impact of colistin and colistin-loaded on alginate nanoparticles on pigs infected with a colistin-resistant enterotoxigenic Escherichia coli strain.

Vet Microbiol. 2022-3

[7]
Preparation and Evaluation of the Antibacterial Effect of Chitosan Nanoparticles Containing Ginger Extract Tailored by Central Composite Design.

Adv Pharm Bull. 2021-9

[8]
The Epidemiology and Pathogenesis and Treatment of Pseudomonas aeruginosa Infections: An Update.

Drugs. 2021-12

[9]
Preparation of chitosan-SiO nanoparticles by ultrasonic treatment and its effect on the properties of starch film.

Int J Biol Macromol. 2021-10-31

[10]
Factors Influencing the Antibacterial Activity of Chitosan and Chitosan Modified by Functionalization.

Int J Mol Sci. 2021-7-12

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