» Articles » PMID: 39696307

Chitosan-casein As Novel Drug Delivery System for Transferring Phyllanthus Emblica to Inhibit Pseudomonas Aeruginosa

Overview
Journal BMC Biotechnol
Publisher Biomed Central
Specialty Biotechnology
Date 2024 Dec 19
PMID 39696307
Authors
Affiliations
Soon will be listed here.
Abstract

This study investigated the ability of Phyllanthus emblica encapsulated within chitosan-coated casein (CS-casein-Amla) nanoparticles to inhibit the growth of multi-drug-resistant Pseudomonas aeruginosa (P. aeruginosa) bacteria and prevent the formation of biofilms. The MDR strains underwent screening, and the morphological characteristics of the resulting nanoparticles were assessed using SEM, DLS, and FTIR. In addition, the efficacy of encapsulation, stability, and drug release were evaluated. The PpgL, BdlA, and GacA biofilm gene transcription quantities were quantified by quantitative real-time PCR. Simultaneously, the nanoparticles were assessed for their antibacterial and cytotoxic effects using the well diffusion and MTT procedures. CS-casein-Amla nanoparticles with a size of 500.73 ± 13 nm, encapsulation efficiency of 76.33 ± 0.81%, and stability for 60 days at 4 °C (Humidity 30%) were created. The biological analysis revealed that CS-casein-Amla nanoparticles exhibited strong antibacterial properties. This was shown by their capacity to markedly reduce the transcription of PpgL, BdlA, and GacA biofilm genes at a statistically significant value of p ≤ 0.01. The nanoparticles demonstrated decreased antibiotic resistance compared to unbound Amla and CS-casein. Compared to Amla, CS-casein-Amla nanoparticles showed very little toxicity against HDF cells at dosages ranging from 1.56 to 100 µg/mL (p ≤ 0.01). The results highlight the potential of CS-casein-Amla nanoparticles as a significant advancement in combating highly resistant P. aeruginosa. The powerful antibacterial properties of CS-casein-Amla nanoparticles against P. aeruginosa MDR strains, which are highly resistant pathogens of great concern, may catalyze the development of novel antibacterial research approaches.

References
1.
Qin S, Xiao W, Zhou C, Pu Q, Deng X, Lan L . Pseudomonas aeruginosa: pathogenesis, virulence factors, antibiotic resistance, interaction with host, technology advances and emerging therapeutics. Signal Transduct Target Ther. 2022; 7(1):199. PMC: 9233671. DOI: 10.1038/s41392-022-01056-1. View

2.
de Sousa T, Hebraud M, Alves O, Costa E, Maltez L, Pereira J . Study of Antimicrobial Resistance, Biofilm Formation, and Motility of Derived from Urine Samples. Microorganisms. 2023; 11(5). PMC: 10224020. DOI: 10.3390/microorganisms11051345. View

3.
Botelho J, Grosso F, Peixe L . Antibiotic resistance in Pseudomonas aeruginosa - Mechanisms, epidemiology and evolution. Drug Resist Updat. 2019; 44:100640. DOI: 10.1016/j.drup.2019.07.002. View

4.
Alves M, Bouchami O, Tavares A, Cordoba L, Santos C, Miragaia M . New Insights into Antibiofilm Effect of a Nanosized ZnO Coating against the Pathogenic Methicillin Resistant Staphylococcus aureus. ACS Appl Mater Interfaces. 2017; 9(34):28157-28167. DOI: 10.1021/acsami.7b02320. View

5.
Deena S, Kumar G, Vickram A, Singhania R, Dong C, Rohini K . Efficiency of various biofilm carriers and microbial interactions with substrate in moving bed-biofilm reactor for environmental wastewater treatment. Bioresour Technol. 2022; 359:127421. DOI: 10.1016/j.biortech.2022.127421. View