已发表论文

羧甲基壳聚糖修饰的光响应性山茶皂角苷配基衍生物阳离子脂质体的制备及抑菌作用

 

Authors Zhang J, Ye CZ, Liu ZY, Yang Q, Ye Y

Received 2 June 2019

Accepted for publication 4 October 2019

Published 1 November 2019 Volume 2019:14 Pages 8611—8626

DOI https://doi.org/10.2147/IJN.S218101

Checked for plagiarism Yes

Review by Single-blind

Peer reviewers approved by Dr Alexander Kharlamov

Peer reviewer comments 2

Editor who approved publication: Dr Lei Yang

Background: Bacterial resistance to antibiotics is a persistent and intractable problem. The sapogenin isolated from the seeds of Camellia oleifera  can inhibit antibiotic-resistant bacteria after structural modification.
Purpose: This study aims to improve sapogenin’s antibacterial activity and avoid bacterial resistance based on nano-preparation with photo responsiveness.
Methods: The liposome shell material of carboxymethyl chitosan-phosphatidyl ethanolamine (CMC-PE) was prepared using amidation reaction, and photo-responsive cationic (PCC) liposomes containing Camellia  sapogenin derivative (CSD) and photosensitizer pheophorbide-a were prepared by film dispersion method. Encapsulation efficiency, drug loading, zeta potential, particle size distribution, morphology and stability of the PCC liposomes were determined by HPLC, particle size analyzer, transmission electron microscopy (TEM) and fluorescence microscopy. Photo-responsive release of CSD in the PCC liposomes was determined by laser (0.5 mW/cm2) at 665 nm. Antibacterial activity of the PCC liposomes with or without irradiation was analyzed by MIC50, MBC, MBIC50, and bacterial morphology to evaluate the antibacterial effects on amoxicillin resistant Escherichia coli  and Staphylococcus aureus .
Results: Size distribution, zeta potential, encapsulation efficiency and drug loading of the PCC liposomes were 189.23 ± 2.12 nm, 18.80 ± 1.57 mV, 83.52 ± 1.53% and 2.83 ± 0.05%, respectively. The PCC liposomes had higher storage stability and gastrointestinal stability, and no obvious hemolytic toxicity to rabbit red blood cells and no cytotoxicity after incubation with Hela cells. The photosensitizer pheophorbide-a was uniformly dispersed in the phospholipid layer of the PCC liposomes and increased the CSD release after irradiation. The PCC liposomes could bind to bacteria and impaired their morphology and structure, and had significant bactericidal effect on amoxicillin resistant E. coli  and S. aureus .
Conclusion: The photo-responsive PCC liposomes are efficient antibacterial agents for avoidance of bacterial resistance against antibiotics.
Keywords: Camellia  sapogenin derivative, photo-responsive cationic liposomes, carboxymethyl chitosan, antibacterial effects, antibiotic substitutes




Figure 1 Structure and drug release mechanism of the PCC liposomes.