Antimicrobial proanthocyanidin-chitosan composite nanoparticles loaded with gentamicin

被引:26
作者
Alfaro-Viquez, Emilia [1 ,2 ]
Esquivel-Alvarado, Daniel [2 ]
Madrigal-Carballo, Sergio [2 ]
Krueger, Christian G. [2 ]
Reed, Jess D. [1 ,2 ]
机构
[1] Univ Wisconsin, Mat Sci & Engn, 1415 Engn Dr, Madison, WI 53706 USA
[2] Univ Wisconsin, Reed Res Grp, Dept Anim Sci, 1675 Observ Dr, Madison, WI 53706 USA
基金
美国食品与农业研究所;
关键词
Proanthocyanidin; Chitosan; Gentamicin; Bacterial agglutination; Bacteriostatic and bactericidal activity; ESCHERICHIA-COLI INVASION; DELIVERY-SYSTEM; CONTROLLED-RELEASE; DRUG-DELIVERY; INFECTIONS;
D O I
10.1016/j.ijbiomac.2020.07.213
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cranberry proanthocyanidin-chitosan nanoparticles (PAC-CHT NPs) loaded with antibiotic gentamicin (GEN) (PAC-CHT-GEN NPs) were formulated and characterized according to size, polydispersity (PDI), surface charge, morphology, and encapsulation efficiency (EE). PAC-CHT-GEN NPs were evaluated for their ability to agglutinate E. coli, S. aureus, and P. aeruginosa and their bacteriostatic and bactericidal activity. Results indicate that the PACCHT-GEN NPs at 0.5:1.0, 1.0:1.0, and 2.0:1.0 weight ratios formed stable nanoparticles with sizes from 242.9 to 277.4 nm, a PDI from 0.344 to 0.391, and a zeta potential from 34.5 to 38.5 mV, and up to 94% EE. Results indicate that PAC-CHT-GEN NPs have the ability to agglutinate E. coli, S. aureus, and P. aeruginosa. Furthermore, PAC-CHTGEN NPs exhibited greater bactericidal activity than GEN alone. Results suggested PAC-CHT-GEN NPs form stable, round-shaped, and bioactive nanoparticles with the potential to be use in the treatment of bacterial infections. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:1500 / 1508
页数:9
相关论文
共 37 条
[1]   Gentamicin-loaded nanoparticles show improved antimicrobial effects towards Pseudomonas aeruginosa infection [J].
Abdelghany, Sharif M. ;
Quinn, Derek J. ;
Ingram, Rebecca J. ;
Gilmore, Brendan F. ;
Donnelly, Ryan F. ;
Taggart, Clifford C. ;
Scott, Christopher J. .
INTERNATIONAL JOURNAL OF NANOMEDICINE, 2012, 7 :4053-4063
[2]   Recent advances on chitosan-based micro- and nanoparticles in drug delivery [J].
Agnihotri, SA ;
Mallikarjuna, NN ;
Aminabhavi, TM .
JOURNAL OF CONTROLLED RELEASE, 2004, 100 (01) :5-28
[3]  
Ahmed SS, 2019, INT J HEALTH SCI-IJH, V13, P48
[4]   Chitosan as biomaterial in drug delivery and tissue engineering [J].
Ahsan, Saad M. ;
Thomas, Mathai ;
Reddy, Kranthi K. ;
Sooraparaju, Sujata Gopal ;
Asthana, Amit ;
Bhatnagar, Ira .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2018, 110 :97-109
[5]   Fluorimetric determination of gentamicin in dosage forms and biological fluids through derivatization with 4-chloro-7-nitrobenzo-2-oxa-1,3-diazole (NBD-Cl) [J].
Al-Majed, AA ;
Belal, F ;
Abounassif, MA ;
Khalil, NY .
MICROCHIMICA ACTA, 2003, 141 (1-2) :1-6
[6]   Characterization of proanthocyanidin-chitosan interactions in the formulation of composite nanoparticles using surface plasmon resonance [J].
Alfaro-Viquez, Emilia ;
Esquivel-Alvarado, Daniel ;
Madrigal-Carballo, Sergio ;
Krueger, Christian G. ;
Reed, Jess D. .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2020, 152 :1068-1076
[7]   Proanthocyanidin-chitosan composite nanoparticles prevent bacterial invasion and colonization of gut epithelial cells by extra-intestinal pathogenic Escherichia coli [J].
Alfaro-Viquez, Emilia ;
Esquivel-Alvarado, Daniel ;
Madrigal-Carballo, Sergio ;
Krueger, Christian G. ;
Reed, Jess D. .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2019, 135 :630-636
[8]   Cranberry proanthocyanidin-chitosan hybrid nanoparticles as a potential inhibitor of extra-intestinal pathogenic Escherichia coli invasion of gut epithelial cells [J].
Alfaro-Viquez, Emilia ;
Esquivel-Alvarado, Daniel ;
Madrigal-Carballo, Sergio ;
Krueger, Christian G. ;
Reed, Jess D. .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2018, 111 :415-420
[9]   An extract from date palm fruit (&ITPhoenix dactylifera&IT) acts as a co-agonist ligand for the nuclear receptor FXR and differentially modulates FXR target-gene expression&IT in vitro &IT [J].
Alfaro-Viquez, Emilia ;
Roling, Brent F. ;
Krueger, Christian G. ;
Rainey, Charlene J. ;
Reed, Jess D. ;
Ricketts, Marie-Louise .
PLOS ONE, 2018, 13 (01)
[10]   Synthesis of pyrazole-based Schiff bases of Chitosan: Evaluation of antimicrobial activity [J].
Anush, S. M. ;
Vishalakshi, B. ;
Kalluraya, B. ;
Manju, N. .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2018, 119 :446-452