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Preparation, characterization and in-vitro efficacy of quercetin loaded liquid crystalline nanoparticles for the treatment of asthma
被引:33
|作者:
Yong, David Ong Cherk
[1
]
Saker, Sanggetha Raja
[1
]
Wadhwa, Ridhima
[2
,3
]
Chellappan, Dinesh Kumar
[4
]
Madheswaran, Thiagarajan
[5
]
Panneerselvam, Jithendra
[5
]
Tambuwala, Murtaza M.
[6
]
Bakshi, Hamid A.
[6
]
Kumar, Pradeep
[7
]
Pillay, Viness
[7
]
Gupta, Gaurav
[8
]
Oliver, Brian G.
[9
]
Wark, Peter
[10
,11
]
Hsu, Alan
[10
,11
]
Hansbro, Philip Michael
[2
,9
,10
,11
]
Dua, Kamal
[2
,3
,10
,11
]
Zeeshan, Farrukh
[5
]
机构:
[1] Int Med Univ, Sch Pharm, Kuala Lumpur 57000, Malaysia
[2] Centenary Inst, Ctr Inflammat, Sydney, NSW 2050, Australia
[3] Univ Technol Sydney, Grad Sch Hlth, Discipline Pharm, Ultimo, NSW 2007, Australia
[4] Int Med Univ, Sch Pharm, Dept Life Sci, Kuala Lumpur 57000, Malaysia
[5] Int Med Univ, Sch Pharm, Dept Pharmaceut Technol, Kuala Lumpur 57000, Malaysia
[6] Ulster Univ, Sch Pharm & Pharmaceut Sci, London, England
[7] Univ Witwatersrand, Fac Hlth Sci, Wits Adv Drug Delivery Platform Res Unit, Dept Pharm & Pharmacol,Sch Therapeut Sci, Johannesburg, South Africa
[8] Suresh Gyan Vihar Univ, Sch Pharm, Mahal Rd, Jaipur 302017, Rajasthan, India
[9] Univ Technol Sydney, Fac Sci, Sch Life Sci, Ultimo, NSW 2007, Australia
[10] Univ Newcastle, Prior Res Ctr Hlth Lungs, Hunter Med Res Inst, Callaghan, NSW 2308, Australia
[11] Univ Newcastle, Sch Biomed Sci & Pharm, Callaghan, NSW 2308, Australia
关键词:
Quercetin;
Liquid crystalline nanoparticles;
Asthma;
Inflammation;
BCi-NS1.1;
NF-KAPPA-B;
DRUG-DELIVERY;
CANCER-CELLS;
MONOOLEIN;
CURCUMIN;
EXPRESSION;
CUBOSOMES;
RELEASE;
NANOTECHNOLOGY;
OPTIMIZATION;
D O I:
10.1016/j.jddst.2019.101297
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
The present study aims to formulate quercetin loaded liquid crystalline nanoparticles (LCN) and surface modified liquid crystalline nanoparticles (sm-LCN) as well as investigate their anti-inflammatory activity in human primary bronchial epithelial cell line (BCi-NS1.1) induced with lipopolysaccharide (LPS). Quercetin LCN were prepared using ultrasonication method. The formulated LCNs and sm-LCNs were characterised in terms of particle size, zeta potential as well as the drug encapsulation efficiency. Furthermore, their morphology and in vitro release profile were also studied. In addition, the anti-inflammatory activity of quercetin LCN and sm-LCNs were evaluated by measuring the concentration of pro-inflammatory markers namely interleukin (IL)-1 beta, IL-6 and IL-8 in BCI-NS1.1 cell lines via cytometric bead array. The molecular mechanism inherent to the inclusion of quercetin into monoolein nanosystem and surface modification of the nanosystem with chitosan was elucidated via molecular mechanics simulations. Quercetin LCN and sm-LCN significantly (p < 0.05) decreased the production of IL-1 beta, IL-6 and IL-8 compared to LPS only group. Encapsulation of quercetin into LCN and sm-LCN further enhanced its anti-inflammatory activity compared to quercetin in dimethyl sulfoxide (DMSO). In addition to that, quercetin LCN and sm-LCN also exhibited comparable activity to fluticasone in terms of significantly (p < 0.05) reducing the production of IL-1 beta and IL-6. Quercetin loaded LCN and sm-LCN could be a potential therapeutic intervention for asthma as they are efficacious in suppressing the production of key pro-inflammatory cytokines associated with the development of asthma.
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