Biogenic gold nanoparticles against wild and resistant type visceral leishmaniasis

被引:6
作者
Das, Suvadra [1 ]
Halder, Asim [1 ]
Roy, Partha [2 ]
Mukherjee, Arup [1 ]
机构
[1] Univ Calcutta, Dept Chem Technol, 92 APC Rd, Kolkata 700009, W Bengal, India
[2] Adamas Univ, Dept Pharmaceut Technol, Kolkata 700126, W Bengal, India
关键词
Gallic acid; gold nanoparticle; visceral leishmaniasis; polyphenols; GALLIC ACID; DRUG-DELIVERY; ANTIOXIDANT; APOPTOSIS; LIPOSOMES; CURCUMIN; SYSTEMS; CELLS;
D O I
10.1016/j.matpr.2018.01.086
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Leishmaniasis is a WHO notified neglected tropical disease and the lethal visceral leishmaniasis variant is endemic in Indian subcontinent. Gold nanoparticles (Aunp) have emerged as veritable tools in drug delivery because of their higher residence time in systemic circulation compared to other nanocarriers. Polyphenolic compound Gallic acid is used for bio-rated synthesis and in situ functionalization for GAunp. Synthesized nanoparticle exhibited surface plasmon response at 530nm and zeta potential of -8.53 mV. The average size of particles in TEM was 12.05 nm. XRD and SAED definite fcc crystalline structure of metallic gold particles and FTIR confirmed gallic acid bioconjugation. Antileishmanial efficiency of GAunp was established against wild type (IC50 4 +/- 1), sodium stibogluconate resistant strain(IC50 4.5 +/- 2). Macrophage uptake of GAunp was complete within one hour as studied in TEM experiments. (c) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2912 / 2920
页数:9
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