Biogenic and hydrothermal synthesis, characterization, antioxidant and anticancer activities of PdNPs using Abutilon indicum leaf extract

被引:0
作者
Sandhya, K. [1 ]
Reddy, G. Bhagavanth [1 ]
Ayodhya, Dasari [2 ,3 ]
Venkatesh, B. [4 ]
Noorjahan, M. [1 ]
Mangatayaru, K. Girija [1 ]
机构
[1] Palamuru Univ, Dept Chem, Mahabubnagar 509001, Telangana, India
[2] Osmania Univ, Dept Chem, Hyderabad 500007, Telangana, India
[3] Intellectual Property India, Chem Grp, Patent Off, Chennai 600032, Tamil Nadu, India
[4] Care Hosp, Dept Clin Pharm, Banjara Hills, Hyderabad 500034, Telangana, India
关键词
Abutilon indicum; Bio-fabrication; Hydrothermal method; Palladium nanoparticles; Antioxidant; Anticancer activity; PALLADIUM NANOPARTICLES; SILVER NANOPARTICLES;
D O I
10.1016/j.inoche.2024.112629
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
In this study, PdNPs are synthesized by using various concentrations of leaf extract of Abutilon indicum (AI), which acts as a reducing, capping, and stabilizing through a hydrothermal method. The synthesized AI leaf extract stabilized PdNPs (AI@PdNPs) were characterized by various analytical techniques such as UV -visible, Powder XRD, DLS, FTIR, and TEM analysis. The formation of PdNPs was primarily confirmed by UV -Vis absorption spectroscopy. The synthesized AI@ PdNPs was found to be FCC crystal structure, spherical, well dispersed, without any agglomeration. PdNPs are highly stable with an average particle size of 7 +/- 4 nm by using powder XRD, DLS and TEM studies respectively. FTIR spectra supports the hypothesis that biomolecules presented in AI extract are effectively involved in the reduction, stabilization and capping of AI@ PdNPs. The AI@ PdNPs were assessed for antioxidant capacity using free radical scavenging activity by DPPH and found to be 76.02 % compared to standard ascorbic acid, which is 96.7 %. The cytotoxicity study was showed that AI@ PdNPs have shown marked cytotoxicity in MCF-7 cells with IC 50 value of 157.5 mu g/mL and did not show marked cytotoxicity in HEK-293 cells. The standard drug (Doxorubicin) was shown the IC 50 value of 18.02 mu M and 66.88 mu M with a maximum inhibition up to 87.26 % and 72.48 % at the highest concentration tested at 100 mu M for MCF-7 and HEK-293 cells, respectively. Therefore, AI@ PdNPs could be a potential candidate for future drug development as an anticancer agent.
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页数:9
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