Reactive oxygen species generating photosynthesized ferromagnetic iron oxide nanorods as promising antileishmanial agent

Author:

Islam Arshad12,Ain Quratul1,Munawar Amna1,Corrêa Junior José Dias3,Khan Ajmal4,Ahmad Farhan4,Demicheli Cynthia5,Shams Dilawar Farhan6,Ullah Ikram1,Sohail Muhammad Farhan7,Yasinzai Masoom1,Frézard Frédéric2,Nadhman Akhtar8

Affiliation:

1. Sulaiman Bin Abdullah Aba Al Khail Centre for Interdisciplinary Research in Basic Sciences, International Islamic University, Islamabad, 44000, Pakistan

2. Postgraduate Program in Physiology & Pharmacology, Institute of Biological Sciences, Federal University of Minas Gerais (UFMG), Belo Horizonte, Minas Gerais, Brazil

3. Departamento of Morphology, Institute of Biological Sciences, Federal University of Minas Gerais (UFMG), Belo Horizonte, Minas Gerais, Brazil

4. Department of Biotechnology, Bacha Khan University, Charsadda, KPK, Pakistan

5. Department of Chemistry, Institute of Exact Sciences, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, Minas Gerais, Brazil

6. Department of Environmental Sciences, Abdul Wali Khan University Mardan, Pakistan

7. Riphah Institute of Pharmaceutical Sciences, Riphah International University, Lahore Campus, Lahore, Pakistan

8. Institute of Integrative Biosciences, CECOS University of IT & Emerging Sciences, Peshawar, Pakistan

Abstract

Aim: To investigate the photodynamic therapeutic potential of ferromagnetic iron oxide nanorods (FIONs), using Trigonella foenum-graecum as a reducing agent, against Leishmania tropica. Materials & methods: FIONs were characterized using ultraviolet visible spectroscopy, x-ray diffraction and scanning electron microscopy. Results: FIONs showed excellent activity against L. tropica promastigotes and amastigotes (IC50 0.036 ± 0.003 and 0.072 ± 0.001 μg/ml, respectively) upon 15 min pre-incubation light-emitting diode light (84 lm/W) exposure, resulting in reactive oxygen species generation and induction of cell death via apoptosis. FIONs were found to be highly biocompatible with human erythrocytes (LD50 779 ± 21 μg/ml) and significantly selective (selectivity index >1000) against murine peritoneal macrophages (CC50 102.7 ± 2.9 μg/ml). Conclusion: Due to their noteworthy in vitro antileishmanial properties, FIONs should be further investigated in an in vivo model of the disease.

Publisher

Future Medicine Ltd

Subject

Development,General Materials Science,Biomedical Engineering,Medicine (miscellaneous),Bioengineering

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