journal article·2021-04

Synthesis of CeO2 nanostructures with its exceptional biological and chemocatalytic activities: a comparative study

Angel Rose Rajan, Vidya Vilas, Anish Rajan, Annamma John, Daizy Philip

Bulletin of Materials Science· Volume 44· Issue 1
Publisher page

Abstract

A comparative study has been carried out on the synthesis of nanostructured CeO2 through chemical and biological methods. CeO2 nanoparticles have been synthesized chemically using oxalic acid. The as-synthesized nanoparticles have been stabilized using the capping agent, polyvinylpyrrolidone. The aqueous leaf extract of Annona reticulata has been utilized for the biofabrication of CeO2 nanoparticles. XRD, TEM and Raman analyses have been carried out to determine the structure and formation of the as-synthesized products. Optical studies have been carried out through UV–visible absorption, photoluminescence, Fourier transform infrared and Raman spectroscopic techniques. The biosynthesized CeO2 nanoparticles exhibit strong antioxidant activity as well as potent antidiabetic and wound healing activities in comparison to their chemically fabricated counterparts, extending the possibility for their application in pharmaceuticals. The biogenic nanoparticles also exhibit superior catalytic activity in the degradation of harmful dyes including methylene blue and eosin yellowish.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Nanoparticles: synthesis and applications · Advanced Nanomaterials in Catalysis · Essential Oils and Antimicrobial Activity

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (48)

Show source-provided references
1. Dhall A and Self W 2018 Antioxidants 7 9710.3390/antiox7080097 ↗
2. Yang Z, Zhou K, Liu X, Tian Q, Lu D and Yang S 2007 Nanotechnology 18 18560610.1088/0957-4484/18/18/185606 ↗
3. Shirke B, Patil A A, Hankare P P and Garadkar K M 2011 J. Mater. Sci.: Mater. Electron. 22 200
4. Pinjari D V and Pandit A B 2011 Ultrason. Sonochem. 18 111810.1016/j.ultsonch.2011.01.008 ↗
5. Darroudi M, Sarani M, Oskuee R K, Zak A K, Hosseini H A and Gholami L 2014 Ceram. Int. 40 204110.1016/j.ceramint.2013.07.116 ↗
6. Farahmandjou M, Zarinkamar M and Firoozabadi T P 2016 Rev. Mex. de Fis. 62 496
7. Xu C, Lin Y, Wang J, Wu L, Wei W, Ren J et al 2013 Adv. Health. Mater. 2 159110.1002/adhm.201200464 ↗
8. Vassie J A, Whitelock J M and Lord M S 2018 Mol. Pharm. 15 99410.1021/acs.molpharmaceut.7b00920 ↗
9. Thovhogi N, Diallo A, Gurib-Fakim A and Maaza M 2015 J. Alloys Compd. 647 39210.1016/j.jallcom.2015.06.076 ↗
10. Maqbool Q, Nazar M, Naz S, Hussain T, Jabeen N, Kausar R et al 2016 Int. J. Nanomed. 11 501510.2147/IJN.S113508 ↗
11. Arumugam A, Karthikeyan C, Haja Hameed A S, Gopinath K, Gowri S and Karthika V 2015 Mater. Sci. Eng. C 49 40810.1016/j.msec.2015.01.042 ↗
12. Kannan S K and Sundrarajan M 2014 Int. J. Nanosci. 13 145001810.1142/S0219581X14500185 ↗
13. Hegazy M A E, Maklad H M, Doaa A, Elmonsif A, Elnozhy F Y, Alqubiea M A et al 2017 J. Med. 53 351
14. Rajeshkumar S and Naik P 2018 Biotechnol. Rep. 17 110.1016/j.btre.2017.11.008 ↗
15. Xiong J, Wu Q, Mei X, Liu J, Wei Y, Zhao Z et al 2018 ACS Catal. 8 791510.1021/acscatal.8b01924 ↗
16. Rajan A R, Rajan A, John A, Vilas V and Philip D 2019 Ceram. Int. 45 2194710.1016/j.ceramint.2019.07.208 ↗
17. Chokshi K, Pancha I, Ghosh T, Paliwal C, Maurya R K, Ghosh A et al 2016 RSC Adv. 6 7226910.1039/C6RA15322D ↗
18. Kumari M M, Jacob J and Philip D 2015 Spectrochim. Acta A 137 18510.1016/j.saa.2014.08.079 ↗
19. Goharshadi E K, Samiee S and Nancarrow P 2011 J. Colloid Interface Sci. 356 47310.1016/j.jcis.2011.01.063 ↗
20. Tsunekawa S, Wang J T, Kawazoe Y and Kasuya A 2003 J. Appl. Phys. 94 365410.1063/1.1600520 ↗
21. Ramjeyanthi N, Alagar M and Muthuraman D 2018 Int. J. Inter. Res. Inn. 6 389
22. Deus R C, Cortes J A, Ramirez M A, Ponce M A, Andres J, Rocha L S R et al 2015 Mater. Res. Bull. 70 41610.1016/j.materresbull.2015.05.006 ↗
23. Gopinath K, Karthika V, Sundaravadivelan C, Gowri S and Arumugam A 2015 J. Nanostruct. Chem. 54 29510.1007/s40097-015-0161-2 ↗
24. Jayanthi S A, Sukanya D, Pragasam A J A and Sagayaraj P 2013 Der. Pharma Chem. 5 90
25. Sreeju N, Rufus A and Philip D 2016 J. Mol. Liq. 221 100810.1016/j.molliq.2016.06.080 ↗
26. Vilas V, Philip D and Mathew J 2016 J. Mol. Liq. 22 1179
27. Sherly E D, Vijaya J J and Kennedy L J 2015 J. Mol. Struct. 1099 11410.1016/j.molstruc.2015.05.057 ↗
28. Kumar S, Srivastava M, Singh J, Layek S, Yashpal M, Materny A et al 2015 AIP Adv. 5 02710910.1063/1.4908003 ↗
29. Gupta R N, Pareek A, Suthar M, Rathore G S, Basniwal P K and Jain D 2010 Int. J. Diabetes Dev. Ctries. 29 170
30. Javed R, Ahmed M, Haq I, Nisa S and Zia M 2017 Mater. Sci. Eng. C 79 10810.1016/j.msec.2017.05.006 ↗
31. Das M S and Devi G 2015 J. Appl. Pharma. Sci. 5 9210.7324/JAPS.2015.501215 ↗
32. Reddy G R, Morais A B and Gandhi N N 2013 Asian J. Chem. 25 924910.14233/ajchem.2013.15215 ↗
33. Phull A R, Abbas Q, Ali A, Raza H, Kim S J, Zia M et al 2016 Future J. Pharma. Sci. 2 3110.1016/j.fjps.2016.03.001 ↗
34. Nagaich U, Gulati N and Chauhan S 2016 J. Pharma. (Cairo) 2016 7141523
35. Sudha A, Jeyakanthan J and Srinivasan P 2017 Res. Effic. Technol. 3 50610.1016/j.reffit.2017.07.002 ↗
36. Esmaeili M A and Sonboli A 2010 Food Chem. Toxicol. 48 84610.1016/j.fct.2009.12.020 ↗
37. Xue Y, Luan Q, Yang D, Yao X and Zhou K 2011 J. Phys. Chem. 115 4433
38. Sandhir R, Yadav A, Sunkaria A and Singhal N 2015 Neurochem. Int. 89 20910.1016/j.neuint.2015.08.011 ↗
39. Diaconeasa Z, Rugina D, Coman C, Socaciu C, Leopold L F, Vulpoi A et al 2017 Colloids Surf. A 5 13210.1016/j.colsurfa.2017.05.081 ↗
40. Rajendran N K, Dhilip K S S, Houreld N N and Abrahamse H 2018 J. Drug Deliv. Sci. Technol. 44 42110.1016/j.jddst.2018.01.009 ↗
41. Pawar R S, Chaurasiya P K, Rajak H, Singour P K, Toppo F A and Jain A 2013 Indian J. Pharmacol. 45 47410.4103/0253-7613.117759 ↗
42. Rather H A, Thakore R, Singh R, Jhala D, Singh S and Vasita R 2018 Bioact. Mater. 3 20110.1016/j.bioactmat.2017.09.006 ↗
43. Chigurupati S, Mughal M R, Okun E, Das S, Kumar A, McCaffery M et al 2013 Biomaterials 34 219410.1016/j.biomaterials.2012.11.061 ↗
44. Rajan A, Vilas V and Philip D 2015 J. Mol. Liq. 207 23110.1016/j.molliq.2015.03.023 ↗
45. Vasantharaj S, Sathiyavimal S, Saravanan M, Senthilkumar P, Kavitha G, Shanmugavel M et al 2019 J. Photochem. Photobiol. B 191 14310.1016/j.jphotobiol.2018.12.026 ↗
46. Arasu M V, Arokiyaraj S, Viayaraghavan P, JebaKumar T S, Duraipandiyan V, Al-Dhabi N A et al 2019 J. Photochem. Photobiol. B 190 15410.1016/j.jphotobiol.2018.11.020 ↗
47. Abraham N, Rufus A, Unni C and Philip D 2019 Spectrochim. Acta A 200 11610.1016/j.saa.2018.04.015 ↗
48. Princy K F and Gopinath A 2018 J. Nanostruct. Chem. 8 33310.1007/s40097-018-0277-2 ↗