Antimalarial silver and gold nanoparticles: Green synthesis, characterization and in vitro study

Biomedicine and Pharmacotherapy

Volumn 91, Issue , 2017, Pages 567-580

  Dutta, Partha P ^a   Bordoloi, Manobjyoti ^a   Gogoi, Kabita ^b   Roy, Sonali ^a   Narzary, Bardwi ^a   Bhattacharyya, Dibya R ^b   Mohapatra, Pradyumna K ^b   Mazumder, Bhaskar ^c  

^a CSIR NORTH EAST INSTITUTE OF SCIENCE AND TECHNOLOGY   (India)

^b REGIONAL MEDICAL RESEARCH CENTRE   (India)

^c DIBRUGARH UNIVERSITY   (India)

Author keywords

Cytotoxicity; Gold and silver nanoparticle; Green synthesis; Schizontocidal activity; Syzygium jambos

Indexed keywords

ANTIMALARIAL AGENT; CHLOROQUINE; DOXORUBICIN; GOLD NANOPARTICLE; PLANT EXTRACT; SILVER NANOPARTICLE; SYZYGIUM JAMBOS EXTRACT; UNCLASSIFIED DRUG; GOLD; METAL NANOPARTICLE; SILVER; SORBITOL;

ANIMAL CELL; ANTIMALARIAL ACTIVITY; ARTICLE; BARK; BIOCOMPATIBILITY; CANCER CELL LINE; CERVICAL CANCER CELL LINE; CONTROLLED STUDY; CYTOTOXICITY; CYTOTOXICITY ASSAY; DRUG SCREENING; DRUG SYNTHESIS; ERYTHROCYTE; FEMALE; GREEN SYNTHESIS; HUMAN; HUMAN CELL; IN VITRO STUDY; INFRARED SPECTROSCOPY; NONHUMAN; PLANT LEAF; PLASMODIUM FALCIPARUM; PRIORITY JOURNAL; RAT; REACTION OPTIMIZATION; SKELETAL MUSCLE CELL; SYZYGIUM; SYZYGIUM JAMBOS; TRADITIONAL MEDICINE; TRANSMISSION ELECTRON MICROSCOPY; ULTRAVIOLET SPECTROSCOPY; X RAY DIFFRACTION; ZETA POTENTIAL; ANIMAL; CHEMISTRY; DRUG EFFECTS; GREEN CHEMISTRY; HELA CELL LINE; PARTICLE SIZE; PH; PROCEDURES; STATIC ELECTRICITY; TEMPERATURE; TIME FACTOR; ULTRASTRUCTURE;

ANIMALS; ANTIMALARIALS; GOLD; GREEN CHEMISTRY TECHNOLOGY; HELA CELLS; HUMANS; HYDROGEN-ION CONCENTRATION; METAL NANOPARTICLES; PARTICLE SIZE; PLASMODIUM FALCIPARUM; RATS; SILVER; SORBITOL; SPECTROSCOPY, FOURIER TRANSFORM INFRARED; STATIC ELECTRICITY; SYZYGIUM; TEMPERATURE; TIME FACTORS; X-RAY DIFFRACTION;

EID: 85018352154     PISSN: 07533322     EISSN: 19506007     Source Type: Journal    
DOI: 10.1016/j.biopha.2017.04.032     Document Type: Article

References (60)

1. [1] WHO, Status Report on Artemisinin and ACT Resistance 2015., 2015 ([cited 2016 March 20]. Available from:) http://www.who.int/malaria/publications/atoz/status-rep-artemisinin-resistance-sept2015.pdf.
2. [2] Patra, S., Mukherjee, S., Barui, A.K., Ganguly, A., Sreedhar, B., Patra, C.R., Green synthesis, characterization of gold and silver nanoparticles and their potential application for cancer therapeutics. Mater Sci. Eng. C 53 (2015), 298–309, 10.1016/j.msec.2015.04.048.
3. [3] Gurunathan, S., Kalishwaralal, K., Vaidyanathan, R., Venkataraman, D., Pandian, S.R., Muniyandi, J., Hariharan, N., Eom, S.H., Biosynthesis, purification and characterization of silver nanoparticles using Escherichia coli. Coll Surf B: Bioint. 74 (2009), 328–335, 10.1016/j.colsurfb.2009.07.048.
4. [4] Guangquan, L., Dan, H., Yongqing, Q., Buyuan, G., Song, G., Yan, C., Koji, Y., Li, W., Fungus-mediated green synthesis of silver nanoparticles using Aspergillus terreus. Int. J. Mol. Sci. 13 (2012), 466–476, 10.3390/ijms13010466.
5. [5] Rangnekar, T.K., Sarma, A.K., Singh, J., Deka, A., Ramesh, A., Chattopadhyay, A., Retention of enzymatic activity of α-amylase in the reductive synthesis of gold nanoparticles. Langmuir 273 (2007), 5700–5706, 10.1021/la062749e.
6. [6] Mishra, A., Sardar, M., Alpha-amylase mediated synthesis of silver nanoparticles. Sci. Adv. Mater. 1 (2012), 143–146, 10.1166/sam.2012.1263.
7. [7] Tripathy, A., Raichur, A.M., Chandrasekaran, N., Prathna, T.C., Mukherjee, A., Process variables in biomimetic synthesis of silver nanoparticles by aqueous extract of Azadirachta indica (Neem) leaves. J. Nanopart. Res. 12 (2009), 237–246, 10.1007/s11051-009-9602-5.
8. [8] Sharma, V.K., Yagard, R.A., Lin, Y., Silver nanoparticles: green synthesis and their antimicrobial activities. Adv. Colloid Interface Sci. 145 (2009), 83–96, 10.1016/j.cis.2008.09.002.
9. [9] Dwivedi, A.D., Gopal, K., Biosynthesis of silver and gold nanoparticles using Chenopodium album leaf extract. Colloids Surf. A: Physicochem. Eng. Aspects 369 (2010), 27–33, 10.1016/j.colsurfa.2010.07.020.
10. [10] Ávila-Peña, D., Peña, N., Quintero, L., Suárez-Roca, H., Antinociceptive activity of Syzygium jambos leaves extract on rats. J. Ethnopharmacol. 112 (2007), 380–385, 10.1016/j.jep.2007.03.027.
11. [11] Hossain, H., Rahman, S.E., Akbar, P.N., Khan, T.A., Rahman, M.M., Jahan, I.A., profiling, H.P.L.C., antioxidant and in vivo anti-inflammatory activity of the ethanol extract of Syzygium jambos available in Bangladesh. BMC Res. Notes, 9, 2016, 191, 10.1186/s13104-016-2000-z.
12. [12] Gavillán-Suárez, J., Aguilar-Perez, A., Rivera-Ortiz, N., Rodríguez-Tirado, K., Figueroa-Cuilan, W., Morales-Santiago, L., Maldonado-Martínez, G., Cubano, L.A., Martínez-Montemayor, M.M., Chemical profile and in vivo hypoglycemic effects of Syzygium jambos, Costus speciosus and Tapeinochilos ananassae plant extracts used as diabetes adjuvants in Puerto Rico. BMC Complement. Altern. Med., 15, 2015, 244, 10.1186/s12906-015-0772-7.
13. [13] Donatini, R.S., Ishikawa, T., Barros, S.B.M., Bacchi, E.M., Antiulcerogenic and antioxidant activities of leaf extract of Syzygium jambos (L.) Alston (Myrtaceae). Braz. J. Pharm. 19 (2009), 89–94, 10.1590/S0102-695x2009000100018.
14. [14] Yang, L.L., Lee, C.Y., Yen, K.Y., Induction of apoptosis by hydrolyzable tannins from Eugenia jambos L. on human leukemia cells. Cancer Lett. 157 (2000), 65–75, 10.1016/S0304-3835(00)00477-8.
15. [15] Lin, D.D., Liu, J.W., Li, W.G., Luo, W., Cheng, J.L., Chen, W.W., Chemical constituents from stems of Syzygium jambos var. jambos and their in vitro cytotoxicity. Chin. Trad. Herb. Drugs 45 (2014), 1993–1997.
16. [16] Mohanty, S., Cock, I.E., Bioactivity of Syzygium jambos methanolic extracts: antibacterial activity and toxicity. Pharm. Res. 2 (2010), 4–9, 10.4103/0974-8490.60577.
17. [17] Sharma, R., Kishore, N., Hussein, A., Lall, N., Antibacterial and anti-inflammatory effects of Syzygium jambos L. (Alston) and isolated compounds on acne vulgaris. BMC Complement. Altern. Med., 13, 2013, 292, 10.1186/1472-6882-13-292.
18. [18] Kuiate, J.R., Mouokeu, S., Wabo, H.K., Tane, P., Antidermatophytic triterpenoids from Syzygium jambos (L.) alston (Myrtaceae). Phytother. Res. 21 (2007), 149–152, 10.1002/ptr.2039.
19. [19] Sakander, H., Akhilesh, B., Koteshwara, A.R., Evaluation of antifungal potential of selected medicinal plants against human pathogenic fungi. Int. J. Green Pharm. 9 (2015), 110–117.
20. [20] Das, S., De, B., Evaluation of Angiotensin I-Converting Enzyme (ACE) inhibitory potential of some underutilized indigenous fruits of West Bengal using an in vitro model. Fruits 68 (2013), 499–506, 10.1051/fruits/2013092.
21. [21] Tang, W., Chen, N.H., Li, G.Q., Wang, G.C., Li, Y.L., Crystal structure of betulinic acid methanol monosolvate. Acta Cryst. E 70 (2014), o1242–o1243, 10.1107/S1600536814023848.
22. [22] Slowing, K., Sollhuber, M., Carretero, E., Villar, A., Flavonoid glycosides from Eugenia jambos. Phytochem 37 (1994), 255–258.
23. [23] Slowing, K., Carretero, E., Villar, A., Anti-inflammatory compounds of Eugenia jambos. Phytother. Res. 10:SUPPL. 1 (1996), S126–S127.
24. [24] Hoang, V.L., Nguyen, Q.T., Chemical compositions of Syzygium jambos (Linn)​·Alston, tap chi phan tich hoa. Ly Va Sinh Hoc, 9(20–23), 2004, 19.
25. [25] Jayasinghe, U.L.B., Ratnayake, R.M.S., Medawala, M.M.W.S., Fujimoto, Y., Dihydrochalcones with radical scavenging properties from the leaves of Syzygium jambos. Nat. Prod. Res. 21 (2007), 551–554, 10.1080/14786410601132238.
26. [26] Li, G.Q., Zhang, Y.B., Wu, P., Chen, N.H., Wu, Z.N., Yang, L., Qiu, R.X., Wang, G.C., Li, Y.L., New phloroglucinol derivatives from the fruit tree Syzygium jambos and their cytotoxic and antioxidant activities. J. Agric. Food Chem. 63 (2015), 10257–10262, 10.1021/acs.jafc.5b04293.
27. [27] Zheng, N., Wang, Z., Chen, F., Lin, J., Evaluation to the antioxidant activity of total flavonoids extract from Syzygium jambos seeds and optimization by response surface methodology. Afr. J. Pharm. Pharmacol. 5 (2011), 2411–2419, 10.5897/AJPP11.691.
28. [28] Bonfanti, G., Bitencourt, P.R., De Bona, K.S., Da Silva, P.S., Jantsch, L.B., Pigatto, A.S., Boligon, A., Athayde, M.L., Gonçalves, T.L., Moretto, M.B., Syzygium jambos and Solanum guaraniticum show similar antioxidant properties but induce different enzymatic activities in the brain of rats. Molecules 18 (2013), 9179–9194, 10.3390/molecules18089179.
29. [29] Bonfanti, G., De Bona, K.S., de Lucca, L., Jantsch, L., Pigatto, A.S., Boligon, A.A., Athayde, M.L., Moretto, M.B., Gonçalves, T.L., Delta-ALA-D inhibitory potential and protective action of Syzygium jambos and Solanum guaraniticum leaf extracts on oxidatively stressed erythrocytes. Redox Rep. 19 (2014), 206–213, 10.1179/1351000214Y.0000000092.
30. [30] Prasad, R., Satyanarayana, S.V., Prasad, K.S., Varma, A., Biogenic synthesis of silver nanoparticles from the leaf extract of Syzygium cumini (L.) and its antibacterial activity. Int. J. Pharm. Biol. Sci. 3 (2012), 745–752.
31. [31] Gupta, K., Barua, S., Hazarika, S.N., Manhar, A.K., Nath, D., Karak, N., Namsa, N.D., Mukhopadhyay, R., Kalia, V.P., Mandal, M., Green silver nanoparticles: enhanced antimicrobial and antibiofilm activity with effects on DNA replication and cell cytotoxicity. RSC Adv. 4 (2014), 52845–52855, 10.1039/c4ra08791g.
32. [32] Logeswari, P., Silambarasan, S., Abraham, J., Synthesis of silver nanoparticles using plants extract and analysis of their antimicrobial property. J. Saudi Chem. Soc. 19 (2015), 311–317, 10.1016/j.jscs.2012.04.007.
33. [33] Kumar, V., Yadav, S.K., Characterisation of gold nanoparticles synthesised by leaf and seed extract of Syzygium cumini L. J. Exp. Nanosci. 7 (2012), 440–451, 10.1080/17458080.2010.543989.
34. [34] Karthick, V., Kumar, V.G., Dhas, T.S., Govindaraju, K., Sinha, S., Singaravelu, G., Biosynthesis of gold nanoparticles and identification of capping agent using gas chromatography-mass spectrometry and matrix assisted laser desorption ionization-mass spectrometry. J. Nanosci. Nanotechnol. 15 (2015), 4052–4057, 10.1166/jnn.2015.9157.
35. [35] Thampi, N., Shalini, J.V., Bio-prospecting the in-vitro antioxidant and anti-cancer activities of silver nanoparticles synthesized from the leaves of Syzygium samarangense. Int. J. Pharm. Sci. 7 (2015), 269–274.
36. [36] Thampi, N., Veronica, S.J., Anti-proliferative and apoptotic activities of Syzygium samarangense (wax apple) fruits extract against human A549 lung cancer cell lines. Int. J. Pharm. Sci. 7 (2015), 361–365.
37. [37] Thampi, N., Jeyadoss, V.S., Biogenic synthesis and characterization of silver nanoparticles using Syzygium samarangense (Wax apple) Leaves extract and their antibacterial activity. Int. J. Pharm. Tech. Res. 8 (2015), 426–433.
38. [38] Jeevika, A., Ravi Shankaran, D., Seed-free synthesis of 1D silver nanowires ink using clove oil (Syzygium aromaticum) at room temperature. J. Colloid Interface Sci. 458 (2015), 155–159, 10.1016/j.jcis.2015.07.045.
39. [39] Yugandhar, P., Savithramma, N., Leaf assisted green synthesis of silver nanoparticles from Syzygium alternifolium (Wt.) walp. characterization and antimicrobial studies. Nano Biomed. Eng. 7 (2015), 29–37, 10.5101/nbe.v7i2.p29-37.
40. [40] Yugandhar, P., Savithramma, N., Biosynthesis, characterization and antimicrobial studies of green synthesized silver nanoparticles from fruit extract of Syzygium alternifolium (Wt.) Walp. an endemic, endangered medicinal tree taxon. Appl. Nanosci. 6 (2016), 223–233, 10.1007/s13204-015-0428-4.
41. [41] Kimling, J., Maier, M., Okenve, B., Kotaidis, V., Ballot, H., Plech, A., Turkevich method for gold nanoparticle synthesis revisited. J. Phys. Chem. B 110 (2006), 15700–15707, 10.1021/jp061667w.
42. [42] Li, K., Jia, X., Tang, A., Zhu, X., Meng, H., Wang, Y., Preparation of spherical and triangular silver nanoparticles by a convenient method. Integr. Ferroelectr. 136 (2012), 9–14, 10.1080/10584587.2012.686405.
43. [43] Singleton, V.L., Orthofer, R., Lamuela-Raventos, R.M., Analysis of total phenols and other oxidation substrates and antioxidants by means of Folin Ciocalteau reagent. Methods Enzymol. 299 (1999), 152–178.
44. [44] Trager, W., Jensen, J.B., Human malaria parasites in continuous culture. Science 193 (1976), 673–675.
45. [45] WHO in Vitro Micro-test (mark Iii) for the Assessment of the Response of Plasmodium Falciparum to Chloroquine, Mefloquine, Quinine, Amodiaquine, Sulfadoxine/pyrimethamine and Artemisinin. ([cited 2016 March 15]. Available from:) http://www.who.int/malaria/publications/atoz/markiii.pdf.
46. [46] Waako, P.J., Smith, P., Folb, P.I., In vitro interactions of Aspilia africana Pers. C.D. Adams, a traditional antimalarial medicinal plant, with artemisinin against Plasmodium falciparum. J. Ethnopharmacol. 102 (2005), 262–268, 10.1016/j.jep.2005.06.021.
47. [47] Mosmann, T., Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. J. Immunol. Methods 65 (1983), 55–63.
48. [48] Nayak, D., Ashe, S., Rauta, P.R., Kumari, M., Nayak, B., Bark extract mediated green synthesis of silver nanoparticles: evaluation of antimicrobial activity and antiproliferative response against osteosarcoma. Mater. Sci. Eng. C 58 (2016), 44–52, 10.1016/j.msec.2015.08.022.
49. [49] Dhamecha, D., Jalalpure, S., Jadhav, K., Sajjan, D., Green synthesis of gold nanoparticles using Pterocarpus marsupium: Characterization and biocompatibility studies. Particul. Sci. Technol. 34 (2016), 156–164, 10.1080/02726351.2015.1054972.
50. [50] Mishra, A., Kaushik, N.K., Sardar, M., Sahal, D., Evaluation of antiplasmodial activity of green synthesized silver nanoparticles. Colloids Surf. B: Biointerfaces 111 (2013), 713–718, 10.1016/j.colsurfb.2013.06.036.
51. [51] Clogston, J.D., Patri, A.K., Zeta potential measurement. Methods Mol. Biol. 697 (2011), 63–70, 10.1007/978-1-60327-198-1_6.
52. [52] Oluwafemi, O.S., Lucwaba, Y., Gura, A., Masabeya, M., Ncapayi, V., Olujimi, O.O., Songca, S.P., A facile completely ‘green’ size tunable synthesis of maltose-reduced silver nanoparticles without the use of any accelerator. Colloids Surf. B: Biointerfaces 102 (2013), 718–723, 10.1016/j.colsurfb.2012.09.001.
53. [53] Mehta, S.K., Chaudhary, S., Gradzielski, M., Time dependence of nucleation and growth of silver nanoparticles generated by sugar reduction in micellar media. J. Colloid Interface Sci. 343 (2010), 447–453, 10.1016/j.jcis.2009.11.053.
54. [54] Kim, T.Y., Cha, S.H., Cho, S., Park, Y., Tannic acid-mediated green synthesis of antibacterial silver nanoparticles. Arch. Pharm. Res. 39 (2016), 465–473, 10.1007/s12272-016-0718-8.
55. [55] Guo, D., Dou, D., Ge, L., Huang, Z., Wang, L., Gu, N., A caffeic acid mediated facile synthesis of silver nanoparticles with powerful anti-cancer activity. Colloids Surf. B: Biointerfaces 134 (2015), 229–234, 10.1016/j.colsurfb.2015.06.070.
56. [56] Murugan, K., Samidoss, C.M., Panneerselvam, C., Higuchi, A., Roni, M., Suresh, U., Chandramohan, B., Subramaniam, J., Madhiyazhagan, P., Dinesh, D., Rajaganesh, R., Alarfaj, A.A., Nicoletti, M., Kumar, S., Wei, H., Canale, A., Mehlhorn, H., Benelli, G., Seaweed-synthesized silver nanoparticles: an eco-friendly tool in the fight against Plasmodium falciparum and its vector Anopheles stephensi?. Parasitol. Res. 114 (2015), 4087–4097, 10.1007/s00436-015-4638-1.
57. [57] Jaganathan, A., Murugan, K., Panneerselvam, C., Madhiyazhagan, P., Dinesh, D., Vadivalagan, C., Aziz, A.T., Chandramohan, B., Suresh, U., Rajaganesh, R., Subramaniam, J., Nicoletti, M., Higuchi, A., Alarfaj, A.A., Munusamy, M.A., Kumar, S., Benelli, G., Earthworm-mediated synthesis of silver nanoparticles: a potent tool against hepatocellular carcinoma, Plasmodium falciparum parasites and malaria mosquitoes. Parasitol. Int. 65 (2016), 276–284, 10.1016/j.parint.2016.02.003.
58. [58] Rajakumar, G., Rahuman, A.A., Chung, I.M., Kirthi, A.V., Marimuthu, S., Anbarasan, K., Antiplasmodial activity of eco-friendly synthesized palladium nanoparticles using Eclipta prostrata extract against Plasmodium berghei in swiss albino mice. Parasitol. Res. 114 (2015), 397–406, 10.1007/s00436-015-4318-1.
59. [59] Sannella, A.R., Casini, A., Gabbiani, C., Messori, L., Bilia, A.R., Vincieri, F.F., Majori, G., Severini, C., New uses for old drugs. Auranofin, a clinically established antiarthritic metallo drug, exhibits potent antimalarial effects in vitro: mechanistic and pharmacological implications. FEBS Lett. 582 (2008), 844–847, 10.1016/j.febslet.2008.02.028.
60. [60] Lambros, C., Vanderberg, J.P., Synchronization of Plasmodium falciparum erythrocytic stages in culture. J. Parasitol. 65 (1979), 418–420.