اخبار و اعلانات

 آمار

تعداد نشریات41
تعداد شماره‌ها1,138
تعداد مقالات9,757
تعداد مشاهده مقاله17,870,149
تعداد دریافت فایل اصل مقاله12,484,781
Rahimi, Rahmatollah, Fayyaz, Fatemeh, Rassa, Mehdi, Rabbani, Mahboubeh. (1395). Microwave-assisted synthesis of 5,10,15,20-tetrakis(4-nitrophenyl)porphyrin and zinc derivative and study of their bacterial photoinactivation. فصلنامه علمی زیست فناوری گیاهان زراعی, 4(Issue 2, pp. 133-235, Serial No. 11), 175-185.
Rahmatollah Rahimi; Fatemeh Fayyaz; Mehdi Rassa; Mahboubeh Rabbani. "Microwave-assisted synthesis of 5,10,15,20-tetrakis(4-nitrophenyl)porphyrin and zinc derivative and study of their bacterial photoinactivation". فصلنامه علمی زیست فناوری گیاهان زراعی, 4, Issue 2, pp. 133-235, Serial No. 11, 1395, 175-185.
Rahimi, Rahmatollah, Fayyaz, Fatemeh, Rassa, Mehdi, Rabbani, Mahboubeh. (1395). 'Microwave-assisted synthesis of 5,10,15,20-tetrakis(4-nitrophenyl)porphyrin and zinc derivative and study of their bacterial photoinactivation', فصلنامه علمی زیست فناوری گیاهان زراعی, 4(Issue 2, pp. 133-235, Serial No. 11), pp. 175-185.
Rahimi, Rahmatollah, Fayyaz, Fatemeh, Rassa, Mehdi, Rabbani, Mahboubeh. Microwave-assisted synthesis of 5,10,15,20-tetrakis(4-nitrophenyl)porphyrin and zinc derivative and study of their bacterial photoinactivation. فصلنامه علمی زیست فناوری گیاهان زراعی, 1395; 4(Issue 2, pp. 133-235, Serial No. 11): 175-185.

Microwave-assisted synthesis of 5,10,15,20-tetrakis(4-nitrophenyl)porphyrin and zinc derivative and study of their bacterial photoinactivation

Iranian chemical communication
مقاله 6، دوره 4، Issue 2, pp. 133-235, Serial No. 11، تیر 2016، صفحه 175-185    اصل مقاله (209.86 K)
نوع مقاله: Original Research Article
نویسندگان
Rahmatollah Rahimi* 1؛ Fatemeh Fayyaz1؛ Mehdi Rassa2؛ Mahboubeh Rabbani3
1Bioinorganic Chemistry Laboratory, Department of Chemistry, Iran University of Science and Technology
2Department of Biology, Faculty of Science, University of Guilan, Rasht, Iran
3Department of Chemistry, Iran University of Science and Technology,
چکیده
In this study, 5,10,15,20-tetrakis(4-nitrophenyl)porphyrin (TNPP) and its zinc porphyrin complex (ZnTNPP) were synthesized in situ using the microwave method and identified by UV-Vis, FT-IR and 1H NMR. The photostability and photodynamic antimicrobial activity (PACT) of these compounds were investigated on Pseudomonas aeruginosa and Bacillus subtilis under visible light irradiation. MIC, MBC and inhibition zones produced by these compounds were determined and the number of bacteria counted. The results indicated that both compounds have significant stability when illuminated for various illumination periods in nutrient broth media. Both compounds exhibited more effective activity against P. aeruginosa than B. subtilis in nutrient agar.
کلیدواژه‌ها
Antimicrobial activity؛ Bacillus subtilis؛ photoinactivation؛ pseudomonas aeruginosa؛ TNPP
مراجع
[1] E. Feese, H. Sadeghifar, H.S. Gracz, D.S. Argyropoulos, R.A. Ghiladi, Biomacromolecules, 2011, 12, 3528–3539.

[2] A.M. Munoz-Bonilla, Prog. Polym. Sci., 2012, 37, 281– 339.

[3] X. Ragàs, X. He, M. Agut, M. Roxo-Rosa, A. Rocha Gonsalves, A.C. Serra, S. Nonell, Molecules, 2013, 18, 2712-2725.

[4] X.Y. Liu, H.M. Wang, J.Q. Jiang, J.H. Xiao, R.L. Gao, F.Y. Lin,  Chem. Biol. Interact, 2008, 172, 154–158.

[5] K.G. Yu, D.H. Li, C.H. Zhou, Chin. Chem. Lett, 2009, 20, 411–414.

[6] H. Kim, W. Kim, Y. Mackeyev, G-S Lee, H-J Kim, T. Tachikawa, S. Hong, S. Lee, J. Kim, L.J. Wilson, T. Majima, P.J.J. Alvarez, W. Choi, J. Lee  Environ. Sci. Technol., 2012, 46, 9606−9613.

[7] C. Spagnul, L.C. Turner, R.W. Boyle, J. Photochem. Photobiol. B: Biol, 2015, 150, 11–30.

[8] R. Dosselli, C. Tampieri, R. Ruiz-González, S.D. Munari, X. Ragàs, D. Sánchez-García, M. Agut, S. Nonell, E. Reddi, M. Gobbo, J. Med. Chem, 2013, 56, 1052−1063.

[9] M.A. Latief, T. Chikama, M. Shibasaki, T. Sasaki,  J.A. Ko, Y. Kiuchi, T. Sakaguchi, A. Obana, Lasers in Med. Sci., 2015, 30(1), 383-387.

[10] F. Fayyaz, R. Rahimi, M. Rassa, A. Maleki, Water sci. technol. Water Supply, 2015, 15(5), in press.

[11] E. Alves, M.A. F. Faustino, J.P.C. Tomé, M.G.P.M.S. Neves, A.C. Tomé, J.A.S. Cavaleiro, Â. Cunha, N.C.M. Gomes, A. Almeid, Bioorg. Med. Chem., 2013, 21(14), 4311–4318.

[12] S-F. Jin, P. Zhao, L-C. Xu, M. Zheng, J-Z. Lu, P-L. Zhao, Q-L. Su, H-X. Chen, D-t. Tang, J. Chen, J-Q. Lin, Bioorg. Chem., 2015, 60, 110–117.

[13] D.C.S. Costa, V.F. Pais, A.M.S. Silva, J.A.S. Cavaleiro, U. Pischel, J.P.C. Tomé, Tetrahedron Let., 2014, 55(30), 4156–4159.

[14] D.  Drozd, K. Szczubiałka, M. Skiba, M. Kepczynski, M. Nowakowska, J. Phys. Chem. C, 2014, 118, 9196−9202.

[15] B. Pudžiuvytė, R. Daugelavičius, V. kirveliene, A. Sasnauskienė, R. Bonnett, E. Bakienė, Biologija, 2008, 54, 198–201.

[16] N.S. Gsponer, M.B. Spesia, E.N. Durantini, Photodiag. Photodyn. Therap.,2015, 12(1), 67–75.

[17] S. Meng,  Z. Xu,  G. Hong, L. Zhao, Z. Zhao, J. Guo,  H. Ji, T. Liu, Europ. J. Med.Chem. 2015, 92, 35–48.

[18] S.A.G. Lambrechts, M.C.G . Aalders, F.D. Verbraak, J.W.M. Lagerberg, J.B. Dankert, J.J. Schuitmaker, J. Photochem. Photobiol. B, Biol, 2005, 79, 51–57.

[19] E.V. Alopina, T.A. Ageeva, A.V. Lyubimtsev,  O. Yu. Kuznetsovc, S.A. Syrbu, Os. I. Koifman, Macroheterocycles, 2012, 5, 76–80.

[20] R. Luguya, L. Jaquinod, F.R. Fronczek, M. Graca, H. Vicente, K.M. Smith, Tetrahedron, 2004, 60, 2757–2763.

[21] M.A. Schiavon, L.S. Iwamoto, A.G. Ferreira, Y. Iamamoto,  MV.B. Zanoniand, M.D. Assis,J. Braz. Chem. Soc., 2000, 11, 458–466.

[22] K. Rajesh, R.A. Kalilur, B.K. Shanmuga, S. Sreedaran, V. Gangadevi,  V. Narayanan,  Bull. Korean Chem. Soc., 2010, 31, 2656–2664.

[23] X.G. Liu, Y.Q. Feng, F. Li, X.G. Chen, X. Li, C.Y. Zhang, Chin. Chem. Lett., 2005, 16, 1181-1184.

[24] J. Zhang, X. Wu, X. Cao, F. Yang, J. Wang, X. Zhoua, X.L. Zhang, Bioorg. Med. Chem. Lett., 2003, 13, 1097–1100.

[25] H. Ashkenazi, Y. Nitzan, D. Ga, Photochem. Photobiol., 2003, 77, 186–191.

[26] V. Sol, P. Branland, V. Chaleix, R. Granet, M. Guilloton, F. Lamarche, B. Verneuil, P. Krausz, Bioorg. Med. Chem. Lett., 2004, 14, 4207–4211.

[27] D. Lazzeri, M. Rovera, L. Pascual,  E.N. Durantini, Photochem. Photobiol., 2004, 80, 286–293.

[28] V.T. Orlandi, E. Caruso, S. Banfi, P. Barbieri, Photochem. Photobiol., 2012, 88, 557–564.

[29] H. Xing-qing, F. Yan-lin, W. Tian-jiao, W. La-mei, C. Lian-qing, J. Jiangxi Normal University, Natural Sciences, 2009, Edition 6.

[30] T. Kangwanwong, W. Pluempanupat, W. Parasuk, H.E. Keenan, A. Songsasen, Scienceasia, 2012, 38, 278–282.

[31] L. Jayashankar, B. Syama Sundar, R. Vijayaraghavan, K. S. AJM Betanabhatla, C. Athimoolam, J. Sundara Saravanan, K. Sundara Saravanan, Pharmacologyonline, 2008, 1, 66-77.

[32] N. Drogat, R. Granet, C.L. Morvan, G. Bégaud-Grimaud, P. Krausz, V. Sol, Bioorg. Med. Chem. Let., 2012, 22, 3648–3652.

[33] S. Mordon, C. Cochrane, J.B. Tylcz, N. Betrouni, L. Mortier, V. Koncar, Photodiag. Photodyn. Therap., 2015, 12(1), 1–8.

[34] S. Senthilkumar, R. Hariharan, A. Suganthi, M. Ashokkumar, M. Rajarajan, K. Pitchumani, Powder Technology, 2013, 237, 497–505.

[35] M. Krouit, R. Granet, P. Krausz, Photobactericidal Films from Porphyrins Grafted to Alkylated Cellulose–Synthesis and Bactericidal Properties. Eur. Polym. J., 2009, 45, 1250–1259.

آمار
تعداد مشاهده مقاله: 2,803
تعداد دریافت فایل اصل مقاله: 2,302


سامانه مدیریت نشریات علمی. قدرت گرفته از سیناوب