Morphology, optical, thermal and antimicrobial studies of ibuprofen-based hyperbranched polyester
Source abstract
Abstract
Herein we report the synthesis of ibuprofen-based hyperbranched polyester ranging from morphological, thermal and fluorescent behaviour. The proposed synthesis of ibuprofen-based hyperbranched polyester was achieved by a simple acid chloride approach. The formation of aromatic ester linkage in the product was confirmed using Fourier transform infrared and nuclear magnetic resonance spectroscopy. The morphology of ibuprofen-based hyperbranched polyester was investigated by using the X-ray diffraction, scanning electron microscopy and differential scanning calorimetry (DSC) analyses. The glass transition temperature (~78°C) and double melting peaks of ibuprofen-based hyperbranched polyester were observed using DSC. The liquid chromatography-mass spectrometry analysis confirmed the chemical structure and the molecular weight of the ibuprofen-based hyperbranched polyester. The presence of broad absorption peak at 301 nm in UV region indicated the fluorescent property of ibuprofen-based hyperbranched polyester. The antimicrobial tests of ibuprofen-based hyperbranched polyester were carried against Gram-negative organisms such as Escherichia coli MCIM 2065 and Salmonella paratyphi MCIM 2501, Gram-positive organisms such as Bacillus subtilis NCIM 2063 and Staphylococcus aureus NCIM 2079 and fungi such as Aspergillus niger MTCC 1344 and Candida albicans MTCC 3100. The result of agar disc diffusion method showed that the polymer had higher antimicrobial potential towards fungi than bacteria.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Dendrimers and Hyperbranched Polymers · Antimicrobial agents and applications · Luminescence and Fluorescent Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (36)
Show source-provided references
1. Karpagam S and Venkateswaran M 2014 Int. J. Pharm. Invest. 44 110.1007/s40005-013-0086-z ↗
2. Saeed H A M, Eltahir Y A, Xia Y and Yimin W 2014 Russ. J. Appl. Chem. 87 148110.1134/S1070427214100140 ↗
3. Gregorwicz J, Wawrzynska E P, Parzuchowski P G, Fras Z, Rokicki G, Wojciechowski K et al 2013 Macromolecules 46 718010.1021/ma401086m ↗
4. Xie A, Chen H, Xu C, Chen H, Zhou Y, Lin Y et al 2015 J. Coat. Technol. Res. 12 32510.1007/s11998-014-9636-1 ↗
5. Saeed H A M and Yimin W 2013 Russ. J. Appl. Chem. 86 156910.1134/S1070427213100157 ↗
6. Kavitha C and Priya Dasan K 2013 J. Coat. Technol. Res. 10 66910.1007/s11998-013-9499-x ↗
7. Yang D, Chen Z, Rong X, Zhang H and Qiu F 2014 J. Polym. Res. 21 33110.1007/s10965-013-0331-1 ↗
8. Chattopadhyay D K, Sreedhar B and Raju K V S N 2006 J. Polym. Sci. Part B: Polym. Phys. 44 10210.1002/polb.20586 ↗
9. Li X, Essawy H A, Pizzi A, Delmotte L, Rode K, Nouen D L et al 2012 J. Polym. Res. 19 2110.1007/s10965-012-0021-4 ↗
10. Postnova I, Silant’ev V, Kim M H, Song G Y, Kim I L, Ha C et al 2013 Colloids Surf. B 103 3110.1016/j.colsurfb.2012.10.026 ↗
11. Krukiewicz K and Zak J K 2014 J. Mater. Sci. 49 573810.1007/s10853-014-8292-2 ↗
12. Sivakumar C and Nasar A S 2009 J. Polym. Sci. Part A: Polym. Chem. 47 333710.1002/pola.23404 ↗
13. Shanmugam T, Sivakumar C and Nasar A S 2008 J. Polym. Sci. Part A: Polym. Chem. 46 541410.1002/pola.22861 ↗
14. Wu L, Lu S, Pan L, Luo Q, Yang J, Hou L et al 2016 Fiber Polym. 17 215310.1007/s12221-016-6257-6 ↗
15. Mahdavi H, Hosseinzadeh M T and Shahalizade T 2015 J. Iran. Chem. Soc. 12 146510.1007/s13738-015-0615-y ↗
16. Wei D, Ge L and Guo R 2010 J. Phys. Chem. B 114 347210.1021/jp910315e ↗
17. Kolhe P, Khandare J, Pillai O, Kannan S, Lieh-Lai M and Kannan R 2004 Pharm. Res. 21 218510.1007/s11095-004-7670-x ↗
18. Rosario-Melendez R, Yu W and Uhrich K E 2013 Biomacromolecules 14 354210.1021/bm400889a ↗
19. Ali H A, Omar S N, Daraesheh M D and Fares H 2016 J. Coord. Chem. 69 111010.1080/00958972.2016.1149819 ↗
20. Kamari Y and Ghiaci M 2016 Microporous Mesoporous Mater. 234 36110.1016/j.micromeso.2016.07.030 ↗
21. Obad J, Suskovic J and Kos B 2015 Eur. J. Pharm. Sci. 71 9310.1016/j.ejps.2015.02.011 ↗
22. Hasegawa U, Van der Viles A J, Wandrey C and Hubbell J A 2013 Biomacromolecules 14 331410.1021/bm4009149 ↗
23. Garcia-Arguelles S, Serrano M C, Gutierrez M C, Ferrer M L, Yuste L, Rojo F et al 2013 Langmuir 29 952510.1021/la401353r ↗
24. Stebbins N D, Yu W and Uhrich K E 2015 Biomacromolecules 16 363210.1021/acs.biomac.5b01088 ↗
25. Pereira e Silva I M, Profirio D M, Ferraz de Paiva R E, Lancellotti M, Formiga A L B and Corbi P P 2013 J. Mol. Struct. 1049 110.1016/j.molstruc.2013.06.034 ↗
26. Prabu S and Sivakumar C 2018 J. Coat. Technol. Res. 15 105910.1007/s11998-017-0041-4 ↗
27. Prabu S, Nasar A S and Sivakumar C 2018 Macromol. Res. 26 83110.1007/s13233-018-6116-y ↗
28. Makvandi P, Ghaemy M, Ghadiri A A and Mohseni M 2015 J. Dent. Res. 94 140110.1177/0022034515599973 ↗
29. Jianmei P, Yuxia L, Feifei L, Xiaoqing C, Jimin D and Li Z 2011 Int. J. Nanomed. 6 65910.2217/nnm.11.22 ↗
30. Safaa M Y, Ali H A and Mahmoud A M 2016 J. Chem. Eng. Process Technol. 7 1
31. Ming-Yih J and Feng-Chih D C 2001 Polymer 42 503710.1016/S0032-3861(00)00888-0 ↗
32. Xianzhen L, Wenjin Z, Yong Z, Qioong H, Wei Y and Yong C 2005 Eur. Polym. J. 41 292310.1016/j.eurpolymj.2005.05.039 ↗
33. Elvers K T and Wright S J L 1995 Lett. Appl. Microbiol. 20 8210.1111/j.1472-765X.1995.tb01291.x ↗
34. Shah P N, Marshall-Batty K R, Smolen J A, Tagaev J A, Chen Q, Rodesney C A et al 2018 Antimicrob. Agents Chemother. 62 110.1128/AAC.01574-17 ↗
35. Karpagam S and Guhanathan S 2014 Prog. Org. Coat. 77 190110.1016/j.porgcoat.2014.06.022 ↗
36. Kenawy E R, Worley S D and Broughton R 2007 Biomacromolecules 8 135910.1021/bm061150q ↗