Synthesis, characterization and drug release activity of poly(ε-caprolactone)/Fe₃O₄–alizarinred nanocomposites

References

• B. J. Ireland, C. A. Wheaton and P. G. Hayes: ‘Cationic organo magnesium complexes as highly active initiators for the ring opening polymerization of ε-caprolactone’, Organometallics, 2010, 29, 1079–1084.10.1021/om900669y
   Web of Science ®Google Scholar
• M. L. Gou, Z. Y. Qian, H. Wang, Y. B. Tang and M. J. Huang: ‘Preparation and characterization of magnetic poly (ε-caprolactone)-poly (ethyleneglycol) -poly (ε-caprolactone) microspheres’, J. Mater. Sci. Mater. Med., 2008, 19, 1033–1041.10.1007/s10856-007-3230-3
   PubMed Web of Science ®Google Scholar
• X. Deliang and J. Bian: ‘Study on the ring opening polymerization of ε-caprolactone initiated by hydroxyl acids’, Acta Polym. Sinica., 2000, 5, 532–537.
   Google Scholar
• H. Liu, Z. Shen, S. E. Stiriba and Y. Chen: ‘Coreshell type multiarm star PEI-b-PCL: synthesis and guest encapsulation potential’, J. Polym. Sci. Part A Polym. Chem., 2006, 44, 4165–4173.10.1002/(ISSN)1099-0518
   Web of Science ®Google Scholar
• R. S. Lee, W. H. Chen and J. H. Lin: ‘Polymer grafted MWCNT through surface initiated ring opening polymerization and click reaction’, Polymer, 2001, 52, 2180–2188.
   Google Scholar
• A. Sowkath, A. Mansur and R. Anbarasan: ‘Synthesis, characterization and application of a novel Schiff base’, J. Chem. Bio. Phy. Sci. Sec A., 2014, 4, 1930–1940.
   Google Scholar
• B. Meenarathi, S. Palanikumar, L. Kannammal and R. Anbarasan: ‘Synthesis and characterizations of Fe3O4-acidfuchsin tagged poly (ε-caprolactone) nanocomposites’, Mater. Res. Exp., 2014, 1, 1–16.
   Google Scholar
• L. Kannammal, S. Palanikumar, B. Meenarathi, A. Yelilarasi and R. Anbarasan: ‘Synthesis, characterization and band gap energy of poly(ε-caprolactone)/Sr-MSA nanocomposite’, J. Phys. D: Appl. Phys., 2014, 47, 1–10.
   Web of Science ®Google Scholar
• K. Agathian, P. Siva, B. Meenarathi and R. Anbarasan: ‘Luminol intiated ring opening polymerization of ε-caprolactone’, Ind. J. Sci., 2013, 5, 37–40.
   Google Scholar
• B. Meenarathi, H. H. Chen, P. H. Chen and R. Anbarasan: ‘Near infrared dye functionalized MWCNT as an effective initiator for the ring opening polymerization of ε-caprolactone’, J. Polym. Res., 2013, 20, 118–130.10.1007/s10965-013-0118-4
   Web of Science ®Google Scholar
• B. Wu, R. W. Lenz and B. Hazer: ‘Synthesis, characterization and drug delivery activity of poly (anthranilicacid) based triblock copolymer’, Macromolecules, 1999, 32, 6856–6859.10.1021/ma990166o
   Web of Science ®Google Scholar
• B. A. Rozenberg: ‘Kinetics and mechanism of ε-caprolactone anionic polymerization under the influence of amines’, Pure Appl. Chem., 1981, 53, 1715–1727.
   Web of Science ®Google Scholar
• V. T. Lipik and M. J. M. Asadie: ‘Process optimization of poly(ε-caprolactone) synthesizing ring opening polymerization’, Iran. Polym. J., 2010, 19, 885–893.
   Web of Science ®Google Scholar
• G. Wu, J. Liu, W. Sun and Z. Shen: ‘Ring opening polymerization of ε-caprolactone by a new yuttium complex’, Polym. Int., 2010, 59, 431–436.10.1002/pi.v59:4
   Web of Science ®Google Scholar
• A. Kiersnowski, P. Dąbrowski, H. Budde and J. Kressler: ‘Synthesis and structure of poly(caprolactone)/synthetic montmorillonite nanointercalates’, Eur. Polym. J., 2004, 40, 2591–2598.10.1016/j.eurpolymj.2004.06.014
   Web of Science ®Google Scholar
• T. F. Al-Azemi, L. Kondaveti and K. S. Bisht: ‘Solventless enantioselective ring opening polymerization of substituted ε-caprolactone by enzymatic catalysis’, Macromolecules, 2002, 35, 3380–3386.10.1021/ma012016v
   Web of Science ®Google Scholar
• G. Carrot, J. G. Hilborn and M. Trollsås: ‘Two general methods for the synthesis of thiol functionalized poly (ε-caprolactone)’, Macromolecules, 1999, 32, 5264–5269.10.1021/ma990198b
   Web of Science ®Google Scholar
• I. Lin, C. G. Cheng, Y. -C. Yen and F. C. Chang: ‘Synthesis and assembly behavior of heteronucleobase-functionalized of poly (ε-caprolactone)’, Macromolecules, 2010, 43, 1245–1252.10.1021/ma9026614
   Web of Science ®Google Scholar
• M. Oshimura and A. Takasu: ‘Controlled ring opening polymerization of ε-caprolactone by rare earth perfluoroalkanesulfonates and perfluoroalkanesulfonimides’, Macromolecules, 2010, 43, 2283–2290.10.1021/ma902557t
   Web of Science ®Google Scholar
• Y. C. Wang, X. Q. Liu, T. M. Sun, M. H. Xiong and J. Wang: ‘Functionalized micelles from block co polymer of polyphosphoester and poly(ε-caprolactone) for receptor mediated drug delivery’, J. Contr. Rel., 2008, 128, 32–40.10.1016/j.jconrel.2008.01.021
   PubMed Web of Science ®Google Scholar
• M. J. Kim, D. H. Jang and Y. H. Choa: ‘Preparation and characterization of carboxyl functionalization of magnetic nanoparticles for oligo nucleotide immobilization’, Phys. Ser., 2010, 139, 1–4.
   Google Scholar
• H. Lida, K. Takayanagi, T. Nakanishi and T. Osaka: ‘Synthesis of Fe3O4 nanoparticles with various sizes and magnetic properties by controlled hydrolysis’, J. Colloid Inter. Sci., 2007, 314, 274–280.
   PubMed Web of Science ®Google Scholar
• S. Ahmad, U. Riaz, A. Kaushik and J. Alam: ‘Soft template synthesis of superparamagnetic Fe3O4 nanoparticles a novel technique’, J. Inorg. Organomet. Polym., 2009, 19, 355–360.10.1007/s10904-009-9276-6
   Web of Science ®Google Scholar
• S. Palanikumar, L. Kannammal, B. Meenarathi and R. Anbarasan: ‘Effect of folic acid functionalized magnetic fluorescent nanoparticles on the sedimentation of starch molecules’, Int. Nano Lett., 2014, 4, 104–113.10.1007/s40089-014-0104-9
   Google Scholar
• Z. Li, H. Chen, H. Bao and M. Gao: ‘One pot reaction to synthesize water soluble magnetic nanocrystals’, Chem. Mater., 2004, 16, 1391–1393.10.1021/cm035346y
   Web of Science ®Google Scholar
• A. Kayrak, R. C. Foitzik and M. Pfeffer: ‘Fluorescence and conductivity studies on wool’, Mater. Chem. Phys., 2009, 113, 480–484.
   Web of Science ®Google Scholar
• V. Kohila, M. G. Sribala, L. Kannammal, B. Meenarathi, T. Dhanalakshmi and R. Anbarasan: ‘Synthesis and spectral characterization of poly(congored) grafted silk fibre: A kinetic Approach’, Ind. J. Fibre. Text. Res., 2014, 9, 172–179.
   Google Scholar
• A. Khazaoi, S. Saedina, M. K. Borazjgani and F. Abbasi: ‘Synthesis and characterization of novel polymer drug conjugates based on the poly(Styrene-alt-maleic anhydride) as a potential method for drug release’, Acta Chim. Slov., 2013, 60, 724–731.
   PubMed Web of Science ®Google Scholar
• J. Sultana, M. S. Hossaih, S. M. A. Islam and M. S. Islam: ‘Synthesis and characterizations of Fe3O4-acidfuchsin tagged poly (ε- caprolactone) nanocomposites’, Ind. J. Novel Drug Del., 2012, 4, 145–150.
   Google Scholar
• H. J. Liu, H. C. Chu, L. H. Lin and S. Y. Hsu: ‘Effect of MWCNT and Au nanoparticle on the structure-property relationship of poly (N-isopropylacrylamide)’, Int. J. Polym. Mater. Polym. Biomater., 2015, 64, 7–14.10.1080/00914037.2014.886238
   Web of Science ®Google Scholar
• A. C. Salome, C. O. Godswil and I. O. Ikecha: ‘Kinetics and mechanisms of drug release from swellable and non-swellable matrices: a review’, Res. J. Pharm. Biol. Chem. Sci., 2013, 4, 97–103.
   Google Scholar
• M. Olukman, O. Şanlı and E. K. Solak: ‘Release of anticancer drug 5-fluorouracil form different ionically cross linked alginate beads’, J. Biomater. Nanobiotechnol., 2012, 3, 469–479.10.4236/jbnb.2012.34048
   Google Scholar
• S. Palanikumar, B. Meenarathi, L. Kannammal and R. Anbarasan: ‘Effect of Fe3O4 on the sedimentation and structure-property relationship of starch under different pHs’, Int. J. Biol. Macromol., 2014, 67, 91–98.10.1016/j.ijbiomac.2014.03.012
   PubMed Web of Science ®Google Scholar
• B. Meenarathi, S. Palanikumar, L. Kannammal and R. Anbarasan: ‘Synthesis, characterization and catalytic activity of Ag-acidfuchsin nanohybrid system towards the ring opening polymerization of ɛcaprolactone’, Spectrochim. Acta Part A, 2015, 135, 93–100.10.1016/j.saa.2014.06.136
   PubMed Web of Science ®Google Scholar
• R. Rahimi, A. Tadjarodi, M. Imani, M. Rabbani, S. Safalou and H. Kerdari: ‘Synthesis of tetrakis(carboxyphenyl)porphyrin coated paramagnetic iron oxide nanoparticles via amino acid for photodegradation of methylene blue’, Turk. J. Chem., 2013, 37, 879–888.10.3906/kim-1204-19
   Web of Science ®Google Scholar
• A. M. Demin, V. P. Krasnov and V. N. Charushin: ‘Covalent surface modification of Fe3O4 magnetic nanoparticles with alkoxy silanes and amino acids’, Mendaleev Commun., 2013, 23, 14–16.10.1016/j.mencom.2013.01.004
   Web of Science ®Google Scholar
• R. Anbarasan and C. A. Peng: ‘Effect of MWCNT and Au nanoparticle on the structure-property relationship of poly (N-isopropylacrylamide)’, J. Appl. Polym. Sci., 2012, 124, 3996–4006.10.1002/app.v124.5
   Web of Science ®Google Scholar
• S. Kailash, B. Meenarathi, L. Kannammal, S. Palanikumar and R. Anbarasan: ‘Synthesis, characterization, drug delivery, and splinting activity of folic acid bridged poly(ε-caprolactone-co-tetrahydrofuran)’, Int. J. Polym. Mater. Polym. Biomater., 2015, 64, 620–627.10.1080/00914037.2014.996711
   Web of Science ®Google Scholar
• B. Meenarathi, H. H. Chen, P. H. Chen and R. Anbarasan: ‘Synthesis and characterization of fluorescent bio-degradable poly(ε-caprolactone)’, Int. J. Plast. Technol., 2014, 18, 135–145.10.1007/s12588-014-9070-3
   Google Scholar