Dergiler / Hittite Journal of Science and Engineering / 2022 / Cilt: 9 - Sayı: 4

Design, Synthesis and Characterization of 1,2-Phenylenediamine Functionalized Poly (Maleic Anhydride-alt-Vinyl Acetate) as a Potential New Bioactive Formulation

Sayfa
305–311
Yayın Tarihi
2022-12-31
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Spectroscopic methods and water solubility results confirmed that the conjugation took place successfully after the ring opening reaction by the amidation mechanism.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:This study includes the design, synthesis and characterization of 1,2-phenylenediamine (o-PDA) functionalized maleic anhydride (MA)-vinyl acetate (VA) copolymer-based conjugate to develop a new formulation.
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Temel Bulgular & Veri:The 1,2-phenylenediamine molecule is a fluorescent dye that allows designing new chemotherapeutic polymeric molecules.
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Sonuç & Katkı:Spectroscopic methods and water solubility results confirmed that the conjugation took place successfully after the ring opening reaction by the amidation mechanism.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:poli(MA-alt-VA) · Surface modification · 2-phenylenediamine

Abstract

This study includes the design, synthesis and characterization of 1,2-phenylenediamine (o-PDA) functionalized maleic anhydride (MA)-vinyl acetate (VA) copolymer-based conjugate to develop a new formulation. The 1,2-phenylenediamine molecule is a fluorescent dye that allows designing new chemotherapeutic polymeric molecules. Poly(maleic anhydride-alt-vinyl acetate) [Poly(MA-alt-VA)] was obtained via charge transfer complex (CTC) radical polymerization presence of methyl ethyl ketone (MEK), utilizing benzoyl peroxide (BPO) free-radical initiator at 80 °C, as a potential functional polymeric carrier. Structural characterization of the surface functionalized poly(MA-alt-VA)/1,2-PDA conjugate was performed by Attenuated Total Reflectance-Fourier Transform Infrared (ATR-FTIR) and Nuclear Magnetic Resonance (1H-NMR). Spectroscopic methods and water solubility results confirmed that the conjugation took place successfully after the ring opening reaction by the amidation mechanism.

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Bu Makaleye Atıf Yap

KARAKUŞ, G. (2022). Design, Synthesis and Characterization of 1,2-Phenylenediamine Functionalized Poly (Maleic Anhydride-alt-Vinyl Acetate) as a Potential New Bioactive Formulation. Hittite Journal of Science and Engineering, Cilt: 9 - Sayı: 4, 305–311. https://ajindex.com/articles/859842

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Kaynakça (14)

  1. I.D. Ibrahim, T. Jamiru, E.R. Sadiku, W.K. Kupolati, S.C. Agwuncha, Mechanical properties of sisal fibre-reinforced polymer composites: a review, Compos. Interface., 23(1) (2016) 15-36
  2. E.R. Fuchs, F.R. Field, R. Roth, R.E. Kirchain, Strategic materials selection in the automobile body: Economic opportunities for polymer composite design, Compos. Sci. Technol., 68 (2008) 1989-2002
  3. S.P. Victor, J. Muthu, Bioactive mechanically favorable, and biodegradable copolymer nanocomposites for orthopedic applications, Mater. Sci. Eng. C. Mater. Biol. Appl., 39 (2014) 150-160
  4. Z. Ma, Z. Mao, C. Gao, Surface modification and property analysis of biomedical polymers used for tissue engineering, Colloids. Surf. B. Biointerfaces., 60 (2007) 137-157
  5. F. Scognamiglio, A. Travan, I. Rustighi, P. Tarchi, S. Palmisano, Adhesive and sealant interfaces for general surgery applications, J. Biomed. Mater. Res. B. Appl. Biomater., 104(3) (2016) 626-639
  6. H. Ringsdorf, Structure and properties of pharmacologically active polymers, J. Polym. Sci., 51 (1975) 135–153
  7. R. Duncan, Polymer conjugates for tumour targeting and intracytoplasmic delivery. The EPR effect as a common gateway?, Res. Focus. Rev., 2 (1999) 441–449
  8. D. Spridon, L. Panaitescu, D. Ursu, C.V. Uglea, Synthesis and biocompatibility of maleic anhydride copolymers: 1. Maleic anhydride–vinyl acetate, maleic anhydride methyl methacrylate and maleic anhydride-styrene, Polym. Int., 43 (1997) 175–181
  9. G.R. Saad, R.E. Morsi, S.Z. Mohammady, M.Z. Elsabee, Dielectric relaxation of monoesters based poly(styrene-co-maleic anhydride) copolymer, J. Polym. Res., 15 (2008) 115–123
  10. H.Y. Liu, K. Cao, Z. Yao, B.G. Li, G.H. Hu, Variations of the glass-transition temperature in the imidization of poly(styrene-co-maleic anhydride), J. Appl. Polym. Sci., 104 (2007) 2418–2422
  11. R-J. Yu, J-J. Sun, H. Song, J-Z. Tian, D-W. Li, Y-T. Long, Real-Time Sensing of O-Phenylenediamine Oxidation on Gold Nanoparticles, Sensors., 17 (2017) 530. 12.
  12. G. Karakus, H.B. Zengin, Z. Akin-Polat, A.F. Yenidunya, S. Aydin, Cytotoxicity of three maleic anhydride copolymers and common solvents used for polymer solvation, Polym. Bull., 70 (2013) 1591–1612
  13. G. Karakus, Z. Akin-Polat, A.F. Yenidunya, H.B. Zengin, C.B. Karakus, Synthesis, characterization and cytotoxicity of novel modified poly[(maleic anhydride)-co-(vinyl acetate)]/noradrenaline conjugate, Polym. Int., 62 (2013) 492–500
  14. H. Kapl