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Synthesis, characterization and antiproliferative activities of novel modified poly (maleic anhydride-co-vinyl acetate)/cytosine β-Darabinofuranoside hydrochloride conjugate

Year 2015, Volume: 19 Issue: 1, 73 - 81, 07.01.2015

Abstract

ABSTRACT
Poly (maleic anhydride-co-vinyl acetate) (MAVA) copolymer
was synthesized by free-radical- polymerization reaction in
methyl ethyl ketone (MEK) at 80 ºC using benzoyl-peroxide
(BPO) as the radical-initiator. MAVA was then modified with
anti-leukemic chemotherapy-agent cytosine β-Darabinofuranoside
hydrochloride (CF). Modification was
performed at 70 oC in dimethylformamide (DMF) containing
triethylamine (Et3N) as the catalyst. Structural characterization
of the copolymer and copolymer/drug couple (MAVA/CF) was
carried out by Fourier Transform Infrared (FTIR) and Nuclear
Magnetic Resonance (1H-NMR). FTIR and 1H-NMR spectra
confirmed the modification reaction. UV-Spectrophotometric
measurements indicated that MAVA/CF kept its molecular
integrity in physiological-body-fluid, PBS, for first four days.
Antiproliferative activities of MAVA/CF were also determined
by BrdU-cell-proliferation-ELISA assays using C6 and HeLa
cell lines (cisplatin and 5-fluorouracil used as positive control).
MAVA/CF appeared to have little antiproliferative activity
against C6 cell line while samples didn’t have antiproliferative
activity against HeLa cell line at low concentrations (< 100
μg/ml). Reaction mechanism was also recommended for
modification product MAVA/CF.
Keywords: Antiproliferative activity, copolymer modification,
cytosine β-D-arabinofuranoside hydrochloride, physiological
body fluid PBS, poly(maleic anhydride-co-vinyl acetate).

References

  • Saad GR, Morsi RE, Mohammady SZ, Elsabee MZ Dielectric relaxation of monoesters based poly(styrene-co-maleic anhydride) copolymer. J Polym Res 2008; 15:115-23
  • Atıcı OG, Akar A, Rahimian R Modification of poly(maleic anhydride-co- styrene) with hydroxyl containing compounds. Turk J Chem 2001; 25:259-66.
  • Patel H, Raval DA, Madamwar D, Patel SR Polymeric prodrug: Synthesis, release study and antimicrobial property of poly(styrene-co-maleic anhydride)-bound acriflavine. Angew Makromol Chem 1998; 263:25-30.
  • Liu HY, Cao K, Yao Z, Li BG, Hu GH Variations of the glass- transition temperature in the imidization of poly(styrene-co- maleic anhydride). J Appl Polym Sci 2007; 104:2418-22
  • Jain JP, Modi S, Domb AJ, Kumar N. Role of Polyanhydrides as localized Drug Carriers. Control Release 2005; 103:541- 63.
  • Breslow DS Biologically active synthetic polymers. Pure & Appl Chem 1976; 46:103-13.
  • Dhal PK, Holmes-Farley SR, Huval CC, Jozefiak TH. Polymers as drugs. Adv Polym Sci 2006;192:9-58.
  • Duncan R. The dawning era of polymer therapeutics. Nat Rev Drug Discov 2003; 2:347-60.
  • Greish K, Sawa T, Fang J, Akaika T, Maeda H SMA- doxorubicin, a new polymeric micellar drug for effective targeting to solid tumors. J Control Release 2004; 97:219-30.
  • Maeda H, Ueda M, Morinaga T, Matsumoto T Conjugation of poly(styrene-co-maleic acid) derivatives to the antitumor protein neocarzinostatin: pronounced improvements in pharmacological properties. J Med Chem 1985; 28:455-61.
  • Kobayashi A, Oda T, Maeda H Protein binding of macromolecular anticancer agent SMANCS: Characterization of poly(styrene-co-maleic acid) derivatives as an albumin binding ligand. J Bioact Compat Pol 1988; 3:319-33.
  • Ohtsuka N, Konno T, Myauchi Y, Meada H Anticancer effects of arterial administration of the anticancer agent SMANCS with lipiodol on metastatic lymph nodes. Cancer 1987; 59:1560-65.
  • Maeda H, Matsumoto T, Konno T, Iwai K, Ueda M Tailor- making of protein drugs by polymer conjugation for tumor targeting: A brief review on Smancs. J Protein Chem 1984; 3:181-93.
  • Greish K, Fang J, Inutsuka T, Nagamitsu A, Maeda H Macromolecular Therapeutics: Advantages and prospects with special emphasis on solid tumour targeting. Clin Pharmacokinet 2003; 42:1089-105.
  • Maeda H. SMANCS and polymer-conjugated macromolecular drugs: advantages in cancer chemotherapy. Adv Drug Deliv Rev 1991; 6:181-202.
  • Spridon D, Panaitescu L, Ursu D, and Uglea CV. Synthesis and biocompatibility of maleic anhydride copolymers: 1. maleic anhydride-vinyl acetate, maleic anhydride methyl methacrylate and maleic anhydride-styrene. Polym Int 1997; 43:175-81.
  • Vardanyan RS, Hruby VJ. Synthesis of Essential Drugs. Elsevier. Amsterdam. 2006.
  • Karakus G, Zengin HB, Akin Polat Z, Yenidunya AF, Aydin S Cytotoxicity of three maleic anhydride copolymers and common solvents used for polymer solvation. Polym Bull 2013; 70:1591-612.
  • Karakus G, Yenidunya AF, Zengin HB, Malatyali E, Ozcelik S Amoebicidal effect of poly(maleic anhydride-co-vinyl acetate) copolymer on entamoeba histolytica trophozoites. Med Chem 2011; 1:1-4.
  • Nguyen V, Yoshida W, Cohen Y. Graft polymerization of vinyl acetate onto silica. J Appl Polym Sci 2003; 87:300-10.
  • Karakus G, Akin Polat Z, Yenidunya AF, Zengin HB, Karakus CB. Synthesis, characterization and cytotoxicity of novel modified poly[(maleic anhydride)-co-(vinyl acetate)]/ noradrenaline conjugate. Polym Int 2013; 62: 492-500.
  • Kaplan Can H, Doğan AL, Rzaev ZMO, Uner AH, Güner A. Synthesis and antitumor activity of poly(3,4-dihydro-2H- pyran-co-maleic anhydride-co-vinyl acetate). J Appl Polym Sci 2005; 96:2352-9.
  • Sundell AM, Luttikhedde HJG. Drug release from ionomer cements based on hydrolyzed poly(vinylacetate-maleic anhydride). Pure Appl Chem 1999;A361045-59
  • Demirtas I, Sahin A, Ayhan B, Tekin S, Telci I. Antiproliferative effects of the methanolic extracts of sideritis libanotica labill. subsp. linearis. Rec Natural Prod 2009; 3:104–9.
  • Demirtas I, Sahin A. Bioactive volatile content of the stem and root of Centaurea carduiformis DC. subsp. carduiformis var. carduiformis. J Chem 2013; 125286: 6 pages.
  • Pal J, Singh H, Ghosh AK. Modification of LLDPE using esterified styrene maleic anhydride copolymer: Study of its properties and environmental degradability. J Appl Polym Sci 2004; 92:102-8.
  • Popa I, Offenberg H, Beldie C, Uglea CV. Benzocaine modified maleic anhydride copolymers-I. Synthesis and characterization of benzocaine modified poly(maleic anhydride-co-vinyl acetate), poly(maleic anhydride-co- methyl methacrylate) and poly(maleic anhydride-co-styrene). Eur Polym J 1997; 33:1511-14.
  • Chitanu GC, Popescu I, Carpov A. Synthesis and characterization of maleic anhydride copolymers and their derivatives. 2. New data on the copolymerization of maleic anhydride with vinyl acetate1. Rev Roum Chim 2006; 51: 923-9.
  • Coskun M, Seven P. Synthesis, characterization and investigation of dielectric properties of two-armed graft copolymers prepared with methyl methacrylate and styrene onto PVC using atom transfer radical polymerization. React Funct Polym 2011; 71: 395-401.
  • Qiao Z, Xie Y, Chen M, Xu J, Zhu Y, Qian Y. Synthesis of lead sulfide/(polyvinyl acetate) nanocomposites with controllable morphology. Chem Phys Lett 2000; 321: 504-7.
  • Barakat MF, Abdelkerim FM. Investigation of the polymers formed in reactor irradiated aniline and pyridine. Can J Chem 1973; 51:3860-5.
  • Tripp RA, Dluhy RA, Zhao Y. Novel nanostructures for SERS biosensing. Nanotoday (Review) 2008; 3:31-7.
  • Jeong JH, Byoun YS, Ko SB, Lee YS Chemical modification of poly(styrene-alt-maleic anhydride) with antimicrobial 4-aminobenzoic acid and 4-hydroxybenzoic acid. J Ind Eng Chem 2001; 7:310-5.
  • Ferruti P, Ranucci E, Trotta F, Gianasi E, G. Evagorou E, Wasil M, Wilson G, Duncan R. Synthesis, characterization and antitumour activity of platinum (II) complexes of novel functionalized poly(amido amine)s. Macromol Chem Phys 1999; 200:1644-54.
  • Kim SY, Kim C, Han IS, Lee SC, Kim SH, Lee KS, Choi Y, Byun Y. Inhibition effect of new farnesol derivatives on all- trans-retinoic acid metabolism. Metabolism 2001; 50:1356-60.
  • Kenawy ER, Abdel-Hay F, El-Newehy M, Ottenbrite RM. Effect of pH on the drug release rate from a new polymer- drug conjugate system. Polym Int 2008; 57: 85-91.
  • Balaji R, Nanjundan S. Copolymerization of 3-methoxy-4- methacryloyloxybenzal phenylimine with methyl methacrylate. Eur Polym J 1999; 35:1133-8.
  • Rzayev ZMO. Graft copolymers of maleic anhydride and its isostructurel analogues: High performance engineering materials. Int Rev Chem Eng 2011; 3:153-215.
  • Yoon KJ, Woo JH, Seo YS. Formaldehyde free cross-linking agents based on maleic anhydride copolymers. Fiber Polym 2003; 4:182-7.
  • Nemtoi G, Beldie C, Tircolea C, Popa I, Cretescu I, Humelnicu I, Humelnicu D. Behaviour of the poly(maleic anhydride-co- vinyl acetate) copolymer in aqueous solutions. Eur Polym J 2001; 37:729-35.
  • Ranjbar-Karimi R, Loghmani-Khouzani H. Synthesis of new azines in various reaction conditions and investigation of their cycloaddition reaction. J Iran Chem Soc 2011; 8: 223-30.
  • Sanmathi CS, Prasannakumar S, Sherigara BS. Terpolymerization of 2-ethoxy ethylmethacrylate, styrene and maleic anhydride:determination of the reactivity ratios. Bull Mater Sci 2004; 27:243-9.
  • Bruch M, Mäder D, Bauers F, Loontjens T, Mülhaupt R. Melt modification of poly(styrene-co-maleic anhydride) with alcohols in the presence of 1,3-oxazolines. J Polym Sci 2000; 38:1222-31.
  • Cox CJ, Dutta K, Petri ET, Hwang WC, Lin Y, Pascal SM, Basavappa R. The regions of securing and cyclin B proteins recognized by the ubiquitination machinery are natively unfolded. Febs Lett 2002; 527:303-8.

ORIGINAL RESEARCH

Year 2015, Volume: 19 Issue: 1, 73 - 81, 07.01.2015

Abstract

References

  • Saad GR, Morsi RE, Mohammady SZ, Elsabee MZ Dielectric relaxation of monoesters based poly(styrene-co-maleic anhydride) copolymer. J Polym Res 2008; 15:115-23
  • Atıcı OG, Akar A, Rahimian R Modification of poly(maleic anhydride-co- styrene) with hydroxyl containing compounds. Turk J Chem 2001; 25:259-66.
  • Patel H, Raval DA, Madamwar D, Patel SR Polymeric prodrug: Synthesis, release study and antimicrobial property of poly(styrene-co-maleic anhydride)-bound acriflavine. Angew Makromol Chem 1998; 263:25-30.
  • Liu HY, Cao K, Yao Z, Li BG, Hu GH Variations of the glass- transition temperature in the imidization of poly(styrene-co- maleic anhydride). J Appl Polym Sci 2007; 104:2418-22
  • Jain JP, Modi S, Domb AJ, Kumar N. Role of Polyanhydrides as localized Drug Carriers. Control Release 2005; 103:541- 63.
  • Breslow DS Biologically active synthetic polymers. Pure & Appl Chem 1976; 46:103-13.
  • Dhal PK, Holmes-Farley SR, Huval CC, Jozefiak TH. Polymers as drugs. Adv Polym Sci 2006;192:9-58.
  • Duncan R. The dawning era of polymer therapeutics. Nat Rev Drug Discov 2003; 2:347-60.
  • Greish K, Sawa T, Fang J, Akaika T, Maeda H SMA- doxorubicin, a new polymeric micellar drug for effective targeting to solid tumors. J Control Release 2004; 97:219-30.
  • Maeda H, Ueda M, Morinaga T, Matsumoto T Conjugation of poly(styrene-co-maleic acid) derivatives to the antitumor protein neocarzinostatin: pronounced improvements in pharmacological properties. J Med Chem 1985; 28:455-61.
  • Kobayashi A, Oda T, Maeda H Protein binding of macromolecular anticancer agent SMANCS: Characterization of poly(styrene-co-maleic acid) derivatives as an albumin binding ligand. J Bioact Compat Pol 1988; 3:319-33.
  • Ohtsuka N, Konno T, Myauchi Y, Meada H Anticancer effects of arterial administration of the anticancer agent SMANCS with lipiodol on metastatic lymph nodes. Cancer 1987; 59:1560-65.
  • Maeda H, Matsumoto T, Konno T, Iwai K, Ueda M Tailor- making of protein drugs by polymer conjugation for tumor targeting: A brief review on Smancs. J Protein Chem 1984; 3:181-93.
  • Greish K, Fang J, Inutsuka T, Nagamitsu A, Maeda H Macromolecular Therapeutics: Advantages and prospects with special emphasis on solid tumour targeting. Clin Pharmacokinet 2003; 42:1089-105.
  • Maeda H. SMANCS and polymer-conjugated macromolecular drugs: advantages in cancer chemotherapy. Adv Drug Deliv Rev 1991; 6:181-202.
  • Spridon D, Panaitescu L, Ursu D, and Uglea CV. Synthesis and biocompatibility of maleic anhydride copolymers: 1. maleic anhydride-vinyl acetate, maleic anhydride methyl methacrylate and maleic anhydride-styrene. Polym Int 1997; 43:175-81.
  • Vardanyan RS, Hruby VJ. Synthesis of Essential Drugs. Elsevier. Amsterdam. 2006.
  • Karakus G, Zengin HB, Akin Polat Z, Yenidunya AF, Aydin S Cytotoxicity of three maleic anhydride copolymers and common solvents used for polymer solvation. Polym Bull 2013; 70:1591-612.
  • Karakus G, Yenidunya AF, Zengin HB, Malatyali E, Ozcelik S Amoebicidal effect of poly(maleic anhydride-co-vinyl acetate) copolymer on entamoeba histolytica trophozoites. Med Chem 2011; 1:1-4.
  • Nguyen V, Yoshida W, Cohen Y. Graft polymerization of vinyl acetate onto silica. J Appl Polym Sci 2003; 87:300-10.
  • Karakus G, Akin Polat Z, Yenidunya AF, Zengin HB, Karakus CB. Synthesis, characterization and cytotoxicity of novel modified poly[(maleic anhydride)-co-(vinyl acetate)]/ noradrenaline conjugate. Polym Int 2013; 62: 492-500.
  • Kaplan Can H, Doğan AL, Rzaev ZMO, Uner AH, Güner A. Synthesis and antitumor activity of poly(3,4-dihydro-2H- pyran-co-maleic anhydride-co-vinyl acetate). J Appl Polym Sci 2005; 96:2352-9.
  • Sundell AM, Luttikhedde HJG. Drug release from ionomer cements based on hydrolyzed poly(vinylacetate-maleic anhydride). Pure Appl Chem 1999;A361045-59
  • Demirtas I, Sahin A, Ayhan B, Tekin S, Telci I. Antiproliferative effects of the methanolic extracts of sideritis libanotica labill. subsp. linearis. Rec Natural Prod 2009; 3:104–9.
  • Demirtas I, Sahin A. Bioactive volatile content of the stem and root of Centaurea carduiformis DC. subsp. carduiformis var. carduiformis. J Chem 2013; 125286: 6 pages.
  • Pal J, Singh H, Ghosh AK. Modification of LLDPE using esterified styrene maleic anhydride copolymer: Study of its properties and environmental degradability. J Appl Polym Sci 2004; 92:102-8.
  • Popa I, Offenberg H, Beldie C, Uglea CV. Benzocaine modified maleic anhydride copolymers-I. Synthesis and characterization of benzocaine modified poly(maleic anhydride-co-vinyl acetate), poly(maleic anhydride-co- methyl methacrylate) and poly(maleic anhydride-co-styrene). Eur Polym J 1997; 33:1511-14.
  • Chitanu GC, Popescu I, Carpov A. Synthesis and characterization of maleic anhydride copolymers and their derivatives. 2. New data on the copolymerization of maleic anhydride with vinyl acetate1. Rev Roum Chim 2006; 51: 923-9.
  • Coskun M, Seven P. Synthesis, characterization and investigation of dielectric properties of two-armed graft copolymers prepared with methyl methacrylate and styrene onto PVC using atom transfer radical polymerization. React Funct Polym 2011; 71: 395-401.
  • Qiao Z, Xie Y, Chen M, Xu J, Zhu Y, Qian Y. Synthesis of lead sulfide/(polyvinyl acetate) nanocomposites with controllable morphology. Chem Phys Lett 2000; 321: 504-7.
  • Barakat MF, Abdelkerim FM. Investigation of the polymers formed in reactor irradiated aniline and pyridine. Can J Chem 1973; 51:3860-5.
  • Tripp RA, Dluhy RA, Zhao Y. Novel nanostructures for SERS biosensing. Nanotoday (Review) 2008; 3:31-7.
  • Jeong JH, Byoun YS, Ko SB, Lee YS Chemical modification of poly(styrene-alt-maleic anhydride) with antimicrobial 4-aminobenzoic acid and 4-hydroxybenzoic acid. J Ind Eng Chem 2001; 7:310-5.
  • Ferruti P, Ranucci E, Trotta F, Gianasi E, G. Evagorou E, Wasil M, Wilson G, Duncan R. Synthesis, characterization and antitumour activity of platinum (II) complexes of novel functionalized poly(amido amine)s. Macromol Chem Phys 1999; 200:1644-54.
  • Kim SY, Kim C, Han IS, Lee SC, Kim SH, Lee KS, Choi Y, Byun Y. Inhibition effect of new farnesol derivatives on all- trans-retinoic acid metabolism. Metabolism 2001; 50:1356-60.
  • Kenawy ER, Abdel-Hay F, El-Newehy M, Ottenbrite RM. Effect of pH on the drug release rate from a new polymer- drug conjugate system. Polym Int 2008; 57: 85-91.
  • Balaji R, Nanjundan S. Copolymerization of 3-methoxy-4- methacryloyloxybenzal phenylimine with methyl methacrylate. Eur Polym J 1999; 35:1133-8.
  • Rzayev ZMO. Graft copolymers of maleic anhydride and its isostructurel analogues: High performance engineering materials. Int Rev Chem Eng 2011; 3:153-215.
  • Yoon KJ, Woo JH, Seo YS. Formaldehyde free cross-linking agents based on maleic anhydride copolymers. Fiber Polym 2003; 4:182-7.
  • Nemtoi G, Beldie C, Tircolea C, Popa I, Cretescu I, Humelnicu I, Humelnicu D. Behaviour of the poly(maleic anhydride-co- vinyl acetate) copolymer in aqueous solutions. Eur Polym J 2001; 37:729-35.
  • Ranjbar-Karimi R, Loghmani-Khouzani H. Synthesis of new azines in various reaction conditions and investigation of their cycloaddition reaction. J Iran Chem Soc 2011; 8: 223-30.
  • Sanmathi CS, Prasannakumar S, Sherigara BS. Terpolymerization of 2-ethoxy ethylmethacrylate, styrene and maleic anhydride:determination of the reactivity ratios. Bull Mater Sci 2004; 27:243-9.
  • Bruch M, Mäder D, Bauers F, Loontjens T, Mülhaupt R. Melt modification of poly(styrene-co-maleic anhydride) with alcohols in the presence of 1,3-oxazolines. J Polym Sci 2000; 38:1222-31.
  • Cox CJ, Dutta K, Petri ET, Hwang WC, Lin Y, Pascal SM, Basavappa R. The regions of securing and cyclin B proteins recognized by the ubiquitination machinery are natively unfolded. Febs Lett 2002; 527:303-8.
There are 44 citations in total.

Details

Primary Language English
Journal Section Articles
Authors

Gülderen Karakuş

Ayşe Şahin Yağlıoğlu This is me

Hacı Zengin This is me

Nihat Karakuş This is me

Publication Date January 7, 2015
Published in Issue Year 2015 Volume: 19 Issue: 1

Cite

APA Karakuş, G., Şahin Yağlıoğlu, A., Zengin, H., Karakuş, N. (2015). Synthesis, characterization and antiproliferative activities of novel modified poly (maleic anhydride-co-vinyl acetate)/cytosine β-Darabinofuranoside hydrochloride conjugate. Marmara Pharmaceutical Journal, 19(1), 73-81. https://doi.org/10.12991/mpj.2015198613
AMA Karakuş G, Şahin Yağlıoğlu A, Zengin H, Karakuş N. Synthesis, characterization and antiproliferative activities of novel modified poly (maleic anhydride-co-vinyl acetate)/cytosine β-Darabinofuranoside hydrochloride conjugate. Marmara Pharm J. January 2015;19(1):73-81. doi:10.12991/mpj.2015198613
Chicago Karakuş, Gülderen, Ayşe Şahin Yağlıoğlu, Hacı Zengin, and Nihat Karakuş. “Synthesis, Characterization and Antiproliferative Activities of Novel Modified Poly (maleic Anhydride-Co-Vinyl acetate)/Cytosine β-Darabinofuranoside Hydrochloride Conjugate”. Marmara Pharmaceutical Journal 19, no. 1 (January 2015): 73-81. https://doi.org/10.12991/mpj.2015198613.
EndNote Karakuş G, Şahin Yağlıoğlu A, Zengin H, Karakuş N (January 1, 2015) Synthesis, characterization and antiproliferative activities of novel modified poly (maleic anhydride-co-vinyl acetate)/cytosine β-Darabinofuranoside hydrochloride conjugate. Marmara Pharmaceutical Journal 19 1 73–81.
IEEE G. Karakuş, A. Şahin Yağlıoğlu, H. Zengin, and N. Karakuş, “Synthesis, characterization and antiproliferative activities of novel modified poly (maleic anhydride-co-vinyl acetate)/cytosine β-Darabinofuranoside hydrochloride conjugate”, Marmara Pharm J, vol. 19, no. 1, pp. 73–81, 2015, doi: 10.12991/mpj.2015198613.
ISNAD Karakuş, Gülderen et al. “Synthesis, Characterization and Antiproliferative Activities of Novel Modified Poly (maleic Anhydride-Co-Vinyl acetate)/Cytosine β-Darabinofuranoside Hydrochloride Conjugate”. Marmara Pharmaceutical Journal 19/1 (January 2015), 73-81. https://doi.org/10.12991/mpj.2015198613.
JAMA Karakuş G, Şahin Yağlıoğlu A, Zengin H, Karakuş N. Synthesis, characterization and antiproliferative activities of novel modified poly (maleic anhydride-co-vinyl acetate)/cytosine β-Darabinofuranoside hydrochloride conjugate. Marmara Pharm J. 2015;19:73–81.
MLA Karakuş, Gülderen et al. “Synthesis, Characterization and Antiproliferative Activities of Novel Modified Poly (maleic Anhydride-Co-Vinyl acetate)/Cytosine β-Darabinofuranoside Hydrochloride Conjugate”. Marmara Pharmaceutical Journal, vol. 19, no. 1, 2015, pp. 73-81, doi:10.12991/mpj.2015198613.
Vancouver Karakuş G, Şahin Yağlıoğlu A, Zengin H, Karakuş N. Synthesis, characterization and antiproliferative activities of novel modified poly (maleic anhydride-co-vinyl acetate)/cytosine β-Darabinofuranoside hydrochloride conjugate. Marmara Pharm J. 2015;19(1):73-81.