Design of pH-responsive nanoparticles of terpolymer of poly(methacrylic acid), polysorbate 80 and starch for delivery of doxorubicin

Colloids and Surfaces B: Biointerfaces

Volumn 101, Issue , 2013, Pages 405-413

  Shalviri, Alireza ^a   Chan, Ho Ka ^a   Raval, Gaurav ^a   Abdekhodaie, Mohammad J ^a,b   Liu, Qiang ^c   Heerklotz, Heiko ^a   Wu, Xiao Yu ^a  

^a UNIVERSITY OF TORONTO   (Canada)

^b SHARIF UNIVERSITY OF TECHNOLOGY   (Iran)

^c GUELPH RESEARCH AND DEVELOPMENT CENTRE   (Canada)

Author keywords

Doxorubicin delivery; Nanoparticles; One pot synthesis; PH responsive; Poly(methacrylic acid) polysorbate 80 starch; Terpolymer

Indexed keywords

ANTICANCER DRUG; AQUEOUS MEDIUM; CHEMICAL COMPOSITIONS; CONTROLLED DELIVERY; CROSS LINKING AGENTS; DOXORUBICIN; FTIR; HIGH LOADINGS; IN-VITRO; MONOMER CONCENTRATION; NANOPARTICLE FORMATION; NARROW SIZE DISTRIBUTIONS; ONE-POT METHOD; ONE-POT SYNTHESIS; PH-DEPENDENT SWELLING; PH-RESPONSIVE; PHYSIOLOGICAL PH RANGE; POLY (METHACRYLIC ACID); POLYMER COMPOSITION; POLYSORBATE 80; POLYSORBATES; POROUS MORPHOLOGY; POTENTIOMETRIC TITRATIONS;

CONTROLLED DRUG DELIVERY; CROSSLINKING; EMULSIONS; GRAFTING (CHEMICAL); NANOPARTICLES; PH; STARCH; TERPOLYMERS; TITRATION; VOLTAMMETRY;

SYNTHESIS (CHEMICAL);

DOXORUBICIN; NANOPARTICLE; POLYMETHACRYLIC ACID; POLYSORBATE 80; STARCH; SURFACTANT;

AQUEOUS SOLUTION; ARTICLE; CHEMICAL COMPOSITION; CONTROLLED STUDY; DRUG DELIVERY SYSTEM; DRUG DESIGN; DRUG RELEASE; DRUG SYNTHESIS; INFRARED SPECTROSCOPY; MOLECULAR INTERACTION; PARTICLE SIZE; PH; POTENTIOMETRY; PRIORITY JOURNAL; PROCESS OPTIMIZATION; PROTON NUCLEAR MAGNETIC RESONANCE; TRANSMISSION ELECTRON MICROSCOPY;

ANTIBIOTICS, ANTINEOPLASTIC; CARBOXYLIC ACIDS; DOXORUBICIN; EXCIPIENTS; HYDROGEN-ION CONCENTRATION; LIGHT; MAGNETIC RESONANCE SPECTROSCOPY; MICROSCOPY, ELECTRON, TRANSMISSION; NANOPARTICLES; PARTICLE SIZE; POLYMETHACRYLIC ACIDS; POLYSORBATES; SCATTERING, RADIATION; SPECTROSCOPY, FOURIER TRANSFORM INFRARED; STARCH;

EID: 84865517797     PISSN: 09277765     EISSN: 18734367     Source Type: Journal    
DOI: 10.1016/j.colsurfb.2012.07.015     Document Type: Article

References (46)

1. Gref R., Minamitake Y., Peracchia M.T., Trubetskoy V., Torchilin V., Langer R. Science 1994, 263:1600.
2. Gref R., Domb A., Quellec P., Blunk T., Müller R., Verbavatz J., Langer R. Adv. Drug Deliv. Rev. 1995, 16:215.
3. Lemarchand C., Gref R., Couvreur P. Eur. J. Pharm. Biopharm. 2004, 58:327.
4. Passirani C., Barratt G., Devissaguet J.P., Labarre D. Pharm. Res. 1998, 15:1046.
5. Weissleder R., Bogdanov A., Neuwelt E.A., Papisov M. Adv. Drug Deliv. Rev. 1995, 16:321.
6. Besheer A., Vogel J., Glanz D., Kressler J., Groth T., Mäder K. Mol. Pharm. 2009, 6:407.
7. Stahn R., Zeisig R. Tumor Biol. 2000, 21:176.
8. Ellis H., Ring S. Carbohydr. Polym. 1985, 5:201.
9. Kerr R.W. Chemistry and Industry of Starch 1950, Academic Press, New York, NY.
10. Beliakova M.K., Aly A.A., Abdel Mohdy F.A. Starch/Stärke 2004, 56:407.
11. Celik M., Sacak M. J. Appl. Polym. Sci. 2002, 86:53.
12. Hebeish A., Beliakova M., Bayazeed A. J. Appl. Polym. Sci. 1998, 68:1709.
13. Liu M., Cheng R., Wu J., Ma C. J. Polym. Sci., Part A: Polym. Chem. 1993, 31:3181.
14. Sangramsingh N., Patra B., Singh B., Patra C. J. Appl. Polym. Sci. 2004, 91:981.
15. Trimnell D., Stout E. J. Appl. Polym. Sci. 1980, 25:2431.
16. Zhang L.M., Chen D.Q. Starch/Stärke 2001, 53:311.
17. Nguyen C.C., Martin V.J., Pauley E.P. Starch graft polymers. US 5003022 1991, vol. 5003022. Penford Products Company, Cedar Rapids, Iowa.
18. Athawale V., Rathi S. J. Macromol. Sci., Polym. Rev. 1999, 39:445.
19. Saboktakin M.R., Maharramov A., Ramazanov M.A. Carbohydr. Polym. 2009, 77:634.
20. Strickley R.G. Pharm. Res. 2004, 21:201.
21. Cappel M.J., Kreuter J. Int. J. Pharm. 1991, 69:143.
22. Wohlfart S., Gelperina S., Kreuter J. J. Control. Release 2011, 161:264.
23. Kreuter J. Adv. Drug Deliv. Rev. 2001, 47:65.
24. Kreuter J. Curr. Med. Chem.: Cent. Nerv. Syst. Agents 2002, 2:241.
25. Zhang Z., Feng S.S. Biomacromolecules 2006, 7:1139.
26. Wiersema P., Loeb A., Overbeek J.T.G. J. Colloid Interface Sci. 1966, 22:78.
27. Kawaguchi S., Nishikawa Y., Kitano T., Ito K., Minakata A. Macromolecules 1990, 23:2710.
28. Kitano T., Kawaguchi S., Ito K., Minakata A. Macromolecules 1987, 20:1598.
29. Wu X.Y., Zhang Q., Arshady R. Stimuli sensetive hydrogels: response and release modulation. Introduction to Polymeric Biomaterials 2004, Citus Books, London. R. Arshady (Ed.).
30. Zeman L., Patterson D. J. Phys. Chem. 1972, 76:1214.
31. Aggarwal A., Saxena R., Wang B., Caneba G.T. J. Appl. Polym. Sci. 1996, 62:2039.
32. Donbrow M., Azaz E., Pillersdorf A. J. Pharm. Sci. 1978, 67:1676.
33. Ha E., Wang W., Wang Y.J. J. Pharm. Sci. 2002, 91:2252.
34. Donbrow M. Nonionic Surfactants: Physical Chemistry 1987, Marcel Dekker, New York.
35. Nema S., Washkuhn R., Brendel R. J. Pharm. Sci. Technol. 1997, 51:166.
36. Maeda H., Wu J., Sawa T., Matsumura Y., Hori K. J. Control. Release 2000, 65:271.
37. Tauer K., Ali A.M.I., Sedlak M. Colloid Polym. Sci. 2005, 283:351.
38. Wu X.Y., Lee P.I. Pharm. Res. 1993, 10:1544.
39. Hoare T., Pelton R. Langmuir 2004, 20:2123.
40. Kawaguchi S., Yekta A., Winnik M.A. J. Colloid Interface Sci. 1995, 176:362.
41. Shalviri A., Liu Q., Abdekhodaie M.J., Wu X.Y. Carbohydr. Polym. 2010, 79:898.
42. Tian Y., Bromberg L., Lin S.N., Alan Hatton T., Tam K.C. J. Control. Release 2007, 121:137.
43. Tian Y., Ravi P., Bromberg L., Hatton T.A., Tam K.C. Langmuir 2007, 23:2638.
44. Liu Z., Cheung R., Wu X.Y., Ballinger J.R., Bendayan R., Rauth A.M. J. Control. Release 2001, 77:213.
45. Li X., Hirsh D.J., Cabral-Lilly D., Zirkel A., Gruner S.M., Janoff A.S., Perkins W.R. Biochim. Biophys. Acta 1998, 1415:23.
46. Tannock I.F., Rotin D. Cancer Res. 1989, 49:4373.