A New Hyaluronic Acid Derivative Obtained from Atom Transfer Radical Polymerization as a siRNA Vector for CD44 Receptor Tumor Targeting

Macromolecular Bioscience

Volumn 15, Issue 11, 2015, Pages 1605-1615

  Palumbo, Fabio Salvatore ^a   Bavuso Volpe, Antonella ^a   Bongiovì, Flavia ^a   Pitarresi, Giovanna ^a,b   Giammona, Gaetano ^c  

^a UNIVERSITY OF PALERMO   (Italy)

^b CNR Consiglio Nazionale delle Ricerche   (Italy)

^c CNR   (Italy)

Author keywords

ATRP; CD44; hyaluronic acid; siRNA delivery; tumor targeting

Indexed keywords

ATOMS; CATIONIC POLYMERIZATION; CELL CULTURE; FREE RADICAL REACTIONS; HYALURONIC ACID; LIGHT SCATTERING; ORGANIC ACIDS; POLYMERIZATION; TUMORS;

CD44; DIETHYLAMINOETHYL; DYNAMIC LIGHT SCATTERING MEASUREMENT; GEL-RETARDATION ASSAY; HYALURONIC ACID DERIVATIVES; POTENTIAL VALUES; SIRNA DELIVERY; TUMOR TARGETING;

ATOM TRANSFER RADICAL POLYMERIZATION;

CD44 RECEPTOR; HYALURONIC ACID; HYALURONIC ACID DERIVATIVE; LYMPHOCYTE ANTIGEN RECEPTOR; METHACRYLIC ACID; MONOMER; SMALL INTERFERING RNA; UNCLASSIFIED DRUG; CD44 PROTEIN, HUMAN; DIETHYLAMINOETHYL METHACRYLATE; HERMES ANTIGEN; METHACRYLIC ACID DERIVATIVE; TUMOR PROTEIN;

AQUEOUS SOLUTION; ARTICLE; ATOM TRANSFER RADICAL POLYMERIZATION; CELL INTERACTION; CELL MEMBRANE PERMEABILITY; CELL VIABILITY; CELLS BY BODY ANATOMY; COLORIMETRY; COMPLEX FORMATION; CONCENTRATION RESPONSE; CONTROLLED STUDY; CYTOTOXICITY; DERIVATIZATION; DOWN REGULATION; GENE SILENCING; GENE VECTOR; HCT116 CELL LINE; HETERONUCLEAR MULTIPLE QUANTUM COHERENCE; HUMAN; HUMAN CELL; HYDROLYSIS; IN VITRO STUDY; INTERNALIZATION; LYSOSOME; MOLECULAR WEIGHT; PH; POLYMERIZATION; PRECIPITATION; PROTEIN EXPRESSION; PROTEIN TARGETING; SOLUBILITY; SURFACE CHARGE; SURFACE PROPERTY; ZETA POTENTIAL; CHEMISTRY; DRUG DELIVERY SYSTEM; GENETICS; METABOLISM; NEOPLASMS; PATHOLOGY; PHARMACOLOGY; PROCEDURES; SYNTHESIS; TUMOR CELL LINE;

ANTIGENS, CD44; CELL LINE, TUMOR; DRUG DELIVERY SYSTEMS; GENETIC VECTORS; HUMANS; HYALURONIC ACID; METHACRYLATES; NEOPLASM PROTEINS; NEOPLASMS; RNA, SMALL INTERFERING;

EID: 84945469195     PISSN: 16165187     EISSN: 16165195     Source Type: Journal    
DOI: 10.1002/mabi.201500129     Document Type: Article

References (27)

1. J.-M. Lee, T.-J. Yoon, Y.-S. Cho, BioMed Res. Int. 2013, ID 782041.
2. L. Aagaard, J. J. Rossi, Adv. Drug Deliv. Rev. 2007, 59, 75.
3. J. Wang, Z. Lu, M. G. Wientjes, J. L.-S. Au, AAPS J. 2010, 12, 492.
4. Y.-K. Oh, T. G. Park, Adv. Drug Deliv. Rev. 2009, 61, 850.
5. a) A. J. Ditto, P. N. Shah, Y. H. Yun, Expert. Opin. Drug Deliv. 2009, 6, 1149;
6. b) T. G. Park, J. H. Jeongb, S. W. Kimb, Adv. Drug Deliv. Rev. 2006, 58, 467;
7. c) S. E. Han, H. Kang, G. Y. Shim, S. J. Kim, H. G. Choi, J. Kim, S. K. Hahn, Y. K. Oh, J Drug Target. 2009, 17, 123.
8. F. J. Verbaan, C. Oussoren, I. M. van Dam, Y. Takakura, M. Hashida, D. J. A. Crommelin, W. E. Hennink, G. Storm, Int. J. Pharm. 2001, 214, 99.
9. K. Y. Choi, G. Saravanakumar, J. H. Park, K. Park, Colloids Surf. B Biointerfaces 2012, 99, 82.
10. G. Pasut, Polymers 2014, 6, 160.
11. G. Pitarresi, F. S. Palumbo, A. Albanese, C. Fiorica, P. Picone, G. Giammona, J. Drug Target. 2010, 4, 264.
12. X. B. Xiong, H. Uludag, A. Lavasanifar, Biomaterials 2009, 30, 242.
13. K. Park, S. W. Hong, W. Hur, M.-Y. Lee, J.-A. Yang, S. W. Kim, S. K. Yoon, S. K. Hahn, Biomaterials 2011, 32, 4951.
14. a) M. Licciardi, G. Cavallaro, G. Amato, C. Fiorica, G. Giammona, React. Funct. Polym. 2012, 72, 268;
15. b) N. H. Abd, Ellah, S. J. Potter, L. Taylor, N. Ayres, M. M. Elmahdy, G. N. Fetih, E.-S. A. Ibrahim, G. M. Pauletti, J. Pharm. Technol. Drug Res. 2014, 3, 2.
16. X. Z. Shu, Y. Liu, Y. Luo, M. C. Roberts, G. D. Prestwich, Biomacromolecules 2002, 3, 1304.
17. F. S. Palumbo, G. Pitarresi, D. Mandracchia, G. Tripodo, G. Giammona, Carbohydr. Polym. 2006, 66, 379.
18. E. L. Ferguson, M. J. Alshame, D. W. Thomas, Int. J. Pharm. 2010, 402, 95.
19. F. S. Palumbo, G. Pitarresi, C. Fiorica, P. Matricardi, A. Albanese, G. Giammona, Soft Matter 2012, 8, 4918.
20. G. Pitarresi, C. Fiorica, M. Licciardi, F. S. Palumbo, G. Giammona, Carbohydr. Polym. 2013, 92, 1054.
21. G. Cavallaro, M. Licciardi, G. Amato, C. Sardo, G. Giammona, R. Farra, B. Dapas, M. Grassi, G. Grassi, Int. J. Pharm. 2014, 466, 246.
22. Y. Onishi, Y. Eshita, R.-C. Ji, M. Onishi, T. Kobayashi, M. Mizuno, J. Yoshida, N. Kubota, Beilstein J. Nanotechnol. 2014, 5, 2293.
23. F. S. Palumbo, A. Volpe Bavuso, M. G. Cusimano, G. Pitarresi, G. Giammona, D. Schillaci, Int. J. Pharm. 2015, 478, 70.
24. A. Aied, U. Greiser, A. Pandit, W. Wang, Drug Discov. Today 2013, 18, 1090.
25. a) C. Wang, J. Xie, J. Guo, H. C. Manning, J. C. Gore, N. Guo, Oncol. Rep. 2012, 28, 1301;
26. b) S. H. Sahlberg, D. Spiegelberg, B. Glimelius, B. Stenerlo, M. Nestor, PLoS ONE 2014, 9, e94621.
27. S. Ganesh, A. K. Iyer, D. V. Morrissey, M. M. Amiji, Biomaterials 2013, 34, 3489.