A novel crosslinked hyaluronic acid nanogel for drug delivery

Macromolecular Bioscience

Volumn 14, Issue 11, 2014, Pages 1556-1568

  Pedrosa, Sílvia Santos ^a   Gonçalves, Catarina ^a   David, Laurent ^b   Gama, Miguel ^a  

^a UNIVERSITY OF MINHO   (Portugal)

^b UNIVERSITÉ DE LYON   (France)

Author keywords

[No Author keywords available]

Indexed keywords

DRUG DELIVERY; HYALURONIC ACID; HYDROPHOBICITY; NANOSTRUCTURED MATERIALS; ORGANIC ACIDS;

AMPHIPHILICS; AVERAGE DIAMETER; DRUG-LOADING EFFICIENCY; HYDROPHOBIC DRUG; HYDROPHOBIC MOLECULES; LIPOPHILIC DRUGS; REDOX SENSITIVES; SIMVASTATIN;

LOADING;

1,4 BIS[3 (2 PYRIDYLDITHIO)PROPIONAMIDO]BUTANE; AMPHOPHILE; BUTANE; CROSS LINKING REAGENT; CURCUMIN; HYALURONIC ACID; NANOPARTICLE; POLYSACCHARIDE; SIMVASTATIN; UNCLASSIFIED DRUG; COLLOID; MACROGOL DERIVATIVE; NANOGEL; POLYETHYLENEIMINE;

ARTICLE; CONJUGATE; CROSS LINKING; CRYOELECTRON MICROSCOPY; DISPERSION; DRUG DELIVERY SYSTEM; FIELD EMISSION SCANNING ELECTRON MICROSCOPY; FLUORESCENCE SPECTROSCOPY; GEL; HYDROPHOBICITY; LIGHT SCATTERING; NANOFABRICATION; NANOGEL; OXIDATION REDUCTION POTENTIAL; PARTICLE SIZE; PROTON NUCLEAR MAGNETIC RESONANCE; RADIATION SCATTERING; ULTRAVIOLET SPECTROSCOPY; ZETA POTENTIAL; CHEMISTRY; COLLOID; HYDRODYNAMICS; LIGHT; MOLECULAR WEIGHT; OXIDATION REDUCTION REACTION; SMALL ANGLE SCATTERING; SPECTROFLUOROMETRY; SYNTHESIS; ULTRAVIOLET SPECTROPHOTOMETRY; X RAY DIFFRACTION;

HYA;

BUTANES; COLLOIDS; CROSS-LINKING REAGENTS; CRYOELECTRON MICROSCOPY; CURCUMIN; DRUG DELIVERY SYSTEMS; HYALURONIC ACID; HYDRODYNAMICS; LIGHT; MOLECULAR WEIGHT; OXIDATION-REDUCTION; PARTICLE SIZE; POLYETHYLENE GLYCOLS; POLYETHYLENEIMINE; PROTON MAGNETIC RESONANCE SPECTROSCOPY; SCATTERING, RADIATION; SCATTERING, SMALL ANGLE; SIMVASTATIN; SPECTROMETRY, FLUORESCENCE; SPECTROPHOTOMETRY, ULTRAVIOLET; X-RAY DIFFRACTION;

EID: 84927667186     PISSN: 16165187     EISSN: 16165195     Source Type: Journal    
DOI: 10.1002/mabi.201400135     Document Type: Article

References (37)

1. K. Y. Choi, G. Saravanakumar, J. H. Park, K. Park, Colloids Surf. B, Biointerfaces 2012, 99, 82.
2. K. Y. Choi, K. H. Min, J. H. Na, K. Choi, K. Kim, J. H. Park, I. C. Kwon, S. Y. Jeong, J. Mater. Chem. 2009, 19, 4102.
3. S. Ekici, P. Ilgin, S. Butun, N. Sahiner, Carbohydr. Polym. 2011, 84, 1306.
4. F. Li, B. C. Bae, K. Na, Bioconjug. Chem. 2010, 21, 1312.
5. A. Fakhari, C. Berkland, Acta Biomater. 2013, 9, 7081.
6. E. J. Oh, K. Park, K. S. Kim, J. Kim, J.-A. Yang, J.-H. Kong, M. Y. Lee, A. S. Hoffman, S. K. Hahn, J. Controlled Release 2010, 141, 2.
7. C. Cheng, E. Khoshdel, K. L. Wooley, Macromolecules 2007, 40, 2289.
8. Y.-L. Li, L. Zhu, Z. Liu, R. Cheng, F. Meng, J.-H. Cui, S.-J. Ji, Z. Zhong, Angew. Chem. Int. Ed. 2009, 48, 9914.
9. M. Talelli, M. Iman, A. K. Varkouhi, C. J. Rijcken, R. M. Schiffelers, T. Etrych, K. Ulbrich, C. F. van Nostrum, T. Lammers, G. Storm, W. E. Hennink, Biomaterials 2010, 31, 7797.
10. Y. Xu, F. Meng, R. Cheng, Z. Zhong, Macromol. Biosci. 2009, 9, 1254.
11. J. Li, M. Huo, J. Wang, J. Zhou, J. M. Mohammad, Y. Zhang, Q. Zhu, A. Y. Waddad, Q. Zhang, Biomaterials 2012, 33, 2310.
12. S. Ganesh, A. K. Iyer, D. V. Morrissey, M. M. Amiji, Biomaterials 2013, 34, 3489.
13. Y. Liu, J. Sun, W. Cao, J. Yang, H. Lian, X. Li, Y. Sun, Y. Wang, S. Wang, Z. He, Int. J. Pharm. 2011, 421, 160.
14. Y. Shen, Q. Li, J. Tu, J. Zhu, Carbohydr. Polym. 2009, 77, 95.
15. M. H. M. Oudshoorn, R. Rissmann, J. A. Bouwstra, W. E. Hennink, Polymer 2007, 48, 1915.
16. M. von Smoluchowski, Ann. Phys. 1906, 326, 756.
17. K. D. Wittrup, G. L. Verdine, " Protein Engineering for Therapeutics, " Elsevier Science, USA 2012, DOI: 10.1016/B978-0-12-396962-0.00013-6.
18. G. T. Hermanson, " Bioconjugate Techniques, " Elsevier Science, USA 2010, ISBN: 978-0-12-370501-3.
19. N. C. f. B. Information, "SID: 54454."
20. F. S. Palumbo, G. Pitarresi, D. Mandracchia, G. Tripodo, G. Giammona, Carbohydr. Polym. 2006, 66, 379.
21. M. Bodnár, L. Darõczi, G. Batta, J. Bakõ, J. Hartmann, J. Borbély, Colloid Polym. Sci. 2009, 287, 991.
22. Y.-J. Jin, U. Termsarasab, S.-H. Ko, J.-S. Shim, S. Chong, S.-J. Chung, C.-K. Shim, H.-J. Cho, D.-D. Kim, Pharm. Res. 2012, 29, 3443.
23. G. B. Dutt, S. Doraiswamy, J. Chem. Phys. 1992, 96, 2475.
24. M. M. G. Krishna, J. Phys. Chem. A 1999, 103, 3589.
25. J. Yao, L. Zhang, J. Zhou, H. Liu, Q. Zhang, Mol. Pharm. 2013, 10, 1080.
26. Y. Zhang, M. Huo, J. Zhou, D. Yu, Y. Wu, Carbohydr. Polym. 2009, 77, 231.
27. C. Goncalves, Y. Lalatonne, L. Melro, G. Badino, M. F. M. Ferreira, L. David, C. F. G. C. Geraldes, L. Motte, J. A. Martins, F. M. Gama, J Mater. Chem. B 2013, 1, 5853.
28. S. Mahor, E. Collin, B. C. Dash, A. Pandit, Curr. Drug Delivery 2011, 8, 354.
29. Y. H. Tao, J. Xu, M. Q. Chen, H. Y. Bai, X. Y. Liu, Carbohydr. Polym. 2012, 88, 118.
30. H. Salman, M. Bergman, M. Djaldetti, H. Bessler, Biomed. Pharmacother. =Biomed. Pharmacother. 2008, 62, 41.
31. M. K. Jain, P. M. Ridker, Nat. Rev. Drug Discovery 2005, 4, 977.
32. B. Kwak, F. Mulhaupt, S. Myit, F. Mach, Nat. Med. 2000, 6, 1399.
33. S. Manju, K. Sreenivasan, J. Colloid Interface Sci. 2011, 359, 318.
34. S. Doggui, J. K. Sahni, M. Arseneault, L. Dao, C. Ramassamy, J. Alzheimer's Dis. 2012, 30, 377.
35. S. D. Nath, N. T. Linh, A. Sadiasa, B. T. Lee, J. Biomater. Appl. 2013, 28, 1151.
36. G. Saravanakumar, K. Y. Choi, H. Y. Yoon, K. Kim, J. H. Park, I. C. Kwon, K. Park, Int. J. Pharm. 2010, 394, 154.
37. A. K. Yadav, A. Agarwal, G. Rai, P. Mishra, S. Jain, A. K. Mishra, H. Agrawal, G. P. Agrawal, Drug Delivery 2010, 17, 561.