Block copolypeptide nanoparticles for the delivery of ocular therapeutics

Macromolecular Bioscience

Volumn 15, Issue 1, 2015, Pages 138-145

  Stukenkemper, Timo ^a   Dose, Anica ^a   Gonzalez, Maria Caballo ^a,b   Groenen, Alexander J J ^a   Hehir, Sarah ^a   Andres Guerrero, Vanessa ^b   Vanrell, Rocio Herrero ^b   Cameron, Neil R ^a  

^a DURHAM UNIVERSITY   (United Kingdom)

^b UNIVERSIDAD COMPLUTENSE DE MADRID   (Spain)

Author keywords

Block copolymers; Drug delivery systems; Nanoparticles; Polypeptides; Ring opening polymerization

Indexed keywords

AMINO ACIDS; BLOCK COPOLYMERS; CONTROLLED DRUG DELIVERY; DRUG PRODUCTS; DYNAMIC LIGHT SCATTERING; MICELLES; NANOPARTICLES; ORGANIC SOLVENTS; POLYPEPTIDES; SELF ASSEMBLY; SPHERES; TARGETED DRUG DELIVERY;

AMPHIPHILIC BLOCK COPOLYMERS; ANTI-INFLAMMATORY DRUGS; COPOLYMER COMPOSITIONS; DRUG DELIVERY SYSTEM; NANOPARTICLE PREPARATIONS; NUMBER AVERAGE MOLECULAR WEIGHT; SELECTIVE DEPROTECTION; SYNTHESIZED POLYMERS;

RING OPENING POLYMERIZATION;

COPOLYMER; COPOLYPEPTIDE NANOPARTICLE; DEXAMETHASONE; GLUTAMIC ACID; N CARBOXYANHYDRIDE; NANOCARRIER; POLYANHYDRIDE; UNCLASSIFIED DRUG; ACID ANHYDRIDE; DRUG CARRIER; GAMMA-BENZYLGLUTAMYL-N-CARBOXY ANHYDRIDE; GLUTAMIC ACID DERIVATIVE; MICELLE; NANOPARTICLE; NILE RED; OXAZINE DERIVATIVE; PEPTIDE; POLY-GAMMA-BENZYL-L-GLUTAMATE; POLYGLUTAMIC ACID;

ARTICLE; CHEMICAL STRUCTURE; DRUG DELIVERY SYSTEM; DRUG RELEASE; NANOENCAPSULATION; PROTON NUCLEAR MAGNETIC RESONANCE; RING OPENING METATHESIS POLYMERIZATION; SYNTHESIS; ANALOGS AND DERIVATIVES; CHEMISTRY; DRUG DESIGN; EYE DISEASES; HUMAN; MICELLE; NANOMEDICINE; PROCEDURES; TRENDS;

ANHYDRIDES; DEXAMETHASONE; DRUG CARRIERS; DRUG DESIGN; EYE DISEASES; GLUTAMATES; HUMANS; MICELLES; MOLECULAR STRUCTURE; NANOMEDICINE; NANOPARTICLES; OXAZINES; PEPTIDES; POLYGLUTAMIC ACID;

EID: 84920803868     PISSN: 16165187     EISSN: 16165195     Source Type: Journal    
DOI: 10.1002/mabi.201400471     Document Type: Article

References (20)

1. R. Herrero-Vanrell, I. Bravo-Osuna, V. Andres-Guerrero, M. Vicario-de-la-Torre, I. T. Molina-Martínez, Prog. Retin. Eye Res. 2014, 42, 27.
2. R. Herrero-Vanrell, M. F. Refojo, Adv. Drug Deliv. Rev. 2001, 52, 5.
3. S. Hehir, N. R. Cameron, Polym. Int. 2014, 63, 943.
4. H. R. Kricheldorf, Angew. Chem. Int. Ed. 2006, 45, 5752.
5. J. Cheng, T. J. Deming, Top. Curr. Chem. 2012, 1, 310.
6. T. Aliferis, H. Iatrou, N. Hadjichristidis, Biomacromolecules 2004, 5, 1653.
7. T. J. Deming, Nature 1997, 390, 386.
8. T. J. Deming, J. Am. Chem. Soc. 1997, 119, 2759.
9. H. Lu, J. Cheng, J. Am. Chem. Soc. 2007, 129, 14114.
10. H. Lu, J. Cheng, J. Am. Chem. Soc. 2008, 130, 12562.
11. W. Vayaboury, O. Giani, H. Cottet, S. Bonaric, F. Schue, Macromol Chem. Phys. 2008, 209, 1628.
12. W. Vayaboury, O. Giani, H. Cottet, A. Deratani, F. Schue, Macromol Rapid Commun. 2004, 25, 1221.
13. I. Dimitrov, H. Schlaad, Chem. Commun. 2003, 23, 2944.
14. I. Conejos-Sanchez, A. Duro-Castano, A. Birke, M. Barz, M. J. Vicent, Polym. Chem. 2013, 4, 3182.
15. J. Zou, J. Fan, X. He, S. Zhang, H. Wang, K. L. Wooley, Macromolecules 2013, 46, 4223.
16. F. Checot, J. Rodrguez-Hernandez, Y. Gnanou, S. Lecommandoux, Biomol. Eng. 2007, 24, 81.
17. J. Rodrguez-Hernandez, S. Lecommandoux, J. Am. Chem. Soc. 2005, 127.
18. W. H. Daly, D. Poche, Tetrahedron Lett. 1988, 29, 5859.
19. D. Fischer, Y. X. Li, B. Ahlemeyer, J. Krieglstein, T. Kissel, Biomaterials 2003, 24, 1121.
20. W. Agut, A. Brulet, D. Taton, S. Lecommandoux, Langmuir 2007, 23, 11526.