pH and Redox Dual Responsive Nanoparticle for Nuclear Targeted Drug Delivery

Remant Bahadur K. C.; Bindu Thapa; Peisheng Xu

doi:10.1021/mp300274g

journal article Aug 22, 2012

pH and Redox Dual Responsive Nanoparticle for Nuclear Targeted Drug Delivery

Remant Bahadur K. C. Bindu Thapa Peisheng Xu

Molecular Pharmaceutics Vol. 9 No. 9 pp. 2719-2729 · American Chemical Society (ACS)

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References

43

[1]

Brannon-Peppas L. Adv. Drug Delivery Rev. (2004) 10.1016/j.addr.2004.02.014

[2]

10.3402/nano.v1i0.5705

[3]

Li Z. Science (2004) 10.1126/science.1103350

[4]

Toroidal Triblock Copolymer Assemblies

Darrin J. Pochan, Zhiyun Chen, Honggang Cui et al.

Science 2004 10.1126/science.1102866

[5]

Wiradharma N. Nano Today (2009) 10.1016/j.nantod.2009.06.001

[6]

Duncan R. Nat. Rev. Drug Discovery (2003) 10.1038/nrd1088

[7]

Nanocarriers as an emerging platform for cancer therapy

Dan Peer, Jeffrey M. Karp, Seungpyo Hong et al.

Nature Nanotechnology 2007 10.1038/nnano.2007.387

[8]

Otsuka H. Adv. Drug Delivery Rev. (2003) 10.1016/s0169-409x(02)00226-0

[9]

Chan Y. Biomacromolecules (2008) 10.1021/bm800043n

[10]

Wong L. Biomacromolecules (2008) 10.1021/bm800197v

[11]

Sun P. J. J. Controlled Release (2011) 10.1016/j.jconrel.2011.08.140

[12]

Bauhuber S. Adv. Mater. (2009) 10.1002/adma.200802453

[13]

Bahadur K. C. R. Macromol Biosci. (2012) 10.1002/mabi.201100464

[14]

Jia Z. Biomacromolecules (2009) 10.1021/bm900817a

[15]

Ghosh S. Macromolecules (2006) 10.1021/ma061420x

[16]

Synthesis of Poly(β-amino ester)s with Thiol-Reactive Side Chains for DNA Delivery

Gregory T. Zugates, Daniel G. Anderson, Steven R. Little et al.

Journal of the American Chemical Society 2006 10.1021/ja061570n

[17]

Ryu J. H. J. Am. Chem. Soc. (2010) 10.1021/ja102316a

[18]

Liu J. Macromol. Rapid Commun. (2012) 10.1002/marc.201200029

[19]

Syrett J. A. Chem. Commun. (Cambridge) (2011) 10.1039/c0cc04532b

[20]

Duong H. T. T. Macromolecules (2011) 10.1021/ma201085z

[21]

Klaikherd A. J. Am. Chem. Soc. (2009) 10.1021/ja809475a

[22]

Bird R. Soft Matter (2012) 10.1039/c1sm06507f

[23]

Ganta S. J. Controlled Release (2008) 10.1016/j.jconrel.2007.12.017

[24]

Meng F. H. Biomaterials (2009) 10.1016/j.biomaterials.2009.01.026

[25]

Bae Y. Angew Chem Int Edit (2003) 10.1002/anie.200250653

[26]

Zhou X. J. Am. Chem. Soc. (2004) 10.1021/ja0446496

[27]

Furgeson D. Y. J. Controlled Release (2006) 10.1016/j.jconrel.2005.10.006

[28]

Shi M. Adv. Funct. Mater. (2009) 10.1002/adfm.200801271

[29]

Cheng R. J. Controlled Release (2011) 10.1016/j.jconrel.2011.01.030

[30]

Oba M. Bioconjugate Chem. (2007) 10.1021/bc0700133

[31]

Monnier Y. Cancer Res. (2008) 10.1158/0008-5472.can-08-0841

[32]

Ghosh S. Macromolecules (2006) 10.1021/ma061420x

[33]

Redox environment of the cell as viewed through the redox state of the glutathione disulfide/glutathione couple

Freya Q. Schafer, Garry R. Buettner

Free Radical Biology and Medicine 2001 10.1016/s0891-5849(01)00480-4

[34]

Boyer C. J. Polym. Sci., Part A: Polym. Chem. (2008) 10.1002/pola.23028

[35]

Kim Y. Nanotechnology (2005) 10.1088/0957-4484/16/7/024

[36]

Chen J. Biomacromolecules (2011) 10.1021/bm200804j

[37]

Patel S. K. Biomaterials (2010) 10.1016/j.biomaterials.2009.09.051

[38]

Murthy N. J. Controlled Release (1999) 10.1016/s0168-3659(99)00114-5

[39]

Allen T. M. Nat. Rev. Cancer (2002) 10.1038/nrc903

[40]

Tkachenko A. G. J. Am. Chem. Soc. (2003) 10.1021/ja0296935

[41]

Tkachenko A. G. Bioconjugate Chem. (2004) 10.1021/bc034189q

[42]

Xu P. Angew. Chem., Int. Ed. (2007) 10.1002/anie.200605254

[43]

Xu P. Mol. Pharmaceutics (2009) 10.1021/mp800137z

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References

Details

Published: Aug 22, 2012
Vol/Issue: 9(9)
Pages: 2719-2729

Authors

R

Remant Bahadur K. C.

Department of Pharmaceutical and Biomedical Sciences, South Carolina College of Pharmacy, University of South Carolina, 715 Sumter Street, Columbia, South Carolina 29208, United States

B

Bindu Thapa

Department of Pharmaceutical and Biomedical Sciences, South Carolina College of Pharmacy, University of South Carolina, 715 Sumter Street, Columbia, South Carolina 29208, United States

P

Peisheng Xu

Department of Pharmaceutical and Biomedical Sciences, South Carolina College of Pharmacy, University of South Carolina, 715 Sumter Street, Columbia, South Carolina 29208, United States; Center for Colon Cancer Research, University of South Carolina, 712 Main Street, Columbia, South Carolina 29208, United States; NanoCenter, University of South Carolina, 1212 Greene Street, Columbia, South Carolina 29208, United States

Cite This Article

Remant Bahadur K. C., Bindu Thapa, Peisheng Xu (2012). pH and Redox Dual Responsive Nanoparticle for Nuclear Targeted Drug Delivery. Molecular Pharmaceutics, 9(9), 2719-2729. https://doi.org/10.1021/mp300274g

pH and Redox Dual Responsive Nanoparticle for Nuclear Targeted Drug Delivery

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