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Cited by 984

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Nuclear-Targeted Drug Delivery of TAT Peptide-Conjugated Monodisperse Mesoporous Silica Nanoparticles

Pan, Limin, He, Qianjun, Liu, Jianan, Chen, Yu, Ma, Ming, Zhang, Linlin, Shi, Jianlin·2012·Journal of the American Chemical Society

Abstract

Most present nanodrug delivery systems have been developed to target cancer cells but rarely nuclei. However, nuclear-targeted drug delivery is expected to kill cancer cells more directly and efficiently. In this work, TAT peptide has been employed to conjugate onto mesoporous silica nanoparticles (MSNs-TAT) with high payload for nuclear-targeted drug delivery for the first time. Monodispersed MSNs-TAT of varied particle sizes have been synthesized to investigate the effects of particle size and TAT conjugation on the nuclear membrane penetrability of MSNs. MSNs-TAT with a diameter of 50 nm or smaller can efficiently target the nucleus and deliver the active anticancer drug doxorubicin (DOX) into the targeted nucleus, killing these cancer cells with much enhanced efficiencies. This study may provide an effective strategy for the design and development of cell-nuclear-targeted drug delivery.

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Metadata

Authors
Pan, L., He, Q., Liu, J., Chen, Y., Ma, M., Zhang, L., & Shi, J.
Venue
Journal of the American Chemical Society
Published
2012-03-20
Volume
134
Issue
13
Pages
5722-5725
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W1981053807
Cited by
984
References
0
FWCI
28.74
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Nuclear-Targeted Drug Delivery of TAT Peptide-Conjugated Monodisperse Mesoporous Silica Nanoparticles. https://app.cochat.ai/papers/10.1021/ja211035w
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Pan, L., He, Q., Liu, J., Chen, Y., Ma, M., Zhang, L., & Shi, J. (2012). Nuclear-Targeted Drug Delivery of TAT Peptide-Conjugated Monodisperse Mesoporous Silica Nanoparticles. Journal of the American Chemical Society. https://doi.org/10.1021/ja211035w

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