Interaction between Cell-Penetrating Peptides and Acid-Sensitive Anionic Oligopeptides as a Model for the Design of Targeted Drug Carriers-Reference-Cited by-同舟云学术

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Interaction between Cell-Penetrating Peptides and Acid-Sensitive Anionic Oligopeptides as a Model for the Design of Targeted Drug Carriers

Published:2014-04-15 Issue:5 Volume:11 Page:1583-1590
ISSN:1543-8384
Container-title:Molecular Pharmaceutics
language:en
Short-container-title:Mol. Pharmaceutics

Author:

Sun Chunmeng¹²,Shen Wei-Chiang²,Tu Jiasheng¹,Zaro Jennica L.²

Affiliation:

1. State Key Laboratory of Natural Medicines, Department of Pharmaceutics, School of Pharmacy, China Pharmaceutical University, 24 Tong Jia Xiang, Nanjing 210009, China

2. Department of Pharmacology and Pharmaceutical Science, University of Southern California, 1985 Zonal Ave, Los Angeles, California 90033, United States

Funder

National Institutes of Health

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Pharmaceutical Science,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/mp400747k

Reference40 articles.

1. Cellular uptake of the tat protein from human immunodeficiency virus

2. MAP-mediated nuclear delivery of a cargo protein

3. Cytosolic delivery of a p16-peptide oligoarginine conjugate for inhibiting proliferation of MCF7 cells

4. Comparison of Cationic and Amphipathic Cell Penetrating Peptides for siRNA Delivery and Efficacy

5. Protein Transduction Domain of HIV-1 Tat Protein Promotes Efficient Delivery of DNA into Mammalian Cells

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