Issue 17, 2013

Cell-penetrating albumin conjugates for enhanced doxorubicin delivery

Abstract

Albumin-based drug delivery has been demonstrated to be useful for achieving improved cancer therapy, largely due to its passive target toward tumor via the enhanced permeability and retention effect and the increased demand for albumin by tumor cells as source of energy and amino acids. However, albumin lacks not only the active mechanism to overcome the cell membrane barrier, but also the ability to penetrate into tumor tissues. Herein, a cell-penetrating albumin-based delivery strategy was developed, in which a cell-penetrating peptide was chemically conjugated to albumin in order to enhance the efficiency of intracellular delivery and tumor penetration. Doxorubicin (DOX) molecules were loaded into the carrier via cleavable disulfide bonds, which are responsive to the highly reducing environment in the cytosol of tumor cells, thus archiving prodrug-type targeted drug release. The cell-penetrating albumin–DOX conjugates displayed significantly higher antitumor activity than DOX. More interestingly, the conjugates also efficiently killed the drug-resistant tumor cells, in sharp contrast to the ineffective DOX. The studies with human xenograft tumors in nude mice further demonstrated the enhanced antitumor efficacy and reduced side effects of the cell-penetrating albumin-assisted DOX delivery strategy, indicating the promise of this delivery system.

Graphical abstract: Cell-penetrating albumin conjugates for enhanced doxorubicin delivery

Supplementary files

Article information

Article type
Communication
Submitted
06 Jun 2013
Accepted
09 Jul 2013
First published
10 Jul 2013

Polym. Chem., 2013,4, 4584-4587

Cell-penetrating albumin conjugates for enhanced doxorubicin delivery

Q. Guo, H. Wang, Y. Zhao, H. Wang, F. Zeng, H. Hua, Q. Xu and Y. Huang, Polym. Chem., 2013, 4, 4584 DOI: 10.1039/C3PY00742A

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