Abstract
One of the current challenges in cancer chemotherapy is the ultra-sensitive identification of in vivo tumors. Herein, we report a new class of tumor-identifying polypeptides that can home in on in vivo tumors via an electrostatic charge conversion process occurring in the acidic milieu of a verity of tumors, which can be distinguished from receptor-interacting conventional tumor-homing peptides. We exploit the chemical coupling between polypeptides and therapeutic objects (drugs or particles) to carry out an antitumor study in nude mice, and find a significant increase in the efficiency of polypeptide-tagged objects in tumor uptake and inhibition, which is more significant than any known tumor-homing peptide system thus far developed.
Original language | English |
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Pages (from-to) | 1884-1893 |
Number of pages | 10 |
Journal | Biomaterials |
Volume | 33 |
Issue number | 6 |
DOIs | |
State | Published - Feb 2012 |
Bibliographical note
Funding Information:This work was financially supported by the Research Fund, 2011 of the Catholic University of Korea, the Research Grant funded by the Gyeonggi Regional Research Center (GRRC) , by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science, and Technology (No. 2011-0003874, 2011-0004766 ), and by a grant from the Fundamental R&D Program for Core Technology of Materials funded by the Ministry of Knowledge Economy , Republic of Korea.
Keywords
- Cancer chemotherapy
- Photodynamic therapy
- Tumor extracellular pH
- Tumor-identifying polypeptide