journal article·2017-04-05

MnO2-Based Nanoplatform Serves as Drug Vehicle and MRI Contrast Agent for Cancer Theranostics

Mei Zhang, Lei Xing, Hengte Ke, Yu-Jing He, Peng-Fei Cui, Yong Zhu, Ge Jiang, Jian-Bin Qiao, Na Lu, Huabing Chen, Hu-Lin Jiang

Publisher page

Abstract

Multidrug resistance (MDR) greatly impedes the therapeutic efficacy of chemotherapeutic agents. Overexpression of ATP-binding cassette (ABC) transporters, such as P-gp, on the surface of tumor cells is a major mechanism in MDR. In this study, we fabricated manganese dioxide (MnO 2 )/doxorubicin (DOX)-loaded albumin nanoparticles (BMDN) for magnetic resonance imaging and reversing MDR in resistant tumor. BMDN facilitated the delivery of DOX into MDR tumor cells through their MDR reversal effects including enhanced cellular uptake, reduced drug efflux, and decreased hypoxic tumor microenvironment. BMDN also acted as an effective MRI contrast agent, thereby causing good in vitro and in vivo T 1 -weighted imaging.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Nanoparticle-Based Drug Delivery · Nanoplatforms for cancer theranostics · Drug Transport and Resistance Mechanisms

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

College of Life Sciences and Biotechnology, Dalian University, Dalian, China

Funding

Ministry of Science and Technology of the People's Republic of China · Natural Science Foundation of Jiangsu Province · National Natural Science Foundation of China · State Key Laboratory of Natural Medicines, China Pharmaceutical University · Jiangsu Province

References (30)

Show source-provided references
1. 10.1038/nrc278910.1038/nrc2789 ↗
2. 10.1038/nrc70610.1038/nrc706 ↗
3. 10.1517/14656566.7.8.104110.1517/14656566.7.8.1041 ↗
4. 10.1155/2014/94059110.1155/2014/940591 ↗
5. 10.1016/j.jconrel.2008.05.01010.1016/j.jconrel.2008.05.010 ↗
6. Vogel S. M. · Am. J. Physiol. Lung Cell. Mol. Physiol. · 2001 · 281 · L151210.1152/ajplung.2001.281.6.L1512 ↗
7. 10.1111/j.1365-2990.2010.01072.x10.1111/j.1365-2990.2010.01072.x ↗
8. 10.3892/ijo.17.4.68310.3892/ijo.17.4.683 ↗
9. 10.1158/0008-5472.CAN-10-404910.1158/0008-5472.CAN-10-4049 ↗
10. 10.1007/s10555-007-9058-y10.1007/s10555-007-9058-y ↗
11. 10.1038/nrc70410.1038/nrc704 ↗
12. 10.1111/j.1582-4934.2009.00994.x10.1111/j.1582-4934.2009.00994.x ↗
13. 10.1016/j.gde.2009.10.00910.1016/j.gde.2009.10.009 ↗
14. 10.1021/nn405773r10.1021/nn405773r ↗
15. 10.1002/adma.20140514110.1002/adma.201405141 ↗
16. 10.1016/j.biomaterials.2011.11.08610.1016/j.biomaterials.2011.11.086 ↗
17. 10.1002/anie.20110310810.1002/anie.201103108 ↗
18. 10.1021/ja108409510.1021/ja1084095 ↗
19. 10.1002/anie.20090668910.1002/anie.200906689 ↗
20. 10.1016/j.ccr.2013.03.00710.1016/j.ccr.2013.03.007 ↗
21. 10.1021/cm00008a02110.1021/cm00008a021 ↗
22. 10.1002/sia.740160112010.1002/sia.7401601120 ↗
23. 10.1016/j.actbio.2012.12.02410.1016/j.actbio.2012.12.024 ↗
24. 10.1016/j.actbio.2014.12.00110.1016/j.actbio.2014.12.001 ↗
25. 10.1111/bph.1307910.1111/bph.13079 ↗
26. 10.1021/nn202410f10.1021/nn202410f ↗
27. 10.1517/13543776.2011.56178410.1517/13543776.2011.561784 ↗
28. 10.4137/DTI.S1251910.4137/DTI.S12519 ↗
29. 10.1002/jcb.2412210.1002/jcb.24122 ↗
30. 10.1002/adma.20140257210.1002/adma.201402572 ↗