journal article·2015-05-20

Surface-Eroding Poly(ortho ester amides) for Highly Efficient Oral Chemotherapy

Bing Wei, Yangyang Tao, Xin Wang, Rupei Tang, Jun Wang, Rui Wang, Liying Qiu

Publisher page

Abstract

Two new poly(ortho ester amide) copolymers (POEA-4 and POEA-5) were synthesized via polycondensation of a new ortho ester diamine monomer with active esters of different aliphatic diacids. The kinetics of POEA mass loss and release of 5-FU were both nearly zero-order, suggesting predominantly surface-restricted polymer erosion and drug release. In vitro cytotoxicity tests demonstrated that both copolymers have excellent biocompatibility. In vivo acute toxicity tests suggested that oral administration of POEA-4 and POEA-5 did not cause any adverse effects on mice even at a very high dose (2000 mg/kg). In vivo antitumor efficacy against H22 transplanted tumors of 5-FU-loaded POEA tablets were fully examined. We envision that, with further optimization, POEA-based materials could have great potential as drug carriers for oral chemotherapy.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Dendrimers and Hyperbranched Polymers · Nanoparticle-Based Drug Delivery · Synthesis and properties of polymers

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

Affiliations

Engineering Research Center for Biomedical Materials, School of Life Science, Anhui University, 111 Jiulong Road, Hefei, Anhui Province 230601, P. R. China

School of Pharmaceutical Science, Jiangnan University, 1800 Lihu Road, Wuxi, Jiangsu Province 214122, P. R. China

Funding

Program for New Century Excellent Talents in University · Ministry of Education of the People's Republic of China · Anhui University · National Natural Science Foundation of China · Natural Science Foundation of Anhui Province

References (39)

Show source-provided references
1. Thanki K. · J. Controlled Release · 2013 · 170 · 1510.1016/j.jconrel.2013.04.020 ↗
2. Mei L. · Adv. Drug Delivery Rev. · 2013 · 65 · 88010.1016/j.addr.2012.11.005 ↗
3. Mazzaferro S. · Drug Discovery Today · 2013 · 18 · 9910.1016/j.drudis.2012.08.007 ↗
4. Moghimi S. M. · ACS Nano · 2011 · 5 · 845410.1021/nn2038252 ↗
5. Wu P. · Biomaterials · 2006 · 27 · 245010.1016/j.biomaterials.2005.11.031 ↗
6. Petrus A. K. · Angew. Chem., Int. Ed. · 2009 · 48 · 102210.1002/anie.200800865 ↗
7. Wilson D. S. · Nat. Mater. · 2010 · 9 · 92310.1038/nmat2859 ↗
8. Lv P. P. · Biomacromolecules · 2011 · 12 · 423010.1021/bm2010774 ↗
9. Gamboa J. M. · Adv. Drug Delivery Rev. · 2013 · 65 · 80010.1016/j.addr.2013.01.003 ↗
10. Shin S. C. · Int. J. Pharm. · 2006 · 313 · 14410.1016/j.ijpharm.2006.01.028 ↗
11. Khatun Z. · J. Controlled Release · 2014 · 177 · 6410.1016/j.jconrel.2013.12.034 ↗
12. Kim D. · Mol. Pharmaceutics · 2009 · 6 · 135310.1021/mp900021q ↗
13. Feng S. S. · Biomaterials · 2009 · 30 · 329710.1016/j.biomaterials.2009.02.045 ↗
14. Roy K. · Nat. Med. · 1999 · 5 · 38710.1038/7385 ↗
15. Fletcher J. · Gastroenterology · 2001 · 121 · 77510.1053/gast.2001.27997 ↗
16. Nurunnabi M. · Biomaterials · 2010 · 31 · 543610.1016/j.biomaterials.2010.03.057 ↗
17. Renukuntla J. · Int. J. Pharm. · 2013 · 447 · 7510.1016/j.ijpharm.2013.02.030 ↗
18. Oh J. K. · J. Am. Chem. Soc. · 2007 · 129 · 593910.1021/ja069150l ↗
19. Wang Y. · Biomaterials · 2014 · 35 · 697210.1016/j.biomaterials.2014.04.099 ↗
20. Duran-Lobato M. · Biomacromolecules · 2014 · 15 · 272510.1021/bm500588x ↗
21. He P. · Macromol. Biosci. · 2012 · 12 · 54710.1002/mabi.201100358 ↗
22. Lin Y. · J. Mater. Sci. Mater. Med. · 2012 · 23 · 245310.1007/s10856-012-4723-2 ↗
23. Yin L. · Angew. Chem., Int. Ed. · 2013 · 52 · 575710.1002/anie.201209991 ↗
24. Lam P. L. · J. Microencapsul. · 2014 · 31 · 75410.3109/02652048.2014.918670 ↗
25. Chirra H. D. · Adv. Drug Delivery Rev. · 2012 · 64 · 156910.1016/j.addr.2012.08.013 ↗
26. Roger E. · Mol. Pharmaceutics · 2012 · 9 · 210310.1021/mp2005388 ↗
27. Jain S. · Nanomedicine · 2012 · 7 · 131110.2217/nnm.12.31 ↗
28. Dong Y. · Biomaterials · 2005 · 26 · 606810.1016/j.biomaterials.2005.03.021 ↗
29. DeVolder R. J. · Adv. Mater. · 2011 · 23 · 313910.1002/adma.201100823 ↗
30. El-Sherbiny I. M. · Carbohyd. Polym. · 2011 · 83 · 134510.1016/j.carbpol.2010.09.055 ↗
31. Fattahi P. · Adv. Mater. · 2013 · 25 · 455510.1002/adma.201301033 ↗
32. Faisant N. · Int. J. Pharm. · 2006 · 314 · 18910.1016/j.ijpharm.2005.07.030 ↗
33. Freiberg S. · Int. J. Pharm. · 2004 · 282 · 110.1016/j.ijpharm.2004.04.013 ↗
34. Heller J. · Adv. Drug Delivery Rev. · 2002 · 54 · 101510.1016/S0169-409X(02)00055-8 ↗
35. Heller J. · Biomacromolecules · 2004 · 5 · 162510.1021/bm040049n ↗
36. Heller J. · Adv. Polym. Sci. · 1993 · 107 · 4110.1007/BFb0027551 ↗
37. Rothen-Weinhold A. · J. Controlled Release · 2001 · 71 · 3110.1016/S0168-3659(00)00348-5 ↗
38. Tang R. · Biomacromolecules · 2009 · 10 · 72210.1021/bm9000475 ↗
39. Hahn R. G. · Cancer · 1975 · 35 · 103110.1002/1097-0142(197504)35:4<1031::AID-CNCR2820350403>3.0.CO;2-N ↗