Poly(Caprolactone)-Poly(N-Isopropyl Acrylamide)-Fe3O4Magnetic Nanofibrous Structure with Stimuli Responsive Drug Release

被引:5
|
作者
Gholami, Sanaz [1 ]
Labbaf, Sheyda [1 ]
Kermanpur, Ahmad [1 ]
Houreh, Arezou Baharlou [2 ]
Luo, Chaojie [3 ]
Edirisinghe, Mohan [3 ]
Esfahani, MohammadHossein Nasr [2 ]
机构
[1] Isfahan Univ Technol, Dept Mat Engn, Biomat Res Grp, Esfahan 8415683111, Iran
[2] Royan Inst Biotechnol, ACECR, Cell Sci Res Ctr, Dept Cellular Biotechnol, Esfahan, Iran
[3] UCL, Dept Mech Engn, Torrington Pl, London WC1E 7JE, England
关键词
Fe3O4; hyperthermia; magnetic fibrous structures; poly(caprolactone); poly(N-isopropylacrylamie); TARGETED DELIVERY; NANOPARTICLES; SCAFFOLDS; POLYCAPROLACTONE; FABRICATION; DOXORUBICIN; RESISTANCE; HYDROGELS; MICELLES; DEXTRAN;
D O I
10.1002/mame.202000208
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Poly(caprolactone; PCL)-poly(N-isopropylacrylamie; PNIPAAm)-Fe(3)O(4)fiber, that can be magnetically actuated, is reported. Here, a structure is engineered that can be utilized as a smart carrier for the release of chemotherapeutic drug via magneto-thermal activation, with the aid of magnetic nanoparticles (MNPs). The magnetic measurement of the fibers revealed saturation magnetization values within the range of 1.2-2.2 emu g(-1). The magnetic PCL-PNIPAAm-Fe(3)O(4)scaffold shows a specific loss power value of 4.19 W g(-1)at 20 wt% MNPs. A temperature increase of 40 degrees C led to a 600% swelling after only 3 h. Doxorubicin (DOX) as a model drug, demonstrates a controllable drug release profile. 39% +/- 0.92 of the total drug loaded is released after 96 h at 37 degrees C, while 25% drug release in 3 h at 40 degrees C is detected. Cytotoxicity results show no significant difference in cell attachment efficiency between the MNP-loaded fibers and control while the DOX-loaded fibers effectively inhibited cell proliferation at 24 h matching the drug release profile. The noncytotoxic effect, coupled with the magneto-thermal property and controlled drug release, renders excellent potential for these fibers to be used as a smart drug-release agent for localized cancer therapy.
引用
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页数:9
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