B.E. Li

Dr. B.E. Li

School of Material Science and Engineering, Hebei University of Technology, Tianjin, China

Research Focus & Metrics

Academic Career Length

14Years (2013-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 August 2014 in Materials & Design (1980-2015)
Verified
Journal Article
Closed access
HLHaipeng Li
Haipeng Li
JFJiawei Fan
Jiawei Fan
XGXiaoxin Geng
Xiaoxin Geng
BLB.E. Li
B.E. Li
CLChunyong Liang
Chunyong Liang
JKJianli Kang
Jianli Kang

8 October 2020 in Nanotechnology
Verified
Journal Article
Closed access
BLB.E. Li
B.E. Li
XXXiaomei Xia
Xiaomei Xia
JCJiatian Chen
Jiatian Chen
DXDan Xia
Dan Xia
RXRuodan Xu
Ruodan Xu
CLChunyong Liang
Chunyong Liang
Electrospun composite nanofibrous scaffolds have been regarded as a potential carrier for local drug delivery to prevent tumor recurrence. Herein, a model drug (paclitaxel) was creatively loaded into lignin nanoparticles (PLNPs) and then encapsulated into the polymer of poly (vinyl alcohol)/polyvinyl pyrrolidone which has been fabricated into a composite nanofibrous membrane (PVA/PVP-PLNPs) for use as a drug carrier using the electrospinning technique. The fabricated PVA/PVP-PLNPs membranes exhibited good particle distribution, mechanical properties, thermal stability and biocompatibility. In vitro experiments showed that combining lignin nanoparticles by electrospinning not only improved the drug release profile, but also enhanced the hydrophilicity of nanofibrous membranes which was beneficial to cell adhesion and proliferation. Cellular experiments demonstrated that PVA/PVP-2%PLNPs membrane showed good cell inhibition ability, and the cell survival rate was only 21% at day 7. It indicates that the as-prepared PVA/PVP-PLNPs composite nanofibers are promising candidates for local anticancer therapy.

20 March 2017 in Applied Biochemistry and Biotechnology
Verified
Journal Article
Closed access
PDF file
JHJingzu Hao
Jingzu Hao
YLYing Li
Ying Li
BLB.E. Li
B.E. Li
XWXiaolin Wang
Xiaolin Wang
HLHaipeng Li
Haipeng Li
HWHongshui Wang
Hongshui Wang

16 July 2019 in Biomaterials Science
Verified
Journal Article
Closed access
PDF file
BLB.E. Li
B.E. Li
JMJianwei Ma
Jianwei Ma
DWDonghui Wang
Donghui Wang
XLXuanyong Liu
Xuanyong Liu
HLHaipeng Li
Haipeng Li
HWHongshui Wang
Hongshui Wang
Titanium (Ti) is a widely used implant material in clinics; however, failures still frequently occur due to its bioinertness and poor antibacterial capability. Post-implant infections most likely occur within the first two weeks. Thereafter, the host immune system lowers the infection risk, and biosafety becomes the first consideration. Therefore, endowing biomedical Ti with a time-dependent bactericidal effect is of considerable interest. In this study, Ag nanoparticles (NPs) as the antibacterial agent were incorporated deeply into TiO2 nanotubes prepared on the sandblasted and etched (SLA) Ti surface. The incorporated Ag NPs were verified to automatically transform from a free state to an immobilized state, rendering the constructed platform exhibit a self-adjusting antibacterial effect. It showed strong “release bactericidal” activity in the early phase that gradually changed to the “contact bactericidal” ability. Such a smart alteration could satisfy the varied antibacterial requirements in different periods after biomaterial implantation. Moreover, the nanotubular structure could accelerate apatite formation and improve cell adhesion and proliferation when compared with those of commercially used SLA implants. Based on these results, it can be concluded that Ag-NP-incorporated micro-nanostructured Ti has worthwhile biological and time-dependent antibacterial properties, and it can have promising applications in orthopedics, dentistry, and fabrication of other biomedical devices.


12 March 2020 in Biomedical Microdevices
Verified
Journal Article
Closed access
PDF file
LZLei Zhang
Lei Zhang
BLB.E. Li
B.E. Li
XZXianlin Zhang
Xianlin Zhang
DWDonghui Wang
Donghui Wang
LZLinxi Zhou
Linxi Zhou
HWHongshui Wang
Hongshui Wang