XiuJun Jame Li

Prof. Dr. XiuJun Jame Li

orcid

Research Focus & Metrics

Academic Career Length

25Years (2002-Present)

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

Representative Publications

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8 November 2019 in NPG Asia Materials
Verified
Journal Article
Open access
PDF file
QSQiang Shi
Qiang Shi
HLHao Liu
Hao Liu
DTDeding Tang
Deding Tang
YLYuhui Li
Yuhui Li
XiuJun Jame LiXiuJun Jame Li
XiuJun Jame Li
FXFeng Xu
Feng Xu
The increasingly intimate bond connecting soft actuation devices and emerging biomedical applications is triggering the development of novel materials with superb biocompatibility and a sensitive actuation capability that can reliably function as bio-use-oriented actuators in a human-friendly manner. Stimulus-responsive hydrogels are biocompatible with human tissues/organs, have sufficient water content, are similar to extracellular matrices in structure and chemophysical properties, and are responsive to external environmental stimuli, and these materials have recently attracted massive research interest for fabricating bioactuators. The great potential of employing such hydrogels that respond to various stimuli (e.g., pH, temperature, light, electricity, and magnetic fields) for actuation purposes has been revealed by their performances in real-time biosensing systems, targeted drug delivery, artificial muscle reconstruction, and cell microenvironment engineering. In this review, the material selection of hydrogels with multiple stimulus-responsive mechanisms for actuator fabrication is first introduced, followed by a detailed introduction to and discussion of the most recent progress in emerging biomedical applications of hydrogel-based bioactuators. Final conclusions, existing challenges, and upcoming development prospects are noted in light of the status quo of bioactuators based on stimulus-responsive hydrogels.

1 March 2018 in Advanced Drug Delivery Reviews
Verified
Journal Article
Closed access
SSSharma T. Sanjay
Sharma T. Sanjay
WZWan Zhou
Wan Zhou
MDMaowei Dou
Maowei Dou
HTHamed Tavakoli
Hamed Tavakoli
LMLei Ma
Lei Ma
XiuJun Jame LiXiuJun Jame Li
XiuJun Jame Li

1 April 2017 in Applied Catalysis B: Environment and Energy
Verified
Journal Article
Closed access
SZSihui Zhan
Sihui Zhan
HZHe Zhang
He Zhang
YZYu Zhang
Yu Zhang
QSQiang Shi
Qiang Shi
YLYi Li
Yi Li
XiuJun Jame LiXiuJun Jame Li
XiuJun Jame Li

1 March 2021 in Biosensors and Bioelectronics
Verified
Journal Article
Closed access
MLMengzhen Lv
Mengzhen Lv
WZWan Zhou
Wan Zhou
HTHamed Tavakoli
Hamed Tavakoli
CBCynthia Bautista
Cynthia Bautista
JXJianfei Xia
Jianfei Xia
XiuJun Jame LiXiuJun Jame Li
XiuJun Jame Li

1 June 2012 in Bioanalysis
Verified
Journal Article
Closed access
XiuJun Jame LiXiuJun Jame Li
XiuJun Jame Li
AVAlejandra V Valadez
Alejandra V Valadez
PZPeng Zuo
Peng Zuo
ZNZhihong Nie
Zhihong Nie
Current fundamental investigations of human biology and the development of therapeutic drugs commonly rely on 2D monolayer cell culture systems. However, 2D cell culture systems do not accurately r...

16 July 2013 in Lab on a Chip
Verified
Journal Article
Closed access
PDF file
PZPeng Zuo
Peng Zuo
XiuJun Jame LiXiuJun Jame Li
XiuJun Jame Li
DDDelfina C. Dominguez
Delfina C. Dominguez
BYBang-Ce Ye
Bang-Ce Ye
Infectious pathogens often cause serious public health concerns throughout the world. There is an increasing demand for simple, rapid and sensitive approaches for multiplexed pathogen detection. In this paper we have developed a polydimethylsiloxane (PDMS)/paper/glass hybrid microfluidic system integrated with aptamer-functionalized graphene oxide (GO) nano-biosensors for simple, one-step, multiplexed pathogen detection. The paper substrate used in this hybrid microfluidic system facilitated the integration of aptamer biosensors on the microfluidic biochip, and avoided complicated surface treatment and aptamer probe immobilization in a PDMS or glass-only microfluidic system. Lactobacillus acidophilus was used as a bacterium model to develop the microfluidic platform with a detection limit of 11.0 cfu mL−1. We have also successfully extended this method to the simultaneous detection of two infectious pathogens - Staphylococcus aureus and Salmonella enterica. This method is simple and fast. The one-step ‘turn on’ pathogen assay in a ready-to-use microfluidic device only takes ∼10 min to complete on the biochip. Furthermore, this microfluidic device has great potential in rapid detection of a wide variety of different other bacterial and viral pathogens.