TY - JOUR
T1 - Hemocompatible ɛ-polylysine-heparin microparticles
T2 - A platform for detecting triglycerides in whole blood
AU - Xu, Tingting
AU - Chi, Bo
AU - Chu, Meilin
AU - Zhang, Qicheng
AU - Zhan, Shuyue
AU - Shi, Rongjia
AU - Xu, Hong
AU - Mao, Chun
N1 - Publisher Copyright:
© 2017 Elsevier B.V.
PY - 2018/1/15
Y1 - 2018/1/15
N2 - Triglycerides are clinically important marker for atherosclerosis, heart disease and hypertension. Here, a platform for detecting triglycerides in whole blood directly was developed based on hemocompatible ɛ-polylysine-heparin microparticles. The obtained products of ɛ-polylysine-heparin microparticles were characterized by fourier transform infrared (FT-IR) spectra, transmission electron microscopy (TEM) and ζ-potential. Moreover, the blood compatibility of ɛ-polylysine-heparin microparticles was characterized by in vitro coagulation tests, hemolysis assay and whole blood adhesion tests. Considering of uniform particle size, good dispersibility and moderate long-term anticoagulation capability of the microparticles, a Lipase-(ɛ-polylysine-heparin)-glassy carbon electrode (GCE) was constructed to detect triglycerides. The proposed biosensor had good electrocatalytic activity towards triglycerides, in which case the sensitivity was 0.40 μA mg−1 dL cm−2 and the detection limit was 4.67 mg dL−1 (S/N = 3). Meanwhile, the Lipase-(ɛ-polylysine-heparin)-GCE electrode had strong anti-interference ability as well as a long shelf-life. Moreover, for the detection of triglycerides in whole blood directly, the detection limit was as low as 5.18 mg dL−1. The new constructed platform is suitable for detecting triglycerides in whole blood directly, which provides new analytical systems for clinical illness diagnosis.
AB - Triglycerides are clinically important marker for atherosclerosis, heart disease and hypertension. Here, a platform for detecting triglycerides in whole blood directly was developed based on hemocompatible ɛ-polylysine-heparin microparticles. The obtained products of ɛ-polylysine-heparin microparticles were characterized by fourier transform infrared (FT-IR) spectra, transmission electron microscopy (TEM) and ζ-potential. Moreover, the blood compatibility of ɛ-polylysine-heparin microparticles was characterized by in vitro coagulation tests, hemolysis assay and whole blood adhesion tests. Considering of uniform particle size, good dispersibility and moderate long-term anticoagulation capability of the microparticles, a Lipase-(ɛ-polylysine-heparin)-glassy carbon electrode (GCE) was constructed to detect triglycerides. The proposed biosensor had good electrocatalytic activity towards triglycerides, in which case the sensitivity was 0.40 μA mg−1 dL cm−2 and the detection limit was 4.67 mg dL−1 (S/N = 3). Meanwhile, the Lipase-(ɛ-polylysine-heparin)-GCE electrode had strong anti-interference ability as well as a long shelf-life. Moreover, for the detection of triglycerides in whole blood directly, the detection limit was as low as 5.18 mg dL−1. The new constructed platform is suitable for detecting triglycerides in whole blood directly, which provides new analytical systems for clinical illness diagnosis.
KW - Biosensor
KW - Electrostatic self-assembly
KW - Hemocompatible ɛ-polylysine-heparin microparticles
KW - Lipase
KW - Triglycerides
UR - http://www.scopus.com/inward/record.url?scp=85027492241&partnerID=8YFLogxK
U2 - 10.1016/j.bios.2017.08.030
DO - 10.1016/j.bios.2017.08.030
M3 - 文章
C2 - 28826001
AN - SCOPUS:85027492241
SN - 0956-5663
VL - 99
SP - 571
EP - 577
JO - Biosensors and Bioelectronics
JF - Biosensors and Bioelectronics
ER -