TY - JOUR
T1 - 异丙基丙烯酰胺水凝胶纳米微球粒径的控制及其对多肽吸附的影响
AU - Hou, Yaqi
AU - Shen, Jingyao
AU - Yi, Da
AU - Wang, Zhe
AU - Kang, Lingling
AU - Meng, Zihui
AU - Xue, Min
N1 - Publisher Copyright:
© 2020, Editorial Board of CIESC Journal. All right reserved.
PY - 2020/10
Y1 - 2020/10
N2 - A library of poly(N-isopropylacrylamide-co-N-tert-butylacrylamide-co-acrylic acid) (P-NIPAm-tBAm-AAc) hydrogel nanoparticles with good dispersion and uniform size were prepared by precipitation polymerization method. Their hydrodynamic diameters were controlled from 71 nm to 304 nm proved by dynamic light scattering (DLS) with adjusting the polymerization formulation, while the PDI values are all below 0.1. Due to the charge repulsion, the particle size increased from 71 nm to 219 nm when the feeding of electrophilic monomer AAc increased from 5% to 50%(mol) in polymerization. Meanwhile, the inverse effect was also revealed on the hydrophobic monomer tBAm, that is, the nanoparticle size decreased along with increasing its feeding ratio. Besides, the increased usage of the surfactant SDS resulted in the microspheres being smaller to 71 nm. It is proved that the NPs size greatly affected their affinity to the target peptides (LEVLFQGP), and the results showed that the adsorption rate increased with decreasing the nanoparticle size. When the molar ratio of AAc was 20% and the diameter was 128 nm, the adsorption rate could reach 90%. Furthermore, the adsorption and desorption experiment was performed with changing the environmental temperature from 35℃ to 5℃ since the volume phase transition temperature (LCST) of NPs is (20±2)℃ proved by DLS. After five times adsorption/desorption circulation experiments, the reduction of NPs adsorption rate on target peptide was below 7%. Therefore, the prepared and screened NPs are size controlled and reusable.
AB - A library of poly(N-isopropylacrylamide-co-N-tert-butylacrylamide-co-acrylic acid) (P-NIPAm-tBAm-AAc) hydrogel nanoparticles with good dispersion and uniform size were prepared by precipitation polymerization method. Their hydrodynamic diameters were controlled from 71 nm to 304 nm proved by dynamic light scattering (DLS) with adjusting the polymerization formulation, while the PDI values are all below 0.1. Due to the charge repulsion, the particle size increased from 71 nm to 219 nm when the feeding of electrophilic monomer AAc increased from 5% to 50%(mol) in polymerization. Meanwhile, the inverse effect was also revealed on the hydrophobic monomer tBAm, that is, the nanoparticle size decreased along with increasing its feeding ratio. Besides, the increased usage of the surfactant SDS resulted in the microspheres being smaller to 71 nm. It is proved that the NPs size greatly affected their affinity to the target peptides (LEVLFQGP), and the results showed that the adsorption rate increased with decreasing the nanoparticle size. When the molar ratio of AAc was 20% and the diameter was 128 nm, the adsorption rate could reach 90%. Furthermore, the adsorption and desorption experiment was performed with changing the environmental temperature from 35℃ to 5℃ since the volume phase transition temperature (LCST) of NPs is (20±2)℃ proved by DLS. After five times adsorption/desorption circulation experiments, the reduction of NPs adsorption rate on target peptide was below 7%. Therefore, the prepared and screened NPs are size controlled and reusable.
KW - Adsorption
KW - Hydrodynamic diameter
KW - Hydrogel nanoparticles
KW - N-isopropylacrylamide
KW - Nanoparticles
KW - Particle size distribution
UR - http://www.scopus.com/inward/record.url?scp=85096491938&partnerID=8YFLogxK
U2 - 10.11949/0438-1157.20200517
DO - 10.11949/0438-1157.20200517
M3 - 文章
AN - SCOPUS:85096491938
SN - 0438-1157
VL - 71
SP - 267
EP - 272
JO - Huagong Xuebao/CIESC Journal
JF - Huagong Xuebao/CIESC Journal
ER -