TY - JOUR
T1 - Preparation and photothermal therapy of hyaluronic acid–conjugated Au nanoparticle-coated poly (glycidyl methacrylate) nanocomposites
AU - Zhang, Hepeng
AU - Zhang, Yonggang
AU - Jin, Ronghua
AU - Wu, Chen
AU - Zhang, Baoliang
AU - Zhang, Qiuyu
AU - Chen, Xin
N1 - Publisher Copyright:
© 2018, Springer Science+Business Media, LLC, part of Springer Nature.
PY - 2018/12/1
Y1 - 2018/12/1
N2 - Nanocomposites are fabricated with poly (glycidyl methacrylate) (PGMA) microspheres, Au nanoparticles and hyaluronic acid (HA) for accurate photothermal therapy. PGMA microspheres are synthesized by emulsifier-free emulsion polymerization followed by amination. The adsorption of gold seeds is successfully achieved through chelation. PGMA@Au-4 nanocomposites (abbreviated as PGMA@Au) are obtained after gold seed growth. The temperature of the 0.3 mg mL−1 PGMA@Au dispersion increases by 10.6 °C when irradiated with a near-infrared (NIR) laser for 5 min. In order to reduce side effects in normal cells and achieve a specific targeting property for cancer cells, HA is further conjugated on the surface of PGMA@Au (denoted as PGMA@Au–HA). The PGMA@Au–HA nanocomposites perform highly selective targeting toward cancer cells and have good photothermal properties, leading to threefold therapeutic efficacy against cancer cells in comparison with normal cells. These results indicate that the PGMA@Au–HA construct could be a promising platform for cancer therapy.
AB - Nanocomposites are fabricated with poly (glycidyl methacrylate) (PGMA) microspheres, Au nanoparticles and hyaluronic acid (HA) for accurate photothermal therapy. PGMA microspheres are synthesized by emulsifier-free emulsion polymerization followed by amination. The adsorption of gold seeds is successfully achieved through chelation. PGMA@Au-4 nanocomposites (abbreviated as PGMA@Au) are obtained after gold seed growth. The temperature of the 0.3 mg mL−1 PGMA@Au dispersion increases by 10.6 °C when irradiated with a near-infrared (NIR) laser for 5 min. In order to reduce side effects in normal cells and achieve a specific targeting property for cancer cells, HA is further conjugated on the surface of PGMA@Au (denoted as PGMA@Au–HA). The PGMA@Au–HA nanocomposites perform highly selective targeting toward cancer cells and have good photothermal properties, leading to threefold therapeutic efficacy against cancer cells in comparison with normal cells. These results indicate that the PGMA@Au–HA construct could be a promising platform for cancer therapy.
UR - http://www.scopus.com/inward/record.url?scp=85051851390&partnerID=8YFLogxK
U2 - 10.1007/s10853-018-2773-7
DO - 10.1007/s10853-018-2773-7
M3 - 文章
AN - SCOPUS:85051851390
SN - 0022-2461
VL - 53
SP - 16252
EP - 16262
JO - Journal of Materials Science
JF - Journal of Materials Science
IS - 24
ER -