TY - JOUR
T1 - Photo- and pH-responsive drug delivery nanocomposite based on o-nitrobenzyl functionalized upconversion nanoparticles
AU - Wang, Xiaotao
AU - Yang, Yebin
AU - Liu, Chuang
AU - Guo, Huiling
AU - Chen, Zhuofan
AU - Xia, Junyong
AU - Liao, Yonggui
AU - Tang, Chak Yin
AU - Law, Wing Cheung
N1 - Funding Information:
This work was supported by the National Natural Science Foundation of China ( 51303049 , 31871442 and 51973072 ).
Publisher Copyright:
© 2021 Elsevier Ltd
PY - 2021/8/16
Y1 - 2021/8/16
N2 - A near infrared (NIR) and pH dual-responsive nanocomposite, composed of a lanthanide-doped upconversion nanoparticle (UCNP) core and a transformable poly-o-nitrobenzyl shell, was prepared by the distillation precipitation polymerization and template method. The poly-o-nitrobenzyl shell can undergo hydrophobic-hydrophilic transformation upon an irradiation of 980 nm, rendering the capability of NIR-activated drug release. The anticancer drug, doxorubicin (DOX), can be loaded into these nanocomposites with a loading efficiency of 7.23 wt%. Furthermore, pH responsiveness caused by the hydrogen bond and charge interactions between DOX and nanocapsules can trigger the release of drugs at low pH. Under visible light irradiation and neutral (pH 7.4) conditions, the cumulative release of DOX was only 8.35% after 300 min, while it reached 59.5% under the synergistic effect of NIR irradiation and acidic conditions. The Baker-Lonsdale model was used to describe the drug release kinetics of this system, and the diffusion coefficient (3DCs/r02C0) and R2 under different conditions were determined to be 4.15 × 10−6 and 0.98 (pH 7.4 and visible light), 2.64 × 10−5 and 0.99 (NIR light), 3.26 × 10−5 and 0.97 (pH 4.5 and visible light), 2.59 × 10−4 and 0.99 (pH 4.5 and NIR light), respectively. This controlled release feature makes the nanocomposite a promising therapeutic agent for treating diseases.
AB - A near infrared (NIR) and pH dual-responsive nanocomposite, composed of a lanthanide-doped upconversion nanoparticle (UCNP) core and a transformable poly-o-nitrobenzyl shell, was prepared by the distillation precipitation polymerization and template method. The poly-o-nitrobenzyl shell can undergo hydrophobic-hydrophilic transformation upon an irradiation of 980 nm, rendering the capability of NIR-activated drug release. The anticancer drug, doxorubicin (DOX), can be loaded into these nanocomposites with a loading efficiency of 7.23 wt%. Furthermore, pH responsiveness caused by the hydrogen bond and charge interactions between DOX and nanocapsules can trigger the release of drugs at low pH. Under visible light irradiation and neutral (pH 7.4) conditions, the cumulative release of DOX was only 8.35% after 300 min, while it reached 59.5% under the synergistic effect of NIR irradiation and acidic conditions. The Baker-Lonsdale model was used to describe the drug release kinetics of this system, and the diffusion coefficient (3DCs/r02C0) and R2 under different conditions were determined to be 4.15 × 10−6 and 0.98 (pH 7.4 and visible light), 2.64 × 10−5 and 0.99 (NIR light), 3.26 × 10−5 and 0.97 (pH 4.5 and visible light), 2.59 × 10−4 and 0.99 (pH 4.5 and NIR light), respectively. This controlled release feature makes the nanocomposite a promising therapeutic agent for treating diseases.
KW - Nanocomposite
KW - Photoresponse
KW - Upconversion nanoparticle
UR - http://www.scopus.com/inward/record.url?scp=85108817851&partnerID=8YFLogxK
U2 - 10.1016/j.polymer.2021.123961
DO - 10.1016/j.polymer.2021.123961
M3 - Journal article
AN - SCOPUS:85108817851
SN - 0032-3861
VL - 229
JO - Polymer
JF - Polymer
M1 - 123961
ER -