TY - JOUR
T1 - A nanoscale porous glucose-based polymer for gas adsorption and drug delivery
AU - Jiang, Xiaowei
AU - Wang, Qiuliang
AU - Liu, Yunfei
AU - Fu, Xiaohui
AU - Luo, Yali
AU - Lyu, Yinong
N1 - Publisher Copyright:
© The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.
PY - 2018
Y1 - 2018
N2 - A glucose-based nanoporous organic polymer (glu-NOP) was designed and synthesized facilely by a Scholl coupling reaction using benzylated glucose as a single monomer. The glu-NOP exhibits a high surface area (682 m2 g−1), large pore volume, and high thermal stability, making it an efficient adsorbent for CO2 capture (2.84 mmol g−1 at 1.0 bar/273 K) and separation. In addition to its capabilities for gas sorption, the highly biocompatible glu-NOP was also evaluated as a drug carrier for the delivery of a hydrophobic drug, ibuprofen (IBU) and a hydrophilic drug, 5-fluorouracil (5-FU). The solution impregnation method was used for drug loading and the drug release kinetics were determined by UV spectroscopy. The results presented here reveal that, for IBU/glu-NOP and 5-FU/glu-NOP complexes, the drug loading efficiency is about 10.7 wt% and 30 wt%, respectively. More importantly, very slow delivery of IBU was achieved under physiological conditions, which is even better than that of its analogue MIL-53(Cr, Fe). This could effectively avoid frequent and invasive dosing and improve patient compliance. This study, therefore, supports the potential of glu-NOP as a simple and stable platform for both gas uptake and drug delivery.
AB - A glucose-based nanoporous organic polymer (glu-NOP) was designed and synthesized facilely by a Scholl coupling reaction using benzylated glucose as a single monomer. The glu-NOP exhibits a high surface area (682 m2 g−1), large pore volume, and high thermal stability, making it an efficient adsorbent for CO2 capture (2.84 mmol g−1 at 1.0 bar/273 K) and separation. In addition to its capabilities for gas sorption, the highly biocompatible glu-NOP was also evaluated as a drug carrier for the delivery of a hydrophobic drug, ibuprofen (IBU) and a hydrophilic drug, 5-fluorouracil (5-FU). The solution impregnation method was used for drug loading and the drug release kinetics were determined by UV spectroscopy. The results presented here reveal that, for IBU/glu-NOP and 5-FU/glu-NOP complexes, the drug loading efficiency is about 10.7 wt% and 30 wt%, respectively. More importantly, very slow delivery of IBU was achieved under physiological conditions, which is even better than that of its analogue MIL-53(Cr, Fe). This could effectively avoid frequent and invasive dosing and improve patient compliance. This study, therefore, supports the potential of glu-NOP as a simple and stable platform for both gas uptake and drug delivery.
UR - http://www.scopus.com/inward/record.url?scp=85054013253&partnerID=8YFLogxK
U2 - 10.1039/c8nj03160f
DO - 10.1039/c8nj03160f
M3 - 文章
AN - SCOPUS:85054013253
SN - 1144-0546
VL - 42
SP - 15692
EP - 15697
JO - New Journal of Chemistry
JF - New Journal of Chemistry
IS - 19
ER -