385-393
Preparation and Release Behavior of Pectin Nanoparticles Loading Doxorubicin
Authors: WEN Shaohong1,†, OU Jinlai2,†, LUO Rui1, LIANG Wenli1, OUYANG Ping1, ZENG Fen1, CHEN Yanwen1, XU Zhenxia1, ZHAO Wen1, LI Sha1,*
Number of views: 724
Doxorubicin (DOX) is a highly efficient
and broad-spectrum antitumor drug in the treatment
of solid tumors. However, DOX can lead to a wide
range of biochemical effects on human including
inevitable toxicity to the normal tissues which has
limited its clinical application. Nanoparticles, as a new
kind of vehicle for antitumor drug delivery, can greatly
enhance the theraputic effect and reduce the drug
toxicity. In this work, we chose pectin (PEC) as carrier
material to prepare DOX loading nanoparticles. The
blank PEC nanoparticles (PEC-NPs) were prepared by
emulsification-ionotropic gelation method and the
formulation was optimized by central composite
design and response surface method. The drug was
loaded in PEC-NPs to obtain DOX loading pectin
nanoparticles (DOX-PEC-NPs) by adsorption. The drug
loading capacity of PEC-NPs was chiefly affected by
ratio of DOX to PEC. The time, pH value and
temperature of adsorption showed some influence on
drug loading. Both PEC-NPs and DOX-PEC-NPs were
sphere-like in shape with a mean diameter of (266.93 ±
1.70) nm and (287.70 ± 1.21) nm, respectively. The
entrapment efficiency and drug loading rate of DOXPEC-
NPs was (91.71 ± 0.50)% and (17.17 ± 0.24) %,
respectively. Compared with DOX, DOX-PEC-NPs
showed apparent sustained release behavior with a
burst release, which followed the double exponential
diphase kinetics equation well.