Supra-molecular assembly and magnetic targeted slow-release effect of "dextran-magnetic layered double hydroxide-fluorouracil" drug delivery system.
- Author:
Guo-jing GOU
1
;
Yan-hong LIU
;
Yue SUN
;
Je HUANG
;
Bing XUE
;
Li-e DONG
Author Information
1. Department of Chemistry, Ningxia Medical University, Yinchuan 750004, China. ggj64@yahoo.com.cn
- Publication Type:Journal Article
- MeSH:
Animals;
Biological Availability;
Delayed-Action Preparations;
Dextrans;
chemistry;
Drug Carriers;
Female;
Fluorouracil;
administration & dosage;
chemistry;
pharmacokinetics;
Half-Life;
Hydroxides;
chemistry;
Magnetics;
Male;
Microscopy, Electron, Transmission;
Rats;
Rats, Sprague-Dawley;
Spectrophotometry, Infrared;
Thermogravimetry;
X-Ray Diffraction
- From:
Acta Pharmaceutica Sinica
2011;46(11):1390-1398
- CountryChina
- Language:Chinese
-
Abstract:
The drug-loading system of DMF (dextran - magnetic layered double hydroxide - fluorouracil) was synthesized by "co-precipitation intercalated assembly - dextran composite in situ - solvent conversion" technology. The crystal-phase characteristic and slow-release performance of DMF were investigated through X-ray diffraction (XRD), infrared spectrum (IR), transmission electron microscopy (TEM), thermogravimetry (TG) and in vitro release experiment. The targeted transshipment and slow-release effect of DMF system were evaluated by in vivo animal experiment. It was showed that the XRD of DMF matched with R-sixtetragonum type layered double hydroxide and Fd-3m cubic type ferrite. IR test demonstrated that the DMF system was a supra-molecular complex consisted of Dextran (DET), magnetic layered double hydroxide (MLDH) and fluorouracil (FU) components. The two-level supra-molecular MLDH-FU presented six-edge lozenge TEM morphology, with layered characteristics. DET on the surface of DMF was capable of protecting the layered structure of MLDH-FU, improving particle dispersion properties, and strengthening the slow-release performance of the drug delivery system. The drug release model of DMF at pH 7.35 of PBS in vitro fit to the zero-order kinetics equation C = 1.1716 x 10(-5) + 4.4626 x 10(-7) t. The drug delivery system DMF could transport drugs principally to in vivo target organs with a local effect, targeted specificity, and excellent circulation transshipment performance. The pharmacokinetic process of DMF presented multi-peak phenomenon with peak attenuation and cyclic growth. The peaks appeared at 0.25, 1, 3, 5 and 9 d separately after dosing intervention. The first peak process of DMF accorded with a pharmacokinetic equation of C(FU) = 14.34 e(-0.530t) + 36.04 e(-0.321t) + 24.18 e(-0.96t), and presented the characteristic of slow absorption and fast elimination. As for subsequent peak processes, half-life increased, bioavailability increased, and plasma clearance decreased. The highest peak value of DMF was 1/37 of original value of FU, and the relative bioavailability was 419% to original FU.
