Research on Tat peptide-polyethylene glycol modified gelatin-siloxane nanoparticles across the blood-brain barrier.
- Author:
Xinhua TIAN
1
;
Feng WEI
;
Xiaoning LIN
;
Wei FENG
;
Peng WANG
Author Information
1. Neurosurgical Department of Affiliated Zhongshan Hospital, Xiamen University, Xiamen 361004, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Blood-Brain Barrier;
metabolism;
Drug Delivery Systems;
Female;
Gelatin;
administration & dosage;
chemistry;
pharmacokinetics;
Male;
Mice;
Mice, Nude;
Nanoparticles;
chemistry;
Peptide Fragments;
chemistry;
Polyethylene Glycols;
chemistry;
Siloxanes;
administration & dosage;
chemistry;
pharmacokinetics;
tat Gene Products, Human Immunodeficiency Virus;
chemistry
- From:
Journal of Biomedical Engineering
2012;29(3):486-500
- CountryChina
- Language:Chinese
-
Abstract:
Gelatin-siloxane nanoparticles (GS NPs) have been considered to be good gene carrier candidate in vitro, since they have several advantages such as low toxicity, easy preparation and surface modification. In this study, the Tat-PEG-GS NPs were synthesized by the gelatin-siloxane, surface-modified with the polyethylene glycol (H2 N-PEG-COOH) and Tat peptide (KYGRRRQRRKKRGC) and thus constructed a delivery system which can cross BBB (Blood-brain barrier). The morphology, diameter, and zeta potential of Tat-PEG-GS NPs carrier system were characterized with transmission electron microscopy (TEM) and Nano-ZS zetasizer dynamic light scattering Detector. The organ distribution and dynamic evolution localized in the brain parenchyma of Tat-PEG-GS NPs in vivo was investigated with Cri in vivo imaging system and TEM. The obtained Tat-PEG-GS NPs were approximately spherical in shape with average particle size of 150-200 nm and zeta potentials of (32.27 +/- 2.47) mV. In vivo imaging results showed that the accumulation of Tat-PEG-GS NPs was higher in the brain than the accumulation of PEG-GS NPs, but the accumulation of Tat-PEG-GS NPs was lower in the liver than the accumulation of PEG-GS NPs. These differences are statistically significant. The nanocomplex could cross the BBB and reach the neural tissues tested with TEM. The Tat-PEG-GS NPs could cross the BBB and escape the arrest of the reticuloendothelial system (RES), and it would be potential nano-carrier systems for central delivery.
