Preparation and Application of Brain Tumor Targeting Liposomes Modified by Glucose and Triphenylphosphonium

A technology targeting liposomes and triphenylphosphonium, applied in liposome delivery, anti-tumor drugs, medical preparations of non-active ingredients, etc., can solve problems such as increased toxicity

Active Publication Date: 2022-05-17
SICHUAN UNIV
View PDF9 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0006] However, triphenylphosphonium-modified liposomes will have a strong positive charge, which will increase toxicity to both normal and tumor cells and be easily cleared by the reticuloendothelial system

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Preparation and Application of Brain Tumor Targeting Liposomes Modified by Glucose and Triphenylphosphonium
  • Preparation and Application of Brain Tumor Targeting Liposomes Modified by Glucose and Triphenylphosphonium
  • Preparation and Application of Brain Tumor Targeting Liposomes Modified by Glucose and Triphenylphosphonium

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0028] Preparation of compound 3

[0029]

[0030] At -5 °C, 3,3'-dithiodipropionic acid (4.054 g, 19.28 mmol) CH 2 Cl 2 (30 mL) solution was added EDCI (4.75 g, 24.1 mmol), DMAP (2.95 g, 24.1 mmol), and DIPEA (3.74 g, 28.92 mmol), and stirred for 30 minutes. Then, CH 2 Cl 2 (30 mL) solution and react overnight at room temperature. The reaction solution was washed sequentially with aqueous HCl (1N, 100 mL×2) and saturated NaCl (100 mL×3). The organic phase was further treated with anhydrous Na 2 SO 4 Dry and remove solvent. Finally, by silica gel column chromatography (CH 2 Cl 2 / CH 3 OH=300 / 1) to obtain light yellow semi-solid (5.067 g), yield 74.06%. 1H-NMR (400 MHz, CDCl3, ppm) δ: 0.67 (s, 3H), 0.86 (dd, 6H, J 1 = 6.6Hz, J 2 = 1.6 Hz), 0.91 (d, 3H, J =6.4 Hz), 0.99 (s, 3H), 0.85-2.39 (remaining cholesterol protons), 2.75-2.79(m, 4H), 2.93 -2.97 (m, 4H), 3.15-3.24 (m, 1H), 3.64- 3.68 (m, 8H), 3.72-3.74(m, 2H), 4.26-4.28 (m, 2H), 5.34 (s, 1H). HRMS (ESI) ...

Embodiment 2

[0032] Preparation of Compound 4

[0033]

[0034] At -5 °C, CH 2 Cl 2 (10 mL) solution, add DCC (257 mg, 1.247 mmol) and DMAP (25 mg, 0.208 mmol) and stir for 30 minutes. Then, PEG (1.039 g, 1.04 mmol) in CH 2 Cl 2(10 mL) solution, stirred overnight at room temperature. After filtering off by-products (DCU), the reaction solution was concentrated. Finally, by silica gel column chromatography (CH 2 Cl 2 / CH 3 OH=70 / 1) to obtain light yellow oil (898 mg), yield 51.05%. 1 H-NMR (400 MHz, CDCl 3 , ppm)δ: 0.67 (s, 3H), 0.86 (dd, 6H, J 1 = 6.8Hz, J 2 = 1.2 Hz), 0.91 (d, 3H, J = 6.4 Hz), 0.99 (s, 3H), 0.85-2.38 (remainingcholesterol protons), 2.75-2.79 (m, 4H), 2.91 -2.94 (m, 4H), 3.10-3.22 (m,2H), 3.47-3.83 (m, 85H), 4.25-4.27 (m, 4H), 5.34 (s, 1H).

Embodiment 3

[0036] Preparation of compound 5

[0037]

[0038] CH 2 Cl 2 (10 mL) solution, DCC (84 mg, 0.41 mmol), DMAP (8 mg, 0.065 mmol) were added and stirred for 30 minutes. Then, compound 4 (200 mg, 0.34 mmol) in CH was added dropwise to the mixture 2 Cl 2 (10 mL), stirred overnight at room temperature. After filtering off DCU, the reaction solution was concentrated. Finally, by silica gel column chromatography (CH 2 Cl 2 / CH 3 OH=100 / 1) to obtain light yellow oil (158 mg), yield 61.24%. 1H-NMR (400 MHz, CDCl 3 , ppm)δ:0.14-0.15 (m, 36H), 0.68 (s, 3H), 0.86 (d, 6H, J = 6.6 Hz), 0.91 (d, 3H, J =6.0 Hz), 0.99 (s, 3H), 0.85-2.39 (remaining cholesterol protons), 2.66-2.67(m, 4H), 2.75-2.79 (m, 4H), 2.91-2.94 (m, 4H), 3.10- 3.21 (m, 2H), 3.64-3.92(m, 95H), 4.03-4.07 (m, 2H) 4.25-4.27 (m, 6H), 4.35-4.38 (m, 1H), 4.42-4.50(m, 1H ), 5.00 (d, 1H, J =2.4 Hz), 5.34 (s, 1H).

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

PUM

No PUM Login to view more

Abstract

The invention discloses the preparation and application of a reduction-sensitive brain tumor targeting liposome co-modified by glucose and triphenylphosphonium, which is used to realize the efficient delivery of brain tumor targeting drugs. The new liposomes are co-modified by glucose and triphenylphosphonium, which can respectively recognize the glucose transporter GLUT1, which is highly expressed on the surface of the blood-brain barrier and brain tumor cells, and electrostatically interact with the mitochondria in the tumor cells, from cells and organelles Two levels, realize multiple targeting functions on the blood-brain barrier, tumor tissue and mitochondria, and play a stronger role in the targeted therapy of brain tumors. The new liposome can be used for combined loading of chemotherapeutic drugs and chemosensitizers acting on mitochondria for synergistic treatment of brain tumors. It has more precise targeting of brain tumors, can improve the effect of chemotherapy and reduce side effects. It has broad application prospects.

Description

technical field [0001] The invention relates to a new type of liposome and its application in drug delivery system, specifically refers to using glucose as a dual targeting ligand for blood-brain barrier and brain tumor, and triphenylphosphonium as a mitochondrial targeting ligand for Co-modify liposomes, and introduce disulfide bonds as reduction-sensitive bonds and make liposomes PEGylated to achieve long-term circulation. This new multifunctional liposome is used to co-encapsulate chemotherapeutic drugs and chemosensitizers. Further improve the targeted therapeutic effect of drugs on brain tumors. The invention includes the preparation and characterization of the material, and its application as a drug carrier in drug delivery, and belongs to the technical field of medicine. Background technique [0002] Glioma is the most common and deadly brain tumor, with a life expectancy of only 12-18 months after diagnosis. However, traditional therapies such as chemotherapy still...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to view more

Application Information

Patent Timeline
no application Login to view more
Patent Type & Authority Patents(China)
IPC IPC(8): A61K47/69A61K47/54A61K47/60A61K45/06A61K47/24A61K47/28A61P35/00
CPCA61K47/6911A61K47/549A61K47/54A61K47/60A61K45/06A61K47/24A61K47/28A61P35/00
Inventor 吴勇海俐彭瑶郭丽李茹卢嘉琪
Owner SICHUAN UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap