Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

DPPA-based therapeutic liposome nanoparticle, and preparation method and application thereof

A nanoparticle and liposome technology, applied in the field of biomedicine, can solve problems such as the inability to further improve the treatment effect of tumors, the difficulty in achieving multiple regulatory functions, and the expensive price of antibody-conjugated drugs, achieving good in vivo stability and significant effect , high security effect

Pending Publication Date: 2021-11-26
SUN YAT SEN MEMORIAL HOSPITAL SUN YAT SEN UNIV
View PDF5 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Compared with traditional chemotherapeutic drugs, antibody-drug conjugates can reduce or avoid drug damage to normal tissues, but they also have major defects: when the linker of antibody-drug conjugates is unstable, it is easy to cause systemic exposure of the drug, It can bind to normal tissues expressing the same antibody, resulting in off-target effects; and antibody-conjugated drugs are expensive, and the range of applicable populations is limited
However, the treatment methods based on nanoparticles loaded with therapeutic substances in the prior art still have shortcomings, that is, the nanocarriers in the nanoparticles only act as targeted delivery, and cannot use components other than the therapeutic substances loaded to play a therapeutic role.
Moreover, the therapeutic substances that nanocarriers can carry are limited, so it is often difficult to achieve multiple regulatory effects when using nano-delivery systems to treat related diseases
Take liposomal doxorubicin, the only nano-drug currently on the market, as an example. Through the superior tumor-targeting performance of nano-carriers, it can effectively reduce its systemic side effects, but its carrier only plays a delivery role and cannot further improve the treatment of tumors. Effect

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
  • DPPA-based therapeutic liposome nanoparticle, and preparation method and application thereof
  • DPPA-based therapeutic liposome nanoparticle, and preparation method and application thereof
  • DPPA-based therapeutic liposome nanoparticle, and preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0053] A DPPA-based therapeutic liposome nanoparticle comprises a main drug and DPPA coupled with or wrapped outside the main drug. The main drug described in this embodiment is a therapeutic drug or antibody or DNA or RNA that acts on tumor cells or target genes to treat tumors.

[0054] In this embodiment, the nanoparticles can cooperate with the killing and / or inhibiting tumor growth and metastasis of the main drug to realize the anti-tumor angiogenesis effect and realize the synergistic anti-tumor effect.

[0055] The nanoparticles described in this example can be applied to the actual production of drugs, including anti-angiogenesis drugs and anti-tumor drugs, and can be applied to diseases that require anti-angiogenesis, including cancer, after processing.

[0056] The nanoparticles in this example are prepared by the nanoprecipitation method based on the main drug and DPPA.

Embodiment 2

[0058] A DPPA-based therapeutic liposome nanoparticle comprises a main drug and DPPA coupled with or wrapped outside the main drug. The main drug described in this example is a therapeutic drug or antibody or DNA that acts on tumor cells or target genes to treat tumors, and the nanoparticles are also connected with modifiers, and the modifiers are selected from lipid molecules-polymers At least one of ethylene glycol, lipid molecule-polyethylene glycol-guiding peptide, lipid molecule-polyethylene glycol is DSPE-PEG3000 in this embodiment, lipid molecule-polyethylene glycol-guiding peptide is DSPE-PEG3000-RGD. In this embodiment, the nanoparticles can cooperate with the main drug to kill and / or inhibit tumor growth and metastasis to achieve anti-tumor angiogenesis and achieve a synergistic anti-tumor effect.

[0059] The nanoparticles described in this example can be applied to the actual production of drugs, including anti-angiogenesis drugs and anti-tumor drugs, and can be a...

Embodiment 3

[0062] A DPPA-based therapeutic liposome nanoparticle comprises a main drug and DPPA coupled with or wrapped outside the main drug. The main drug described in this embodiment is siRNA, in order to reflect the effects of DPPA nanoparticles except the main drug effect, the siRNAs used in the embodiment of the present invention are all scrambled siRNAs without biological effects, and the nanoparticles are also connected with Modifier, the modifier is selected from at least one of lipid molecule-polyethylene glycol, lipid molecule-polyethylene glycol-directing peptide, in this embodiment, lipid molecule-polyethylene glycol is DSPE- PEG3000, the lipid molecule-polyethylene glycol-directing peptide is DSPE-PEG3000-RGD. The particle size range is 50-200nm, and the average value is between 100nm and 120nm. In this embodiment, nanoparticles can cooperate with siRNA to kill and / or inhibit tumor growth and metastasis to achieve anti-tumor angiogenesis and achieve a synergistic anti-tumo...

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

PropertyMeasurementUnit
Particle sizeaaaaaaaaaa
Particle sizeaaaaaaaaaa
Login to View More

Abstract

The invention discloses a DPPA-based therapeutic liposome nanoparticle, which comprises a main drug and DPPA coupled with the main drug or wrapping the main drug, and the main drug is selected from at least one of drugs acting on tumor cells or target genes, proteins, DNA or RNA. According to the nanoparticles prepared based on DPPA, by means of the biological activity of the DPPA component, the nanoparticles prepared based on DPPA have the anti-angiogenesis and tumor inhibition effects besides the tumor effect of the main drug, and synergistic treatment and multiple regulation and control are achieved by combining the main drug. The DPPA belongs to a substance existing in an organism, so that the nanoparticles prepared on the basis of the DPPA have good in-vivo stability, small toxic and side effects and high safety. In addition, due to the anti-tumor characteristic of the DPPA component, the dosage of the entrapment substance can be reduced, so that the toxic and side effects possibly caused by the entrapment substance are further reduced.

Description

technical field [0001] The invention relates to the technical field of biomedicine, more specifically, to a DPPA-based therapeutic liposome nanoparticle and its preparation method and application. Background technique [0002] One of the common tumor treatment methods in the prior art is chemotherapeutic drug treatment, which acts on different links of tumor cell growth and reproduction through chemotherapeutic drugs to inhibit or kill various tumors. However, it can also kill normal cells while killing tumor cells, thus causing adverse reactions, including bone marrow suppression, heart damage, etc., that is, it has a defect of lack of targeting. [0003] For this reason, antibody-conjugated drug therapy methods and RNA interference-based therapy methods have also been developed in the prior art, both of which have a certain degree of targeting, and have advantages brought about by targeting compared with chemotherapy drug therapy. Among them, antibody-drug conjugates (ADC...

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
IPC IPC(8): A61K9/52A61K47/24A61K47/18A61K47/55A61K47/54A61K47/60A61K47/62A61K47/69A61K31/661A61K31/7105A61P35/00A61P35/04A61K49/00G01N21/64
CPCA61K9/5123A61K47/55A61K47/544A61K47/60A61K47/62A61K47/6935A61K31/661A61K31/7105A61P35/00A61P35/04A61K49/0039G01N21/64A61K2300/00Y02P20/55
Inventor 蔡佩娥曹舒雯许小丁姚燕丹张文岳
Owner SUN YAT SEN MEMORIAL HOSPITAL SUN YAT SEN UNIV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products