Preparation and application of nano diamond drug with high load and pH capable of controlling release of adriamycin

A nano-diamond and doxorubicin technology, used in drug combinations, medical preparations with inactive ingredients, anti-tumor drugs, etc., can solve the problems of strong cytotoxicity, lack of specific recognition, killing, etc., and achieve stable chemical properties. , good biocompatibility, reducing the effect of toxic and side effects

Inactive Publication Date: 2015-12-02
SHANXI UNIV
View PDF3 Cites 7 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, these clinically used anticancer drugs usually have strong cytotoxicity and lack of specific recognition. While killing cancer cells, they will also kill normal tissue cells
In addition, chemotherapy also has the disadvantage of low bioavailability of drugs, which is manifested in the low efficiency of drug uptake b

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 nano diamond drug with high load and pH capable of controlling release of adriamycin
  • Preparation and application of nano diamond drug with high load and pH capable of controlling release of adriamycin
  • Preparation and application of nano diamond drug with high load and pH capable of controlling release of adriamycin

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0036] (1) Preparation of nanodiamond-polyethylene glycol (ND-PEG-COOH) nanoparticles

[0037] Accurately weigh 1.0 mg of carboxylated nano-diamonds, and pass through dimethyl sulfoxide (DMSO), absolute ethanol (C 2 h 5 OH), distilled water (H 2 O) After washing, place in 1.0mL MES (0.1M, pH5.8) buffer solution, ultrasonically disperse for 30min to form a suspension, then add 0.2mgEDC, 0.25mgNHS, stir at room temperature for 6h, and centrifuge at 15000rpm after the reaction is complete 5min, remove supernatant, obtain the nano-diamond precipitate of activated carboxyl group;

[0038] Quickly disperse the nano-diamond precipitate with activated carboxyl group into 1.0mL BBS (0.1M, pH8.4) buffer solution, ultrasonically disperse for 10min to form a suspension, then add 0.3mg polyethylene glycol (H 2 N-PEG-COOH), continue to stir and react at room temperature for 12 hours. After the reaction is completed, collect the supernatant by high-speed centrifugation at 15,000 rpm for 5...

Embodiment 2

[0043] (1) The preparation of nano diamond-polyethylene glycol (ND-PEG-COOH) nanoparticles is the same as in Example 1

[0044] (2) Nano diamond-polyethylene glycol-doxorubicin / sodium citrate (ND-PEG-DOX / Na 3 Cit) Preparation of Nanomedicine

[0045] Weigh 1 mg of vacuum-dried nano-diamond-polyethylene glycol (ND-PEG-COOH), add 1 mL of sodium citrate (Na 3 Cit, 1.0M) solution, ultrasonically disperse for 1 hour to form a suspension, then add 0.1 mg doxorubicin (DOX), and react on a shaker in the dark for 6 hours. After the reaction is complete, centrifuge at 15,000 rpm for 5 minutes to collect the supernatant solution, and with 1.0M sodium citrate (Na 3 Cit) continue to wash three times with 15000rpm high-speed centrifugation for 5min to obtain nanodiamond-polyethylene glycol-doxorubicin / sodium citrate (ND-PEG-DOX / Na 3 Cit) nanoparticles, placed in a vacuum oven to preserve for subsequent use. All supernatants were collected into a small beaker and left overnight in a refr...

Embodiment 3

[0047] (1) With embodiment 1 step (1).

[0048] (2) Preparation of nanodiamond-polyethylene glycol-doxorubicin / sodium acetate (ND-PEG-DOX / NaAc) nanomedicine

[0049] Weigh 1 mg of vacuum-dried nano-diamond-polyethylene glycol (ND-PEG-COOH), add 1 mL of sodium acetate (NaAc, 1.0 M) solution, and ultrasonically disperse for 1 hour to form a suspension, then add 0.2 mg of doxorubicin ( DOX), avoid light and react on a shaker for 6 hours. After the reaction is completed, collect the supernatant with 15000rpm high-speed centrifugation for 5min, and continue to wash three times with 1.0M sodium acetate (NaAc) with 15000rpm high-speed centrifugation for 5min to obtain nano-diamond-polymer Ethylene glycol-doxorubicin / sodium citrate (ND-PEG-DOX / NaAc) nano-medicine is stored in a vacuum drying oven for future use. All supernatants were collected into a small beaker and left overnight in a refrigerator at 4°C to determine the mass of DOX adsorbed on ND-PEG-COOH nanoparticles. The absor...

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 provides preparation and application of a nano diamond drug with high load and pH capable of controlling release of adriamycin. H2N-PEG-COOH is firstly used for decorating a nano diamond, an ND-PEG-COOH carrier is synthesized, adriamycin is physically absorbed under the condition of Na-citrate and natrium aceticum to obtain target drug nano diamond-polyethylene glycol-adriamycin/sodium citrate (ND-PEG-DOX/Na3Cit) or nano diamond-polyethylene glycol-adriamycin/natrium aceticum (ND-PEG-DOX/NaAc). In vitro drug release experiments, MTT experiments and experiments that flow cytometry tests cell taking in nano diamond drug show that ND-PEG-DOX/Na3Cit and ND-PEG-DOX/NaAc can induce a cancer cell to apoptosis, and the nano diamond drug can be applied in preparation of antineoplastic drugs.

Description

technical field [0001] The invention relates to a nano-medicine, in particular to a nano-diamond drug with high load and pH-controllable release of doxorubicin, a preparation method thereof, and an application of the drug in preparing antitumor drugs. Background technique [0002] Cancer is a serious threat to human life and health, and its morbidity and mortality are second only to heart disease and infectious diseases worldwide. At present, the main treatment methods for cancer are surgical resection, radiotherapy and chemotherapy. If the tumor grows only in a local area or is detected early, both surgical resection and radiation therapy are suitable for treatment. However, usually when the tumor is discovered, the patient is already in the middle and late stage of the cancer, and it is often accompanied by signs of metastasis and spread of the lesion. In this case, chemotherapy is the only hope for the patient to survive. Traditional chemotherapy is to kill cancer cells...

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): A61K47/48A61K47/04A61K47/34A61K9/14A61P35/00A61K47/52A61K47/60A61K47/69
Inventor 李林李英奇杨斌盛
Owner SHANXI 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