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An electric field multi-pulse drug release device and its preparation method and application

A multi-pulse and drug-releasing technology, applied in the direction of drug devices and other medical devices, can solve the problems of complex manufacturing methods, and achieve the effects of low cost, great independence, and precise control of drug release time.

Active Publication Date: 2015-08-26
SOUTHEAST UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the manufacturing method of this device is relatively complicated, so finding a simple and applicable manufacturing method has become the latest topic in the research of multi-pulse drug delivery system.

Method used

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  • An electric field multi-pulse drug release device and its preparation method and application
  • An electric field multi-pulse drug release device and its preparation method and application
  • An electric field multi-pulse drug release device and its preparation method and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0055] Example 1 Preparation of bionic self-assembled multi-pulse drug release device (precipitation ring layer is calcium hydrogen phosphate crystal)

[0056] 1) Weigh a certain amount of gelatin and put it in a container, add double distilled water to fully dissolve, and make a gel solution with a concentration of 1wt% according to the mass volume ratio;

[0057] 2) Mix the above glue solution with calcium nitrate solution with a concentration of 0.01mol / L, the volume ratio is 1:0.5, stir evenly, add a certain volume of glutaraldehyde solution with a mass fraction of 2%, to make the crosslinking degree of gelatin 2% to obtain a mixed cross-linking gel solution;

[0058] 3) Add vitamin C to the above-mentioned mixed cross-linking glue solution. The amount of vitamin C added is 0.5% in terms of weight-to-volume ratio. In the tubular mold, leave a certain space at the mouth of the nozzle, let it stand to make it completely solidified, insert the electrode into the fully solidi...

Embodiment 2

[0061] Example 2 Preparation of bionic self-assembled multi-pulse drug release device (precipitation ring layer is barium sulfate crystal)

[0062] 1) Weigh a certain amount of sodium silicate and put it in a container, add double distilled water to fully dissolve, and make a glue solution with a concentration of 80wt% according to the mass volume ratio;

[0063] 2) Mix the above glue solution with barium nitrate solution with a concentration of 5mol / L, the volume ratio is 1:2, after mixing evenly, stir for 1 hour to obtain a mixed crosslinking glue solution;

[0064] 3) Add vitamin C to the above mixed cross-linking gel solution. The amount of rifampicin added is 5% in terms of weight to volume ratio. Mix evenly. Draw a certain amount with the syringe. After standing for 1-2 hours, slowly push it into the opening In the spherical mold tube, leave a certain space at the opening, let it stand to make it completely solidified, insert the electrode into the fully solidified gel, ...

Embodiment 3

[0067] Example 3 Preparation of bionic self-assembled multi-pulse drug release device (precipitation ring layer is calcium hydrogen phosphate crystal)

[0068] 1) Weigh a certain amount of gelatin, put it in a container, add double distilled water to fully dissolve, and make a gel solution with a concentration of 3% according to the mass-volume ratio;

[0069] 2) Mix the above glue solution with calcium chloride solution with a concentration of 0.02mol / L, the volume ratio is 1:1, after mixing evenly, add a certain volume of glutaraldehyde solution with a mass fraction of 1%, and stir for 1 hour to make the gelatin The degree of cross-linking is 1%, and the mixed cross-linking gel solution is obtained;

[0070] 3) Add vitamin C to the above mixed cross-linking glue solution. The amount of vitamin C added is 2% in terms of weight to volume ratio, mix well, draw a certain amount from the syringe, and after standing for 1.5 hours, slowly push it into the open spherical In the mol...

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Abstract

The invention discloses an electric fieldmulti-pulse drug release device which comprises an adhesive medium layer, a precipitation ring layer, drugs and an electrode. The adhesive medium layer and the precipitation ring layer are arranged at an interval, the drugs are distributed in the adhesive medium layer or the precipitation ring layer, one end of the electrode is arranged at the central position of the device, and the other end of the electrode is exposed out of the device. The invention further provides a method for manufacturing the self-assembling multi-pulse drug release device by exerting an electric field, and finally the invention further provides an application of the electric field multi-pulse drug release device in the preparation process of control release type preparations. Compared with the prior art, the self-assembling multi-pulse drug release device can achieve long-time and periodic release of the drugs, and overcome the defects of short-time and one-time drug release of a drug release device. In the manufacturing and release process, the electric field influence is exerted, and the number and period of pulses of the drugs can be effectively controlled. Therefore, the method with the wide application prospect is provided for molecule or drug conveying, and the method has the higher independence of controlling the drug release and drug reliability.

Description

technical field [0001] The invention belongs to the field of pharmaceutical preparations, and in particular relates to an electric field multi-pulse drug release device and a preparation method and application thereof. Background technique [0002] In the field of pharmaceutical preparations, the application of polymer materials has a long history. In the process of seeking survival and fighting against diseases since ancient times, human beings have widely used natural animal and plant-derived polymer materials, such as starch, polysaccharides, proteins, colloids, etc., as binders, excipients, Suspending agent, emulsifying agent. After the 1930s, a large number of synthetic polymer materials emerged, and their applications in the research and production of pharmaceutical preparations became increasingly widespread. It can be said that any dosage form requires the use of polymer materials, and the application of each suitable polymer material will improve the internal or e...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): A61M31/00
Inventor 倪恨美张慧吴敏周晓梅陈雨露詹侃陈国霞
Owner SOUTHEAST UNIV