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Preparation and application of florfenicol slowly-releasing micropill for treating animal digestive canal infection

A technology of digestive tract infection and florfenicol, which is applied in the field of preparation of sustained-release pellets, can solve the problems of drug side effects and drug concentration reduction, and achieve the effect of reducing treatment costs and reducing drug absorption

Inactive Publication Date: 2010-04-14
TIANJIN SHENGJI GRP CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

For such gastrointestinal diseases, the existing treatment methods are mostly oral premixes of sensitive antibacterial drugs, or intramuscular injections. Although the above treatment methods can kill pathogenic bacteria in the intestinal tract to a certain extent, At the same time, there are two disadvantages: after injection or oral administration, the systemic distribution of the drug leads to a decrease in the concentration of the drug at the treatment site; in addition, the accumulation of the drug in the non-treatment site will produce unnecessary toxic side effects

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0014] A preparation method of florfenicol oral sustained-release pellets for treating animal digestive tract diseases, the implementation steps are as follows: according to the ratio of 0.1 to 10:1 by weight, take pharmaceutical excipients and florfenicol raw materials, first prepare The micropills are formed into micropills with particle diameters ranging from 0.5 to 3 mm, and the micropills are wrapped with a pH-independent high-molecular polymer film, and the film contains low-molecular water-soluble substances. After the coated pellets come into contact with water or body fluids in the intestinal tract, the water-soluble substances on the membrane, such as mannitol, glucose or sodium chloride, dissolve immediately, forming small pores on the membrane, and the drugs in the pellets are released in a certain amount. It is released slowly from the pores at a high speed and has a long-lasting therapeutic effect in the intestinal tract. The release rate of the drug is related t...

Embodiment 2

[0018] Take florfenicol raw materials and pharmaceutical excipients acceptable to pharmacy, mix them evenly according to the mass ratio of 1:0.5, and make ball cores according to conventional methods. Take a pH-independent, mass ratio concentration of 15% cellulose acetate acetone solution, in which glucose with a mass ratio of 0.01:1 is dispersed. The above-mentioned ball cores are coated with this coating solution, and the mass ratio of the weight gain of the coating to the weight of the ball cores is controlled to be 0.05:1.

[0019] Others are with embodiment 1.

Embodiment 3

[0021] Take florfenicol raw materials and pharmaceutical excipients acceptable to pharmacy, mix them uniformly according to the ratio of mass ratio 1:5, and make ball cores according to conventional methods. Take a pH-independent aqueous dispersion of acrylic resin with a mass ratio concentration of 35%, in which sodium chloride is dissolved in a mass ratio of 0.02:1. The above-mentioned ball cores are coated with this coating solution, and the mass ratio of the weight gain of the coating to the weight of the ball cores is controlled to be 0.05:1.

[0022] Others are with embodiment 1.

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PUM

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Abstract

The invention relates to preparation and application of florfenicol slowly-releasing micropills for treating animal digestive canal infection. The implementation comprises the following steps: weighing drug accessories and florfenicol raw materials according to the proportion of weight ratio 0.1-10:1, preparing micropills whose grain size dimension is between 0.5 to 3mm, wrapping a non-pH dependency high molecular polymer film outside the micropills, wherein the film contains low molecular water-soluble materials. Slowly-releasing micropills containing florfenicol is wrapped by non-pH dependency high molecular polymer materials, water-soluble materials such as mannidex, antacidin or natrii chloridum are added in the wrapping film, after people take the wrapped micropill orally, the water-soluble component in the wrapping film is dissolved to form a pore passage, and the drug is slowly released from the pore passage and exerts the long-term curative effect in the intestinal tract. The drug is different from traditional drug feeding modes in that higher drug concentration can be kept in intestinal tracts for long time, directional distribution of the drug in the intestinal tract can lower the side effects of drug to other organs and tissues, and the treatment cost can be lowered due to less drug dosage.

Description

technical field [0001] The invention relates to a preparation method of sustained-release pellets, in particular to the preparation and application of florfenicol sustained-release pellets for treating animal digestive tract infections. Background technique [0002] At present, digestive tract diseases caused by bacteria are common diseases in mammals, such as diarrhea and enteritis. For such gastrointestinal diseases, the existing treatment methods are mostly oral premixes of sensitive antibacterial drugs, or intramuscular injections. Although the above treatment methods can kill pathogenic bacteria in the intestinal tract to a certain extent, At the same time, there are two disadvantages: after injection or oral administration, the systemic distribution of the drug leads to a decrease in the concentration of the drug at the treatment site. In addition, the accumulation of the drug at the non-treatment site will cause unnecessary side effects. [0003] Therefore, to provid...

Claims

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Application Information

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IPC IPC(8): A61K9/16A61K31/165A61K47/32A61K47/38A61P1/00
Inventor 田杏芳
Owner TIANJIN SHENGJI GRP CO LTD
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