Piroxicam belta-cyclodextrin inclusion compound micro-pill capsules

A technology of cyclodextrin inclusion compound and piroxicam, which is applied in the direction of microcapsules, nanocapsules, capsule delivery, etc., can solve problems in the production process of complex preparations, avoid process difficulties, simplify process flow, and reduce production costs Effect

Active Publication Date: 2009-07-29
上海微丸医药开发有限公司 +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

This patented technology allows for faster dissolution time without adding any extra ingredient that makes up part of its formula. It also improves upon existing methods by reducing manufacturing costs while still providing effective treatment with less harmful chemical compounds like ppirolimus (a type of medication).

Problems solved by technology

This patented technical problem addressed in this patents describes how to prepare stable and efficient compositions containing various types of active ingredient called beta-cyclic oxymerazoline derivative(BZ)-pirolacinonbodiester salt ((EMI)).

Method used

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  • Piroxicam belta-cyclodextrin inclusion compound micro-pill capsules
  • Piroxicam belta-cyclodextrin inclusion compound micro-pill capsules
  • Piroxicam belta-cyclodextrin inclusion compound micro-pill capsules

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0042] Preparation of piroxicam β-cyclodextrin inclusion complex pellets with a molar ratio of 1∶2.7 by spray coating

[0043] (1) Dissolve 32.3g of piroxicam, 300g of β-cyclodextrin, and 32.3g of 25% ammonia water in a dissolving tank pre-added with 1800g of pure water and preheated to above 65°C, and stir fully while heating until all the materials are dissolved to Clarify and keep warm at 75-85°C for later use;

[0044](2) Spray the hot solution onto 200g pellet cores under the atomization pressure of 0.05-0.5MPa, control the airflow temperature at 80-85°C, and spray the solution at a flow rate of 30-120ml / min. After spraying, piroxicam β-cyclodextrin inclusion complex pellets were prepared.

Embodiment 2

[0046] Preparation of piroxicam β-cyclodextrin inclusion compound pellets with a molar ratio of 1∶3.2 by spray coating

[0047] (1) Dissolve 33g of piroxicam, 363g of β-cyclodextrin, and 33g of 25% ammonia water in a dissolving tank pre-added with 1900g of pure water and preheated to above 65°C, fully stir while heating until the materials are completely dissolved until clarified, Keep warm at 75-85°C for later use;

[0048] (2) Spray the hot solution onto 200g pellet cores at an atomization pressure of 0.05-0.5MPa, control the airflow temperature at 80-85°C, and spray the solution at a flow rate of 20-110ml / min. After spraying, piroxicam β-cyclodextrin inclusion complex pellets were prepared.

Embodiment 3

[0050] Preparation of piroxicam β-cyclodextrin inclusion complex pellets with a molar ratio of 1∶3.8 by spray coating

[0051] (1) Dissolve 33 g of piroxicam, 431 g of β-cyclodextrin, and 33 g of 25% ammonia water in a dissolving tank pre-added with 2000 g of pure water and preheated to above 65° C., fully stir while heating until the materials are completely dissolved until clarified, Keep warm at 75-80°C for later use;

[0052] (2) Spray the hot solution onto 200g pellet cores under the atomization pressure of 0.05-0.5MPa, control the airflow temperature at 80-85°C, and spray the solution at a flow rate of 10-100ml / min. After spraying, piroxicam β-cyclodextrin inclusion complex pellets were prepared.

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Abstract

The invention relates to a method for preparing a piroxicam beta-cyclodextrin inclusion compound micropill capsule, which comprises the following steps that: (1) in ammonia water with a mass percent concentration of between 23 and 25 percent, piroxicam and beta-cyclodextrin are dissolved into water with a temperature of between 65 and 85 DEG C according to a mol ratio of 1: 2.7-3.8; and (2) under the atomizing pressure of between 0.05 and 0.5MPa, the airflow temperature is controlled to be between 75 and 85 DEG C, the flow rate is between 10 and 150ml/min, a piroxicam beta-cyclodextrin solution is sprayed on a pill core for spraying and coating, and a piroxicam beta-cyclodextrin inclusion compound micropill is prepared after immediate drying. The method does not need to add any auxiliary materials or excipients so as to reduce the relative process difficulty when including a piroxicam beta-cyclodextrin powder preparation, simplifies process flow, and reduces production cost.

Description

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Claims

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Application Information

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Owner 上海微丸医药开发有限公司
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