RU2552346C1 - Fenbendazole encapsulation method - Google Patents

Abstract

FIELD: chemistry.

SUBSTANCE: invention provides a method of encapsulating a medicinal preparation via non-solvent addition, characterised by that the core of the microcapsules used is fenbendazole, the envelope used is sodium carboxymethyl cellulose which is deposited from a solution in toluene by adding, as the nonsolvent, carbinol and water at 25°C.

EFFECT: simpler and faster process of producing microcapsules and reduced losses when producing microcapsules.

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Description

The invention relates to the field of encapsulation, and in particular the production of fenbendazole microcapsules.

Previously known methods for producing microcapsules of drugs. So, in Pat.2092155, IPC A61K 047/02, A61K 009/16, published on 10/10/1997 The Russian Federation proposed a method of microencapsulation of drugs based on the use of ultraviolet radiation.

The disadvantages of this method are the duration of the process and the use of ultraviolet radiation, which can affect the process of formation of microcapsules.

In US Pat. 2091071, IPC A61K 35/10 Russian Federation, published 09/27/1997, a method for producing the preparation by dispersion in a ball mill to obtain microcapsules is proposed.

The disadvantage of this method is the use of a ball mill and the duration of the process.

Patent 2101010, IPC A61K 9/52, A61K 9/50, A61K 9/22, A61K 9/20, A61K 31/19 Russian Federation, published January 10, 1998, proposes a chewing form of a taste-masked drug with controlled release properties the drug contains microcapsules 100-800 microns in diameter in diameter and consists of a pharmaceutical core with crystalline ibuprofen and a polymer coating including a plasticizer flexible enough to withstand chewing. The polymer coating is a methacrylic acid based copolymer.

The disadvantages of the invention: the use of a copolymer based on methacrylic acid, as these polymer coatings can cause cancerous tumors; complexity of execution; the duration of the process.

Pat.2173140, IPC A61K009 / 50, A61K009 / 127 Russian Federation, published September 10, 2001. A method for producing silicon organolipid microcapsules using a rotary-cavitation unit with high shear forces and powerful sonar acoustic and ultrasonic dispersion ranges is proposed.

The disadvantage of this method is the use of special equipment - a rotary-quittance installation, which has an ultrasonic effect, which affects the formation of microcapsules and can cause adverse reactions due to the fact that ultrasound destructively affects polymers of a protein nature, therefore, the proposed method is applicable when work with polymers of synthetic origin.

Pat. 2,359,662, IPC A61K 009/56, A61J 003/07, B01J 013/02, A23L 001/00, published June 27, 2009. The Russian Federation proposes a method for producing microcapsules using spray cooling in a Niro spray cooling tower under the following conditions: air temperature at the inlet 10 ° C, the air temperature at the outlet 28 ° C, the rotation speed of the spray drum 10,000 rpm. The microcapsules of the invention have improved stability and provide controlled and / or prolonged release of the active ingredient.

The disadvantages of the proposed method are the duration of the process and the use of special equipment, a set of certain conditions (air temperature at the inlet 10 ° C, air temperature at the outlet 28 ° C, rotation speed of the spray drum 10,000 rpm).

The closest method is the method proposed in Pat.2134967, IPC A01N 53/00, A01N 25/28, published on 08.27.1999, Russian Federation (1999). A solution of a mixture of natural lipids and a pyrethroid insecticide in a weight ratio of 2-4: 1 in an organic solvent is dispersed in water, which simplifies the microencapsulation method.

The disadvantage of this method is dispersion in an aqueous medium, which makes the proposed method inapplicable for producing microcapsules of water-soluble preparations in water-soluble polymers.

The technical task is to simplify and accelerate the process of obtaining microcapsules, reducing losses when receiving microcapsules (increase in yield by mass).

The solution to the technical problem is achieved by the method of encapsulation of fenbendazole, characterized in that sodium carboxymethyl cellulose is used as the shell of the microcapsules when they are obtained by the physicochemical method of precipitation with a non-solvent using two precipitators - carbinol and toluene, the production process is carried out without special equipment.

A distinctive feature of the proposed method is the use of sodium carboxymethyl cellulose as the shell of microcapsules, fenbendazole as their core, as well as the use of two precipitants - carbinol and toluene.

The result of the proposed method is the production of fenbendazole microcapsules in sodium carboxymethyl cellulose at 25 ° C for 20 minutes. The output of microcapsules is more than 90%.

EXAMPLE 1. Obtaining microcapsules of fenbzindazole with dissolution of the drug in dioxane, the ratio of core / polymer 1: 3

100 mg of fenbendazole is dissolved in 1 ml of dioxane and the resulting mixture is dispersed in a solution of sodium carboxymethyl cellulose in toluene containing the indicated 300 mg of polymer in the presence of 0.01 g of the preparation E472 s with stirring 1000 rps. Then pour 2 ml of carbinol and 1 ml of distilled water. The resulting suspension is filtered and dried at room temperature.

Received 0.396 g of a white with a yellowish tinge of powder. The yield was 99%.

EXAMPLE 2. Obtaining microcapsules of fenbendazole with dissolution of the drug in dimethyl sulfoxide (DMSO), the ratio of core / polymer 1: 3

100 mg of fenbendazole is dissolved in 1 ml of DMSO and the resulting mixture is dispersed in a solution of sodium carboxymethyl cellulose in toluene containing the indicated 300 mg of polymer in the presence of 0.01 g of the preparation E472 s with stirring 1000 rps. Then pour 2 ml of carbinol and 1 ml of distilled water. The resulting suspension is filtered and dried at room temperature.

Received 0.396 g of a white with a yellowish tinge of powder. The yield was 99%.

EXAMPLE 3. Obtaining microcapsules of fenbendazole with the dissolution of the drug in dimethylformamide (DMF), the ratio of core / polymer 1: 3

100 mg of fenbendazole is dissolved in 1 ml of DMF and the resulting mixture is dispersed in a solution of sodium carboxymethyl cellulose in toluene containing the indicated 300 mg of polymer in the presence of 0.01 g of the preparation E472 s with stirring 1000 rps. Then pour 2 ml of carbinol and 1 ml of distilled water. The resulting suspension is filtered and dried at room temperature.

Received 0.396 g of a white with a yellowish tinge of powder. The yield was 99%.

Fenbendazole microcapsules were obtained by the physicochemical non-solvent precipitation method using two precipitants — carbinol and toluene, which increased the yield and accelerated the microencapsulation process. The process is simple to execute and lasts for 20 minutes, does not require special equipment.

The proposed technique is suitable for the veterinary industry due to minimal losses, speed, ease of obtaining and isolation of microcapsules.

Claims (1)

A method of encapsulating a drug using a non-solvent precipitation method, characterized in that fenbendazole is used as the microcapsule core, and sodium carboxymethyl cellulose is used as a shell, which is precipitated from the solution in toluene by adding carbinol and water as a solvent at 25 ° C.