WO2007029159A1

WO2007029159A1 - A process for the preparation of lyophilized sodium bicarbonate

Info

Publication number: WO2007029159A1
Application number: PCT/IB2006/053085
Authority: WO
Inventors: M. V. Rama KRISHNA; Bhupendra Vashista; Sanjay Gade
Original assignee: Ranbaxy Laboratories Limited
Priority date: 2005-09-05
Filing date: 2006-09-01
Publication date: 2007-03-15
Also published as: CN101282908A

Abstract

The present invention provides a process for the preparation of crystalline lyophilized sodium bicarbonate.

Description

A PROCESS FOR THE PREPARATION OF LYOPHILIZED SODIUM

BICARBONATE

Field of the Invention The present invention provides a process for the preparation of crystalline lyophilized sodium bicarbonate.

Background of the Invention

Sodium bicarbonate is used as an inactive ingredient in injectable pharmaceutical preparations such as ertapenem, octreotide acetate, fomivirsen sodium, mannitol, and poractant alfa and in oral tablets such as ESTRATEST® (Esterified Estrogens and Methyltestosterone) and terfenadine. Sterile water for injection containing sodium bicarbonate is used for reconstituting certain drugs such as ceftizoxime, cefazolin, cimetidine hydrochloride, cefoxitin sodium and ceftriaxone sodium. Sodium bicarbonate is also used in the preparation of sodium salts of the drugs such as cilastatin and cefotetan. Sodium bicarbonate is also an ingredient in oral solutions for gastrointestinal lavage such as COLYTE^®. It is also used for pH neutralization of drugs such as metronidazole and ascorbic acid prior to parenteral administration.

Sodium bicarbonate of higher purity is commercially produced by injecting gaseous carbon dioxide into a sodium carbonate solution of such composition that results in crystallization of sodium bicarbonate as the solution becomes fully saturated with carbon dioxide. The crystals are separated by centrifuging and filtering, and then dried to remove the traces of moisture.

As detailed in PCT Patent Publication No. WO 94/14705, sodium bicarbonate wet cake is traditionally dried by using conventional rotary steam tube dryers. Such methods involve high temperature dehydration and steam pressure up to thirty five atmosphere. The dried material usually has high bulk density and the crystals resulting from this process usually have irregular particle size distribution and dendritic structures, which are physically weak and readily disintegrate into finer fragments on handling. Further, at higher temperatures, sodium bicarbonate tends to be converted into sodium carbonate.

U.S. Patent No 3,647,365 describes a method to obtain hollow beads of sodium bicarbonate having bulk density of 25 - 32 pounds per cubic foot, and the process involves drying of the product by warming under carbon dioxide environment. Such methods of drying by warming consume considerable time for complete removal of the moisture. U.S. Patent No. 5,290,322 provides a method to prepare sodium bicarbonate crystals having regular particle size distribution by mobile bed crystallization method. However, the method needs to be carried out at a temperature of about 70⁰C under carbon dioxide environment and results in a mean particle size of about 900 microns.

Summary of the Invention

The present inventors have now surprisingly found that crystalline sodium bicarbonate with high purity; optimum bulk density and uniform particle size distribution can be prepared in comparatively a shorter reaction time by lyophilizing a solution of sodium bicarbonate. The method does not require carbon dioxide atmosphere, high pressure or temperature conditions, and yet results in a pure product with moisture content less than about 0.25 % w/w. The present method is suitable for industrial preparation of pharmaceutical grade crystalline sodium bicarbonate.

Detailed Description of the Invention

A first aspect of the present invention provides a crystalline lyophilized sodium bicarbonate. The crystalline lyophilized sodium bicarbonate of the present invention has bulk density ranging from about 0.10 to about 0.25 g/ml and tapped density ranging from 0.30 to about 0.40 g/ml.

A second aspect of the invention provides crystalline lyophilized sodium bicarbonate having particle size wherein 90% of the particles (do ₉) have particle diameter 40 microns or less. A third aspect of the present invention provides a process for the preparation of crystalline sodium bicarbonate, wherein the process comprises a) lyophilizing the solution of sodium bicarbonate in lyophilizer having tray thickness of about 15 mm or less, and b) isolating crystalline sodium bicarbonate from the reaction mass thereof.

Sodium bicarbonate of any morphology or particle size range prepared by any of the prior art methods can be used as a starting substrate. The sodium bicarbonate is dissolved in water at a temperature of about 5° to about 15°C. The solution is optionally filtered through a micron filter and transferred to lyophilizer trays having the temperature of about 0° to about -10⁰C. The thickness of the solution layer on the lyophilizer trays is less than about 15 millimeter. The solution is cooled to a temperature of -20⁰C or less under vacuum. Then the temperature is raised to about 0⁰C, and then to about 10⁰C. The product can further be dried at a temperature of about 15°C or above.

While the present invention has been described in terms of its specific embodiments, certain modifications and equivalents will be apparent to those skilled in the art and are included within the scope of the present invention.

Example 1: Preparation of Crystalline Lyophilized Sodium Bicarbonate:

Deionised water (3.5 L) was cooled at a temperature of 5° to 10⁰C. Sodium bicarbonate (250 g) was added slowly to the deionised water at a temperature of 5° to 10⁰C and stirred until complete dissolution of the solid. The solution was filtered using 0.45 micron filter and transferred to lyophilizer trays, pre-cooled to 0° to -5°C, to form a layer of 8 to 10 millimeter thickness. The solution was frozen to -40⁰C and held at the same temperature for 180 minutes, followed by the application of vacuum (150 mTorr). The temperature was raised to 0⁰C in 300 minutes and held at the same temperature for 600 minutes. The temperature was further raised to 10⁰C in 120 minutes and held at the same temperature for 600 minutes. The temperature of the reaction mixture so obtained was raised to 15°C in 60 minutes and held at the same temperature for 360 minutes. The temperature was further raised to 25°C in 120 minutes and held at the same temperature for 300 minutes, followed by the release of vacuum to obtain the title compound. Yield: 225 g

Purity: 99.6 % w/w

Loss on Drying: 0.08%

Bulk Density: 0.24 g/ml

Tapped Bulk Density: 0.34 g/ml

Particle Size (measured by Malvern Mastersizer):

D (0.1) D (0.5) D (0.9)

3μ 15μ 37μ

Claims

WE CLAIM: 1. A crystalline lyophilized sodium bicarbonate. 2. A crystalline lyophilized sodium bicarbonate having a bulk density ranging from about 0.10 to about 0.25 g/ml. 3. A crystalline lyophilized sodium bicarbonate having a tapped density ranging from about 0.30 to about 0.40 g/ml. 4. A crystalline lyophilized sodium bicarbonate having particle size wherein 90% of the particles (do ₉) have particle diameter of 40 microns or less. 5. A process for the preparation of crystalline lyophilized sodium bicarbonate, wherein the process comprises, a) lyophilizing the solution of sodium bicarbonate in lyophilizer having tray thickness of about 15 mm or less, and b) isolating crystalline sodium bicarbonate from the reaction mass thereof. 6. A process as claimed in claim 5, wherein the solution of sodium bicarbonate is obtained by dissolving sodium bicarbonate in water. 7. A process as claimed in claim 6, wherein sodium bicarbonate is dissolved at a temperature of about 15°C or less. 8. A process as claimed in claim 5, wherein step a) is carried out at a temperature of about -20⁰C or less. 9. A process as claimed in claim 5, wherein the reaction mixture is filtered before lyophilizing. 10. A process as claimed in claim 5, wherein step a) is carried out under vacuum.