GB1566346A

GB1566346A - Sterilizing a particulate solid material

Info

Publication number: GB1566346A
Application number: GB4687077A
Authority: GB
Original assignee: Individual
Current assignee: Individual
Priority date: 1977-11-10
Filing date: 1977-11-10
Publication date: 1980-04-30

Description

(54) STERILIZING A PARTICULATE SOLID MATERIAL (71) I, IRWIN MADDLIN STONE, a citizen of the United States of America, San Jose, California, United States of America, do hereby declare the invention for which I pray that a patent may be granted to me, and the method by which it is to be performed to be particularly described in and by the following statement: Conventional sterilization methods for injectable solutions or suspensions generally comprise the exposure of the preformed mixture to high temperatures or ionizing radiation sufficient to kill any microorganisms present. This approach cannot be used with materials that will be adversely affected by the sterilizing conditions. Another approach is the sterile membrane filtration system in which the solution is passed through a sterile Millipore (Registered Trade Mark) filter system. This technique can be cumbersome, involved and expensive. Both approaches, however, fail to come to grips with the problem associated with solutions which tend to decompose relatively rapidly thereby having an intolerably low shelf life. Such materials as sodium ascorbate, for example, are available in 50 ml vials containing 25% sodium ascorbate solution (12.5 g sodium ascorbate) preserved with sodium sulfite and benzyl alcohol. When such materials are used, for example, in the treatment of humans and animals in the manner described by F.R.

Klenner (J. International Acad. Prev.

Med., vol. 1, No. 1, pages 49-65 (1974) and W.O. Belfield et al (J. International Acad.

Prev. Med. vol. 2, No. 3, pages 10-26 (1975) and E. Cameron et al, J. Internat. Res.

Commun., vol. 1, No. 6 page 38 (1973), the sulfite produced adverse side effects resembling those of beri-beri as a result of the reaction of the sulfite with the patient's vitamin B. The manufacturer, upon request, has produced vials without the sulfite but the manufacturer believes the shelf life is so short that they do not distribute the product through normal channels. What is needed is an inexpensive means for sterilizing sensitive materials in the solid state so that they can be stored for long periods and mixed with sterile water immediately prior to use. This invention describes such as approach.

According to the present invention, there is provided a method for sterilizing a particulate solid material, the method comprising: a) placing a charge of the particulate solid material, which must be non-reactive with ethyl alcohol, in a sealable container, b)adding to said container an amount of ethyl alcohol sufficient to produce a sterilizing ethyl alcohol vapor in said container, c)sealing said container, and d)storing said sealed container for a period of time at least sufficient to sterilize said material.

The present invention also comprehends biologically active solid particulate material sterilized in accordance with the method of the invention, for parenteral or hypodermic introduction into the body of humans or animals, in a sealed container, wherein the material is maintained, in the container in an atmosphere of sterilizing ethyl alcohol vapor.

Thus, in accordance with this invention a stable sterile particulate solid material can be prepared by a simple, non-toxic, inexpensive means in a convenient cheap disposable container. The container and contents can have a long shelf life and can be capable of being simply and rapidly used by the physician or nurse in the preparation of fresh injectable solutions immediately before injection into the patient.

The following description will be directed to the preferred embodiment of sodium ascorbate but it should be recognized that the invention can be used with combinations of sodium ascorbate with other materials or with any other pharmaceutical material (without the presence of sodium ascorbate) that is non-reactive with ethyl alcohol.

Sodium ascorbate, for example, is rather unstable to heat both in the dry state and in solution, so that the temperatures required for heat sterilization causes destruction and loss of activity of the ascorbate. Sterilization by sterile membrane filtration through a completely sterile system such as that manufactured by the Millipore Corporation can be done, but is limited to solutions. This is an expensive and time consuming operation, especially if it is necessary to first get the sodium ascorbate into solution, membrane filter this solution and then freeze-dry the sterile solution under sterile conditions to obtain a sterile dry powder for permanent shelf life stability in the dry state in the sterile packaged product.

Another method of sterilization, by high energy radiation, requires a tremendous investment in special equipment and there is no data available on the effect of such high energy radiation on an unstable material like sodium ascorbate as to loss in activity and the shelf life stability of radiated ascorbate.

I have overcome all these objections to present customary sterilization procedures by the provision of a very simple, elegant and inexpensive, non-toxic procedure in accordance with the invention for the lowtemperature, vapor phase sterilization, which can produce a stable particulate material suitable for injection purposes, with no loss of activity.

The principle of the method is to place a weighed charge of, for example sodium ascorbate (fine crystals preferred) into a suitable sealable container (glass, plastic or other) and add a quantity of ethyl alcohol sufficient to produce a high enough concentraton of alcoholic vapor to effectively kill and inactivate any viable microorganisms adhering to the sodium ascorbate during the shelf-life storage time on the package containing it. At the time the physician or nurse wants to prepare the solution for injection, they either remove or penetrate the seal with a sterile hypodermic syringe and add the required amount of sterile water for injection needed for the preparation of the solution. The sodium ascorbate quickly dissolves and the solution is ready for injection into the patient or for further dilution for parenteral drip therapy. No attempt is made to remove the ethyl alcohol as the amount originally added is so small and harmless and will be normally metabolized after injection into the patient, with no deleterious side effects or toxicity. The patient is thus assured a perfectly fresh solution of the paper ascorbate strength as the time between preparation and administration is so short that no loss of ascorbate activity can take place.

The amount of ethyl alcohol required in this treatment is very small and is easily calculated from the volume of the container and the fact that 100 mg of ethyl alcohol (100%) will produce approximately 50 ml of saturated vapor at room temperature. If a 6 ounce (170 ml) container is used, then aout 360 mg of ethyl will be required to fill the container with ethyl alcohol vapor. Less quantities than that giving 100% saturation, like 50% saturation, will also be effective, but I prefer to use an amount giving about 150% saturation. Substantially larger amounts of ethyl alcohol beyond about 150% are unnecessary and only add to the costs. The amounts of ethyl alcohol needed are so small that they do not "wet" the powder, with visible liquid in the interstices of the particulate materials. Besides, keeping the ethyl alcohol levels minimal is desirable, to avoid unnecessary increases in the alcohol blood levels of the patients. The adult blood volume is about 4 liters so that the ethyl alcohol added in the above example would produce an insignificant rise of about 0.01% in the alcohol blood level.

The ethyl alcohol concentration in the alcoholic liquid added to the dry particulate material is not critical, but should be preferably high to avoid adding excessive water to the mixture along with the alcohol. 100% or absolute alcohol may be employed, but the less expensive azeotropic concentration of about 95% ethyl alcohol is preferred. Lesser concentrations can be used but require more liquid to generate the required vapor volumes.

The costs of the finished sterile product of this invention will be low, being not much more than the costs of the raw materials and package, as there are no involved expensive processing operations to produce sterility.

This results in substantial savings to the patient in the cost of medical care.

Other materials like soluble vitamins, minerals or other drugs that are required to be injected along with the ascorbate may be added to the sodium ascorbate in the package and the ethyl alcohol added to the mixture before the package is sealed. In this way the other additives for injection are sterilized at the same time as the sodium ascorbate.

Sterile water "For Injection" is the preferred liquid for dissolving the treated sodium ascorbate of this invention. I have found that if this injectable grade of water is not available, particularly in veterinary medicine, boiled and cooled distilled water or even plain tap water may be used for dilution, without harmful effect on the patient.

The following are typical examples of the procedure of this patent: Example 1 Into a clean 6 ounce screw capped bottle weigh 15 g of sodium ascorbate fine crystals.

Add 360 mg of ethyl alcohol (0.46 ml 95% ethyl alcohol), seal tightly and shake vigorously to distribute the alcohol and permit rapid vaporization throughout the sealed bottle. Allow to stand.

Example 2 Weigh 30 g of sodium ascorbate into a dry 1 liter plastic a renteral bag add 600 mg of ethyl alcohol (0.8 ml of 90% ethyl alcohol) and mix thoroughly with the contained powder. Fold the bag and store flat (to limit the internal volume) until ready to use.

Dilute with 1 liter of sterile water "For Injection" immediately before connecting to the patient. This will produce a fresh sterile isotonic parenteral solution of sodium ascorbate suitale for continuous intravenous drip therapy.

Example 3 Weigh 20 g of sodium ascorbate (fine crystals) into a 100 ml sealable vial and add 300 mg of ethyl alcohol (0.48 ml 70% ethyl alcohol). Shake thoroughly and seal with a closure that can be sterily penetrated by a hypodermic needle. Allow to stand. When ready for use, draw 100 ml of sterile water for injection into a sterile hypodermic syringe. Penetrate the cap with the hypodermic needle and add sufficient water to dissolve the sodium ascorbate by swirling, without removing the hypodermic from the vial. When dissolved with solution is sucked back into the hypodermic syringe, mixed and is ready for injection.

Example 4 10 g of sodium ascorbate (fine crystals) are weighed into a 100 ml sealable vial and 300 mg of ethyl alcohol is added (0.38 ml absolute alcohol) and the vial is sealed and shaken as in Example 3 and is handled similarly.

WHAT WE CLAIM IS: 1. A method for sterilizing a particulate solid material, the method comprising: a) placing a charge of the particulate solid material, which must be non-reactive with ethyl alcohol, in a sealable container, b)adding to said container an amount of ethyl alcohol sufficient to produce a sterilizing ethyl alcohol vapor in said container, c) sealing said container, and d) storing said sealed container for a period of time at least sufficient to sterilize said material.

2. A method according to claim 1, wherein the ethyl alcohol is added in an amount sufficient to produce a sterilizing ethyl alcohol vapor saturation of at least 50%.

3. A method according to claim 1 or claim 2, wherein the ethyl alcohol is added in an amount sufficient to produce a sterilizing ethyl alcohol vapor saturation of about 150%.

4. A method according to any one of claims 1 to 3, wherein said solid material comprises sodium ascorbate.

5. A method for sterilizing a particulate solid material, the method being substantially as described in any one of the foregoing Examples 1 to 4.

6. Biologically active solid particulate material, sterilized in accordance with the method of any one of claims 1 to 5, for parenteral or hypodermic introduction into the body of humans or animals, in a sealed container, wherein the material is maintained, in the container in an atmosphere of sterilizing ethyl alcohol vapor.

**WARNING** end of DESC field may overlap start of CLMS **.

Claims

**WARNING** start of CLMS field may overlap end of DESC **.

The following are typical examples of the procedure of this patent: Example 1 Into a clean 6 ounce screw capped bottle weigh 15 g of sodium ascorbate fine crystals.

Add 360 mg of ethyl alcohol (0.46 ml 95% ethyl alcohol), seal tightly and shake vigorously to distribute the alcohol and permit rapid vaporization throughout the sealed bottle. Allow to stand.

Example 2 Weigh 30 g of sodium ascorbate into a dry 1 liter plastic a renteral bag add 600 mg of ethyl alcohol (0.8 ml of 90% ethyl alcohol) and mix thoroughly with the contained powder. Fold the bag and store flat (to limit the internal volume) until ready to use.

Dilute with 1 liter of sterile water "For Injection" immediately before connecting to the patient. This will produce a fresh sterile isotonic parenteral solution of sodium ascorbate suitale for continuous intravenous drip therapy.

Example 3 Weigh 20 g of sodium ascorbate (fine crystals) into a 100 ml sealable vial and add 300 mg of ethyl alcohol (0.48 ml 70% ethyl alcohol). Shake thoroughly and seal with a closure that can be sterily penetrated by a hypodermic needle. Allow to stand. When ready for use, draw 100 ml of sterile water for injection into a sterile hypodermic syringe. Penetrate the cap with the hypodermic needle and add sufficient water to dissolve the sodium ascorbate by swirling, without removing the hypodermic from the vial. When dissolved with solution is sucked back into the hypodermic syringe, mixed and is ready for injection.

Example 4

10 g of sodium ascorbate (fine crystals) are weighed into a 100 ml sealable vial and 300 mg of ethyl alcohol is added (0.38 ml absolute alcohol) and the vial is sealed and shaken as in Example 3 and is handled similarly.

WHAT WE CLAIM IS: 1. A method for sterilizing a particulate solid material, the method comprising: a) placing a charge of the particulate solid material, which must be non-reactive with ethyl alcohol, in a sealable container, b)adding to said container an amount of ethyl alcohol sufficient to produce a sterilizing ethyl alcohol vapor in said container, c) sealing said container, and d) storing said sealed container for a period of time at least sufficient to sterilize said material.
2. A method according to claim 1, wherein the ethyl alcohol is added in an amount sufficient to produce a sterilizing ethyl alcohol vapor saturation of at least 50%.
3. A method according to claim 1 or claim 2, wherein the ethyl alcohol is added in an amount sufficient to produce a sterilizing ethyl alcohol vapor saturation of about 150%.
4. A method according to any one of claims 1 to 3, wherein said solid material comprises sodium ascorbate.
5. A method for sterilizing a particulate solid material, the method being substantially as described in any one of the foregoing Examples 1 to 4.
6. Biologically active solid particulate material, sterilized in accordance with the method of any one of claims 1 to 5, for parenteral or hypodermic introduction into the body of humans or animals, in a sealed container, wherein the material is maintained, in the container in an atmosphere of sterilizing ethyl alcohol vapor.