The present invention relates to a syringe barrel to be used for a syringe formulation which has preliminarily been filled with drug solution and sealed it in an injection barrel (hereinafter referred to as “a pre-filled syringe formulation”), a process for producing the barrel, and a syringe formulation which has been filled with a drug solution and sealed it (i.e. “pre-filled syringe formulation”).
Of the conventional syringe barrels for pre-filled syringe formulations, a specific one made of synthetic resins is widely used because of its simplicity of use.
However, such conventional syringe barrels are problematic in that air bubbles tend to easily adhere to their interior surfaces. This could lead to a serious consequence (e.g. air embolism), if such air bubbles actually intrude into the blood vessels during the administering of a drug solution. For this reason, whenever the administration of a drug solution is performed by use of a conventional pre-filled syringe formulation, a physician has been required to take extra care, lest air bubbles intrude into the blood vessels. For example, a physician used to rely upon a method by which air bubbles adhering to the inner can be accumulated into one area by striking the syringe tube with fingers in advance. However, such a method has another problem, because an extreme delay would be invited on the treatment or checkup of patients, if this method is taken at a busy clinical scene.
So far, there has been a report on a technology which enables the adhesion of air bubbles to be reduced in order to prevent the above-mentioned problems before they occur, by subjecting the interior surface of the syringe tube to an oxygen plasma treatment to increase hydrophilicity (e.g. Patent Document 1).
However, this oxygen plasma treatment requires massive amounts of equipments and also is not suitable for continuous treatment in terms of the production line, so that the realization of efficient production stays difficult as it now stands.
The present invention was made in light of such longstanding problems and circumstances as described above, and it is an object of the invention to provide a syringe barrel for pre-filled syringe formulation, which is capable of suppressing the adhesion of air bubbles to the interior surface, a pre-filled syringe which is capable of suppressing the adhesion of air bubbles, and a process for efficiently producing the syringe barrel.
The inventors of the present invention conducted various studies intended to solve the problems described above, and as a result, they found that when the interior surface of a syringe barrel is treated by corona discharge, the adhesion of air bubbles to the interior surface is significantly suppressed. Thus the present invention was completed.
The present invention has solved the above-described problems by means of a syringe barrel for drag solution filled and sealed syringe formulation, which is characterized by having the interior surface treated by corona discharge.
The present invention has also solved the above-described problems by means of a pre-filled syringe formulation, which is characterized by having a drug solution filled and sealed in the aforementioned syringe barrel.
The present invention has also solved the above-described problems by means of a process for producing a syringe barrel for pre-filled syringe formulation, which is characterized by having a process of subjecting the interior surface of the syringe barrel to a corona discharge treatment.
By use of the syringe barrel of the present invention, a pre-filled syringe formulation capable of suppressing the adhesion of air bubbles to the interior surface can be provided.
Furthermore, since the adhesion of air bubbles to the interior surface can be suppressed by use of the pre-filled syringe formulation of the present invention, there is no need to perform an operation of collecting the air bubbles adhering to the interior surface of the syringe barrel to one area when a physician injects a drug solution at a clinical scene, and thus administration of drug solution can be performed more efficiently and safely.
Moreover, according to the present invention, since massive amounts of equipments are not required, and continuous treatment is facilitated, highly efficient production of syringe barrels which are capable of suppressing the adhesion of air bubbles is made possible.
a is a schematic explanatory diagram showing the contact angle at the surface of a syringe barrel which has not been subjected to corona discharge treatment.
b is a schematic explanatory diagram showing the contact angle at the surface of a syringe barrel which has been subjected to corona discharge treatment.
10: Pre-filled syringe formulation
11: Syringe barrel
12: Cap
13: Plunger
P: Drug solution
θ: Contact angle
Hereinafter, embodiments of the present invention will be described with reference to the drawings.
In
The interior surface of the syringe barrel 11 has been subjected to a corona discharge treatment, so that a contact angle θ of 50 to 80° is obtained for a fluid droplet on the surface (see
As for the condition of corona discharge treatment resulting in such a contact angle θ, it is desirable to carry out the treatment with a corona discharge treatment apparatus, for which an output power and a duration of treatment sufficient for obtaining the aforementioned effect have been appropriately set in accordance with the size or shape of the syringe barrel 11, but for example, in the case of a syringe barrel for contrast agents, it is preferable to carry out the treatment at an output power of 50 to 400 W for about 5 to 10 seconds.
Furthermore, the corona discharge treatment apparatus is not particularly limited, but for example, corona discharge treatment apparatuses manufactured by Kasuga Electric Works, Ltd. are suitably used.
The material of the syringe barrel 11 is not particularly limited, but the material is preferably a synthetic resin. Examples of such synthetic resin include polypropylene resins, polyethylene resins, cyclic polyolefin resins and the like, but a product molded from a cyclic polyolefin resin is preferred from the viewpoint that the resin has excellent transparency, and it can be confirmed by visual inspection as to whether generation of air bubbles is suppressed. As for the cyclic polyolefin resin, there may be mentioned, for example, synthetic resins “tradename: ZEONEX (registered trademark)” manufactured by Zeon Corporation; synthetic resins “trade name: APEL (registered trademark)” manufactured by Mitsui Chemicals, Inc.; synthetic resins “trade name: TOPAS (registered trademark)” manufactured by Topas Advanced Polymers GmbH; and the like.
The drug solution P is a solution or suspension of a drug which is applicable as the pre-filled syringe formulation, and is not particularly limited as long as it is an injectable solution prepared for injection. For example, an injectable solution such as a contrast agent, a cardiovascular agent, an antispasmodic, a local anesthetic drug, an infusion formulation, a vitamin formulation, a vaccine for prophylactic inoculation, an antiplasmin agent, or a hyaluronan formulation can be used.
Here, examples of the contrast agent include injectable solutions of nonionic iodinated X-ray contrast agents such as iopromide, iomeprol, iopamidol, ioversol, iohexol, ioxilan, iotrolan and iodixanol; ionic iodinated X-ray contrast agents such as sodium meglumine amidotrizoate, sodium iolactamate, meglumine iolactamate, ioxaglic acid and meglumine iotroxate; nonionic MRI contrast agents such as gadodiamide hydrate and gadoteridol; ionic MRI contrast agents such as meglumine gadoterate and meglumine gadopentetate; and the like.
Examples of the cardiovascular agent include injectable solutions of anticoagulants such as heparin, heparin sodium and argatrovan; cardiotonic agents such as epinephrine and norepinephrine; and the like.
Examples of the antispasmodic include injectable solutions of butylscopolamine bromide, and the like.
Examples of the local anesthetic drug include injectable solutions of lidocaine hydrochloride, dibucaine hydrochloride, bupivacaine hydrochloride, lopivacaine hydrochloride, and the like.
Examples of the infusion formulation include injectable solutions of calcium chloride, glucose, sodium chloride, magnesium sulfate, dipotassium phosphate, and the like.
Examples of the vitamin formulation include injectable solutions of vitamin A, vitamin B1, vitamin B2, vitamin B6, vitamin B12, vitamin C, vitamin D, vitamin E, calcium pantothenate, nicotinic acid amide, retinol palmitate, mixed vitamins combining these, and the like.
Examples of the vaccine for prophylactic inoculation include injectable solutions of influenza HA vaccine, adsorbed diphtheria-purified pertussis-tetanus combined vaccine (DPT), rubella vaccine, mumps vaccine, varicella vaccine, hepatitis B vaccine, and the like.
Examples of the antiplasmin agent include injectable solutions of tranexamic acid and the like.
According to the present invention, among the drug solutions as described above, the injectable solutions of nonionic iodinated X-ray contrast agents, inter alia, the injectable solution of iohexol and the injectable solution of iodixanol are particularly preferred.
Hereinafter, the present invention will be described in more detail by way of Examples.
The entire interior surface of a syringe barrel made of a cyclic polyolefin resin (capacity 100 mL) was treated by means of a corona discharge treatment apparatus manufactured by Kasuga Electric Works, Ltd. at an output power of 250 W for about 5 seconds, and thus a syringe barrel for pre-filled syringe formulation of the present invention was obtained.
For each of the syringe barrel of the present invention obtained in Example 1 and a non-corona discharge treated syringe barrel made of a cyclic polyolefin resin, the contact angle θ of a fluid droplet formed on the surface (see
The results are presented in Table 1.
In each of the syringe barrel of the present invention obtained in Example 1 and the non-corona discharge treated syringe barrel made of a cyclic polyolefin resin, an injectable solution of iohexol (“OMNIPAQUE: trade name” manufactured by Daiichi Sankyo Co., Ltd.), which is a contrast agent, was filled and sealed. Air bubbles were completely removed in advance, and then an impact was applied to confirm the state of adhesion of air bubbles.
As a result, air bubbles were nearly not recognized in the syringe barrel of the present invention (
The injectable solution of iohexol according to Test Example 2 was changed to an injectable solution of iodixanol (“VISIPAQUE: trade name”) manufactured by Daiichi Sankyo Co., Ltd.), and the state of adhesion of air bubbles was confirmed in the same manner as in Test Example 2.
As a result, air bubbles were hardly recognized in the syringe barrel of the present invention (
Number | Date | Country | Kind |
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2006-339438 | Dec 2006 | JP | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/JP2007/001416 | 12/17/2007 | WO | 00 | 6/11/2009 |