Polystyrene sulfonate-containing gel preparation

Drug – bio-affecting and body treating compositions – Solid synthetic organic polymer as designated organic active... – Ion exchange resin

Reexamination Certificate

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C514S944000

Reexamination Certificate

active

06703013

ABSTRACT:

TECHNICAL FIELD
The present invention relates to a polystyrene sulfonate-containing preparation which can be easily taken with a drastically reduced intake of water for ingestion, and particularly to a gel therapeutic agent for hyperpotassemia, which comprises polystyrene sulfonate as an active ingredient.
BACKGROUND ART
Conventional therapies applied to patients with hyperpotassemia include calcium gluconate therapy, glucose-insulin therapy, sodium bicarbonate therapy, saline therapy or a combination thereof for relative emergency cases, or dialysis therapy and cation-exchange therapy based on administration of cation-exchange resin such as polystyrene sulfonate for non-emergency cases. Among these therapies, the cation-exchange therapy involving removing potassium from the body by replacement of potassium ions in intestinal tracts is generally conducted for patients with chronic renal insufficiency, and in this therapy, a daily dosage of 15 to 30 g polystyrene sulfonate for an adult person is divided into 2 to 3 portions and each portion is suspended in 30 to 50 ml water and orally administered. However, polystyrene sulfonate is a powder which is hardly dissolved in water and it should be taken in a large amount, so it feels strongly unpleasant in the oral cavity upon ingestion, and it is noted that there are many cases where compliance with clinician's instructions is not obeyed.
The polystyrene sulfonate when suspended in water is easily precipitated at the bottom of a cup, thus making it difficult to take the whole dose all at once, so some patients take powdery sulfonate polystyrene with water in the oral cavity without previously suspending it. In this case, there is a possibility that the polystyrene sulfonate is not uniformly dispersed in digestive tracts and forms agglomerates, thus failing to bring about the desired pharmaceutical effect. Further, the polystyrene sulfonate when taken in the form of powder feels strongly unpleasant in the oral cavity, to become a great mental burden on the patient. Hence, the polystyrene sulfonate gives a remarkably unpleasant feeling in the oral cavity, and according to the present application method, it is difficult to take the whole of a prescribed dose all at once, so under the present circumstances, the patient drinks a large amount of water to take it, which is contraindicated for renal insufficiency.
Recently, the method of administering the pharmaceutical preparation is recently devised in some hospitals, and it is reported that the improvement of compliance is attempted by manufacturing calcium polystyrene sulfonate etc. into jelly preparations {“Shinryo To Shinyaku”, Vol. 29, No. 2, p. 514 (1992), “Shinryo To Shinyaku”, Vol. 31, No. 11, p. 1911 (1994); and “Iyaku No Mon”, Vol. 31, No. 3, p. 190 (1991)}.
However, even in the above-described polystyrene sulfonate-containing jelly preparations, there remain the following problems:
(a) The polystyrene sulfonate-containing jelly preparations reported in the above literatures feel rough like sand, and are inferior in a sense of ingestion. This sense of roughness remains considerably in the oral cavity, and especially 50% or more polystyrene sulfonate is precipitated at the bottom of a vessel at the time of manufacturing the jelly preparation, and thus a sense of significant roughness is felt upon ingestion of the jelly preparation sedimented at the bottom of the vessel, and the removal of this unpleasant sense or sense of foreign matter requires drinking water, which results in an excessive intake of water to cause a great problem for patients with renal insufficiency.
(b) While the variability of contents in jelly confectionery as general food is acceptable at certain degrees, the amounts of contents in the jelly preparation as a pharmaceutical preparation should be strictly guaranteed. However, the majority of polystyrene sulfonate is precipitated upon introduction into a solution before gelation, so it is difficult to set a predetermined content of said salt in the jelly preparation, and accordingly it is almost impossible to produce a large amount of a jelly preparation with a constant content of said salt. To prepare a large amount of a jelly preparation with a constant content of polystyrene sulfonate, it is conceivable that a predetermined amount of said salt is introduced into each vessel and then a solution for gelation is poured into it. However, the polystyrene sulfonate in the vessel is poor in uniform dispersibility, and thus upon ingestion of a part containing a large content of said salt, those who take it feel significantly unpleasant in the oral cavity. Therefore, manual manufacturing of the jelly preparation, such as dispensing it little by little rapidly with stirring, is necessary under the present circumstances, but this makes the operation complicated and productivity lowered. After all, it is very difficult or impossible to prevent the polystyrene sulfonate from being unevenly distributed in the jelly preparation.
(c) The amount of water in the conventional polystyrene sulfonate-containing jelly preparation is at least 100 ml/preparation, and accordingly if it is administered 3 times every day, the intake of water will be at least 300 ml/day. Further, if water is taken in an amount of 50 ml for each administration to relieve the significant unpleasant feeling, the amount of water taken for the administration is further increased to be more than 450 ml/day. However, the daily intake of water for a patient with renal insufficiency is limited to 400-700 ml in order to relieve the burden on the kidney. Accordingly, if the polystyrene sulfonate-containing jelly preparation is administered, the amount of water (including drinking water) which can be taken from other materials than said preparation is made less than half of the usual amount or is very small in some cases, thus significantly impairing the life or quality of life (QOL) of the patient and bringing about a mental burden on the patient.
DISCLOSURE OF INVENTION
An object of the present invention is to solve the above-described prior art problems all at once. That is, the problem to be solved by the invention is to provide polystyrene sulfonate-containing gel preparations with a reduced content of water and with a reduced unpleasant feeling at the time of administration or ingestion, whereby the amount of water taken for administration, as a great problem in patients with renal insufficiency, can be reduced. A further object is to guarantee the content of polystyrene sulfonate in a pharmaceutical preparation and to enable production thereof in a large amount at the industrial level.
The polystyrene sulfonate-containing gel preparation according to the present invention is characterized in that the particle diameter of polyethylene sulfonate is made uniform within the range of at least 5-100&mgr;m. Further, it is characterized in that the viscosity before gelation is adjusted depending on its particle size by adding a thickening agent and the polystyrene sulfonate particles after gelation are uniformly dispersed. More preferably, it is characterized in that a part of contained water is replaced by containing a water-displacing agent.
Hereinafter, the gel preparation of the present invention is described in more detail.
At the time of preparing the polystyrene sulfonate-containing gel preparation of the present invention, adjustment of the viscosity of its solution before gelation is conducted so that a prescribed amount of the active ingredient is contained in an uniformly dispersed state in the preparation without deteriorating the ability of said salt on ion exchange, and simultaneously the unpleasant sense of roughness in the oral cavity upon administration is reduced. As a result of reduction of the unpleasant sense of roughness in the oral cavity, the patient can reduce water intake for ingestion of said preparation.
The viscosity of the solution at 50° C. before gelation is adjusted by the thickening agent specifically to 50 cP or more in case where the particle diameter of polystyre

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