Drug – bio-affecting and body treating compositions – In vivo diagnosis or in vivo testing – Magnetic imaging agent
Reexamination Certificate
2000-04-28
2003-02-04
Hartley, Michael G. (Department: 1616)
Drug, bio-affecting and body treating compositions
In vivo diagnosis or in vivo testing
Magnetic imaging agent
C424S009400, C424S009100
Reexamination Certificate
active
06514480
ABSTRACT:
This application is a 371 of PCT/EP98/05305, filed Aug. 20, 1998.
The invention relates to a method for producing contrast agents largely free side-effects, in particular nonionic, monomeric or dimeric radiological contrast agents, in which the contrast agent is put into contact with a reactive medium having molecules larger than in the contrast agent, so that reactive contaminants contained in the contrast agent from the production process react with the reactive medium, and the reaction products, which are distinguished from the contrast agent by their molecular size, are separated off from the contrast agent.
Such methods, in which contrast agent is cleaned with activated charcoal as a reactive medium or with the aid of ionic exchangers, are known.
Contrast agents are introduced purposefully into the human body, for instance by injection into the bloodstream, in order to make certain parts of the body or the blood flow visible by means of X-rays, which in radioscopy are attenuated especially markedly by the contrast agent. After performing this function, the contrast agent remains in the body and is gradually excreted again via the applicable organs. Hence there is intensive body contact, with the risk of undesired side-effects. In the human being, allergic and pseudoallergic reactions, which can occur spontaneously or after some time, have been observed as a consequence of the administration of contrast agents. Nor can these reactions be substantially lessened by cleaning the contrast agents in a known way.
Earlier, ionic substances (salts) such as iodides, which have two osmotically active particles per iodine molecule, were employed as contrast agents. Later on, nonionic monomeric contrast agents have come onto the market, which contain three iodine atoms covalently on a benzene ring as the basic skeleton, and whose water solubility is attained by means of a plurality of OH groups on side chains. As a result of this arrangement, three iodine molecules are present per osmotically active particle. The most recent development, known as dimeric nonionic contrast agents, are created in principle by the linkage of two nonionic monomeric basic skeletons, and thus they double the number of iodine atoms per osmotically active particle to six. Although the side effects for the nonionic contrast agents compared with the ionic contrast agents have dropped markedly, nevertheless when these substances are administered, side effects and late reactions of an allergic and pseudoallergic nature must be expected, which in rare cases can be so severe as to cause the death of the patient. In the case of nonionic dimeric contrast agents in particular, a trend to pseudoallergic late reactions has been observed. It would therefore be medically relevant to reduce side effects for all radiological contrast agents.
For the present invention, it is significant that allergic reactions are not tripped directly by the contrast agent, since its molecules are much too small to be detected by the body as an allergen. The allergenic effect thus comes into play only once a contrast agent molecule has bonded to a larger molecule, such as an albumin molecule. Pseudoallergic reactions, whose triggers and mechanism are still unexplained at present, are also more likely tripped by a small quantity of reactive contaminant or contaminants than by the contrast agent itself. If the contrast agent caused these reactions, then quantities of up to 300 ml and more should lead to far greater rates of side effects. It should be remembered that injecting 300 ml of a contrast agent available on the market, with a purity of 99.5%, at the same time means the administration of a quantity of 1.5 ml of unknown contaminants. It can therefore be assumed that the substances that trip the undesired reactions are not the contrast agent itself, but rather slight traces present in it of contaminants, which occur in the synthesis of the contrast agent and as is known cannot be removed absolutely completely even with careful cleaning.
This is the point of departure for the invention. It is based on the concept of performing the reaction, which previously took place in the body, outside the body beforehand instead, and separating off the reaction products that occur from the contrast agent before the contrast agent is used. This means cleaning of the contrast agent by preincubation.
Accordingly, the method of the invention is characterized in that substances of human, animal or vegetable origin are used as the reactive medium.
Thus according to the invention, in vitro preincubation is performed, which makes for markedly enhanced tolerance of the thus-treated and separated contrast agent.
Expedient provisions in performing the method of the invention are recited in the dependent claims. Accordingly, as reactive substances, proteins or albumins of human, animal or vegetable origin and in particular blood proteins or blood, and specifically including human blood, can be used, which to a marked extent simulates the conditions and processes that until now occurred in the body when contrast agents were administered.
REFERENCES:
patent: 5204005 (1993-04-01), Doran, III
patent: 5779905 (1998-07-01), Morandi et al.
patent: WO-94/14478 (1994-07-01), None
Amersham Health AS
Chisholm Robert F.
Ronning, Jr. Royal N.
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