Iopamidol

The steric bulk of the three iodine atoms in the 2,4,6-triiodoben2ene system and the amide nature of the 1,3,5-substituents yield rotational isomers of the 5-A/-acyl-substituted 2,4,6-triiodoisophthalamides. Rotational motion in the bonds connecting the side chains and the aromatic ring is restricted. These compounds also exhibit stereoisomerism when chiral carbon atoms are present on side chains. (R,5)-3-Amino-l,2-propanediol is incorporated in the synthesis of iohexol (11) and ioversol (12) and an (3)-2-hydroxypropanoyl group is used in the synthesis of iopamidol (10). Consequendy, the resulting products contain a mixture of stereoisomers, ie, meso-isomers, or an optical isomer. 

Sutton AG, Finn P, Grech ED, et al Early and late reactions after the use of iopamidol 340, ioxaglate 320, and iodixanol 320 in cardiac catheterization. 

Brass, O., J.M. Letoffe, A. Bakkali, J.C. Bureau, C. Corot, and P. Claudy. 1995. Involvement of protein solvation in the interaction between a contrast medium (iopamidol) and fibrinogen or lysozyme. Biophys Chem 54 83-94. 

Recently, Duirk et al. [34] showed evidence that iodinated X-ray contrast media (ICM), such as iopamidol, constitute an iodine source to form iodo-THM DBFs, e.g., dichloroiodomethane, and iodo-acid DBFs, e.g., iodoacetic acid, in chlorinated and chloraminated drinking waters. However, the complete reaction pathway is not fully understood yet, and it is under further investigation. Chloraminated and chlorinated source waters with iopamidol were genotoxic and cytotoxic in mammalian cells. This is in agreement with the previously reported high genotoxicity and cytotoxicity of the iodo-acids and iodo-THMs [20, 21]. 

Lorusso et al. [109] described an HPLC method for assaying iomeprol in plasma and urine samples. Before chromatography, the biological fluids were treated with ion-exchange resins and iopamidol was added as internal standard. Detection was by UV spectrometry at 245 nm. 

The concentration of the X-ray contrast agents, diatrizoate, iopamidol, iopromide, and iomeprol, derived from radiological examinations in municipal sewage, sewage treatment plant efQuents, rivers, and groundwater was investigated by Ternes and Hirsch using LC-electrospray tandem MS detection [119,120]. 

The aggregation of metrizamide in solution further reduced its osmolality to about 485 mOsm kg at 300 mgl mL [ 1 ]. Unfortunately, this agent could not be sterilized by autoclaving and, consequently, had to be lyophilized and reconstituted extemporaneously. In the mid-1970s, stable nonionic compounds such as iopamidol or iohexol superseded metrizamide. Further improvement was reached by stabilization of the hydrophilic sphere against external disruption, as shown with iobitridol [2]. 

Many radiocontrast media contain iodine. These include iodixonal, iohexol, iomeprole, iopamidole, iopanoic acid, iopitridole, iopromide, iothalamate, iotrolan, ioversol, and ioxaglate. 

TI 7790-99-0) see Bunamiodyl locetamic acid Iopamidol lopanoic acid lophenoic acid, lotalamic acid Rizatriptan benzoate... 

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