Pharmacokinetics and whole-body distribution of the new chemotherapeutic agent beta-D-glucosylisophosphoramide mustard and its effects on the incorporation of [methyl-3H]-thymidine in various tissues of the rat.

beta-D-Glucosylisophosphoramide mustard (beta-D-Glc-IPM) is a new, potential chemotherapeutic agent currently under investigation. Its pharmacokinetics in plasma and elimination of the parent drug and its metabolites via urine, bile, and exhaled air were studied in female Sprague-Dawley rats after bolus injection of 315 mg/kg. Typically, the drug's disposition from plasma follows a linear two-compartment model with half-lives (t1/2) of 1.

Antitumor-activity and distribution of Beta-d-lactosylisophosphoramide mustard - a potential cytostatic agent exploiting lectin mediated transport.

Affinity chromatography of the Walker carcinosarcoma 256 B tumor revealed a lactose-specific lectin of 24 kDa. In a chemotherapeutical experiment, B-D-lactosylisophosphoramide mustard (corresponding lectin present in tumor tissue) proved to be significantly more active than B-D-maltosylisophosphoramide mustard (no corresponding lectin present), although both compounds differ only marginally in their sugar parts. Whole body autoradiography after application of C-14-labeled B-D-lactosylisophosphoramide mustard in tumor bearing rats shows an accumulation of radioactivity in kidneys, thymus, central nervous system and in the tumor.

D-19575--a sugar-linked isophosphoramide mustard derivative exploiting transmembrane glucose transport.

D-19575 is a glucose derivative of ifosfamide mustard with a broad spectrum of antitumor activity in animal models. In comparison with ifosfamide, D-19575 is less toxic and is better tolerated by tumor-bearing animals, achieving a better therapeutic efficacy. D-19575 is directly cytotoxic in vitro--in contrast to ifosfamide--and it is possible to modulate this cytotoxicity by inhibition of transmembrane glucose transporters.

[The limits of root planing in the furcation area. A mathematical comparison of the radii of curvature on the root surfaces and on the curettes].

In order to draw some conclusions about the furcation region accessibility for periodontal instruments and their cleaning effect, the curvature radii of the root faces of 31 lower molars were mathematically determined and compared with the curvature radii of the working end of normally available curettes. From the results of this work it can be seen, that the Gracey curettes have an essential greater curvature radius as the curvature radius of the root faces. On the other site the special curettes for root planing in the furcation region have a smaller curvature radius as that of the root faces.