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Biomedical subjects

M Wenzel

Publications and source records attributed to M Wenzel.

243 records · Page 14Linked to original sources

Experimental in vitro and in vivo studies of epithelium formation on biomaterials seeded with isolated respiratory cells.

Extensive tracheal defects after intensive care medicine, trauma, or large resections in tumor surgery remain a major challenge in plastic and reconstructive surgery. Defects that cannot be satisfactorily treated by complicated and costly reconstructive techniques reveal a need for an alloplastic tracheal replacement. Recent experimental and clinical studies in the development of alloplastic tracheal prostheses proved that the lack of an epithelial lining on the luminal surfaces and inadequate biophysical properties and shapes of the prostheses were the main causes for failure of these prostheses. In this study a cell-seeding technique has been used. Adhesion, spreading, and differentiation of seeded mucosa cells on biomaterials in vitro were observed by scanning electron microscopy (SEM). Chemical properties and surface structure of the material influenced the differentiation process. Epithelium formation of incorporated tracheal prostheses was tested in animal experiments. Isolated respiratory cells were seeded into implanted tubular prostheses of porous polyurethane or expanded polytetrafluorethylene. Light microscopy and SEM showed the tendency of epithelium formation on the surface of the lumen. Vigorous cell layers, predominantly as multiple cell layers of squamous epithelium, were observed. Ciliated or mucus cells were not detected. It can be stated that the epithelium formation on incorporated porous implants is possible. Further studies of the stability and the differentiation process of the epithelium on such implants is needed before an introduction of tracheal replacements into the clinical practice can be considered.

Biocompatible Materials↗

[Biochemistry of metallocenes, II. Organ-distribution and thymus affinity of cinnamoyl-[103Ru]ruthenocene (author's transl)].

Metallocenes, labelled with 103Ru, are potential radiopharmaceuticals for use in nuclear medicine diagnosis. Ruthenocene derivatives with oxopropene side-chains were administered to mice and rats to study their biochemical properties. Excretion rates and organ distributions of 103RuCl3 and Cinnamoyl-[103Ru]ruthenocene were very different. While 103RuCl3 was relatively evenly distributed in the body, the metallocene derivative was concentrated in liver, lungs and spleen after intravenous (i.v.) injection. After i.p. injection however a high thymus affinity was observed and autoradiography proved that the site of 103Ru accumulation was in thymocytes. The thymus affinity can be diminished by corticoid pretreatment and raised by inhibition of phagocytosis (BeSO4). The mechanism of accumulation in the thymus and a possible clinical application are discussed.

Animals↗

[Heavy water (D2O) as a protective protein containing medium. Example: human cholinesterase].

Looking for a possible protective effect of heavy water on proteins, cholinesterase and lactate dehydrogenase in combination with D2O and further protective substances were exposed to a temperature of 60 degrees C (for 10 min) and about 45 degrees C (for several days). In combination with glycerine there resulted an additive protective effect; with NaCl and/or albumin being added the individual effects raised to a higher level. In the cold D2O protects cholinesterase only against acid denaturation, but in combination with warmth also against basic denaturation.

Cholinesterases↗

[Protective effect of D20 in bacteria (E. coli)].

E. coli suspended in D2O showed a better survival than in H2O when the bacteria were treated with various damaging agents like UV, heat and freezing. On the contrary E. coli grown in D2O-containing media - therefore being fully deuterated - were more sensitive than normally grown bacteria.

Deuterium↗

[Stability of ferricinium cations and their cytostatic effect].

The relative stabilities of different ferricinium cations were studied in buffer or serum-containing solution and in vivo and compared with their cytostatic effects in cultures of Yoshida ascites tumor cells. Although the ferricinium cation itself was the most unstable cation compared with the dimethyl-ferricinium cation and the deuterated ferricinium derivatives it showed the highest cytostatic effect.

Animals↗

[Analog of hippuran: (103 Ru)ruthenocenoyl-glycine derivative. Synthesis, organ distribution and clearance].

The analogue of hippuric acid, ruthenocenoyl-glycine was synthesized and labelled with the gamma-emitter 103Ru. As a by-product of the synthesis the labelled diamide from ruthenocene-dicarbonic acid and glycine was gained. With these ruthenocene derivatives the organ distributions in mice and rats were measured. All ruthenocene-glycine derivatives showed primary a high kidney accumulation followed by very rapid renal excretion. After application of the cytostatic PtCl2(NH3)2, causing toxic effects in the kidney of mice, the excretion of ruthenocenoyl-glycine is decreased. Biochemical data suggest the use of labelled ruthenocenoyl-glycine as a substitute for Iodo-labelled hippuran.

Animals↗

[Enzymatic hydroxylation of ruthenocene and osmocene by liver microsomes].

In buffer solution (pH 7,4) ruthenocene and osmocene are far more stable than ferrocene. The metallocenes ruthenocene and osmocene are metabolized by microsomes of mouse liver in the presence of NADPH and O2. The Km-values are similar for both metallocenes, the rate of metabolism is higher for osmocene that for ruthenocene.

Animals↗

[In vivo and in vitro hydroxylation of testosterone and dihydrotestosterone in rats after liver damage and starvation (author's transl)].

The in vivo C-2-hydroxylation of testosterone and 5-dihydrotestosterone in rats was measured by labilisation of tritium as HTO after injection of [1 alpha, 2 alpha-T]testosterone or [1 alpha, 2 alpha-T]5 alpha-dihydrotestosterone (radiospirometry). After experimental liver damage caused by CCl4 or after starvation for 60 h the hydroxylation of the androgens decreased. Similar results were gained by measuring the C-2-hydroxylation of testosterone, 5 alpha-dihydrotestosterone and estradiol.

Animals↗