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Biomedical subjects

G Grisanti

Publications and source records attributed to G Grisanti.

At least 19 recordsLinked to original sources

Radioactivity in human milk.

A brief introduction outlines the sources of radionuclides in the environment, their diffusion and transfer to different environmental compartments and their pathways to individuals; definitions of the main quantities and measurement units used in the study are included. A review is given on published data concerning the radioactive contamination of human milk after the Chernobyl accident. The authors' investigation on breast milk contamination in Italy in the same period is discussed together with an examination of the natural radioactive content. Finally, possible future developments and prospects of the research on this issue are explored.

Accidents

An automatic test for frequency discrimination.

Békésy audiometry has been applied to the determination of the frequency discrimination threshold. The automatic test for frequency discrimination is performed by means of a modified automatic audiometer at fixed frequencies, each administered for a duration of 60 s. The test involves the stimulus of a series of pairs of tone bursts of 500 ms duration: the frequency of one of the tone bursts (f0) is constant, while the other (f0 + delta f) gradually increases and decreases according to the subject's response. The tracings obtained facilitate the evaluation of the discrimination capability of the subject. The pattern obtained from a sample of normally hearing people was analysed in order to evaluate the precision of this procedure.

Adolescent

Frequency discrimination for pure-tone and modulated stimuli: an evaluation of automatic and computerized test versions.

Monaural differential frequency discrimination (delta f/f) was investigated in the 32 ears of 16 normal-hearing young adults, using an automated test of pitch-memory (the AFTD of Grisanti, Boll. Ital. Audiol. Foniatr., 1978, 1, 166-169) wherein S, in analogy with Bekesy audiometry, continuously adjusts the frequency of alternating pure-tone bursts between discriminable-nondiscriminable, and using a computer-driven test of discrimination of frequency modulation (the CTFD of Biondi, E. et al, Comm. LXV Congr. Soc. Ital. ORL Modena, 1978), wherein S presses a button, within a criterion time window, to a brief episode of frequency modulation in a pure tone. F was either 0.5, 1, or 2 kc/s at 40 db HL. An estimate of delta f/f for every test by the CTFD was printed out by the apparatus, while 4 indices of delta f/f by the ATFD were abstracted by hand from various features of the Bekesy-type tracings. Estimates of delta f/f by the CTFD were close to those of the classic study of Shower and Biddulph, but those by the ATFD were rather larger than reported in previous studies of pitch-memory. Student "t" tests revealed that only 5 of 24 comparisons between tests (4 ATFD variables vs 1 CTFD estimate X 2 ears X 3 frequencies) reached the 95% confidence level, while Pearson r's also showed little evidence of significant relationships between the two tests. While the CTFD yields a more precise delta f/f and has other virtues as a research tool, it demands 40-200 min to explore a listener's discriminability in both ears at 5 frequencies. Thus, although the ATFD yields less precise data, and has inherent within it the possibility of the intrusion of undesired psychological factors, it is to be preferred for clinical use since it demands only 15 min of experimental time.

Adult

High-performance liquid chromatographic determination of cephacetrile.

A rapid and accurate quantitative determination of cephacetrile in finished bulk and dosage forms is reported. The high-performance liquid chromatographic method is free of interference by acetyl hydrolysis products and synthesis by-products. The assay can be performed in about 15 min, affording less than 0.7% coefficients of variation within and between days. The chromatographic results are in good agreement with the microbiological assay requested by the "Code of Federal Regulations" for certification of cephacetrile sodium.

Cephacetrile

Female-to-male transsexuals compared to lesbians: behavioral patterns of childhood and adolescent development.

We report detailed interview data on a clinical sample (N = 15) of female-to-male transsexuals (FTs) compared to a matched research sample (N = 15) of lesbians (Ls). Both groups were relatively young, with a mean age of 21 years 10 months (FTs) and 23 years 8 months (Ls), respectively, and were of middle or lower SES. Both groups did not differ from each other in respect to frequency of tomboyish behavior or interest in doll play and other aspects of materanl rehearsal. Male peer preference was more often remembered among the FTs, but the difference between the groups was only of borderline significance. The groups differed significantly regarding childhood cross-dressing (80% for FTs, 0% for Ls), gender identity confusion in adolescence (absent among Ls), and negative reaction to breast development and menarche (approximately 70% for FTs, 10% for Ls). The similarities and differences between the two groups in childhood and adolescent development are relevant for clinical management and the differential diagnosis of transsexualism vs. lesbianism.

Adolescent

Synthesis and topical antiinflammatory properties of 17,21-bis(acetyloxy)-6beta,9-difluoro-11beta-hydroxypregna-1,4-diene-3,20-dione and related 2-halogenated compounds.

Introduction of a halogen atom at C-2 of steroid 3-ketofluorohydrins, obtained from the corresponding 5alpha,6alpha-epoxides by trans-diaxial opening with hydrofluoric acid, prevents the 6beta-fluorine atom from undergoing rearrangement to the more stable 6alpha configuration when the 5-tert-hydroxyl is split off to yield to yield a conjugated double bond. Two processes were investigated for the synthesis of 17,21-bis(acetyloxy)-6beta-fluoro-1,4,9(11)-triene-3,20-dione (24a) and the related 2-bromo compound 24b starting from the known 21-(acetyloxy)-6beta-fluoro-5alpha,11alpha,17-trihydroxypregnane-3,20-dione (13). Successive reaction with hypobromous acid, epoxidation, and fluorination converted 24a and 24b into the title compound 27a and the analogue 2-bromo compound 27b. In addition, a synthesis of 17,21-bis(acetyloxy)-2-chloro-6beta,9-difluoropregna-1,4-diene-3,20-dione (27c) is reported. The antiinflammatory activity of 17,21-bis-(acetyloxy)-6beta,9-difluoropregna-1,4-diene-3,20-dione (27a) and its 2-halogenated analogues 27b and 27c in comparison with the corresponding 6alpha,9-difluoro epimers was studied. Some 6beta-fluoro compounds displayed high topical antiinflammatory activity without systemic effects.

Administration, Oral

Derivatives of 2-bromo-6beta-fluoropregna-1,4-diene-3,20-dione and their antiinflammatory activity.

As part of a systematic study of the effects of chemical modifications on the antiinflammatory activity of 17,21-bis(acetyloxy)-2-bromo-6beta,9-difluoro-11beta-hydroxypregna-1,4-diene-3,20-dione (halopredone acetate, Topicon), a new potent antiinflammatory, a series of derivatives of 2-bromo-6beta-fluoropregna-1,4-diene-3,20-dione was prepared for pharmacological screening. Different synthetic approaches are described. All the synthesized compounds had topical antiinflammatory activity, with no side effects, but were lower in activity than halopredone acetate. Most of them showed topical antiinflammatory activity comparable to that of fluocinolone acetonide. Only two of the synthesized compounds were found to have systemic anti-inflammatory activity comparable to that of betamethasone.

Animals

New esters of Halopredone for topical antiinflammatory use.

A series of new halopredone esters has been prepared and screened for local and systemic antiinflammatory activity. High local activity with no side effects, equivalent to that of 17,21-bis(acetyloxy)-2-bromo-6beta,9-difluoro-11beta-hydroxypregna-1,4-diene-3,20-dione (halopredone acetate; Topicon), is obtained when either the 17- or 21-OH of halopredone are benzoylated.

Administration, Topical

Physico-chemical and analytical studies on Halopredone acetate.

Physico-chemical, spectroscopic (UV, CD, ORD, IR-1H-DMR, 19F-NMR, PFT13C-NMR, MS), and chromatographic (TLC, HPLC) properties of 17,21-bis(acetyloxy)-2-bromo-6beta,9-difluoro-11beta-hydroxypregna-1,4-diene-3,20-dione (halopredone acetate; Topicon) are reported. Densitometric and high-pressure liquid chromatographic quantitative analytical methods are described. The usual descriptive data, purity tests, potential impurities arising from the synthesis and stability tests are given.

Anti-Inflammatory Agents

Basic derivatives of 6,7-dihydroindolo(1,7-ab)(1) benzazepine and 6H-indolo(7,1-cd)(1,5) benzoxazepine as potential antidepressant agents.

Basic derivatives of 6,7-dihydroindolo[1,7-ab][1]benzazepine and 6H-indolo[7,1-cd][1,5]benzoxazepine incorporating the imipramine basic side chain were synthesized and screened for antidepressant activity in mice. With few exceptions, the compounds unsubstituted at C-2 antagonized reserpine-induced ptosis and hypothermia showing negligible anticholinergic and antihistaminic properties. The compound 1-[2-(N-methyl-N-benzylamino)ethyl]-6,7-dihydroindolo[1,7-ab][1]benzazepine had the highest toxicity-activity ratio.

Animals