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1.
Regul Toxicol Pharmacol ; 123: 104926, 2021 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-33862169

RESUMEN

The ICH M7(R1) guideline describes a framework to assess the carcinogenic risk of mutagenic and carcinogenic pharmaceutical impurities following less-than-lifetime (LTL) exposures. This LTL framework is important as many pharmaceuticals are not administered for a patient's lifetime and as clinical trials typically involve LTL exposures. While there has been regulatory caution about applying LTL concepts to cohort of concern (COC) impurities such as N-nitrosamines, ICH M7 does not preclude this and indeed literature data suggests that the LTL framework will be protective of patient safety for N-nitrosamines. The goal was to investigate if applying the LTL framework in ICH M7 would control exposure to an acceptable excess cancer risk in humans. Using N-nitrosodiethylamine as a case study, empirical data correlating exposure duration (as a percentage of lifespan) and cancer incidence in rodent bioassays indicate that the LTL acceptable intake (AI) as derived using the ICH M7 framework would not exceed a negligible additional risk of cancer. Therefore, controlling N-nitrosamines to an LTL AI based on the ICH M7 framework is thus demonstrated to be protective for potential carcinogenic risk to patients over the exposure durations typical of clinical trials and many prescribed medicines.


Asunto(s)
Dietilnitrosamina/toxicidad , Mutágenos/toxicidad , Carcinógenos , Relación Dosis-Respuesta a Droga , Humanos , Mutagénesis , Nitrosaminas/toxicidad , Pruebas de Toxicidad
2.
Anticancer Agents Med Chem ; 17(13): 1777-1785, 2017.
Artículo en Inglés | MEDLINE | ID: mdl-28403779

RESUMEN

BACKGROUND: Chronic myeloid leukemia (CML) is currently treated with imatinib, a Bcr-Abl inhibitor. However, resistance to this drug usually develops over time. Triptolide, a diterpenoid triepoxide, has been shown active against CML cells resistant to imatinib, acting mainly on the level of Bcr-Abl transcription inhibition. OBJECTIVE: Here, we used the triterpene betulinic acid, a known proteasome inhibitor with potential antileukemic activity, as a scaffold for the generation of analogues with predicted triptolide biological activity. METHOD: Betulinic acid derivatives were designed based on the structure-activity relationship of triptolide and evaluated for their cytotoxic effects in CML cells, lymphocytes and human keratinocytes (HaCaT), as well as against the proteasome complex. The main modification performed on betulinic acid was fluorination at C-28 and epoxidation, both of which are responsible for enhancing activity of triptolide. A total of 10 compounds were obtained: 6 previously described and 4 novel compounds. The cytotoxic activity over a CML cell line (K562) was assessed using flow cytometry and compared to lymphocytes and HaCaT. RESULT: The results show that betulinic acid was the most cytotoxic compound against CML cells, showing a good selectivity index for cancer over normal cells. The most important trend for the activity in betulinic acid derivatives is the presence of a free hydroxyl group at C-3 and a carboxyl group at C-28. Results also indicated that the epoxide is important for enhancing the activity, while modification at C-28 worsens the activity. CONCLUSION: Proteasome inhibition assays suggest that proteasome is the main target for betulinic acid and its derivatives.


Asunto(s)
Antineoplásicos/síntesis química , Antineoplásicos/farmacología , Diseño de Fármacos , Leucemia Mielógena Crónica BCR-ABL Positiva/tratamiento farmacológico , Leucemia Mielógena Crónica BCR-ABL Positiva/patología , Triterpenos/síntesis química , Triterpenos/farmacología , Antineoplásicos/uso terapéutico , Ensayos de Selección de Medicamentos Antitumorales , Humanos , Células K562 , Triterpenos Pentacíclicos , Análisis Espectral/métodos , Relación Estructura-Actividad , Triterpenos/uso terapéutico , Ácido Betulínico
3.
RSBO (Impr.) ; 6(1)20/03/2009.
Artículo en Portugués | LILACS | ID: lil-509355

RESUMEN

Introdução e Objetivo: O presente estudo teve por objetivo avaliar e comparar as medidas do diâmetro D1 de cones estandardizados e secundários calibrados com régua calibradora através da medição do primeiro milímetro dos cones, com um paquímetro digital. Material e Métodos: utilizou-se dez cones de guta-percha estandardizados de cada calibre #25, #30, #35 e #40 das marcas Dentsply/Maillefer e Tanari, e cones secundários B8 calibrados por régua calibradora, perfazendo um total de 160 cones. Com o auxílio de um paquímetro digital eletrônico foi verificado o diâmetro a um milímetro da ponta do cone (D1). Resultados: obteve-se que em uma das marcas houve diferença significativa entre os cones padronizados e os calibrados. Quando comparado o calibre dos cones padronizados das duas marcas, também ocorreu diferença estatística, não ocorrendo quando os cones foram calibrados por régua calibradora. Conclusão: os cones Tanari, em média, tiveram um resultado superior aos cones calibrados e Dentsply, nessa ordem.


Introduction and Objective: The present study had for objective to evaluate and to compare the measures of the D1 diameter of calibrated standardized and secondary cones calibrated using a special scale through the measurement of the first millimeter of the cones, with one digital caliper. Material and Methods: Ten standardized gutta-percha cones of each type had been used: #25, #30, #35 and #40. The manufacturers were Dentsply/Maillefer and Tanari, and secondary cones B8 calibrated by a special scale, making a total of 160 cones. With the aid of a digital electronic caliper was verified the diameter to the one millimeter back from the tip of the cone (D1). Results: one of the manufacturers brand had significant difference between the standardized cones and the calibrated ones. When compared, the caliber of the standardized cones of both brands presented difference in statistics, not occurring when the cones had been calibrated by the special scale. Conclusion: the Tanari cones, on average, had a superior result compared to the calibrated cones and Dentsply, in this order.

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