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1.
Food Chem ; 300: 125168, 2019 Dec 01.
Artigo em Inglês | MEDLINE | ID: mdl-31330368

RESUMO

This study reports a clear-cut relationship of the technological use of specific filter aids with highly variable vanadium levels in beer, wine, and fruit juices. First, the previously reported broad range of vanadium levels was confirmed in 68 commercial beverages by ICP-MS. Since cloudy apple juices exhibited significantly lower vanadium amounts than clear apple juices, filter aids used for clarification were analyzed and found to contain substantial and highly variable amounts of vanadium, particularly in all analyzed diatomite (38-368 mg vanadium per kg filter aid), but not in perlite products (<4 mg/kg). Subsequent pilot-scale precoat filtration experiments (170 L/batch) proved vanadium to be released from diatomite (Kieselguhr), increasing its levels from ca. 2.1-2.6 µg/kg unfiltered to 27-201 µg/kg filtered juice, depending on the use of diatomites high or low in vanadium. Thus, filter aid selection was shown to modulate the vanadium concentrations in clarified beverages.


Assuntos
Bebidas/análise , Filtração/instrumentação , Vanádio/análise , Óxido de Alumínio , Cerveja/análise , Terra de Diatomáceas/análise , Terra de Diatomáceas/química , Filtração/métodos , Contaminação de Alimentos/análise , Sucos de Frutas e Vegetais/análise , Malus , Dióxido de Silício , Vinho/análise
2.
ChemMedChem ; 10(1): 164-72, 2015 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-25338544

RESUMO

Peptidic ligands selectively targeting distinct G protein-coupled receptors that are highly expressed in tumor tissue represent a promising approach in drug delivery. Receptor-preferring analogues of neuropeptide Y (NPY) bind and activate the human Y1 receptor subtype (hY1 receptor), which is found in 90% of breast cancer tissue and in all breast-cancer-derived metastases. Herein, novel highly boron-loaded Y1 -receptor-preferring peptide analogues are described as smart shuttle systems for carbaboranes as (10) B-containing moieties. Various positions in the peptide were screened for their susceptibility to carbaborane modification, and the most promising positions were chosen to create a multi-carbaborane peptide containing 30 boron atoms per peptide with excellent activation and internalization patterns at the hY1 receptor. Boron uptake studies by inductively coupled plasma mass spectrometry revealed successful uptake of the multi-carbaborane peptide into hY1 -receptor-expressing cells, exceeding the required amount of 10(9) boron atoms per cell. This result demonstrates that the NPY/hY receptor system can act as an effective transport system for boron-containing moieties.


Assuntos
Boranos/química , Neuropeptídeo Y/metabolismo , Receptores de Neuropeptídeo Y/metabolismo , Sequência de Aminoácidos , Animais , Boranos/síntese química , Terapia por Captura de Nêutron de Boro , Neoplasias da Mama/radioterapia , Células COS , Chlorocebus aethiops , Feminino , Células HEK293 , Humanos , Dados de Sequência Molecular , Neuropeptídeo Y/análogos & derivados , Receptores de Neuropeptídeo Y/genética
3.
Anal Bioanal Chem ; 407(9): 2365-71, 2015 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-25015045

RESUMO

An analytical method using laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) was developed and applied to assess enrichment of 10B-containing p-boronophenylalanine-fructose (BPA-f) and its pharmacokinetic distribution in human tissues after application for boron neutron capture therapy (BNCT). High spatial resolution (50 µm) and limits of detection in the low parts-per-billion range were achieved using a Nd:YAG laser of 213 nm wavelength. External calibration by means of 10B-enriched standards based on whole blood proved to yield precise quantification results. Using this calibration method, quantification of 10B in cancerous and healthy tissue was carried out. Additionally, the distribution of 11B was investigated, providing 10B enrichment in the investigated tissues. Quantitative imaging of 10B by means of LA-ICP-MS was demonstrated as a new option to characterise the efficacy of boron compounds for BNCT.


Assuntos
Compostos de Boro/química , Boro/química , Frutose/análogos & derivados , Isótopos/química , Neoplasias Hepáticas/radioterapia , Fígado/química , Compostos Radiofarmacêuticos/química , Terapia por Captura de Nêutron de Boro , Frutose/química , Humanos , Fígado/efeitos da radiação , Neoplasias Hepáticas/química , Imagem Molecular
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