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1.
Appl Radiat Isot ; 166: 109404, 2020 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-32956924

RESUMO

The shortcomings in Boron neutron capture therapy (BNCT) and Hyperthermia for killing the tumor cell desired for the synthesis of a new kind of material suitable to be first used in BNCT and later on enable the conditions for Hyperthermia to destroy the tumor cell. The desire led to the synthesis of large band gap semiconductor nano-size Boron-10 enriched crystals of hexagonal boron nitride (10BNNCs). The contents of 10BNNCs are analyzed with the help of x-ray photoelectron spectroscopy (XPS) and counter checked with Raman and XRD. The 10B-contents in 10BNNCs produce 7Li and 4He nuclei. A Part of the 7Li and 4He particles released in the cell is allowed to kill the tumor (via BNCT) whereas the rest produce electron-hole pairs in the semiconductor layer of 10BNNCs suggested to work in Hyperthermia with an externally applied field.


Assuntos
Compostos de Boro/síntese química , Terapia por Captura de Nêutron de Boro/métodos , Nanopartículas/química , Animais , Boro/química , Boro/uso terapêutico , Compostos de Boro/química , Compostos de Boro/uso terapêutico , Humanos , Hipertermia Induzida/métodos , Isótopos/química , Isótopos/uso terapêutico , Microscopia Eletrônica de Transmissão , Nanopartículas/uso terapêutico , Nanopartículas/ultraestrutura , Nanotecnologia , Neoplasias/radioterapia , Neoplasias/terapia , Espectroscopia Fotoeletrônica , Pontos Quânticos/química , Pontos Quânticos/uso terapêutico , Pontos Quânticos/ultraestrutura , Análise Espectral Raman , Difração de Raios X
2.
Phytother Res ; 33(10): 2661-2684, 2019 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-31453659

RESUMO

Several reviews have been published on Artemisia's derived natural products, but it is the first attempt to review the chemistry and pharmacology of more than 80 alkaloids and allied nitrogen compounds obtained from various Artemisia species (covering the literature up to June 2018). The pharmacological potential and unique skeleton types of certain Artemisia's alkaloids provoke the importance of analyzing Artemisia species for bioactive alkaloids and allied nitrogen compounds. Among the various types of bioactive Artemisia's alkaloids, the main classes were the derivatives of rupestine (pyridine-sesquiterpene), lycoctonine (diterpene), pyrrolizidine, purines, polyamine, peptides, indole, piperidine, pyrrolidine, alkamides, and flavoalkaloids. The rupestine derivatives are Artemisia's characteristic alkaloids, whereas the rest are common alkaloids found in the family Asteraceae and chemotaxonomically links the genus Artemisia with the tribes Anthemideae. The most important biological activities of Artemisia's alkaloids are including hepatoprotective, local anesthetic, ß-galactosidase, and antiparasitic activities; treatment of angina pectoris, opening blocked arteries, as a sleep-inducing agents and inhibition of HIV viral protease, CYP450, melanin biosynthesis, human carbonic anhydrase, [3H]-AEA metabolism, kinases, and DNA polymerase ß1 . Some of the important nitrogen metabolites of Artemisia include pellitorine, zeatin, tryptophan, rupestine, and aconitine analogs, which need to be optimized and commercialized further.


Assuntos
Alcaloides/farmacologia , Artemisia/química , Alcaloides/análise , Humanos , Compostos de Nitrogênio/farmacologia , Extratos Vegetais/farmacologia
3.
Nat Prod Res ; 26(5): 484-8, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-21809956

RESUMO

Vitex negundo Linn. (Verbenaceae) is used in traditional medical system for respiratory disorders. This study was carried out to investigate its cough-relieving potential. The antitussive effect of the butanolic extract of V. negundo (Vn) on sulphur dioxide (SO(2))-induced cough was examined in mice. Safety profile of Vn was carried out by observing acute neurotoxicity, median lethal dose (LD(50)) and behavioural signs. Vn dose-dependently (250-1000 mg kg(-1)) inhibited the cough provoked by SO(2) gas in mice and exhibited maximum protection after 60 min of administration. At 1000 mg kg(-1), Vn caused maximum cough-suppressive effects i.e. cough inhibition at 60 min was 67.4%, as compared to codeine (10 mg kg(-1)), dextromethorphan (10 mg kg(-1)) and saline having cough-inhibitory potential 75.7%, 74.7% and 0%, respectively. LD(50) value of V. negundo was found to be greater than 5000 mg kg(-1). In toxicity tests, no signs of neural impairment and acute behavioural toxicity were observed at antitussive doses and extract has been well tolerated at higher doses. These results indicate that V. negundo exhibits antitussive effect and it was found devoid of toxicity.


Assuntos
Antitussígenos/uso terapêutico , Tosse/tratamento farmacológico , Extratos Vegetais/uso terapêutico , Vitex/química , Animais , Antitussígenos/efeitos adversos , Antitussígenos/química , Camundongos , Extratos Vegetais/efeitos adversos , Extratos Vegetais/química
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