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1.
ScientificWorldJournal ; 2012: 495970, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22623901

RESUMO

While many natural and synthetic compounds exhibit auxin-like activity in bioassays, indole-3-acetic acid (IAA) is recognized as the key auxin in most plants. IAA has been implicated in almost all aspects of plant growth and development and a large array of bacteria have been reported to enhance plant growth. Cells of Klebsiella oxytoca isolated from the rhizosphere of Aspidosperma polyneuron and immobilized by adsorption on different inorganic matrices were used for IAA production. The matrices were prepared by the sol-gel method and the silica-titanium was the most suitable matrix for effective immobilization. In operational stability assays, IAA production was maintained after four cycles of production, obtaining 42.80 ± 2.03 µg mL(-1) of IAA in the third cycle, which corresponds to a 54% increase in production in relation to the first cycle, whereas free cells began losing activity after the first cycle. After 90 days of storage at 4°C the immobilized cells showed the slight reduction of IAA production without significant loss of activity.


Assuntos
Ácidos Indolacéticos/metabolismo , Klebsiella oxytoca/metabolismo , Adsorção , Biomassa , Células Imobilizadas/metabolismo , Raízes de Plantas/microbiologia , Rizosfera , Dióxido de Silício , Titânio
2.
J Pharm Biomed Anal ; 33(4): 581-7, 2003 Nov 24.
Artigo em Inglês | MEDLINE | ID: mdl-14623583

RESUMO

This work reports the separation of FTC enantiomers using an amylose tris[(S)-1-phenylethylcarbamate] coated onto APS-Nucleosil (7 microm particle size, 500 A pore size, 20% w/w, 15 x 0.46 cm ID) chiral column under polar organic elution mode. Good enantioselectivity (alpha=1.9) with excellent enantioresolution (R(S)=3.3) was achieved by the use of methanol with 0.02% of triethylamine acetate as mobile phase. The method allows the accurate determination of as low as 0.2% of each enantiomer as an impurity. The validated method proved to be reliable and sensitive for the quantification of both enantiomers as impurity in different batches of emtricitabine and beta-D-(+)-FTC.


Assuntos
Fármacos Anti-HIV/análise , Desoxicitidina/análogos & derivados , Desoxicitidina/análise , Polissacarídeos/análise , Fármacos Anti-HIV/química , Cromatografia Líquida de Alta Pressão/métodos , Desoxicitidina/química , Emtricitabina , Nucleosídeos/análise , Nucleosídeos/química , Polissacarídeos/química , Estereoisomerismo
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