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1.
Chem Asian J ; 16(5): 409-422, 2021 Mar 01.
Artículo en Inglés | MEDLINE | ID: mdl-33443291

RESUMEN

In accordance with the recent studies, Raman spectroscopy is well experimented as a highly sensitive analytical and imaging technique in biomedical research, mainly for various disease diagnosis including cancer. In comparison with other imaging modalities, Raman spectroscopy facilitate numerous assistances owing to its low background signal, immense spatial resolution, high chemical specificity, multiplexing capability, excellent photo stability and non-invasive detection capability. In cancer diagnosis Raman imaging intervened as a promising investigative tool to provide molecular level information to differentiate the cancerous vs non-cancerous cells, tissues and even in body fluids. Anciently, spontaneous Raman scattering is very feeble due to its low signal intensity and long acquisition time but new advanced techniques like coherent Raman scattering (CRS) and surface enhanced Raman scattering (SERS) gradually superseded these issues. So, the present review focuses on the recent developments and applications of Raman spectroscopy-based imaging techniques for cancer diagnosis.


Asunto(s)
Neoplasias/diagnóstico , Espectrometría Raman/métodos , Animales , Línea Celular Tumoral , Humanos , Neoplasias/química , Neoplasias/patología
2.
J Photochem Photobiol B ; 212: 112043, 2020 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-33022468

RESUMEN

Alkaline phosphatase (ALP) is an enzyme that actively plays a significant role in the various metabolic processes by transferring a phosphate group to the protein, nucleic acid, etc. The elevated level of ALP in blood plasma is the hallmark of inflammation/cancer. The hyperactive mitochondria in cancer cells produce an excess of ATP to fulfill the high energy demand. Thus, we have developed a fluorescent probe Mito-Phos for ALP, which can detect phosphatase expression in mitochondria in live cells. The probe Mito-Phos has shown ~15-fold fluorescence intensity increments at 450 nm in the presence of 500 ng/mL of ALP. It takes about 60 min to consume the whole amount of ALP (500 ng/mL) in physiological buffer saline. It can selectively react with ALP even in the presence of other probable cellular reactive components. It is highly biocompatible and nontoxic to the live cells. It has shown ALP expression in a dose-dependent manner by providing concomitant fluorescence images in the blue-channel region. It has localized exclusively in the mitochondria in live cells. The probe Mito-Phos is highly biocompatible with the ability to assess ALP expression in mitochondria in live cells.


Asunto(s)
Fosfatasa Alcalina/metabolismo , Materiales Biocompatibles/química , Colorantes Fluorescentes/química , Mitocondrias/enzimología , Fosfatasa Alcalina/química , Supervivencia Celular , Regulación Enzimológica de la Expresión Génica , Células HeLa , Humanos , Cinética
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