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1.
Mar Drugs ; 18(4)2020 Apr 17.
Artículo en Inglés | MEDLINE | ID: mdl-32316578

RESUMEN

Current anticancer drugs exhibit limited efficacy and initiate severe side effects. As such, identifying bioactive anticancer agents that can surpass these limitations is a necessity. One such agent, curcumin, is a polyphenolic compound derived from turmeric, and has been widely investigated for its potential anti-inflammatory and anticancer effects over the last 40 years. However, the poor bioavailability of curcumin, caused by its low absorption, limits its clinical use. In order to solve this issue, in this study, curcumin was encapsulated in chitosan-coated nanoliposomes derived from three natural lecithin sources. Liposomal formulations were all in the nanometric scale (around 120 nm) and negatively charged (around -40 mV). Among the three lecithins, salmon lecithin presented the highest growth-inhibitory effect on MCF-7 cells (two times lower growth than the control group for 12 µM of curcumin and four times lower for 20 µM of curcumin). The soya and rapeseed lecithins showed a similar growth-inhibitory effect on the tumor cells. Moreover, coating nanoliposomes with chitosan enabled a higher loading efficiency of curcumin (88% for coated liposomes compared to 65% for the non-coated liposomes) and a stronger growth-inhibitory effect on MCF-7 breast cancer cells.


Asunto(s)
Antineoplásicos/farmacología , Curcumina/farmacología , Composición de Medicamentos/métodos , Sistemas de Liberación de Medicamentos/métodos , Liposomas/farmacología , Animales , Disponibilidad Biológica , Brassica rapa , Neoplasias de la Mama/tratamiento farmacológico , Quitosano , Portadores de Fármacos , Femenino , Humanos , Lecitinas , Células MCF-7 , Nanopartículas , Salmón , Células Tumorales Cultivadas/efectos de los fármacos
2.
Mar Drugs ; 16(7)2018 Jun 25.
Artículo en Inglés | MEDLINE | ID: mdl-29941790

RESUMEN

Curcumin (diferuloylmethane) is a natural bioactive compound with many health-promoting benefits. However, its poor water solubility and bioavailability has limited curcumin’s biomedical application. In the present study, we encapsulated curcumin into liposomes, formed from natural sources (salmon lecithin), and characterized its encapsulation efficiency and release profile. The proposed natural carriers increased the solubility and the bioavailability of curcumin. In addition, various physico-chemical properties of the developed soft nanocarriers with and without curcumin were studied. Nanoliposome-encapsulated curcumin increased the viability and network formation in the culture of primary cortical neurons and decreased the rate of apoptosis.


Asunto(s)
Curcumina/química , Curcumina/metabolismo , Liposomas/química , Nanopartículas/química , Neuronas/efectos de los fármacos , Salmón/metabolismo , Animales , Apoptosis/efectos de los fármacos , Disponibilidad Biológica , Portadores de Fármacos/química , Lecitinas/química , Solubilidad/efectos de los fármacos
3.
Sci Rep ; 6: 25777, 2016 05 27.
Artículo en Inglés | MEDLINE | ID: mdl-27228907

RESUMEN

Phospholipids in the brain cell membranes contain different polyunsaturated fatty acids (PUFAs), which are critical to nervous system function and structure. In particular, brain function critically depends on the uptake of the so-called "essential" fatty acids such as omega-3 (n-3) and omega-6 (n-6) PUFAs that cannot be readily synthesized by the human body. We extracted natural lecithin rich in various PUFAs from a marine source and transformed it into nanoliposomes. These nanoliposomes increased neurite outgrowth, network complexity and neural activity of cortical rat neurons in vitro. We also observed an upregulation of synapsin I (SYN1), which supports the positive role of lecithin in synaptogenesis, synaptic development and maturation. These findings suggest that lecithin nanoliposomes enhance neuronal development, which may have an impact on devising new lecithin delivery strategies for therapeutic applications.


Asunto(s)
Lecitinas/farmacología , Red Nerviosa/fisiología , Animales , Liposomas , Microelectrodos , Mitocondrias/efectos de los fármacos , Mitocondrias/metabolismo , Nanopartículas/química , Nanopartículas/ultraestructura , Red Nerviosa/efectos de los fármacos , Neuronas/efectos de los fármacos , Neuronas/metabolismo , ARN Mensajero/genética , ARN Mensajero/metabolismo , Ratas , Sinapsinas/genética , Sinapsinas/metabolismo
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