Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 5 de 5
Filtrar
Más filtros











Base de datos
Intervalo de año de publicación
1.
J Family Med Prim Care ; 13(6): 2200-2208, 2024 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-39027867

RESUMEN

Cystic fibrosis (CF) is a life-threatening genetic disorder caused by mutations in the CFTR gene. This leads to a defective protein that impairs chloride transport, resulting in thick mucus buildup and chronic inflammation in the airways. The review discusses current and future therapeutic approaches for CFTR dysfunction and airway dysbiosis in the era of personalized medicine. Personalized medicine has revolutionized CF treatment with the advent of CFTR modulator therapies that target specific genetic mutations. These therapies have significantly improved patient outcomes, slowing disease progression, and enhancing quality of life. It also highlights the growing recognition of the airway microbiome's role in CF pathogenesis and discusses strategies to modulate the microbiome to further improve patient outcomes. This review discusses various therapeutic approaches for cystic fibrosis (CFTR) mutations, including adenovirus gene treatments, nonviral vectors, CRISPR/cas9 methods, RNA replacement, antisense-oligonucleotide-mediated DNA-based therapies, and cell-based therapies. It also introduces airway dysbiosis with CF and how microbes influence the lungs. The review highlights the importance of understanding the cellular and molecular causes of CF and the development of personalized medicine to improve quality of life and health outcomes.

4.
Drug Dev Ind Pharm ; 38(9): 1152-8, 2012 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-22204306

RESUMEN

Wedelolactone is isolated from the dried leaves of Eclipta alba (L.) and reported to be effective as a potential hepatoprotective, antibacterial and anti hemorrhagic. Pharmacokinetic studies of wedelolactone reveal its poor absorption through the intestine. The objective of the present study is to enhance bioavailability of wedelolactone by its complexation with phosphatidyl choline and then formulating it as phyto-vesicles for hepatoprotective activity. The complex of wedelolactone rich fraction was prepared with phosphatidyl choline and characterized on the basis of solubility, melting point, thin layer chromatography (TLC), UV, IR and NMR spectroscopy. The complex was further converted into phyto-vesicles and characterized. The hepatoprotective potential of phyto-vesicles was compared with complex, wedelolactone rich fraction and physical mixture of wedelolactone rich fraction and phosphatidyl choline by in vitro method. The results revealed that hepatoprotective activity is better in case of phyto-vesicles as compared to the complex, physical mixture and the wedelolactone itself. Enhanced bioavailability of the wedelolactone complex may be due to the amphiphillic nature of the complex, which greatly enhance the water and lipid solubility of the compound. The present study clearly indicates the superiority of phyto-vesicles over the complex and wedelolactone, in terms of better absorption and improved hepatoprotective activity.


Asunto(s)
Cumarinas/química , Sistemas de Liberación de Medicamentos , Hepatocitos/efectos de los fármacos , Sustancias Protectoras/química , Animales , Antibacterianos/administración & dosificación , Antibacterianos/química , Antibacterianos/aislamiento & purificación , Antibacterianos/farmacología , Tetracloruro de Carbono , Supervivencia Celular/efectos de los fármacos , Células Cultivadas , Cumarinas/administración & dosificación , Cumarinas/aislamiento & purificación , Cumarinas/farmacología , Eclipta/química , Hemostáticos/administración & dosificación , Hemostáticos/química , Hemostáticos/aislamiento & purificación , Hemostáticos/farmacología , Hepatocitos/enzimología , Hepatocitos/metabolismo , Interacciones Hidrofóbicas e Hidrofílicas , India , Micelas , Fosfatidilcolinas/química , Extractos Vegetales/administración & dosificación , Extractos Vegetales/química , Extractos Vegetales/aislamiento & purificación , Extractos Vegetales/farmacología , Hojas de la Planta/química , Sustancias Protectoras/administración & dosificación , Sustancias Protectoras/aislamiento & purificación , Sustancias Protectoras/farmacología , Ratas , Solubilidad , Temperatura de Transición
5.
Arch Dermatol Res ; 304(7): 511-9, 2012 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-22160579

RESUMEN

Alopecia is a psychologically distressing phenomenon. Androgenetic alopecia (AGA) is the most common form of alopecia, which affects millions of men and women worldwide, and is an androgen driven disorder. To study the effect of ß-sitosterol phyto-vesicles on AGA, the testosterone-induced alopecia model was used. For the study, the albino rats were used and the period of study was 21 days. ß-Sitosterol is a phytosterol which is chemically similar to cholesterol. This compound was found suitable for the preparation of phyto-vesicles by the process involving its complexation with phosphatidyl choline. Pharmacokinetic studies of ß-sitosterol reveal its poor absorption through the intestine. The objective of the present study is to enhance the bioavailability of ß-sitosterol by its complexation with phosphatidyl choline and then to formulate it as phyto-vesicles for the treatment of alopecia. The complex of ß-sitosterol was prepared with phosphatidyl choline and characterized on the basis of solubility, melting point, TLC, UV, IR and NMR spectroscopy. This complex was then formulated as phyto-vesicles and then characterized. The results revealed that effect on alopecia is better in case of phyto-vesicles as compared to the complex, physical mixture and the ß-sitosterol itself. Enhanced bioavailability of the ß-sitosterol complex may be due to the amphiphilic nature of the complex, which greatly enhance the water and lipid solubility of the compound. The present study clearly indicates the superiority of phyto-vesicles over the complex and ß-sitosterol, in terms of better absorption and improved activity for the treatment of alopecia.


Asunto(s)
Alopecia/tratamiento farmacológico , Sistemas de Liberación de Medicamentos , Sitoesteroles/administración & dosificación , Absorción/efectos de los fármacos , Alopecia/inducido químicamente , Animales , Disponibilidad Biológica , Modelos Animales de Enfermedad , Humanos , Intestinos/efectos de los fármacos , Masculino , Fosfatidilcolinas/administración & dosificación , Fosfatidilcolinas/farmacocinética , Ratas , Ratas Wistar , Sitoesteroles/farmacocinética , Solubilidad/efectos de los fármacos , Testosterona/administración & dosificación
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA