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1.
Molecules ; 25(23)2020 Dec 01.
Artículo en Inglés | MEDLINE | ID: mdl-33271831

RESUMEN

Curcumin is a natural compound that has many medical applications. However, its low solubility and poor stability could impede its clinical applications. The present study aimed to formulate dry proniosomes to overcome these pitfalls and improve the therapeutic efficacy of Curcumin. Curcumin-loaded proniosomes were fabricated by the slurry method according to 32 factorial design using Design-Expert software to demonstrate the impact of different independent variables on entrapment efficiency (EE%) and % drug released after 12 h (Q12h). The optimized formula (F5) was selected according to the desirability criteria. F5 exhibited good flowability and appeared, after reconstitution, as spherical nanovesicles with EE% of 89.94 ± 2.31% and Q12h of 70.89 ± 1.62%. F5 demonstrated higher stability and a significant enhancement of Q12h than the corresponding niosomes. The docking study investigated the ability of Curcumin to bind effectively with the active site of DNA polymerase of Herpes simplex virus (HSV). The antiviral activity and the safety of F5 were significantly higher than Curcumin. F5 improved the safety of Acyclovir (ACV) and reduced its effective dose that produced a 100% reduction of viral plaques. Proniosomes could be promising stable carriers of Curcumin to be used as a safe and efficient antiviral agent.


Asunto(s)
Antivirales/farmacología , Curcumina/farmacología , Sistemas de Liberación de Medicamentos , Herpes Simple/tratamiento farmacológico , Liposomas/administración & dosificación , Nanopartículas/administración & dosificación , Simplexvirus/efectos de los fármacos , Animales , Antineoplásicos/química , Antineoplásicos/farmacología , Antivirales/química , Chlorocebus aethiops , Curcumina/química , Herpes Simple/inducido químicamente , Técnicas In Vitro , Liposomas/química , Nanopartículas/química , Células Vero
2.
J Adv Periodontol Implant Dent ; 14(2): 76-83, 2022.
Artículo en Inglés | MEDLINE | ID: mdl-36714082

RESUMEN

Background. The aim of this study was the clinical and laboratory evaluation of using polycaprolactone (PCL) nanofibers loaded with oxytetracycline hydrochloride (OTC) and zinc oxide (ZnO) as an adjunct to mechanical therapy in managing stage II grade A periodontitis patients concerning GCF lipocalin2- levels. Methods. Fifty stage II grade A periodontitis patients (27 women and 23 men, with an age range of 30‒60) were enrolled in the study. The patients were randomly assigned to five equal groups and treated with scaling and root planing (SRP), followed by local application of PCL nanofibers: group I: SRP + PCL loaded with OTC and ZnO, group II: SRP + PCL loaded with OTC, group III: SRP + PCL loaded with ZnO, group IV: SRP + unloaded PCL, and group V: SRP alone. Additionally, 10 healthy subjects with healthy periodontium (group VI) (age- and gender-matched) served as the negative control. Nanofibers were applied in the selected pockets of periodontitis patients in groups I to IV once weekly for two months. All the participants were examined clinically by assessing periodontal indices (gingival index, plaque index, pocket depth, and clinical attachment level), and biochemically by assessing GCF lipocalin-2 levels. Results. Compared to controls, periodontitis groups (I, II, III, IV, and V) showed significant elevation of both clinical parameters and GCF lipocalin2- levels at baseline. In addition, these parameters improved significantly after treatment, which was more pronounced in groups I, II-, and III) compared to groups IV and V. However, it did not reach normal values. Conclusion. In association with SRP, PCL nanofibers loaded with OTC and ZnO had beneficial therapeutic effects at both clinical and laboratory levels.

3.
J Med Food ; 7(3): 381-4, 2004.
Artículo en Inglés | MEDLINE | ID: mdl-15383236

RESUMEN

Selected natural compounds were evaluated for their effects on dental caries due to different strains of Streptococcus mutans bacteria. Out of 39 tested compounds, four (catechol, emetine, quinine, and flavone) showed potent inhibitory activity on different strains of S. mutans at 6.25 microg/mL or less with inhibition of adherence <50%, two compounds (5,7-dihydroxy-4'-methoxy isoflavone and ellagic acid) exhibited a moderate inhibitory effect at 12.5 microg/mL with inhibition to adherence <50%, and 12 compounds exhibited weak antibacterial activity at 125 microg/mL or more with inhibition of adherence <25%. These compounds represent three major classes of natural products: tannins, alkaloids, and flavonoids. Further study for possible application of these compounds as inhibitors for dental caries is underway.


Asunto(s)
Catecoles/farmacología , Caries Dental/prevención & control , Emetina/farmacología , Flavonoides/farmacología , Quinina/farmacología , Streptococcus mutans/efectos de los fármacos , Antibacterianos/farmacología , Adhesión Bacteriana/efectos de los fármacos , Recuento de Colonia Microbiana , Caries Dental/microbiología , Relación Dosis-Respuesta a Droga , Flavonas , Humanos , Pruebas de Sensibilidad Microbiana , Streptococcus mutans/crecimiento & desarrollo
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