2014
DOI: 10.1016/j.ejps.2014.07.010
|View full text |Cite
|
Sign up to set email alerts
|

Solid self-emulsifying phospholipid suspension (SSEPS) with diatom as a drug carrier

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
19
0
2

Year Published

2014
2014
2023
2023

Publication Types

Select...
6
2
1

Relationship

0
9

Authors

Journals

citations
Cited by 32 publications
(21 citation statements)
references
References 32 publications
0
19
0
2
Order By: Relevance
“…While the physical mixture procedure was more efficient, mixing with the ethanolic extract deemed faster. Both processes, however, showed prolonged longevity (Milovic et al, 2014). Diatom has also been used for transport of siRNA into tumor cells (Rea et al, 2014).…”
Section: Nanomedicine and Medical Applicationsmentioning
confidence: 99%
“…While the physical mixture procedure was more efficient, mixing with the ethanolic extract deemed faster. Both processes, however, showed prolonged longevity (Milovic et al, 2014). Diatom has also been used for transport of siRNA into tumor cells (Rea et al, 2014).…”
Section: Nanomedicine and Medical Applicationsmentioning
confidence: 99%
“…Además de mejorar los aspectos farmacocinéticos, estos BA-PEG mostraron una mejora significativa en lo concerniente a seguridad, obteniendo valores de su concentración de inhibición media (IC50) mayores y porcentaje de hemólisis menores en comparación con Tween 80, usado comúnmente en la industria farmacéutica [106], ratificando así el potencial de los BA-PEG como buenos candidatos como excipientes farmacéuticos. Asimismo, los fosfolípidos que tienen una mayor biocompatibilidad han sido empleados como cotensioactivos en diversas investigaciones sobre SEDDS logrando obtener una mayor estabilidad y capacidad de solubilización del sistema, ya que promueven la formación de micelas mezcladas permitiendo así la reducción en la concentración de los tensioactivos y sus efectos adversos [63,116].…”
Section: Tensioactivounclassified
“…Principally, two steps of drug release from the frustules were observed: the first over 6 h was rapid due to the surface deposition of the drug, and the second was slow and sustained over two weeks with zero order kinetics ascribed to the release from the internal hallow structure. Zhang reported, for the first time, the application of diatom as a solid carrier for water insoluble carbamazepine drug (CBZ) applied in oral drug delivery system based on the self-emulsifying drug delivery system (SEDDS) [49]. Different solid samples of CBZ suspension in SEDDS, were prepared using two methods.…”
Section: Micro-nano Carriers For Delivery Of Therapeuticsmentioning
confidence: 99%