2016
DOI: 10.1016/j.msec.2015.10.039
|View full text |Cite
|
Sign up to set email alerts
|

Mesoporous silica sub-micron spheres as drug dissolution enhancers: Influence of drug and matrix chemistry on functionality and stability

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

1
2
0

Year Published

2016
2016
2019
2019

Publication Types

Select...
4
1
1

Relationship

0
6

Authors

Journals

citations
Cited by 8 publications
(3 citation statements)
references
References 42 publications
1
2
0
Order By: Relevance
“…4 shows the TEM images and EDS elemental analysis result of the agar/5 wt.% silica aerogel nanocomposite film. The TEM images revealed that the film showed a mesoporous microstructure that is typically observed in silica aerogels [15]. As is evident from Fig.…”
Section: Resultssupporting
confidence: 55%
“…4 shows the TEM images and EDS elemental analysis result of the agar/5 wt.% silica aerogel nanocomposite film. The TEM images revealed that the film showed a mesoporous microstructure that is typically observed in silica aerogels [15]. As is evident from Fig.…”
Section: Resultssupporting
confidence: 55%
“…Empirical knowledge on adsorption phenomena in nanomaterials has been continuously progressing for more than one century. 1 Today, their importance in the chemical industry is considerable, owing to the large number of upmost challenging applications that range from nanofiltration and water desalination, 2-4 health [5][6][7] and food science, 8 and CO 2 storage 9 to shale gas extraction. 10 The understanding of the actual adsorption mechanisms is still however hampered by the increasing complexity of the adsorbed multicomponent systems relevant for these applications.…”
Section: Introductionmentioning
confidence: 99%
“…Ibuprofen, ((RS)-2-(4-(2-methylpropyl) phenyl) propanoic acid), is a non-steroidal anti-inflammatory drug (NSAID), with recognised low oral bioavailability attributed to its insolubility in water (0.12 mg/ml R-(-)-enantiomer; 0.08 mg/ml S-(+)-enantiomer) Nerurkar et al, 2005. It is an acidic compound (p K a = 4.49), showing therefore higher solubility in neutral-basic environment (Brigo et al, 2016), and in a set of organic solvents e.g. ethanol (0.20 mg/ml) Rashid et al, 2014, chloroform (618 mg/ml) n -octanol (394 mg/ml) and cyclohexane (193 mg/ml) Garzón and Martínez, 2004.…”
Section: Introductionmentioning
confidence: 99%