2009
DOI: 10.1166/sam.2009.1009
|View full text |Cite
|
Sign up to set email alerts
|

Controlled Release of Phenytoin from Nanostructured TiO<SUB>2</SUB> Reservoirs

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

0
24
0

Year Published

2011
2011
2020
2020

Publication Types

Select...
4
4
1

Relationship

1
8

Authors

Journals

citations
Cited by 23 publications
(24 citation statements)
references
References 0 publications
0
24
0
Order By: Relevance
“…The primary particles almost immediately aggregate, forming the primary aggregates of about 50 nm size. 13 The primary aggregates almost do not have porosity as one can see from TEM micrographs discussed below. Thus, slitlike micropores of 2.5 nm are most likely the result of aggregation of the primary aggregates with the formation of the secondary aggregates.…”
Section: Resultsmentioning
confidence: 94%
See 1 more Smart Citation
“…The primary particles almost immediately aggregate, forming the primary aggregates of about 50 nm size. 13 The primary aggregates almost do not have porosity as one can see from TEM micrographs discussed below. Thus, slitlike micropores of 2.5 nm are most likely the result of aggregation of the primary aggregates with the formation of the secondary aggregates.…”
Section: Resultsmentioning
confidence: 94%
“…10,[13][14][15][16] Since the majority of these factors may be controlled by the parameters of the sol-gel synthesis, the drug release kinetics, therefore, may be tuned by tailoring the processing parameters during the sol-gel reaction. [17][18][19][20][21][22][23] One of the parameters to control is the water/alkoxide ratio r w .…”
Section: Introductionmentioning
confidence: 99%
“…Indeed, it was shown that the hydrothermal treatment of titania during the sol-gel synthesis resulted in different particle sizes of titania, which was reflected later in different release rates of phenytoin. 10 However, in that case phenytoin was incorporated by adsorption after the temperature treatment, which is less effective than its incorporation during the synthesis. The main problem of calcination of the matrix with an encapsulated drug is the thermal lability of many drugs.…”
Section: Introductionmentioning
confidence: 99%
“…Recently the hierarchical structures based on the assembly of nanoscale building blocks absorb our attention. For instance, hierarchically structured nanowires or nanorods made of TiO 2 [14][15][16][17][18][19][20][21][22][23][24][25][26][27][28], ZnO [29][30][31][32], SnO 2 [33], ZnO/TiO 2 [34], SnO 2 /Fe 2 O 3 [35], and V 2 O 5 /TiO 2 [36] have been prepared via various routes. No doubt that abundant voids deriving from the stacking or parallel growth of the building blocks increase the specific surface area to a large extent.…”
Section: Introductionmentioning
confidence: 99%