2003
DOI: 10.1023/a:1022628826404
|View full text |Cite
|
Sign up to set email alerts
|

Untitled

Abstract: Vacuum freeze-drying is not a preferred technique in the pharmaceutical industry because of scalability and high-cost concerns. The ATMFD process enables commercialization of the SFL particle-engineering technology as a micronization method to enhance dissolution of hydrophobic drugs.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2

Citation Types

0
17
0

Year Published

2006
2006
2016
2016

Publication Types

Select...
5
4

Relationship

0
9

Authors

Journals

citations
Cited by 90 publications
(17 citation statements)
references
References 21 publications
0
17
0
Order By: Relevance
“…These include particle size reduction/ milling, [5][6][7][8] solution-based precipitation, solid dispersion by hot melt extrusion 9) or spray-drying, 10,11) complexation with cyclodextrins 12,13) and so on, as also described extensively in reviews. 14,15) Cryogenic technologies such as freeze drying 16) and spray freezing into liquid (SFL), [17][18][19] in particular, have lately attracted considerable attention for BCS class II compounds. These processes use cryogen, particularly liquid nitrogen, to form a solid dispersion composed of nano-dispersed domains of API within the hydrophilic polymer matrix.…”
mentioning
confidence: 99%
“…These include particle size reduction/ milling, [5][6][7][8] solution-based precipitation, solid dispersion by hot melt extrusion 9) or spray-drying, 10,11) complexation with cyclodextrins 12,13) and so on, as also described extensively in reviews. 14,15) Cryogenic technologies such as freeze drying 16) and spray freezing into liquid (SFL), [17][18][19] in particular, have lately attracted considerable attention for BCS class II compounds. These processes use cryogen, particularly liquid nitrogen, to form a solid dispersion composed of nano-dispersed domains of API within the hydrophilic polymer matrix.…”
mentioning
confidence: 99%
“…However, it is not always appropriate for thermolabile compounds because the spray-drying process requires elevated temperatures. Although lyophilization or freeze-drying is a promising technique to produce pharmaceutical powders with improved solubility, the freezing rate is so slow that this technique is often difficult to apply in the pharmaceutical industry.Spray freezing into liquid nitrogen (SFL) is a novel cryogenic atomization technology, developed by Williams et al [7][8][9][10][11] in which either an aqueous or an aqueous-organic cosolvent solution containing an active pharmaceutical ingredient (API) and a pharmaceutical excipient is atomized directly into cryogenic liquid nitrogen. This method via atomization resulted in production of fine particles with a significant large specific surface area, with high yields, and has also been found to prevent interparticle aggregation.…”
mentioning
confidence: 99%
“…Spray freezing into liquid nitrogen (SFL) is a novel cryogenic atomization technology, developed by Williams et al [7][8][9][10][11] in which either an aqueous or an aqueous-organic cosolvent solution containing an active pharmaceutical ingredient (API) and a pharmaceutical excipient is atomized directly into cryogenic liquid nitrogen. This method via atomization resulted in production of fine particles with a significant large specific surface area, with high yields, and has also been found to prevent interparticle aggregation.…”
mentioning
confidence: 99%
“…In contrast to jet-milling, particles with precisely engineered physical properties were, for instance, engineered using antisolvent crystallization (Kaialy et al, 2014(Kaialy et al, , 2010, batch cooling crystallization (Kaialy et al, 2012), spray drying (Vehring, 2008), spray-freeze drying (Rogers et al, 2003), etc. Freeze-drying (lyophilisation) is a technical procedure that involves the removal of frozen water by sublimation.…”
Section: Introductionmentioning
confidence: 99%