model 110 microfluidiser (Microfluidics Inc)
90
Structured Review
Microfluidics Inc
model 110 microfluidiser
Model 110 Microfluidiser, supplied by Microfluidics Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/microfluidiser/model+110+microfluidiser/pm24945139-49-6-9
Average 90 stars, based on 1 article reviews
Model 110 Microfluidiser, supplied by Microfluidics Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/microfluidiser/model+110+microfluidiser/pm24945139-49-6-9
Average 90 stars, based on 1 article reviews
model 110 microfluidiser - by Bioz Stars,
2026-09
90/100 stars
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Emulsion:Article Title: A continuous flow method for estimation of drug release rates from emulsion formulations. Article Snippet: We present a continuous-flow method that allows the release of drugs from submicron colloidal carriers to be estimated on a millisecond timescale.. The technique is applied to the study of release of a model drug (tetracaine) from lipid emulsions, and shows that the solute drug is released in this timescale, and thus is primarily controlled by the rapid diffusion of the drug within the oil droplet.. This confirms our previous claims that existing methods, such as dialysis or centrifugation, are too slow to provide useful release data for drug-containing emulsions, and demonstrates that it is unlikely that a simple emulsion could be used as a circulating sustained-release formulation, as has been suggested by some workers. ã 2014 Elsevier B.V. All rights reserved. Formulation:Article Title: A continuous flow method for estimation of drug release rates from emulsion formulations. Article Snippet: We present a continuous-flow method that allows the release of drugs from submicron colloidal carriers to be estimated on a millisecond timescale.. The technique is applied to the study of release of a model drug (tetracaine) from lipid emulsions, and shows that the solute drug is released in this timescale, and thus is primarily controlled by the rapid diffusion of the drug within the oil droplet.. This confirms our previous claims that existing methods, such as dialysis or centrifugation, are too slow to provide useful release data for drug-containing emulsions, and demonstrates that it is unlikely that a simple emulsion could be used as a circulating sustained-release formulation, as has been suggested by some workers. ã 2014 Elsevier B.V. All rights reserved. |