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https://hal.archives-ouvertes.fr/hal-00706176/file/Microemulsion%20oral%20delivery.pdf
The reference treatment was a single oral dose of 300 mg of Sandimmune® and the test treatment was a single oral dose of 180 mg of Sandimmune Neoral® [62]. Gibaud, S., & Attivi, D. (2012). Microemulsions for oral administration and their therapeutic applications. Expert Opinion on Drug Delivery, 9(8), 937–951.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3399350/
Jul 08, 2012 · Microemulsion (ME), a novel drug delivery system, has been reported to improve the rate and extent of absorption of lipophilic drugs. As a modern drug carrier system, microemulsions are defined as single optically isotropic and thermodynamically stable solution with droplet sizes in the submicron range.Author: Shailendra Singh Solanki, Brajesh Sarkar, Rakesh Kumar Dhanwani
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2750519/
A Labrafac-based microemulsion formulation with Labrasol as surfactant and Plurol Oleique as cosurfactant was developed for oral delivery of acyclovir. Phase behavior and solubilization capacity of the microemulsion system were characterized, and in vivo oral absorption of acyclovir from the microemulsion was investigated in rats.Author: Pradip Kumar Ghosh, Rita J. Majithiya, Manish L. Umrethia, Rayasa S. R. Murthy
https://www.semanticscholar.org/paper/Microemulsions-%3A-As-drug-delivery-system-Mishra-Panola/ef0ad1eb16ad9bb07458dfc5115ebd017c063840
Microemulsions are excellent candidates as potential drug delivery systems because of their improved drug solubilization, long shelf life, and ease of preparation and administration. The formulation of microemulsion for pharmaceutical use requires a thorough understanding of the properties, uses, and limitations of microemulsion.
https://journal.pda.org/content/62/1/66
Jan 01, 2008 · Microemulsions as Potential Drug Delivery Systems: A Review M. J. Ansari , Kanchan Kohli and Nitin Dixit PDA Journal of Pharmaceutical Science and Technology January 2008, 62 (1) 66-79;Author: M. J. Ansari, Kanchan Kohli, Nitin Dixit
https://www.sciencedirect.com/science/article/pii/S0001868606000650
Microemulsions as transdermal drug delivery vehicles Transdermal drug delivery has many advantages over the oral route of administration: it avoids hepatic metabolism, the administration is easier and more convenient for the patient, and there is the possibility of immediate withdrawal of the treatment if necessary.Author: Anna Kogan, Nissim Garti
https://www.researchgate.net/publication/23656786_Microemulsions_A_Novel_Approach_to_Enhanced_Drug_Delivery
Microemulsions: A Novel Approach to Enhanced Drug Delivery. Microemulsions are isotropic, thermodynamically stable transparent (or translucent) systems of oil, water and surfactant, frequently in combination with a cosurfactant with a droplet size usually in the range of 20-200 nm.
http://www.ijpmr.org/pdf/Microemulsions-A-potential-novel-drug-delivery-system.pdf
microemulsion formulations are widely used for the delivery of hydrophilic as well as lipophilic drug as drug carriers due to their improved drug solubilisation capacity, long shelf life, ease of preparation and improvement of bioavailability. In this present review, we willAuthor: Naresh Mandavi, Nazneen Ansari, Ravi Bharti, N Syed Abdul Kader, Gyanesh Kumar Sahu, Harish Sharma
https://www.sciencedirect.com/topics/pharmacology-toxicology-and-pharmaceutical-science/microemulsion
Microemulsion Oral Delivery of Proteins and Peptides. Microemulsions may be used as the carrier for protein... Topical and Transdermal Drug Delivery. Microemulsions are clear, thermodynamically stable,... Emulsions and Microemulsions for Topical and Transdermal Drug Delivery. Nanotechnology ...
http://www.ijpsnonline.com/Issues/1214_full.pdf
Surjyanarayan Mandal and Snigdha. S. Mandal : Microemulsion Drug Delivery System: A Platform for Improving… 1219 Fig. 4 In vitro intestinal permeability data. In Vitro Intestinal Permeability Study: In vitro intestinal permeability data are shown in Figure 4.
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