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https://www.sciencedirect.com/science/article/pii/S0378517310004035
The mean plasma concentration profile of fexofenadine from the intranasal delivery of fexofenadine microemulsion formulations and fexofenadine powder is displayed in Fig. 4B. The corresponding bioavailability and pharmacokinetic parameters are shown in Table 4. At 1.0 mg/kg dose, the nasal delivery of F1 and F2 showed similar bioavailability of ...Author: Hong-Mei Piao, Prabagar Balakrishnan, Hyun-Jong Cho, Hyunjun Kim, You-Sun Kim, Suk-Jae Chung, Chang-...
https://www.researchgate.net/publication/45201046_Preparation_and_evaluation_of_fexofenadine_microemulsion_for_intranasal_delivery
Preparation and evaluation of fexofenadine microemulsion for intranasal delivery Article in International Journal of Pharmaceutics 395(1-2):309-16 · August 2010 with 504 Reads How we measure 'reads'
https://www.ncbi.nlm.nih.gov/pubmed/20685383
Jun 02, 2010 · Preparation and evaluation of fexofenadine microemulsion for intranasal delivery. Piao HM(1), Balakrishnan P, Cho HJ, Kim H, Kim YS, Chung SJ, Shim CK, Kim DD. Author information: (1)College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul 151-742, Korea.Author: Hong-Mei Piao, Prabagar Balakrishnan, Hyun-Jong Cho, Hyunjun Kim, You-Sun Kim, Suk-Jae Chung, Chang-...
https://www.ncbi.nlm.nih.gov/pubmed/20635476
Aug 16, 2010 · Preparation and evaluation of fexofenadine microemulsions for intranasal delivery. Piao HM(1), Balakrishnan P, Cho HJ, Kim H, Kim YS, Chung SJ, Shim CK, Kim DD. Author information: (1)College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul 151-742, Republic of Korea.Author: Hong-Mei Piao, Prabagar Balakrishnan, Hyun-Jong Cho, Hyunjun Kim, You-Sun Kim, Suk-Jae Chung, Chang-...
https://www.academia.edu/12696645/Preparation_and_evaluation_of_fexofenadine_microemulsion_for_intranasal_delivery
To enhance the solubility and bioavailability of poorly absorbable fexofenadine, microemulsion system composed of oil, surfactant and co-surfactant was developed for intranasal delivery. Phase behavior, particle size, viscosity and solubilization
https://www.deepdyve.com/lp/elsevier/preparation-and-evaluation-of-fexofenadine-microemulsions-for-KMmTXu87dr
Aug 16, 2010 · Read "Preparation and evaluation of fexofenadine microemulsions for intranasal delivery, International Journal of Pharmaceutics" on DeepDyve, the largest online rental service for scholarly research with thousands of academic publications available at your fingertips.
https://www.researchgate.net/publication/318037857_Formulation_development_and_characterization_of_oxcarbazepine_microemulsion_for_intranasal_delivery
To enhance the solubility and bioavailability of poorly absorbable fexofenadine, microemulsion system composed of oil, surfactant and co-surfactant was developed for intranasal delivery.
https://www.sciencedirect.com/science/article/pii/S1818087613000093
Preparation and evaluation of transnasal microemulsion of carbamazepine ... The objective of this study was to develop novel transanasl microemulsion containing carbamazepine for treatment of epilepsy. ... J. Xinguo, J. Wenming, et al.Preparation of nimodipine-loaded ME for intranasal delivery and evaluation on the targeting efficiency to the ...Author: Sheetal Porecha Acharya, K. Pundarikakshudu, Aashish Panchal, Anita Lalwani
http://www.allindianpatents.com/patents/251593-a-microemulsion-based-intranasal-drug-delivery-system-and-method-for-preparation-thereof
Title of Invention: A MICROEMULSION BASED INTRANASAL DRUG DELIVERY SYSTEM AND METHOD FOR PREPARATION THEREOF: Abstract: The present invention discloses a microemulsion based intranasal drug delivery system comprising an oil phase; a long chain surfactant component; a short chain cosurfactant component, a combination of long chain thermosensitive polymers, a …Grant Date: 26-Mar-2012
http://www.globalsciencebooks.info/Online/GSBOnline/images/2013/IJBPS_7(1)/IJBPS_7(1)20-27o.pdf
This paper describes formulation considerations and in vitro evaluation of an oleic acid-based polyelectrolytic polymer-containing microemulsion drug delivery system designed for intranasal administration of a hydrophobic model drug Olanzapine. Drug-loaded microemulsions were successfully prepared by a water titration method.
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