2004
DOI: 10.1016/j.ijpharm.2003.10.036
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Intestinal absorption of penclomedine from lipid vehicles in the conscious rat: contribution of emulsification versus digestibility

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Cited by 71 publications
(34 citation statements)
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“…The significantly greater bioavailability of lutein nanoemulsions could have two explanations: (i) nano-sized lutein particles and (ii) micelle-like matrix of the nano particles. The lutein nanoparticles have a greater probability of being absorbed as they have a greater surface to volume ratio as opposed to lutein in a pill form [31,32]. The 6 mg lutein supplement pill in the present study was in a powder, not oil form.…”
Section: Discussionmentioning
confidence: 91%
“…The significantly greater bioavailability of lutein nanoemulsions could have two explanations: (i) nano-sized lutein particles and (ii) micelle-like matrix of the nano particles. The lutein nanoparticles have a greater probability of being absorbed as they have a greater surface to volume ratio as opposed to lutein in a pill form [31,32]. The 6 mg lutein supplement pill in the present study was in a powder, not oil form.…”
Section: Discussionmentioning
confidence: 91%
“…27,30) In conclusion, the optimal formulation of SMEDDS containing daidzein (high drug loading and small particle size) was as following: Ethyl oleate (10%), Cremophor RH 40 (60%), and PEG400 (30%) due to high affinity for the continuous phase and forming the smallest particle size. In vitro dissolution studies revealed that dissolution of daidzein from SMEDDS was faster than the conventional tablet.…”
Section: Discussionmentioning
confidence: 99%
“…(Patel et al, 2008;Vogt et al, 2008;Yavuz et al, 2010). All these techniques yield limited fruition when the drug exhibits low bioavailability, owing to metabolism by the cytochrome P450 family of enzymes present in the gut enterocytes and liver hepatocytes, instability in gastrointestinal (GI) fluids, restricted intestinal permeability, and/ or P-glycoprotein (P-gp) efflux (de Smidt et al, 2004;Sha et al, 2005;Koga et al, 2006;Constantinides & Wasan, 2007;Hauss, 2007;Singh et al, 2009a). Self-emulsifying drug delivery systems (SEDDS), in this regard, have been gaining world-wide acceptance to improve the bioavailability potential of lipophilic drugs by augmenting their dissolution and permeation, and for bypassing hepatic first-pass effect (Humberstone & Charman, 1997;Porter & Charman, 2001;Sha et al, 2005;Koga et al, 2006).…”
Section: Original Articlementioning
confidence: 99%