2020
DOI: 10.1016/j.bcab.2020.101638
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Bioavailability of curcumin in nanoemulsions stabilized with mono- and diacylglycerols structured with conjugated linoleic acid and n-3 fatty acids

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Cited by 21 publications
(4 citation statements)
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“…37 Nevertheless, the disadvantage of using curcumin is its low oral bioavailability; this is due to a combination of efficient first-step metabolism via the glucuronidation and sulfation pathway, leading to low gastrointestinal absorption and rapid elimination. 38 Due to this, various studies have been carried out, and successful advances have been made in the design of formulations to improve the oral bioavailability of curcumin, [39][40][41][42][43][44][45][46][47][48][49][50][51][52][53] as shown in Table 1.…”
Section: Therapeutic Properties and Bioavailability Of Curcuminmentioning
confidence: 99%
“…37 Nevertheless, the disadvantage of using curcumin is its low oral bioavailability; this is due to a combination of efficient first-step metabolism via the glucuronidation and sulfation pathway, leading to low gastrointestinal absorption and rapid elimination. 38 Due to this, various studies have been carried out, and successful advances have been made in the design of formulations to improve the oral bioavailability of curcumin, [39][40][41][42][43][44][45][46][47][48][49][50][51][52][53] as shown in Table 1.…”
Section: Therapeutic Properties and Bioavailability Of Curcuminmentioning
confidence: 99%
“…Other authors enzymatically prepared monoacylglycerides and diacylglycerides structured with conjugated linoleic acid (CLA), medium chain fatty acids (MCFA), and ω-3 fatty acids (ω-3 FA), used to assemble nanoemulsions employed as carrier systems of lipophilic active compounds with a low bioavailability, such as CUR, which need to be protected from the environment [ 124 ]. Contextually, Richa et al [ 129 ] developed polysaccharide-based nanoemulsions for the stabilization and entrapment of CUR (see Figure 5 ).…”
Section: Phenolic Compoundsmentioning
confidence: 99%
“…Lower surface tension values of KO and LED could be attributed to the presence of other compounds such as MAG and DAG which are non-ionic and amphipathic molecules with interfacial activity, that confer outstanding emulsifying properties. [45] A surfactant with these characteristics could produce mixed micelles; the size, shape, and the CMC of mixed micelles are usually different from those formed by a single surfactant. Therefore, these changes in the CMC micelles directly influence emulsion stability.…”
Section: Critical Micellar Concentrationmentioning
confidence: 99%