2017
DOI: 10.1016/j.ejpb.2016.10.003
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Pharmacokinetics and in vivo delivery of curcumin by copolymeric mPEG-PCL micelles

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Cited by 84 publications
(62 citation statements)
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“…In our experiment, CUR was still detectable in plasma after 6 h, in accordance with literature data (Reza Kheiri Manjili et al, 2016), although at very low concentrations.…”
Section: Resultssupporting
confidence: 93%
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“…In our experiment, CUR was still detectable in plasma after 6 h, in accordance with literature data (Reza Kheiri Manjili et al, 2016), although at very low concentrations.…”
Section: Resultssupporting
confidence: 93%
“…A simultaneous fivefold increase of the maximum experimental plasma concentration ( C max ) and reduction of the corresponding peak time ( T max ) from 120 to 90 min were registered ( Figure 5 ). In particular, the increase of C max obtained after the oral administration of microparticles was not far from the improvement recently registered upon multiple oral administration of CUR-loaded polymeric nano-sized micelles (Reza Kheiri Manjili et al, 2016). Most noteworthy, CUR plasma levels after the administration of microparticles remained at values just below the T max (400-450 μg/ml) for the entire duration of the experiment (6 h) ( Figure 5 ), indicating a sustained release of the drug from the polymeric carrier and a prolonged gastro-intestinal absorption.…”
Section: Resultsmentioning
confidence: 61%
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“…Shukla and Gupta (2010) demonstrated that apigenin could support the improvement of cardiovascular disorders, excite immune system and deliver some defense alongside skin, thyroid, endometrial, gastric, liver, and adrenal cortical cancers (21). Patel et al (2007) suggested that in the future, apigenin owns high possibility for progress as a capable cancer chemopreventive factor (22).…”
Section: Introductionmentioning
confidence: 99%
“…Micelles formed by mono methoxy poly (ethylene glycol)-block-poly (ε-caprolactone) (mPEG-PCL) diblock copolymers are able to encapsulate curcumin with a high drug loading capacity of 20 wt.% and with a remarkably enhanced drug half-life t 1/2 and low cytotoxicity compared to curcumin in solution [8]. Rhamnolipids have been explored as nanocarriers for dermal treatment mimicking bacterial bio-surfactants [9].…”
mentioning
confidence: 99%