2018
DOI: 10.1016/j.ijpharm.2018.08.010
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Redox sensitive lipid-camptothecin conjugate encapsulated solid lipid nanoparticles for oral delivery

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Cited by 52 publications
(32 citation statements)
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“…Camptothecins constitute a class of anticancer alkaloid traditionally from Chinese medicine that possesses potential anticancer activity against colon, breast, colorectal, stomach, liver, leukemia, and ovarian cancers. Their mechanism of action involves inhibition of tumor-specific topoisomerase I, a critical enzyme responsible for cutting and re-ligating single DNA strands, which results in DNA damage 4043. The pharmacokinetic profile and anticancer activity of nanocrystals and PEG-PBLG loaded into hydroxycamptothecin (HCPT) were evaluated in rats and rabbits 40,41.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Camptothecins constitute a class of anticancer alkaloid traditionally from Chinese medicine that possesses potential anticancer activity against colon, breast, colorectal, stomach, liver, leukemia, and ovarian cancers. Their mechanism of action involves inhibition of tumor-specific topoisomerase I, a critical enzyme responsible for cutting and re-ligating single DNA strands, which results in DNA damage 4043. The pharmacokinetic profile and anticancer activity of nanocrystals and PEG-PBLG loaded into hydroxycamptothecin (HCPT) were evaluated in rats and rabbits 40,41.…”
Section: Resultsmentioning
confidence: 99%
“…The increased bioavailability was associated with enhanced cytotoxic activity against SKOV3 cancer cells. Similarly, the bioavailability of the solid lipid nanoparticles (SLN) delivering camptothecin (CPT) was shown to be improved by 2.38-fold 43…”
Section: Resultsmentioning
confidence: 99%
“…[ 35 ] Disulfide bond linked CPT and palmitic acid prodrug conjugates can formed NPs and achieved high oral absorption and reduced intestinal side effect for cancer treatment. [ 36 ] To improve the clinical potential of CPT based nanoformulaiton in tumor therapy, phosphorylcholine was introduced into CPT prodrug conjugates. [ 37 , 38 , 39 ]…”
Section: Small Molecule Prodnmsmentioning
confidence: 99%
“…Another interesting strategy to solve the inconveniences of camptothecin and facilitate its oral administration would be its encapsulation in nanocarriers, including lipid-based nanoparticles ( Yang et al, 1999 ; Du et al, 2018 ), dendrimers ( Sadekar et al, 2013 ), and polymer nanoparticles ( Huarte et al, 2016 ; Ünal et al, 2020 ). In this context, an alternative to increase the oral absorption of this drug may be its encapsulation in nanoparticles capable of diffusing through the mucus layer and, then, of reaching the mucosal epithelium surface in order to increase their residence time in close contact with the absorptive membrane.…”
Section: Introductionmentioning
confidence: 99%