2016
DOI: 10.1016/j.colsurfb.2016.09.044
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Soluble curcumin amalgamated chitosan microspheres augmented drug delivery and cytotoxicity in colon cancer cells: In vitro and in vivo study

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Cited by 51 publications
(15 citation statements)
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“…Hence, high single doses of CUR are required to achieve detectable levels in serum of healthy volunteers [6]. Thus, different strategies were tested to overcome these limits, such as liposome-based formulations, and emulsion or microsphere preparations of CUR [7,8,9], all of which were developed with the ultimate goal of optimizing its bioavailability.…”
Section: Introductionmentioning
confidence: 99%
“…Hence, high single doses of CUR are required to achieve detectable levels in serum of healthy volunteers [6]. Thus, different strategies were tested to overcome these limits, such as liposome-based formulations, and emulsion or microsphere preparations of CUR [7,8,9], all of which were developed with the ultimate goal of optimizing its bioavailability.…”
Section: Introductionmentioning
confidence: 99%
“…In vitro experiments demonstrated that the curcumin complex-chitosan microspheres released 95.7% of their curcumin after 24 h in simulated colonic fluid. The concentration of curcumin in colon tissue was significantly higher (44.32 g/g) in mice that received 100 mg/kg of curcumin complex loaded chitosan microspheres by oral gavage than those that received unformulated curcumin (5.3 g/g) [163]. Microparticles containing a curcumin solid dispersion were prepared by the spray drying technique using Gelucire ® 50/13 (stearoyl macrogol-32 EP) and the colloidal silicon dioxide Aerosil ® as a carrier for curcumin delivery.…”
Section: Microcarriers For Curcumin Deliverymentioning
confidence: 91%
“…Wei et al 28 demonstrated that cholesteryl-hyaluronic acid nanogel of CUR exhibited excellent solubility and sustained drug release under physiological conditions and effectively inhibited human pancreatic adenocarcinoma MiaPaCa-2 cells. Jyoti et al 29 investigated chitosan (CS) microspheres of CUR and showed that the microspheres improved solubility and therapeutic index of CUR in HT-29 cells. In addition, it was reported that a series of mesoporous silica material-loaded CUR exhibited higher oral bioavailability and cellular uptake and significantly increased A549, MCF-7 and B16F10 cell apoptosis compared to CUR.…”
Section: Introductionmentioning
confidence: 99%