Preparation of Chitosan Particles as a Delivery System for Tetrahydrocurcumin: β-cyclodextrin Inclusive Compound for Colorectal Carcinoma

2021 ◽  
Vol 16 ◽  
Author(s):  
Tan Kin Fai ◽  
Goh Hui Yee ◽  
Palanirajan Vijayaraj Kumar ◽  
Manogaran Elumalai

Background: Tetrahydrocurcumin is a hydrogenated active metabolite of curcumin that exhibits similar pharmacological effects to curcumin. However, its hydrophobic nature has limited its aqueous solubility and bioavailability. By incorporating the tetrahydro curcumin into β-cyclodextrin, its physiochemical property can be improved. Objective: To develop a chitosan composite loaded with tetrahydro curcumin inclusive complex, characterize the developed composites, and evaluate its effectiveness on cancer cells. Methods: Tetrahydrocurcumin was formulated into an inclusive complex with β-cyclodextrin in the ratio of 1:2 (Tetrahydrocurcumin: β-cyclodextrin). The tetrahydro curcumin inclusive complex loaded chitosan particles (THC IC-loaded CPs) were prepared using ionic gelation and later characterized using FTIR. Cytotoxicity of THC IC-loaded CPs in human colon cancer cells, Caco-2 cells, was examined using RTCA xCELLigence technology. The uptake of these particles by Caco-2 cells was also evaluated via fluorescing microscopy. Results: FTIR results confirmed the formation of the tetrahydrocurcumin inclusive complex and the loading of this complex into chitosan composites. The cytotoxic effect of THC IC-loaded CPs showed a dose-dependent relationship, and the IC50 found was 1.117mM and 0.959mM after 48 and 72 hours, respectively. THC IC-loaded CPs showed an immediate uptake by CaCo-2 cells, and the maximum uptake was observed after 1 hour of incubation. Conclusion: This study showed that THC IC-loaded CPs is a potential drug carrier to deliver tetrahydrocurcumin into cancer cells and able to produce a cytotoxic effect on cancer cells.

Materials ◽  
2021 ◽  
Vol 14 (8) ◽  
pp. 1824
Author(s):  
Yu-Jyuan Wang ◽  
Pei-Ying Lin ◽  
Shu-Ling Hsieh ◽  
Rajendranath Kirankumar ◽  
Hsin-Yi Lin ◽  
...  

The purpose of this study was to use agar as a multifunctional encapsulating material to allow drug and ferromagnetism to be jointly delivered in one nanoparticle. We successfully encapsulated both Fe3O4 and doxorubicin (DOX) with agar as the drug carrier to obtain DOX-Fe3O4@agar. The iron oxide nanoparticles encapsulated in the carrier maintained good saturation of magnetization (41.9 emu/g) and had superparamagnetism. The heating capacity test showed that the specific absorption rate (SAR) value was 18.9 ± 0.5 W/g, indicating that the ferromagnetic nanoparticles encapsulated in the gel still maintained good heating capacity. Moreover, the magnetocaloric temperature could reach 43 °C in a short period of five minutes. In addition, DOX-Fe3O4@agar reached a maximum release rate of 85% ± 3% in 56 min under a neutral pH 7.0 to simulate the intestinal environment. We found using fluorescent microscopy that DOX entered HT-29 human colon cancer cells and reduced cell viability by 66%. When hyperthermia was induced with an auxiliary external magnetic field, cancer cells could be further killed, with a viability of only 15.4%. These results show that agar is an efficient multiple-drug carrier, and allows controlled drug release. Thus, this synergic treatment has potential application value for biopharmaceutical carrier materials.


2018 ◽  
Vol 8 (6) ◽  
pp. 394-399 ◽  
Author(s):  
Ibrahim Turan ◽  
Selim Demir ◽  
Kagan Kilinc ◽  
Serap Ozer Yaman ◽  
Sema Misir ◽  
...  

2017 ◽  
Vol 9 (2) ◽  
pp. 204-207 ◽  
Author(s):  
Shenai Ashwini ◽  
Devaraj Ezhilarasan ◽  
Roy Anitha

2005 ◽  
Vol 34 (1) ◽  
pp. 8-11 ◽  
Author(s):  
Joshua D. Lambert ◽  
Mao-Jung Lee ◽  
Lauren Diamond ◽  
Jihyeung Ju ◽  
Jungil Hong ◽  
...  

2020 ◽  
Vol 85 (1) ◽  
pp. 1-8 ◽  
Author(s):  
Asma Mehrez ◽  
Ibtissem Chakroun ◽  
Dalila Mtat ◽  
Mansour Ben ◽  
Ridha Touati

A series of novel optically pure oxime pseudoesters derivatives were synthesized by the reaction of substitute keto oximes with various N-substituted ?-amino acids chlorides in the presence of triethylamine and dichloromethane at 0?C, and their structures were characterized by IR and 1D-NMR methods. The synthesized compounds were tested for their ability to inhibit the proliferation of human colon cancer cells and human epithelial cells. Some of them were revealed to have a significant cytotoxic effect.


2001 ◽  
Vol 120 (5) ◽  
pp. A493-A493
Author(s):  
J HARDWICK ◽  
G VANDENBRINK ◽  
S VANDEVENTER ◽  
M PEPPELENBOSCH

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