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Drug Delivery Letters

Editor-in-Chief

ISSN (Print): 2210-3031
ISSN (Online): 2210-304X

Research Article

Colon Targeted Delivery and In Vitro Evaluation of Curcumin for Colon Cancer

Author(s): Amit Kumar Pandey* and Udaivir Singh Sara

Volume 13, Issue 4, 2023

Published on: 11 September, 2023

Page: [296 - 303] Pages: 8

DOI: 10.2174/2210303113666230830125337

Price: $65

Abstract

Background: The second most common cause of mortality by cancer is thought to be colorectal cancer, which is one of the most prevalent tumours in the world. Many health advantages have been linked to curcumin, which is the key component of turmeric. The goal of the current study was to create a colon-targeted microbead method coated with Eudragit S100 to improve curcumin targeting in the colon by speeding up the rate of its dissolution.

Methods: The ionotropic gelation process was used to create the formulations. The surface phenomena, bead shape, entrapment effectiveness, drug loading, and in vitro drug release were all assessed for formulations. Moreover, calcium alginate beads with an improved core were enteric coated with Eudragit S100. The polymer concentration and curing duration significantly affected particle size and entrapment effectiveness, respectively.

Results: The particle size of the improved formulation was 705 μm, drug entrapment efficiency was 83.56%, drug loading was 28.64%, and in vitro release was 81.66% after 6 hours in phosphate buffer at pH 6.8. After 10 hours, enteric coating with Eudragit S100 of optimized calcium alginate microbeads revealed a 64.09 ± 0.16% drug release. The calculated values of the regression coefficients for the Higuchi, first-order, and zero-order models were 0.9494, 0.8913, and 0.9579, respectively. The 50% inhibitory concentration value was 2.676 based on the percentage of cell viability.

Conclusion: To effectively treat colorectal cancer, the enteric-coated calcium alginate microbeads can deliver curcumin selectively to the colon when taken orally.

Graphical Abstract

[1]
Goel, A.; Kunnumakkara, A.B.; Aggarwal, B.B.; Bharat, B. Curcumin as “Curecumin”: From kitchen to clinic. Biochem. Pharmacol., 2008, 75(4), 787-809.
[http://dx.doi.org/10.1016/j.bcp.2007.08.016] [PMID: 17900536]
[2]
Pricci, M.; Girardi, B.; Giorgio, F.; Losurdo, G.; Ierardi, E.; Di Leo, A. Curcumin and colorectal cancer: From basic to clinical evidences. Int. J. Mol. Sci., 2020, 21(7), 2364.
[http://dx.doi.org/10.3390/ijms21072364] [PMID: 32235371]
[3]
Castelló, A.; Amiano, P.; Fernández de Larrea, N.; Martín, V.; Alonso, M.H.; Castaño-Vinyals, G.; Pérez-Gómez, B.; Olmedo-Requena, R.; Guevara, M.; Fernandez-Tardon, G.; Dierssen-Sotos, T.; Llorens-Ivorra, C.; Huerta, J.M.; Capelo, R.; Fernández-Villa, T.; Díez-Villanueva, A.; Urtiaga, C.; Castilla, J.; Jiménez-Moleón, J.J.; Moreno, V.; Dávila-Batista, V.; Kogevinas, M.; Aragonés, N.; Pollán, M. Low adherence to the western and high adherence to the mediterranean dietary patterns could prevent colorectal cancer. Eur. J. Nutr., 2019, 58(4), 1495-1505.
[http://dx.doi.org/10.1007/s00394-018-1674-5] [PMID: 29582162]
[4]
Aggarwal, B.B.; Kumar, A.; Bharti, A.C. Anticancer potential of curcumin: Preclinical and clinical studies. Anticancer Res., 2003, 23(1A), 363-398.
[PMID: 12680238]
[5]
Johnson, J.J.; Mukhtar, H. Curcumin for chemoprevention of colon cancer. Cancer Lett., 2007, 255(2), 170-181.
[http://dx.doi.org/10.1016/j.canlet.2007.03.005] [PMID: 17448598]
[6]
Anand, P.; Kunnumakkara, A.B.; Newman, R.A.; Aggarwal, B.B. Bioavailability of curcumin: Problems and promises. Mol. Pharm., 2007, 4(6), 807-818.
[http://dx.doi.org/10.1021/mp700113r] [PMID: 17999464]
[7]
Chourasia, M.K.; Jain, S.K. Pharmaceutical approaches to colon targeted drug delivery systems. J. Pharm. Pharm. Sci., 2003, 6(1), 33-66.
[PMID: 12753729]
[8]
Asghar, L.F.; Chandran, S. Multiparticulate formulation approach to colon specific drug delivery: Current perspectives. J. Pharm. Pharm. Sci., 2006, 9(3), 327-338.
[PMID: 17207416]
[9]
Prajakta, D.; Ratnesh, J.; Chandan, K.; Suresh, S.; Grace, S.; Meera, V.; Vandana, P. Curcumin loaded pH-sensitive nanoparticles for the treatment of colon cancer. J. Biomed. Nanotechnol., 2009, 5(5), 445-455.
[http://dx.doi.org/10.1166/jbn.2009.1038] [PMID: 20201417]
[10]
Jain, S.K.; Jain, A.; Gupta, Y.; Ahirwar, M. Design and development of hydrogel beads for targeted drug delivery to the colon. AAPS PharmSciTech, 2007, 8(3), E34-E41.
[http://dx.doi.org/10.1208/pt0803056] [PMID: 17915806]
[11]
Bagyalakshmi, J.; Arun, R.R.; Ravi, T.K. Formulation and evaluation of prednisolone tablets using bio-degradable natural polysaccharides as a carrier in colon targeted drug delivery. Int. J. Pharm. Sci. Res., 2013, 4(6), 2274-2279.
[12]
Girhepunje, K.M.; Krishnapiillai, P.R.S.; Gevariya, H.B.; Thirumoorthy, N. Celecoxib loaded microbeads: A targeted drug delivery for colorectal cancer. Int. J. Curr. Pharm. Res., 2010, 2(1), 46-55.
[13]
Pandey, A.K.; Choudhary, N.; Rai, V.K.; Dwivedi, H.; Kymonil, K.M.; Saraf, S.A. Fabrication and evaluation of tinidazole microbeads for colon targeting. Asian Pac. J. Trop. Dis., 2012, 2, S197-S201.
[http://dx.doi.org/10.1016/S2222-1808(12)60151-0]
[14]
Nappinnai, M.; Kishore, V.S. Formulation and evaluation of microspheres of diltiazem hydrochloride. Indian J. Pharm. Sci., 2007, 69(4), 511-516.
[http://dx.doi.org/10.4103/0250-474X.36935]
[15]
Mosmann, T. Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays. J. Immunol. Methods, 1983, 65(1-2), 55-63.
[http://dx.doi.org/10.1016/0022-1759(83)90303-4] [PMID: 6606682]
[16]
Hu, C.; Lu, W.; Mata, A.; Nishinari, K.; Fang, Y. Ions-induced gelation of alginate: Mechanisms and applications. Int. J. Biol. Macromol., 2021, 177, 578-588.
[http://dx.doi.org/10.1016/j.ijbiomac.2021.02.086]

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