Skip to content
2000
Volume 1, Issue 1
  • ISSN: 2210-299X
  • E-ISSN: 2210-3007

Abstract

Background and Objective

After lung cancer and breast cancer, colorectal cancer (CRC) is the third most common type of cancer and has the second-highest fatality rate. Curcumin is one such naturally occurring dietary compound that demonstrated promise to treat colon cancer. For that, the goal of the current study was to coat curcumin with Eudragit S100 to treat colorectal cancer in the distal intestine release. The multiparticulate dosage form can increase the solubility of curcumin in the colon environment, sustain the drug release, and protect the drug from abrupt degradation in the colon environment. All of these alterations can enhance the colon tissue levels, especially in the colon cancer cells in the patients, and thereby can enhance the utility of the therapy.

Methods

By using the ionotropic gelation technique, the formulations were made. Moreover, Design Expert 13 used a three-factor, three-level Box-Behnken design (BBD) in this work to optimize the formulation for colon-targeted drug delivery. The concentration of potassium alginate, the concentration of calcium chloride, and the curing duration were considered independent variables, and prepared microbeads were refined to study their impacts on entrapment effectiveness and particle size. Eudragit S100 was enteric coated on Calcium alginate beads with an improved core.

Results

Regarding particle size and entrapment effectiveness, respectively, the polymer concentration and curing duration had a substantial impact. The ideal concentrations of calcium chloride and potassium alginate were 15% w/v and 6% w/v, respectively, with a 20-minute curing time. With a drug entrapment efficiency of 88.4%, the improved formulation had particles with a size of 708 µm. After 12 hours, 79.23±0.32% of the drug was released following an enteric coating of Eudragit S100 of optimized calcium alginate microbeads (10% weight gain).

Conclusion

The present study conclusively demonstrates the usefulness of a Box-Behnken design in the optimization of colon-targeted formulations. To effectively treat colorectal cancer, enteric-coated calcium alginate microbeads can be administered orally to deliver curcumin precisely to the colon.

This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International Public License (CC-BY 4.0), a copy of which is available at: https://creativecommons.org/licenses/by/4.0/legalcode. This license permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Loading

Article metrics loading...

/content/journals/cis/10.2174/012210299X250021230925041855
2023-01-01
2025-09-16
Loading full text...

Full text loading...

/deliver/fulltext/cis/1/1/CIS-1-E2210299X250021.html?itemId=/content/journals/cis/10.2174/012210299X250021230925041855&mimeType=html&fmt=ahah

References

  1. ValentineC.I. RichardA.K. AbduhlW.B. Drug delivery to the Colon. Technology/Industry overviewsPharma Ventures Ltd.20042730
    [Google Scholar]
  2. UraJ. ShirachiD. FerrillM. The chronotherapeutic approach to pharmaceutical treatment.California Pharmacist1992234653
    [Google Scholar]
  3. MinkoT. Drug targeting to the colon with lectins and neoglycoconjugates.Adv. Drug Deliv. Rev.200456449150910.1016/j.addr.2003.10.01714969755
    [Google Scholar]
  4. WongK.E. NgaiS.C. ChanK.G. LeeL.H. GohB.H. ChuahL.H. Curcumin nanoformulations for colorectal cancer: A review.Front. Pharmacol.20191015216910.3389/fphar.2019.0015230890933
    [Google Scholar]
  5. MariaP. GirardiB. GiorgioF. LosurdoG. IerardiE. Curcumin and colorectal cancer: From basic to clinical evidences.Int. J. Mol. Sci.20202172359236432235371
    [Google Scholar]
  6. JainS.K. JainA. GuptaY. AhirwarM. Design and development of hydrogel beads for targeted drug delivery to the colon.AAPS PharmSciTech200783E34E4110.1208/pt080305617915806
    [Google Scholar]
  7. KundlikG. PalR. HiteshB. Celecoxib loaded microbeads: A targeted drug delivery for colorectal cancer.Int. J. Curr. Pharm. Res.201024655
    [Google Scholar]
  8. SridharB.K. SrinathaA. KhanM.S. Development and evaluation of pH-dependent micro beads for colon targeting.Indian J. Pharm. Sci.2010721182310.4103/0250‑474X.6223020582185
    [Google Scholar]
  9. PatelH. NagleA. MurthyR.S.R. Characterization of calcium alginate beads of 5-fluorouracil for colon delivery.Asian J. Pharm.20082424124510.4103/0973‑8398.45039
    [Google Scholar]
  10. GhosalK. GhoshD. DasS.K. Preparation and evaluation of naringin-loaded polycaprolactone microspheres based oral suspension using Box-Behnken design.J. Mol. Liq.2018256495710.1016/j.molliq.2018.02.024
    [Google Scholar]
  11. MosmannT. Rapid colorimetric assay for cellular growth and survival: Application to proliferation and cytotoxicity assays.J. Immunol. Methods1983651-2556310.1016/0022‑1759(83)90303‑46606682
    [Google Scholar]
  12. DasS.K. YuvarajaK. KhanamJ. NandaA. Formulation development and statistical optimization of ibuprofen-loaded polymethacrylate microspheres using response surface methodology.Chem. Eng. Res. Des.20159611410.1016/j.cherd.2015.01.014
    [Google Scholar]
  13. GadaS.G. AnandY. SettyM. Design and optimization of zidovudine loaded uriddall mucilage microspheres, using box behnken method.Int. J. Pharm. Sci. Res.201918561864
    [Google Scholar]
  14. BhandareS.B. LaddhaK.S. Optimization of extraction parameters for total flavonoids from gardenia gummifera gum resin by response surface methodology.Int. J. Pharm. Pharm. Sci.2016811646810.22159/ijpps.2016v8i11.11134
    [Google Scholar]
  15. SolankiA.B. ParikhJ.R. ParikhR.H. Formulation and optimization of piroxicam proniosomes by 3-factor, 3-level box-behnken design.AAPS PharmSciTech2007844310.1208/pt080408618181547
    [Google Scholar]
  16. NutanM.T.H. SolimanM.S. TahaE.I. KhanM.A. Optimization and characterization of controlled release multi-particulate beads coated with starch acetate.Int. J. Pharm.20052941-28910110.1016/j.ijpharm.2005.01.01315814233
    [Google Scholar]
  17. DasS.K. KhanamJ. NandaA. Optimization of preparation method for ketoprofen-loaded microspheres consisting polymeric blends using simplex lattice mixture design.Mater. Sci. Eng. C20166959860810.1016/j.msec.2016.07.01027612752
    [Google Scholar]
  18. PandeyA.K. ChoudharyN. RaiV.K. DwivediH. KymonilK.M. SarafS.A. Fabrication and evaluation of tinidazole microbeads for colon targeting.Asian Pac. J. Trop. Dis.20122S197S20110.1016/S2222‑1808(12)60151‑0
    [Google Scholar]
  19. LiW. ZhouJ. XuY. Study of the in vitro cytotoxicity testing of medical devices.Biomed. Rep.20153561762010.3892/br.2015.48126405534
    [Google Scholar]
  20. ShaikhS. ShaikhJ. NabaY.S. DokeK. AhmedK. YusufiM. Curcumin: Reclaiming the lost ground against cancer resistance.Cancer Drug Resist.20214229832010.20517/cdr.2020.9235582033
    [Google Scholar]
  21. The importance of IC50 determination.Available From: https://visikol.com/blog/2022/06/07/the-importance-of-ic50-determination/ (Accessed on: July 20, 2023).
/content/journals/cis/10.2174/012210299X250021230925041855
Loading
/content/journals/cis/10.2174/012210299X250021230925041855
Loading

Data & Media loading...

This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test