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2000
Volume 15, Issue 1
  • ISSN: 2468-1873
  • E-ISSN: 2468-1881

Abstract

Introduction

The major goal of this work is to develop letrozole nanoparticles using the polymer precipitation technique. Formulations were prepared by using Ethyl cellulose and Eudragit S100 as polymers.

Methods

By varying drug-polymer ratios, a total of ten formulations were prepared. By altering the drug concentration to polymer, five formulations were prepared with Ethyl cellulose and five with Eudragit S100. All ten formulations were evaluated for different characterization and evaluation parameters such as Entrapment efficiency, Loading capacity and drug release studies, particle size, stability (zeta potential), surface morphology, and drug-polymer interaction study.

Result

In comparison, the NEC 2:1 formulation showed the smallest particle size, high stability, good entrapment efficiency, and sustained drug release. This formulation was further studied to determine the anticancer activity in the MCF-7 Breast cancer cell line by MTT assay. The results indicated that the prepared formulation exhibited anticancer activity with an IC50 value of 91.26 micromolar.

Conclusion

Comparatively, Ethyl cellulose was proven to be a better polymer than Eudragit S100, and the nanoprecipitation technique was considered the most suitable technique for preparing letrozole nanoparticles.

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2024-03-18
2024-12-25
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References

  1. NaikJ.B. LokhandeA.B. Development of sustained release micro/nanoparticles using different solvent emulsification techniques: A review.Int J Pharm Bio Sci.201234573590
    [Google Scholar]
  2. AvançoG.B. BruschiM.L. Preparation and characterisation of ethylcellulose microparticles containing propolis.Rev. Cienc. Farm. Basica Apl.2008292129135
    [Google Scholar]
  3. GulbakeA. JainS.K. Colon specific delivery of mesalazine using biocompatible polymeric nanoparticles.Int. J. Pharm. Pharm. Technol.20131219942175
    [Google Scholar]
  4. GaoW. ChanJ. OmidC. pH-Responsive nanoparticles for drug delivery.Mol Pharm20107619131020
    [Google Scholar]
  5. HuD. LiuL. ChenW. LiS. ZhaoY. A novel preparation method for 5-aminosalicylic acid loaded Eudragit S100 nanoparticles.Int. J. Mol. Sci.20121356454646810.3390/ijms1305645422754377
    [Google Scholar]
  6. CostaP. LoboS.J.M. LoboS. Modeling and comparison of dissolution profiles.Eur. J. Pharm. Sci.200113212313310.1016/S0928‑0987(01)00095‑111297896
    [Google Scholar]
  7. RobinsonJ.R. LeeV.H.L. Controlled Drug Delivery2nd edNew YorkMarcel Dekker Inc19872930
    [Google Scholar]
  8. PenaR. Analysis of different parameters of an optimized prolonged release formulation obtained by five processes.Pharmaceutical Technology –Controlled Drug ReleaseLondonEllis Horwood20055770
    [Google Scholar]
  9. MohanrajV.J. ChenY. Nanoparticles – A review.Trop. J. Pharm. Res.200751561573
    [Google Scholar]
  10. KumareshS.S. AminabhaviT.M. AnandraoR. Biodegradable polymeric nanoparticles as drug delivery devices.J. Control. Release2001701–2120
    [Google Scholar]
  11. KoohparK.Z. EntezariM. MovafaghA. HashemiM. Anticancer activity of curcumin on human breast adenocarcinoma: Role of Mcl-1 gene.Iran. J. Cancer Prev.201583e233110.17795/ijcp233126413251
    [Google Scholar]
  12. SenthilrajaP. in vitro cytotoxicity MTT assay in Vero, HepG2 and MCF -7 cell lines study of Marine.Yeast. J. Appl. Pharmaceut. Sci.2015503080084
    [Google Scholar]
  13. JayashreeV. In - vitro anti-proliferative assay and cell viability activity of baicalein using breast cancer cell line.Int. J. Pharm. Sci. Res.20189416201624
    [Google Scholar]
  14. MishraJ. DashA.K. KumarR. Nanotechnology challenges; nanomedicine: Nanorabots.Int. Res. J. Pharm.201224112119
    [Google Scholar]
  15. SailajaA.K. BanuJ. SailajaA.K. BanuJ. Preparation and evaluation of chitosan loaded naproxen nanoparticles by emulsion interfacial reaction method.Drug Deliv. Lett.201992899610.2174/2210303109666190211150117
    [Google Scholar]
  16. SahooS.K. PanyamJ. PrabhaS. LabhasetwarV. Residual polyvinyl alcohol associated with poly (D,L-lactide-coglycolide) nanoparticles affects their physical properties and cellular uptake.J. Control. Release20028210511410.1016/S0168‑3659(02)00127‑X12106981
    [Google Scholar]
  17. SailajaA.K. SwatiP. Preparation and characterization of sulphasalazine loaded nanoparticles by nanoprecipitation and ionotropic gelation techniques using various polymers.Curr. Nanomed.201772125141
    [Google Scholar]
  18. PatelB. ModiV. KomalP.M.P. Preparation and evaluation of ethyl cellulose microspheres prepared by emulsification - Solvent evaporation method.IJRMP20121123202331
    [Google Scholar]
  19. SailajaK.A. Preparation of chitosan coated nanoparticles by emulsion polymerization technique.Asian J. Pharm. Clin. Res.20114117374
    [Google Scholar]
  20. SailajaA.K. AmareshwarA. ChakravartyP. Different techniques used for the preparation of nanoparticles using natural polymers and their application.Int. J. Pharm. Pharm. Sci.2011324550
    [Google Scholar]
  21. KreuterJ. Nanoparticles.Colloidal Drug Delivery SystemsNew YorkMarcel Decker1994261276
    [Google Scholar]
  22. MuellerR.H. Colloidal Carriers for Controlled Drug Delivery and TargetingBostonCRC Press1991379
    [Google Scholar]
  23. KrishnaRSM. Nanoparticles: A novel colloidal drug delivery system.Indian J Pharma Edu Res20064011521
    [Google Scholar]
  24. Le ThiM.H. ChiN.T. TrietN.M. Le NgocT.N. ChienD.M. Preparation of drug nanoparticles by emulsion evaporation method Advanced Materials Science and Nanotechnology (AMSN08).J. Phys. Conf. Ser.20092009187
    [Google Scholar]
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