Folic Acid–Conjugated PLGA Nanoparticles of Eugenol: Development, Characterization, and In Vitro Cytotoxicity Studies on Breast Cancer Cell Line.

Background: The primary goal of the study was to develop folic acid–conjugated eugenol‐loaded PLGA nanoparticles for the treatment of breast cancer. Eugenol is reported to have potent anticancer activity. Entrapment of eugenol in folic acid–conjugated polymeric nanoparticles is expected to enhance i...

Descripción completa

Detalles Bibliográficos
Publicado en:BioMed Research International Vol. 2026; pp. 1 - 14
Autores principales: Kashyap, Bhawna, Khan, Azhar, Malik, Tabarak, Kapoor, Deepak N., Banerjee, Baisakhi
Formato: equations & formulas research tables/charts Journal Article
Publicado: Wiley-Blackwell 4/27/2026
Acceso en línea:Ver este registro en EBSCOhost
fields @attributes:
  recordID: 1
pdfLink:
plink: https://search.ebscohost.com/login.aspx?direct=true&db=ccm&AN=193280603&site=ehost-live
header:
  @attributes:
    shortDbName: ccm
    uiTerm: 193280603
    longDbName: CINAHL Complete
    uiTag: AN
  controlInfo:
    bkinfo:
    dissinfo:
    jinfo:
      jid:
        23146133
        FT2T
      jtl: BioMed Research International
      issn: 23146133
      maglogo: N
    pubinfo:
      dt: 4/27/2026
      vid: 2026
      pid: 480
      pub: Wiley-Blackwell
      place: Malden, Massachusetts
    artinfo:
      ui:
        193280603
        193280603
        193280603
        10.1155/bmri/2898012
        193280603
      ppf: 1
      ppct: 13
      formats:
        fmt:
          – @attributes:
              type: T
          – @attributes:
              type: C
          – @attributes:
              type: P
      tig:
        atl: Folic Acid–Conjugated PLGA Nanoparticles of Eugenol: Development, Characterization, and In Vitro Cytotoxicity Studies on Breast Cancer Cell Line.
      aug:
        au:
          Kashyap, Bhawna
          Khan, Azhar
          Malik, Tabarak
          Kapoor, Deepak N.
          Banerjee, Baisakhi
        affil: Faculty of Applied Sciences and Biotechnology,, Shoolini University,, Solan, Himachal Pradesh,, India, shooliniuniversity.com
      sug:
        subj:
          Breast Neoplasms Drug Therapy
          Folic Acid Administration and Dosage
          Biocompatible Materials
          Essential Oils
          Nanoparticles
          Plant Extracts
          Drug Development Evaluation
          Drug Efficacy Evaluation
          Cell Line, Tumor Drug Effects
          Antineoplastic Agents Pharmacodynamics
          In Vitro Studies
          Chromatography, Liquid
          Magnetic Resonance Spectroscopy
          Antiinflammatory Agents Pharmacodynamics
          Antioxidants Pharmacodynamics
          Chromatography, High Pressure Liquid
          Descriptive Statistics
          Analysis of Variance
          Post Hoc Analysis
          Data Analysis Software
          Cell Viability Drug Effects
          Dose-Response Relationship, Drug
      ab: Background: The primary goal of the study was to develop folic acid–conjugated eugenol‐loaded PLGA nanoparticles for the treatment of breast cancer. Eugenol is reported to have potent anticancer activity. Entrapment of eugenol in folic acid–conjugated polymeric nanoparticles is expected to enhance its availability at the cancer site and improve overall efficacy in breast cancer treatment. Method: Eugenol was isolated by the column chromatography technique. The isolated bioactive fraction was characterized by IR and NMR analyses. Polymeric NPs were prepared by the solvent emulsification–diffusion method and conjugated with FA by the EDC coupling method. The in vitro release profile for FA‐conjugated eugenol‐loaded PLGA NPs was evaluated by the dialysis membrane technique. Further in vitro anti‐inflammatory activity, in vitro antioxidant assays, and cytotoxicity studies were carried out. Results: NPs exhibiting particle size ranging from 444.2 to 928.3 nm, zeta potential ranging from −32.0 to −37.7 mV, entrapment efficiency ranging from 76.97% to 87.51%, and percent conjugation were found to be 72.59%–79.68%. The in vitro drug release profiles of the formulations were most effectively described by the Higuchi kinetic model, indicating that the mechanism governing drug release is primarily attributed to diffusion. The FTIR study indicated that there is no chemical modification of the drug, confirming its compatibility with other excipients. The morphology of the NPs was analyzed by FESEM analysis. The particulate nature of NPs showed homogenous, spherical shapes of NPs. The cell cytotoxicity studies on MDA‐MB‐231 cell lines exhibited enhanced cytotoxicity of the NPs. Conclusion: In conclusion, it was found that FA‐conjugated PLGA NPs can be a suitable platform for the targeted administration of eugenol for BC treatment.
      pubtype: Academic Journal
      doctype:
        equations & formulas
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
    refInfo:
    holdings:
      @attributes:
        islocal: N