Formulation, characterization and cellular toxicity assessment of a novel bee-venom microsphere in prostate cancer

Samia E El-Didamony1, Reham I Amer2,3, Ghada H El-Osaily4

  • 1Zoology and Entomology Department, Faculty of Science, Al-Azhar University, Youssef Abbas St. off Mostafa Elnhhas, 6th District, Nasr City, Cairo, 11751, Egypt.

Scientific Reports
|August 2, 2022
PubMed

Insights

Bee venom microspheres show promise for targeted cancer therapy. This novel formulation effectively targets prostate cancer cells while sparing healthy cells, suggesting potential for improved oral cancer treatment.

Area of Science:

  • Biomaterials Science
  • Pharmacology
  • Oncology

Background:

  • Bee venom (B.V.) possesses therapeutic properties for various cancers, including prostate cancer.
  • B.V. is a protein degraded in the gastrointestinal tract, limiting oral administration.
  • Colon-targeted delivery systems can protect B.V. and enable oral administration.

Purpose of the Study:

  • To develop and evaluate B.V.-loaded enteric-coated cross-linked microspheres for colon targeting.
  • To assess the efficacy and specificity of the microsphere formulation against cancer cells.

Main Methods:

  • Microspheres were prepared using an emulsion cross-linking method.
  • Evaluated parameters included percentage yield, entrapment efficiency, swelling degree, and in-vitro release.
  • Cytotoxic effects were assessed using MTT assay and flow cytometry on prostate cancer cells (PC3) and normal oral epithelial cells (OEC).

Main Results:

  • The optimized microsphere formula (F3) demonstrated effectiveness against PC3 cells, comparable to free B.V. and superior to doxorubicin.
  • Free B.V. and doxorubicin exhibited cytotoxicity on OEC, while microspheres did not affect OEC viability.
  • Flow cytometry indicated that microspheres induced apoptosis and reduced necrosis in cancer cells at IC50 concentration, showing specificity.

Conclusions:

  • The developed B.V.-loaded microspheres exhibit targeted cytotoxic effects on malignant prostate cancer cells.
  • This formulation demonstrates specificity, sparing normal oral epithelial cells.
  • The targeted microsphere delivery system shows potential as a candidate for future clinical trials in cancer therapy.

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