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Updated: Sep 2, 2025

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
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.
Abstract:
Bee venom (B.V.) is a toxin produced naturally by honey bees with several toxic and therapeutic efficacies. It is used in the treatment of different cancer kinds like renal, hepatic, and prostate cancer. Due to its protein nature, it is degraded in the upper gastrointestinal tract. Colon-targeted drug delivery systems represent a useful tool to protect B.V. from degradation and can be administered orally instead of I.V. infusion and traditional bee stinging. In the present study, B.V. loaded enteric-coated cross-linked microspheres were prepared by emulsion cross-linking method. Percentage yield, entrapment efficiency %, swelling degree, and in-vitro release are evaluated for prepared microspheres. Free B.V., optimized microspheres formula (F3), and doxorubicin cytotoxic effects were tested by MTT assay. Results concluded that free B.V. was more effective against the growth of human prostate adenocarcinoma (PC3) cells followed by optimized microspheres than doxorubicin. But both free B.V. and doxorubicin have a cytotoxic effect on normal oral epithelial cells (OEC). According to flow cytometric analysis, the optimized microsphere formula induced apoptosis and reduced necrosis percent at IC50 concentration. Furthermore, microspheres did not affect the viability of OEC. These results revealed that microspheres have a degree of specificity for malignant cells. Therefore, it seems that this targeted formulation could be a good candidate for future clinical trials for cancer therapy.
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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