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Codelivery of Raloxifene and Rutin as PEGylated Nanoliposomes: Formulation, Characterization, and Prophylactic
Maryam Abdulmaged Oleiwi1, Ali Al-Samydai1, Aya Y Al-Kabariti2
1Pharmacological and Diagnostic Research Centre, Faculty of Pharmacy, Al-Ahliyya Amman University, Amman 19328, Jordan.
Advanced Pharmaceutical Bulletin
|September 9, 2025
Summary
PEGylated nanoliposomes loaded with raloxifene and rutin show promise for safer breast cancer treatment. These nanoparticles effectively target cancer cells while improving safety in normal tissues, offering a potential advancement in chemotherapy.
Area of Science:
- Nanomedicine
- Drug Delivery
- Oncology
Background:
- Breast cancer remains a leading cause of cancer-related deaths in women.
- Conventional chemotherapy faces challenges including systemic toxicity and multidrug resistance.
- Nanotechnology offers potential for developing safer and more effective cancer therapies.
Purpose of the Study:
- To synthesize and characterize PEGylated nanoliposomes (NLs) loaded with raloxifene (RLX) and a combination of RLX and rutin.
- To evaluate the in vitro anti-cancer effects and safety profile of these nanoliposomes.
Main Methods:
- Thin-film hydration method for nanoliposome synthesis.
- Characterization using Zetasizer, TEM, and HPLC.
- Cell viability assays (MTT) on breast cancer and normal endothelial cell lines.
Main Results:
- High encapsulation efficiency achieved for RLX (91.28%) and rutin (78.12%) in mixed NLs.
- Nanoliposomes demonstrated stability for up to two months.
- Biphasic drug release observed, with reduced cytotoxicity against cancer cells and improved safety in normal cells.
Conclusions:
- PEGylated NLs loaded with RLX and rutin exhibit safe anti-breast cancer effects.
- The formulation shows potential for targeted and safer cancer treatment compared to mixed NLs.
- Further research is warranted for clinical translation.

