Nanoemulsions as Delivery Systems for Poly-Chemotherapy Aiming at Melanoma Treatment.
Chiara DianzaniChiara MongeGianluca MiglioLoredana SerpeKatia MartinaLuigi CangemiChiara FerrarisSilvia MiolettiSara OsellaCasimiro Luca GigliottiElena BoggioNausicaa ClementeUmberto DianzaniLuigi BattagliaPublished in: Cancers (2020)
Aims: Advanced melanoma is characterized by poor outcome. Despite the number of treatments having been increased over the last decade, current pharmacological strategies are only partially effective. Therefore, the improvement of the current systemic therapy is worthy of investigation. Methods: a nanotechnology-based poly-chemotherapy was tested at preclinical level. Temozolomide, rapamycin, and bevacizumab were co-loaded as injectable nanoemulsions for total parenteral nutrition (Intralipid®), due to suitable devices, and preliminarily tested in vitro on human and mouse cell models and in vivo on the B16-F10 melanoma mouse model. Results: Drug combination was efficiently loaded in the liquid lipid matrix of Intralipid®, including bevacizumab monoclonal antibody, leading to a fast internalization in tumour cells. An increased cytotoxicity towards melanoma cells, as well as an improved inhibition of tumour relapse, migration, and angiogenesis were demonstrated in cell models for the Intralipid®-loaded drug combinations. In preliminary in vivo studies, the proposed approach was able to reduce tumour growth significantly, compared to controls. A relevant efficacy towards tumour angiogenesis and mitotic index was determined and immune response was involved. Conclusions: In these preliminary studies, Intralipid® proved to be a safe and versatile poly-chemotherapy delivery system for advanced melanoma treatment, by acting on multiple mechanisms.
Keyphrases
- endothelial cells
- drug delivery
- immune response
- monoclonal antibody
- wound healing
- cell therapy
- mouse model
- single cell
- locally advanced
- skin cancer
- cancer therapy
- induced apoptosis
- stem cells
- basal cell carcinoma
- dendritic cells
- signaling pathway
- toll like receptor
- cell death
- combination therapy
- rectal cancer
- cell cycle
- cell cycle arrest
- replacement therapy
- endoplasmic reticulum stress
- radiation therapy
- metastatic colorectal cancer
- fatty acid
- induced pluripotent stem cells
- inflammatory response