PLGA Nanoparticles Containing VCAM-1 Inhibitor Succinobucol and Chemotherapeutic Doxorubicin as Therapy against Primary Tumors and Their Lung Metastases

The treatment of malignant tumors is usually accompanied by poor prognosis due to metastasis of tumor cells. Hence, it is crucial to enhance anti-metastasis efficacy when anti-tumor treatments are conducted. It has been reported that the vascular cell adhesion molecule-1 (VCAM-1) is highly expressed on the surface of tumor cells and plays an essential role in the metastasis of tumor cells. Thus, reducing VCAM-1 expression offers hope for inhibiting the metastasis of tumor cells. Evidence has shown that succinobucol (Suc) can selectively and efficiently inhibit VCAM-1 expression. Inspired by these, we designed dual drug-loaded PLGA nanoparticles (Co-NPs) to co-deliver VCAM-1 inhibitor Suc and the chemotherapeutic doxorubicin (Dox) which could both effectively suppress primary melanoma and its lung metastases. Co-NPs were composed of PLGA encapsulated Suc and Dox as hydrophobic cores and DSPE-mPEG(2000) as surface modification materials. With an appropriate particle size (122.4 nm) and a negatively charged surface (-6.77 mV) we could achieve prolonged blood circulation. The in vitro experiments showed that Co-NPs had potent cytotoxicity against B16F10 cells and could significantly inhibit VCAM-1 expression and migration of B16F10 cells. Additionally, the in vivo experiments showed that Co-NPs could efficiently suppress not only primary melanoma but also its lung metastases. In conclusion, PLGA nanoparticles containing VCAM-1 inhibitor Suc and chemotherapeutic Dox as therapy against primary tumors and their lung metastases provides a promising drug delivery strategy for the treatment of metastatic malignant tumors.

Automated summary

The treatment of malignant tumors often leads to poor prognosis due to tumor cell metastasis. Inhibiting VCAM-1 expression, a key factor in tumor cell metastasis, shows promise in inhibiting tumor cell metastasis. This study developed dual drug-loaded PLGA nanoparticles (Co-NPs) that effectively delivered a VCAM-1 inhibitor (Suc) and a chemotherapeutic drug (Dox) to suppress primary melanoma and lung metastases. In vitro experiments demonstrated potent cytotoxicity and inhibition of VCAM-1 expression and migration of B16F10 cells by Co-NPs. In vivo experiments further showed efficient suppression of primary melanoma and lung metastases. These findings suggest that PLGA nanoparticles containing Suc and Dox provide a promising drug delivery strategy for treating metastatic malignant tumors.