摘要
Hybrid-drugs chemotherapy is now one of the widely adopted treatments for cancer prevention with favorable diagnoses. This work has proposed compostable paclitaxel (PTX) and biotin (BT) PCEC nanomaterials (NMs) for the codelivery and to investigate the drug delivery mechanism's efficacy ( [email protected] ) against gastric cancer cells in vitro and in vivo. The fabricated [email protected] were 27.97 ± 1.87 nm in size and had a less polydispersity index (0.156 ± 0.030). PTX and BT were released slowly from the drug delivery without any burst impact. In addition, dose-responsive cytotoxic effects were observed for [email protected] on SGC-791 cells with a higher mortality ratio than free drugs. According to a cellular uptake investigation, drug-loaded PCECs of polymeric liquid nanoparticles were considered better by cancer cells in vitro. To assess the in vivo antitumor activity, [email protected] were administered intravenously injected to xenografted with SGC-791 cells. Substantial inhibition of tumor development was observed with extended survival time and decreased side effects with [email protected] compared to free drugs (PTX + BT). Furthermore, compared to other therapy classes, [email protected] care resulted in lower H&E and Ki67 expressions and improved TUNEL positive in cancer cells, indicating the chemotherapeutic efficiency of drug delivery system. Overall, the current investigation confirmed that DDS [email protected] could be used to successfully combat gastric cancers in the immediate future.
危险品化学品经营许可证(带存储)