Novel co‐delivery of oridonin and docetaxel nanoliposome for an enhanced antitumor effect on esophageal cancer

• Published in: The journal of gene medicine 2024-08, Vol.26 (8), p.e3725-n/a
• Main Authors: Chen, Xi, Mao, Hengyu, Peng, Feng, Fan, Jiang, Yang, Fu
• Format: Article
• Language: English
• Subjects: Animals; Antineoplastic Agents - administration & dosage; Antineoplastic Agents - chemistry; Antineoplastic Agents - pharmacology; Antineoplastic drugs; Antitumor activity; Apoptosis; Cancer; Cancer therapies; Cell Line, Tumor; Chemotherapy; co‐delivery; Diterpenes, Kaurane - administration & dosage; Diterpenes, Kaurane - chemistry; Diterpenes, Kaurane - pharmacology; DNA nucleotidylexotransferase; docetaxel; Docetaxel - administration & dosage; Docetaxel - chemistry; Docetaxel - pharmacology; Drug delivery; Drug Delivery Systems - methods; Drug Liberation; Drugs; Encapsulation; Esophageal cancer; Esophageal Neoplasms - drug therapy; Esophageal Neoplasms - pathology; Esophagus; Ethanolamine; Humans; Light scattering; Liposomes - chemistry; Mice; Mice, Inbred BALB C; Mice, Nude; nanoliposome; Nanoparticle Drug Delivery System - chemistry; Nanoparticles - chemistry; oridonin; Particle Size; Pharmacodynamics; Polyethylene glycol; Transmission electron microscopy; Xenograft Model Antitumor Assays; Zeta potential
• ISSN: 1099-498X; 1521-2254; 1521-2254
• DOI: 10.1002/jgm.3725

Introduction Esophageal cancer is one of the major cancers in China. Most patients with esophageal cancer are diagnosed at an advanced stage, and the 5 year survival rate is discouraging. Combined chemotherapy is a common method for the treatment of esophageal cancer. Methods In this study, distearoyl phosphatidyl ethanolamine polyethylene glycol 2000 (DSPE‐PEG2000) nanoliposomes (NLPs) encapsulating the anticancer drugs docetaxel (DOX) and oridonin (ORD) were prepared, and their ability to enhance the release of anticancer drugs was determined. The NLP system was characterized by transmission electron microscopy, particle size and encapsulation efficiency. In addition, the release characteristics and pharmacodynamics of these drugs were also studied in detail. Results When the DOX/ORD ratio was 2:1, the higher proportion of DOX led to a stronger synergy effect. DOX/ORD NLPs were prepared by the high‐pressure homogenization method and had a uniform spherical morphology. The mean particle size and polydispersity index were determined to be 246.4 and 0.163, respectively. The stability results showed that no significant change was observed in particle size, zeta potential, Encapsulation efficiency and dynamic light scattering for DOX/ORD NLPs during the observation period. The results of in vitro release illustrated that the acidic environment of tumor might be beneficial to drug release. The three‐dimensional tumorsphere showed that DOX/ORD NLPs can reach the interior of tumor spheres, which destroys the structure of cells, resulting in irregular spherical tumor spheres. The in vivo study results indicated that DOX/ORD NLPs had an obvious targeting effect on subcutaneous tumors and have the potential to actively deliver drugs to tumor tissues. Terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) staining was used to detect apoptosis. The results showed that DOX/ORD NLP treatment could significantly induce apoptosis and inhibit tumor growth. Conclusion The DOX/ORD NLPs prepared in this study can enhance the anti‐tumor activity, and are expected to be a promising co‐delivery platform for the treatment of esophageal cancer. Co‐delivery of DOX and ORD in a single NLP could effectively inhibit the proliferation of esophageal cancer (EC) cells and enhance the antitumor effect on esophageal cancer. In vivo tumor inhibition of free DOX/ORD, DOX/ORD liposomes and DOX/ORD NLPs: the tumor volume curves (A), the body weight curves (B) and the tumor weigh