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奥沙利铂和多西紫杉醇共载纳米脂质体用于增强食管癌的抗肿瘤作用。

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

机构信息

Department of Thoracic Surgery, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Department of Pathology Center, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

出版信息

J Gene Med. 2024 Aug;26(8):e3725. doi: 10.1002/jgm.3725.

Abstract

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.

摘要

简介

食管癌是中国的主要癌症之一。大多数食管癌患者在晚期被诊断出来,五年生存率令人沮丧。联合化疗是治疗食管癌的常用方法。

方法

本研究制备了包载抗癌药物多西紫杉醇(DOX)和冬凌草甲素(ORD)的二硬脂酰基磷脂酰乙醇胺聚乙二醇 2000(DSPE-PEG2000)纳米脂质体(NLPs),并测定其增强抗癌药物释放的能力。通过透射电子显微镜、粒径和包封效率对 NLP 系统进行了表征。此外,还详细研究了这些药物的释放特性和药效学。

结果

当 DOX/ORD 比值为 2:1 时,较高比例的 DOX 导致更强的协同作用。采用高压匀质法制备 DOX/ORD NLPs,具有均匀的球形形态。平均粒径和多分散指数分别为 246.4nm 和 0.163。稳定性结果表明,在观察期内,DOX/ORD NLPs 的粒径、Zeta 电位、包封率和动态光散射均无明显变化。体外释放结果表明,肿瘤的酸性环境可能有利于药物释放。三维肿瘤球体实验表明,DOX/ORD NLPs 可以到达肿瘤球体的内部,破坏细胞结构,导致肿瘤球体形状不规则。体内研究结果表明,DOX/ORD NLPs 对皮下肿瘤具有明显的靶向作用,具有主动将药物递送到肿瘤组织的潜力。末端脱氧核苷酸转移酶 dUTP 缺口末端标记(TUNEL)染色用于检测细胞凋亡。结果表明,DOX/ORD NLP 处理可显著诱导细胞凋亡并抑制肿瘤生长。

结论

本研究制备的 DOX/ORD NLPs 可以增强抗肿瘤活性,有望成为治疗食管癌的一种有前途的联合递药平台。

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