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Intraperitoneal administration of doxorubicin-encapsulated Brucea javanica oil nanoemulsion against malignant ascites.
Dai, Jie; Chen, Renjin; Wang, Jie; Zhou, Ping; Wang, Biqiong; Li, Jianmei; Lu, Yun; Pang, Xianlun; Fu, Shaozhi.
Afiliación
  • Dai J; Department of Oncology, the Affiliated Hospital of Southwest Medical University, Luzhou 646000, China.
  • Chen R; Department of Oncology, the Affiliated Hospital of Southwest Medical University, Luzhou 646000, China.
  • Wang J; Department of Pediatrics, School of Clinical Medicine, Southwest Medical University, Luzhou, Sichuan 646000, China.
  • Zhou P; Department of Radiology, the Affiliated Hospital of Southwest Medical University, Luzhou 646000, China.
  • Wang B; Department of Oncology, the Affiliated Hospital of Southwest Medical University, Luzhou 646000, China.
  • Li J; Department of Oncology, the Affiliated Hospital of Southwest Medical University, Luzhou 646000, China.
  • Lu Y; Department of Oncology, the Affiliated Hospital of Southwest Medical University, Luzhou 646000, China.
  • Pang X; Health Management Center, the Affiliated TCM Hospital of Southwest Medical University, Luzhou 646000, China. Electronic address: pangxianlun@126.com.
  • Fu S; Department of Oncology, the Affiliated Hospital of Southwest Medical University, Luzhou 646000, China. Electronic address: shaozhifu513@swmu.edu.cn.
Eur J Pharm Biopharm ; 202: 114422, 2024 Sep.
Article en En | MEDLINE | ID: mdl-39033885
ABSTRACT
Malignant ascites is a common complication of advanced cancers, which reduces survival rates and diminishes patients' quality of life. Intraperitoneal chemotherapy is a conventional method for treating cancer-related ascites, but the poor drug retention of conventional drugs requires frequent administration to maintain sustained anti-tumor effects. In this study, we encapsulated doxorubicin (DOX) into Brucea javanica oil (BJO) to develop a water-in-oil (W/O) nanoemulsion called BJO@DOX for the treatment of malignant ascites through in-situ intraperitoneal administration. BJO significantly induced apoptosis of S180 cells by upregulating the expression of p53 and caspase-3 (cleaved). Additionally, BJO notably downregulated the expression of Bcl-2, further promoting apoptosis of S180 cells. Cell apoptosis significantly inhibited ascites formation and tumor cell proliferation in a mouse model. The combination of DOX and BJO exhibited satisfactory synergistic effects, consequently prolonging the survival period of mice. Histological examination of major organs indicated that the nanoemulsion had excellent biosafety in vivo. The BJO@DOX nanoemulsion represents a promising platform for in-situ chemotherapy of malignant ascites.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Ascitis / Aceites de Plantas / Doxorrubicina / Apoptosis / Brucea / Emulsiones / Nanopartículas Límite: Animals Idioma: En Revista: Eur J Pharm Biopharm Asunto de la revista: FARMACIA / FARMACOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Ascitis / Aceites de Plantas / Doxorrubicina / Apoptosis / Brucea / Emulsiones / Nanopartículas Límite: Animals Idioma: En Revista: Eur J Pharm Biopharm Asunto de la revista: FARMACIA / FARMACOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: China