4.7 Article

Assessment of therapeutic effect of CD20-targeted immunoliposome in primary central nervous system lymphoma

期刊

BIOMEDICINE & PHARMACOTHERAPY
卷 150, 期 -, 页码 -

出版社

ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.biopha.2022.112979

关键词

Lymphoma; CNS; CD20; liposome; rituximab; nanoparticle

资金

  1. National Science and Technology Development Agency (NPT-RNN) [P1851732]
  2. National Research Council of Thailand (NRCT) [N41A640102]
  3. Research Network NANOTEC (RNN) program of the National Nanotechnology Center (NANOTEC)
  4. Ministry of Higher Education, Science, Research and Innovation (MHESI) , Thailand and Siriraj Research Fund
  5. Faculty of Medicine Siriraj Hospital, Mahidol University [R016141027]
  6. NSTDA

向作者/读者索取更多资源

The study demonstrated that liposomes conjugated with RTX and modified with tween-80 can effectively penetrate the blood-brain barrier, targeting lymphoma cells in the CNS. The Lip/RTX showed comparable antitumor activity to free RTX and inhibited tumor aggressiveness. Systemic administration of Lip/RTX significantly prolonged the survival of mice with intracranial lymphoma xenografts.
Primary central nervous system lymphoma (PCNSL) is a form of extranodal non-Hodgkin's B-cell lymphoma limited to the CNS. The treatment of PCNSL is ineffective partly due to the blood-brain barrier (BBB) restriction of delivery of many drugs including anti-CD20 (Rituximab; RTX) which is a standard treatment for systemic B cell lymphomas. In this study, liposome with tween-80 surface modification was fabricated and conjugated with RTX for enhancing BBB penetration to target lymphoma cells in the CNS. Physicochemical characterizations of Lip/RTX were performed and spherical shape liposomes with narrow size distribution were demonstrated by TEM. An average diameter of Lip/RTX was 168.57 +/- 1.57 nm with the percentage of RTX conjugation at 90.94. Cell internalization monitored by flow cytometry confirmed that conjugation of RTX promoted liposome entry into Raji cells expressing CD20. Antitumor activity of Lip/RTX was comparable to free RTX indicating that RTX moieties on liposome remained their therapeutic function. In addition, Lip/RTX inhibited tumor aggressiveness by limiting cell migration and invasion. Systemic administration of Lip/RTX significantly prolonged survival of mice harboring intracranial lymphoma xenografts. Taken together, Lip/RTX presents a new potential treatment for patients with PCNSL.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据