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1.北京市科学技术研究院新材料与先进制造研究所,北京 100089
2.河北蜂桐生物科技有限公司,石家庄 050035
3.河北医科大学药学院,石家庄 050017
助理研究员,博士。研究方向:制药工程。E-mail:zhaoweixuan@bjast.ac.cn
教授,博士生导师,博士。研究方向:药物新剂型与新技术。E-mail:caody3@163.com
收稿日期:2024-07-19,
修回日期:2025-01-15,
录用日期:2025-01-15,
纸质出版日期:2025-02-15
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赵玮璇,卢雪,赵瑞林,等.顺铂脂质体在肿瘤治疗中的研究进展[J].中国药房,2025,36(03):356-361.
ZHAO Weixuan,LU Xue,ZHAO Ruilin,et al.Research advances in cancer therapy of cisplatin liposome[J].ZHONGGUO YAOFANG,2025,36(03):356-361.
赵玮璇,卢雪,赵瑞林,等.顺铂脂质体在肿瘤治疗中的研究进展[J].中国药房,2025,36(03):356-361. DOI: 10.6039/j.issn.1001-0408.2025.03.17.
ZHAO Weixuan,LU Xue,ZHAO Ruilin,et al.Research advances in cancer therapy of cisplatin liposome[J].ZHONGGUO YAOFANG,2025,36(03):356-361. DOI: 10.6039/j.issn.1001-0408.2025.03.17.
以顺铂类药物或其联合应用为基础的化疗是一类常见的肿瘤治疗方法,但出于顺铂的非特异性所导致的副作用、小分子药物的药代动力
学特性较差、易产生耐药等原因,极大地限制了顺铂类药物作为一线抗肿瘤药物的临床应用。随着纳米载体技术的发展,脂质体凭借靶向、减毒、增效的优良特性,成为了递送顺铂类药物的理想载体。本文综述了国内外已进入临床研究的顺铂脂质体现状,包括L-NDDP、SPI-077
®
、Lipoplatin
®
、LiPlaCis、SLIT、ILC等,发现目前只有Lipoplatin
®
和ILC的发展势头良好。虽然顺铂脂质体在降低全身毒性、提高治疗效率等方面取得了一定进展,但在肿瘤靶向性和减少副作用方面仍有待进一步提升。未来可以通过共递送脂质体、刺激响应型脂质体和具有靶向功能的脂质体等制剂技术,开发出更加低毒、高效的顺铂脂质体。
Chemotherapy based on cisplatin or its combination therapy is a common cancer treatment method. However, the non-specific side effects of cisplatin, poor pharmacokinetic properties of small molecule drugs, and susceptibility to drug resistance greatly limit the clinical application of cisplatin as first-line anti-tumor drug. With the development of nanocarrier technology, liposomes have become an ideal carrier for delivering cisplatin drugs due to their excellent properties of targeting, reducing toxicity, and enhancing efficacy. This paper reviews the status of cisplatin liposome both domestically and internationally which have entered clinical trials, including L-NDDP,SPI-077
®
,
Lipoplatin
®
,LiPlaCis,SLIT and ILC, etc. Currently, only Lipoplatin
®
and ILC are showing good potential in cancer therapy. Although cisplatin liposome has made some progress in reducing systemic toxicity and improving treatment efficiency in clinical research, there is still potential for further improvement in tumor targeting and reducing side effects. In the future, more low-toxicity and efficient cisplatin liposomes can be developed through formulation technologies such as co-delivery liposome, stimuli-responsive liposome and targeting liposome.
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