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CD123单克隆抗体修饰的丹参酮ⅡA负载免疫脂质体的制备及其体外评价

[Preparation of CD123 mono-antibody modified tanshinone ⅡA loaded immunoliposome and its in vitro evaluation].

作者信息

Wang Yin, Liu Fu-Rong, Xiang Hong-Lin, Qing Hong, Chen Chen, Mao Sheng-Jun, Li Hui

机构信息

Key Laboratory of Drug Targeting and Drug Delivery System, Ministry of Education, West China School of Pharmacy, Sichuan University, Chengdu 610041, China.

Departmnt of Hematology, Sichuan Provincial People Hospital & Sichuan Academy of Medical Sciences, Chengdu 610072, China.

出版信息

Zhongguo Zhong Yao Za Zhi. 2017 Jun;42(11):2085-2091. doi: 10.19540/j.cnki.cjcmm.20170428.002.

Abstract

In the study, we developed a novel formulation, CD123 mono-antibody (mAb) modified tanshinone ⅡA loaded immunoliposome (CD123-TanⅡA-ILP) to achieve the targeted drug delivery for leukemia cells. Orthogonal test was used to optimize liposome preparation, and the TanⅡA-loaded PEGylated liposomes (TanⅡA-LP) of S100PC-Chol-(mPEG2000-DSPE)-TanⅡA at 19∶5∶1∶1 molar ratio were prepared by the thin film hydration-probe ultrasonic method. A post-insertion method was applied to prepare CD123-TanⅡA-ILP via thiolated mAb conjugated to the terminal of maleimide-PEG2000-DSPE. The cellular uptake assay was measured by flow cytometry, and the inhibitory effect of CD123-TanⅡA-ILP on NB4 cells proliferation was tested by using MTT assay. The results of cellular uptake assay showed that CD123-ILP could significantly increase the drug uptake of NB4 cells as compared with free drugs and LP. The IC₅₀ values at 48 h incubation were 20.87, 11.71, 7.17 μmol•L⁻¹ respectively for TanⅡA,TanⅡA-LP and CD123-TanⅡA-ILP. CD123-ILP demonstrated a potential and promising targeted drug delivery strategy for acute myelogenous leukemia (AML) treatment.

摘要

在本研究中,我们开发了一种新型制剂,即CD123单克隆抗体(mAb)修饰的载丹参酮ⅡA免疫脂质体(CD123-TanⅡA-ILP),以实现白血病细胞的靶向给药。采用正交试验优化脂质体制备工艺,通过薄膜水化-探头超声法制备摩尔比为19∶5∶1∶1的S100PC-胆固醇-(mPEG2000-DSPE)-丹参酮ⅡA载药聚乙二醇化脂质体(TanⅡA-LP)。采用后插入法,通过将硫醇化单克隆抗体与马来酰亚胺-PEG2000-DSPE末端偶联来制备CD123-TanⅡA-ILP。通过流式细胞术测定细胞摄取情况,并使用MTT法检测CD123-TanⅡA-ILP对NB4细胞增殖的抑制作用。细胞摄取试验结果表明,与游离药物和LP相比,CD123-ILP可显著增加NB4细胞的药物摄取。孵育48小时时,丹参酮ⅡA、TanⅡA-LP和CD123-TanⅡA-ILP的IC₅₀值分别为20.87、11.71、7.17 μmol•L⁻¹。CD123-ILP为急性髓性白血病(AML)的治疗展示了一种有潜力且前景广阔的靶向给药策略。

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