Wang Yin, Liu Fu-Rong, Xiang Hong-Lin, Qing Hong, Chen Chen, Mao Sheng-Jun, Li Hui
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.
Zhongguo Zhong Yao Za Zhi. 2017 Jun;42(11):2085-2091. doi: 10.19540/j.cnki.cjcmm.20170428.002.
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.
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。