Zare Mirakabadi Abbas, Moradhaseli Saeed
Dept. of Venomous Animals and Antivenom Production, Razi Vaccine and Serum Research Institute, Karaj, Iran.
Dept. of Venomous Animals and Antivenom Production, Razi Vaccine and Serum Research Institute, Karaj, Iran ; Dept. of Biochemistry, Faculty of Basic Sciences, Payame Noor University, Tehran, Iran.
Iran J Cancer Prev. 2013 Summer;6(3):151-9.
Current anti-cancer drug therapy results in systemic side effects due to non-specific uptake by normal healthy noncancerous tissues. To alleviate this difficulty, many attempts have been devoted to the development of new delivery systems such as polymeric Nanoparticles (NPs). In this study, we prepared ICD-85 NPs based on sodium alginate and analyzed the cytotoxic activity of ICD-85 NPs relative to free ICD-85 on primary lamb kidney cells.
ICD-85 loaded sodium alginate nanoparticles were prepared by ionic gelation method and were characterized by the particle size, size distribution and Fourier Transform Infrared (FT-IR) spectroscopy. The in vitro cytotoxicity was evaluated by MTT assay and membrane integrity was evaluated by measuring Lactate Dehydrogenase (LDH) activity. The morphological alterations of untreated and treated cells were assessed by light inverted microscope.
MTT assay showed that ICD-85 NPs could significantly decrease the in vitro cytotoxicity on primary lamb kidney cells compared to the free ICD-85. The IC10 value at 72 hours was increased from 9±2.7 μg/ml for free ICD-85 to 52±4.3 μg/ml for ICD-85 NPs. LDH assay demonstrated that free ICD-85 had dose-dependent cytotoxicity on primary lamb kidney cells while ICD-85 NPs exhibited significantly decreased cytotoxicity at equivalent concentrations. Moreover, morphological analysis showed no significant difference between control and treated cells with ICD-85 NPs.
Based on the results obtained in the present study it can be concluded that encapsulation of ICD-85 with sodium alginate nanoparticles can reduce its necrotic effect on primary lamb kidney cells.
当前的抗癌药物疗法会导致全身副作用,因为正常健康的非癌组织会非特异性摄取药物。为了缓解这一难题,人们致力于开发新型递送系统,如聚合物纳米颗粒(NPs)。在本研究中,我们制备了基于海藻酸钠的ICD - 85纳米颗粒,并分析了ICD - 85纳米颗粒相对于游离ICD - 85对原代羔羊肾细胞的细胞毒性活性。
通过离子凝胶法制备负载ICD - 85的海藻酸钠纳米颗粒,并通过粒径、粒径分布和傅里叶变换红外(FT - IR)光谱对其进行表征。通过MTT法评估体外细胞毒性,并通过测量乳酸脱氢酶(LDH)活性评估膜完整性。通过倒置光学显微镜评估未处理和处理细胞的形态变化。
MTT法显示,与游离ICD - 85相比,ICD - 85纳米颗粒可显著降低对原代羔羊肾细胞的体外细胞毒性。72小时时的IC10值从游离ICD - 85的9±2.7μg/ml增加到ICD - 85纳米颗粒的52±4.3μg/ml。LDH测定表明,游离ICD - 85对原代羔羊肾细胞具有剂量依赖性细胞毒性,而ICD - 85纳米颗粒在等效浓度下表现出显著降低的细胞毒性。此外,形态学分析显示,用ICD - 85纳米颗粒处理的细胞与对照细胞之间无显著差异。
基于本研究获得的结果,可以得出结论,用海藻酸钠纳米颗粒包裹ICD - 85可降低其对原代羔羊肾细胞的坏死作用。