Construction of 131I-RGDyC-PEG-PAMAM-DTX targeted drug delivery system and study of its physicochemical properties and biological activity.

IF 0.9 4区 医学 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Hellenic journal of nuclear medicine Pub Date : 2023-05-01 Epub Date: 2023-08-04 DOI:10.1967/s002449912574
Qianqian Chen, Jinhe Zhang, Mutu Huang, Peiqi Wang, Xiao Zhang, Mingjun Ma
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Abstract

Objective: To construct a novel targeted drug delivery nanoprobe: iodine-131-arginine-glycine-aspartate-tyrosine-cysteine peptide-polyethylene glycol-fifth generation polyamide-amine-docetaxel (131I-RGDyC-PEG-PAMAM-DTX) and to investigate its physicochemical properties and biological activity.

Materials and methods: Docetaxel was wrapped by solvent volatilization method, and the regression curve of DTX was constructed by high-performance liquid chromatography to determine its drug loading. The particle size of RGDyC-PEG-PAMAM-DTX was detected by dynamic light scattering. The 131I labeling was performed by a chloramine-T method and purified by Sephadex-G50 column chromatography, and it is in vitro stability and lipid-water partition coefficient was investigated. The cytotoxicity of RGDyC-PEG-PAMAM-DTX and 131I-RGDyC-PEG-PAMAM-DTX on A549 cells in vitro was detected by Cell Counting Kit-8 assay.

Results: Arginine-glycine-aspartate-tyrosine-cysteine peptide-PEG-PAMAM-DTX was successfully prepared by solvent volatilization with a loading capacity of about 44μg/mg. The average particle size of RGDyC-PEG-PAMAM-DTX was 57.8nm; the labeling rate of 131I-RGDyC-PEG-PAMAM-DTX by the chloramine-T method was 74.09%-76.09%, and the radiochemical purity was 88.9%-92.6% after purification. The in vitro stability showed that the radiochemical purity was above 80% after 72h in fetal bovine serum and PBS buffer (25oC and 37oC).CCK-8 assay showed that RGDyC-PEG-PAMAM-DTX and 131I-RGDyC-PEG-PAMAM-DTX had more pronounced cytotoxic effects than free DTX and 131I.

Conclusion: Iodine-131-RGDyC-PEG-PAMAM-DTX has good physicochemical properties and apparent cytotoxic effectsandis expected to be used in treating tumors.

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131I-RGDyC-PEG-PAMAM-DTX靶向给药系统的构建及其理化性质和生物活性的研究。
目的:构建一种新型靶向给药纳米探针:碘-131-精氨酸-甘氨酸-酪氨酸-半胱氨酸肽聚乙二醇第五代聚酰胺-胺-多西他赛(131I-RGDyC-PEG-PAMAM-DTX),并研究其理化性质和生物活性。材料与方法:采用溶剂挥发法包裹多西他赛,采用高效液相色谱法构建DTX的回归曲线,测定其载药量。用动态光散射法测定了RGDyC-PEG-PAMAM-DTX的粒径。131I标记采用氯胺-T法,Sephadex-G50柱层析纯化,并考察了其体外稳定性和脂水分配系数。用细胞计数试剂盒-8检测RGDyC-PEG-PAMAM-DTX和131I-RGDyC-PEG PAMAM-DTX对A549细胞的细胞毒性。结果:采用溶剂挥发法制备了精氨酸-甘氨酸-天冬氨酸-酪氨酸半胱氨酸肽PEG-PAMAM-DTX,其负载量约为44μg/mg。RGDyC-PEG-PAMAM-DTX的平均粒径为57.8nm;氯胺-T法对131I-RGDyC-PEG-PAMAM-DTX的标记率为74.09%-76.09%,纯化后的放射化学纯度为88.9%-92.6%。体外稳定性表明,在胎牛血清和PBS缓冲液(25℃和37℃)中72小时后,放射化学纯度达到80%以上用于治疗肿瘤。
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来源期刊
CiteScore
1.40
自引率
6.70%
发文量
34
审稿时长
>12 weeks
期刊介绍: The Hellenic Journal of Nuclear Medicine published by the Hellenic Society of Nuclear Medicine in Thessaloniki, aims to contribute to research, to education and cover the scientific and professional interests of physicians, in the field of nuclear medicine and in medicine in general. The journal may publish papers of nuclear medicine and also papers that refer to related subjects as dosimetry, computer science, targeting of gene expression, radioimmunoassay, radiation protection, biology, cell trafficking, related historical brief reviews and other related subjects. Original papers are preferred. The journal may after special agreement publish supplements covering important subjects, dully reviewed and subscripted separately.
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