Smart bomb AS1411 aptamer-functionalized/PAMAM dendrimer nanocarriers for targeted drug delivery in the treatment of gastric cancer

被引:41
|
作者
Behrooz, Amir Barzegar [1 ]
Nabavizadeh, Fatemeh [1 ]
Adiban, Jamal [2 ]
Ardestani, Mehdi Shafiee [3 ]
Vahabpour, Rouhollah [4 ]
Aghasadeghi, Mohammad Reza [5 ]
Sohanaki, Hamid [1 ]
机构
[1] Univ Tehran Med Sci, Sch Med, Dept Physiol, Tehran, Iran
[2] Shahid Beheshti Univ Med Sci, Dept Med, Biomed Engn & Med Phys, Fac Med, Tehran, Iran
[3] Univ Tehran Med Sci, Dept Radiopharm, Fac Pharm, Tehran, Iran
[4] Shahid Beheshti Univ Med Sci, Sch Allied Med Sci, Med Lab, Dept Technol, Tehran, Iran
[5] Pasteur Inst Iran, Dept Hepatitis & AIDS, Tehran, Iran
来源
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY | 2017年 / 44卷 / 01期
关键词
5-fluorouracil; aptamer; drug delivery; nucleolin; PAMAM; RISK-FACTORS; NANOPARTICLES; THERAPY; PAMAM; 5-FLUOROURACIL; EPIDEMIOLOGY; NUCLEOLIN; CARRIER;
D O I
10.1111/1440-1681.12670
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Chemotherapy, a conventional method assessed in recent oncology studies, poses numerous problems in the clinical environment. To overcome the problems inherent in chemotherapy, an intelligent drug delivery system has come to the forefront of cancer therapeutics. In this study, we designed a dendrimer-based pharmaceutical system together with a single-stranded AS1411 aptamer (APT(AS1411)) as a therapeutic strategy. The polyamidoamine (PAMAM)-polyethylene glycol (PEG) complex was then conjugated with the AS1411 aptamer and confirmed by atomic-force microscopy (AFM) and Fourier transform infrared spectroscopy (FTIR) .In this study, we show that the conjugated PAMAM-PEG-APT(AS1411)complex dramatically increased PAMAM-PEG-5-FU uptake by MKN45 gastric cancer cells. We also demonstrated both the stability of the nanoparticle-5-FU-APT(AS1411) complex, by thin layer chromatography (TLC), and an increase in 5-fluorouracil (5-FU) accumulation in the vicinity of cancerous tumors. This smart drug delivery system is capable of effectively transferring 5-FU to MKN45 gastric cancer cells in consistent and without toxic effects.
引用
收藏
页码:41 / 51
页数:11
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