Polymer coated iron nanoparticles: Radiolabeling & in vitro studies
| Autor: | Çiğdem İçhedef, Selin Yilmaz, Serap Teksöz, Kadriye Busra Karatay |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2021 |
| Předmět: |
Antimetabolites
Antineoplastic Cell Survival Polymers Magnetic drug delivery Nanoparticle In Vitro Techniques Deoxycytidine Polymeric nanoparticles chemistry.chemical_compound Drug Delivery Systems Dynamic light scattering In vitro Cell Line Tumor Zeta potential Humans Radiology Nuclear Medicine and imaging 99mTc Pharmacology Technetium Gemcitabine Tc-99m PLGA chemistry Targeted drug delivery Drug delivery Magnetic Iron Oxide Nanoparticles Radiopharmaceuticals Iron oxide nanoparticles Superparamagnetism Nuclear chemistry Radiolabeling |
| Popis: | Background: Superparamagnetic iron oxide nanoparticles (SPIONs) have been extensively used for targeted drug delivery systems due to their unique magnetic properties. Objective: In this study, it has been aimed to develop a novel targeted Tc-99m radiolabeled polymeric drug delivery system for Gemcitabine (GEM). Methods: Gemcitabine, an anticancer agent, was encapsulated into polymer nanoparticles (PLGA) together with iron oxide nanoparticles via double emulsion technique and then labeled with Tc-99m. SPIONs were synthesized by reduction-coprecipitation method and encapsulated with oleic acid for surface modification. Size distribution and the morphology of the synthesized nanoparticles were characterized by dynamic light scattering (DLS) and scanning electron microscopy (SEM), respectively. The radiolabeling yield of SPION-PLGAGEM nanoparticles was determined via Thin Layer Radio Chromatography (TLRC). Cytotoxicity of GEM loaded SPION-PLGA was investigated on MDA-MB-231 and MCF7 breast cancer cells in vitro. Results: SEM images displayed that the average size of the drug-free nanoparticles was 40 nm and the size of the drug-loaded nanoparticles was 50 nm. The diameter of nanoparticles was deter- mined as 366.6 nm by DLS, while zeta potential was found as 29 mV. SPION was successfully coated with PLGA, which was confirmed by FTIR. GEM encapsulation efficiency of SPION-PLGA was calculated as 4 +/- 0.16% by means of HPLC. Radiolabeling yield of SPION-PLGA-GEM nanoparticles was determined as 97.8 +/- 1.75% via TLRC. Cytotoxicity of GEM loaded SPION-PLGA was investigated on MDA-MB-231 and MCF7 breast cancer cells. SPION-PLGA-GEM showed high uptake on MCF-7, while the incorporation rate was increased for both cell lines with external magnetic field application. Conclusion: Tc-99m labeled SPION-PLGA nanoparticles loaded with GEM may overcome some of the obstacles in anti-cancer drug delivery because of their appropriate size, non-toxic, and super-paramagnetic characteristics Celal Bayar University Scientific Research Projects Coordination Unit [2017-001] Celal Bayar University Scientific Research Projects Coordination Unit (Grant Number: 2017-001). |
| Databáze: | OpenAIRE |
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