Gadolinium labelled nanoliposomes as the platform for MRI theranostics: in vitro safety study in liver cells and macrophages.
Pavlína ŠimečkováFrantišek HubatkaJan KotoučekPavlína Turánek KnötigováJosef MašekJosef SlavíkOndrej KováčJiří NečaPavel KulichDominik HrebíkJana StráskáKateřina PěnčíkováJiřina ProcházkováPavel DivišStuart MacaulayRobert MikulíkMilan RaskaMiroslav MachalaJaroslav TuránekPublished in: Scientific reports (2020)
Gadolinium (Gd)-based contrast agents are extensively used for magnetic resonance imaging (MRI). Liposomes are potential nanocarrier-based biocompatible platforms for development of new generations of MRI diagnostics. Liposomes with Gd-complexes (Gd-lip) co-encapsulated with thrombolytic agents can serve both for imaging and treatment of various pathological states including stroke. In this study, we evaluated nanosafety of Gd-lip containing PE-DTPA chelating Gd+3 prepared by lipid film hydration method. We detected no cytotoxicity of Gd-lip in human liver cells including cancer HepG2, progenitor (non-differentiated) HepaRG, and differentiated HepaRG cells. Furthermore, no potential side effects of Gd-lip were found using a complex system including general biomarkers of toxicity, such as induction of early response genes, oxidative, heat shock and endoplasmic reticulum stress, DNA damage responses, induction of xenobiotic metabolizing enzymes, and changes in sphingolipid metabolism in differentiated HepaRG. Moreover, Gd-lip did not show pro-inflammatory effects, as assessed in an assay based on activation of inflammasome NLRP3 in a model of human macrophages, and release of eicosanoids from HepaRG cells. In conclusion, this in vitro study indicates potential in vivo safety of Gd-lip with respect to hepatotoxicity and immunopathology caused by inflammation.
Keyphrases
- induced apoptosis
- endoplasmic reticulum stress
- magnetic resonance imaging
- contrast enhanced
- oxidative stress
- cell cycle arrest
- dna damage
- drug delivery
- signaling pathway
- computed tomography
- endothelial cells
- magnetic resonance
- high throughput
- transcription factor
- pulmonary embolism
- gene expression
- risk assessment
- ionic liquid
- acute ischemic stroke
- heat stress
- single cell
- combination therapy
- reduced graphene oxide
- cell fate