Correction: Novel cisplatin-magnetoliposome complex shows enhanced antitumor activity via Hyperthermia

The original version of this Article contained an error in Fig. 6, where during figure assembly, the wrong microphotograph was uploaded for the observation under the ML group (liposome + nanoparticles) in kidney tissue.The original Fig. 6 and its accompanying legend appear below.Fig. 6.Analysis of in vivo toxicity of MLs.Representative microphotographs of the histopathological lesions induced in the in vivo toxicity analysis in mice.We observed in the MLC group (liposome+nanoparticles+CDDP) scant acute tubular necrosis, and mild tubular dilation and nuclear dysplasia (arrow) in kidney; diffuse macrovacuolar steatosis (arrows), and moderate chronic inflammatory infiltrate (asterisk) in liver; no injury was detected in lung.In the ML-treated mice (liposome+magnetic nanoparticles) no tissue damage was detected, except a scant intraparenchymal inflammatory infiltrate in liver (asterisk) in some mice.Animals received weekly injections i.p. and 5 mice per group were analyzed at day 35.Hematoxylin-eosin, original magnification 10x.Bar scale: 100 micrometers.

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Publication Details

Journal
Scientific Reports
Published
2026-03-23
DOI
https://doi.org/10.1038/s41598-026-43134-2
Primary Topic
Nanoparticle-Based Drug Delivery
Type
article
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article

Correction: Novel cisplatin-magnetoliposome complex shows enhanced antitumor activity via Hyperthermia

Scientific Reports
Nanoparticle-Based Drug Delivery
article

Correction: Novel cisplatin-magnetoliposome complex shows enhanced antitumor activity via Hyperthermia

article en

Abstract

The original version of this Article contained an error in Fig. 6, where during figure assembly, the wrong microphotograph was uploaded for the observation under the ML group (liposome + nanoparticles) in kidney tissue.The original Fig. 6 and its accompanying legend appear below.Fig. 6.Analysis of in vivo toxicity of MLs.Representative microphotographs of the histopathological lesions induced in the in vivo toxicity analysis in mice.We observed in the MLC group (liposome+nanoparticles+CDDP) scant acute tubular necrosis, and mild tubular dilation and nuclear dysplasia (arrow) in kidney; diffuse macrovacuolar steatosis (arrows), and moderate chronic inflammatory infiltrate (asterisk) in liver; no injury was detected in lung.In the ML-treated mice (liposome+magnetic nanoparticles) no tissue damage was detected, except a scant intraparenchymal inflammatory infiltrate in liver (asterisk) in some mice.Animals received weekly injections i.p. and 5 mice per group were analyzed at day 35.Hematoxylin-eosin, original magnification 10x.Bar scale: 100 micrometers.

Scientific ReportsVol. 16(1)
Universidad de Granada (ES), Instituto de Investigación Biosanitaria de Granada (ES), Instituto de Nanociencia y Materiales de Aragón (ES)
Zero hunger
Openalex Percentile: Top 8%
Nanoparticle-Based Drug Delivery
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