Acute toxicity and biodistribution assessment of quantum dots conjugated to lectins from Schinus terebinthifolia leaves (SteLL) and Punica granatum sarcotesta (PgTeL).
Raquel Cordeiro de Oliveira, Abdênego Rodrigues da Silva, Robson Raion de Vasconcelos Alves, Matheus Cavalcanti de Barros, Talita Giselly Dos Santos Souza, Alisson Macário de Oliveira, Leydianne Leite de Siqueira Patriota, Patrícia Maria Guedes Paiva, Fernanda das Chagas Ângelo Mendes Tenório, Paulo Euzébio Cabral Filho, Adriana Fontes, Thiago Henrique Napoleão, Mércia Liane de Oliveira, Elvis Joacir de França
{"title":"Acute toxicity and biodistribution assessment of quantum dots conjugated to lectins from <i>Schinus terebinthifolia</i> leaves (SteLL) and <i>Punica granatum</i> sarcotesta (PgTeL).","authors":"Raquel Cordeiro de Oliveira, Abdênego Rodrigues da Silva, Robson Raion de Vasconcelos Alves, Matheus Cavalcanti de Barros, Talita Giselly Dos Santos Souza, Alisson Macário de Oliveira, Leydianne Leite de Siqueira Patriota, Patrícia Maria Guedes Paiva, Fernanda das Chagas Ângelo Mendes Tenório, Paulo Euzébio Cabral Filho, Adriana Fontes, Thiago Henrique Napoleão, Mércia Liane de Oliveira, Elvis Joacir de França","doi":"10.1080/01480545.2024.2433074","DOIUrl":null,"url":null,"abstract":"<p><p>This work reports the <i>in vivo</i> investigation of telluride cadmium quantum dots (CdTe QDs) conjugated to plant lectins from <i>Schinus terebinthifolia</i> (SteLL) and <i>Punica granatum</i> (PgTeL) for acute toxicity and genotoxicity in healthy mice and 24-h biodistribution in sarcoma 180-bearing animals. Acute toxicity data indicated their safety, despite some histopathological alterations. Comet assay revealed that the QDs-PgTeL group presented a higher damage index and frequency of damage than the negative control. The micronucleus test did not reveal a genotoxic effect. The 24-h biodistribution study showed a major uptake of cadmium by the liver, spleen, and kidneys. A greater accumulation of cadmium was found in tumors of the QDs-SteLL group. In conclusion, the biodistribution study showed no influence of the studied lectins in the absorption of QDs by different organs and that the conjugation of SteLL resulted in increased targeting of QDs to sarcoma 180 cells, suggesting a potential theranostic application in cancer.</p>","PeriodicalId":11333,"journal":{"name":"Drug and Chemical Toxicology","volume":" ","pages":"1-11"},"PeriodicalIF":2.1000,"publicationDate":"2024-11-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Drug and Chemical Toxicology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/01480545.2024.2433074","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
This work reports the in vivo investigation of telluride cadmium quantum dots (CdTe QDs) conjugated to plant lectins from Schinus terebinthifolia (SteLL) and Punica granatum (PgTeL) for acute toxicity and genotoxicity in healthy mice and 24-h biodistribution in sarcoma 180-bearing animals. Acute toxicity data indicated their safety, despite some histopathological alterations. Comet assay revealed that the QDs-PgTeL group presented a higher damage index and frequency of damage than the negative control. The micronucleus test did not reveal a genotoxic effect. The 24-h biodistribution study showed a major uptake of cadmium by the liver, spleen, and kidneys. A greater accumulation of cadmium was found in tumors of the QDs-SteLL group. In conclusion, the biodistribution study showed no influence of the studied lectins in the absorption of QDs by different organs and that the conjugation of SteLL resulted in increased targeting of QDs to sarcoma 180 cells, suggesting a potential theranostic application in cancer.
期刊介绍:
Drug and Chemical Toxicology publishes full-length research papers, review articles and short communications that encompass a broad spectrum of toxicological data surrounding risk assessment and harmful exposure. Manuscripts are considered according to their relevance to the journal.
Topics include both descriptive and mechanics research that illustrates the risk assessment implications of exposure to toxic agents. Examples of suitable topics include toxicological studies, which are structural examinations on the effects of dose, metabolism, and statistical or mechanism-based approaches to risk assessment. New findings and methods, along with safety evaluations, are also acceptable. Special issues may be reserved to publish symposium summaries, reviews in toxicology, and overviews of the practical interpretation and application of toxicological data.