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Radiolabeled Trastuzumab Solid Lipid Nanoparticles for Breast Cancer Cell: in Vitro and in Vivo Studies
[Image: see text] Radiolabeled trastuzumab (TRZ) loaded solid lipid nanoparticles (SLNs) were prepared by high shear homogenization and sonication techniques. The apoptosis mechanism of TRZ-SLNs was studied only with the MCF-7 cell line, while the cytotoxicity and cell binding capacity were investig...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9435033/ https://www.ncbi.nlm.nih.gov/pubmed/36061662 http://dx.doi.org/10.1021/acsomega.2c03023 |
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author | Ozgenc, Emre Karpuz, Merve Arzuk, Ege Gonzalez-Alvarez, Marta Sanz, Marival Bermejo Gundogdu, Evren Gonzalez-Alvarez, Isabel |
author_facet | Ozgenc, Emre Karpuz, Merve Arzuk, Ege Gonzalez-Alvarez, Marta Sanz, Marival Bermejo Gundogdu, Evren Gonzalez-Alvarez, Isabel |
author_sort | Ozgenc, Emre |
collection | PubMed |
description | [Image: see text] Radiolabeled trastuzumab (TRZ) loaded solid lipid nanoparticles (SLNs) were prepared by high shear homogenization and sonication techniques. The apoptosis mechanism of TRZ-SLNs was studied only with the MCF-7 cell line, while the cytotoxicity and cell binding capacity were investigated using breast cancer cells (MCF-7 and MDA-MB-231) and the human keratinocyte cell line (HaCaT). The particle sizes of TRZ-SLNs were found to be below 100 nm, and they possessed a negative charge. The high radiolabeling efficiency and good radiolabeling stability in saline and a cell culture medium were obtained in the results of radiolabeling studies. According to the in vitro studies, TRZ-SLNs were found to be biocompatible, and they effectively induced apoptosis in MCF-7 cells. After the parenteral injection of TRZ-SLNs into rats, a sustained release profile in blood circulation was achieved compared with free drug solution by the evaluation of pharmacokinetic parameters. As a conclusion, the study reveals that Technetium-99m ((99m)Tc radiolabeled) TRZ loaded SLN formulations could be promising theranostic agents based on their characterization profiles, in vitro cellular uptake and apoptosis induction capacity, and in vivo pharmacokinetic profiles. |
format | Online Article Text |
id | pubmed-9435033 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-94350332022-09-02 Radiolabeled Trastuzumab Solid Lipid Nanoparticles for Breast Cancer Cell: in Vitro and in Vivo Studies Ozgenc, Emre Karpuz, Merve Arzuk, Ege Gonzalez-Alvarez, Marta Sanz, Marival Bermejo Gundogdu, Evren Gonzalez-Alvarez, Isabel ACS Omega [Image: see text] Radiolabeled trastuzumab (TRZ) loaded solid lipid nanoparticles (SLNs) were prepared by high shear homogenization and sonication techniques. The apoptosis mechanism of TRZ-SLNs was studied only with the MCF-7 cell line, while the cytotoxicity and cell binding capacity were investigated using breast cancer cells (MCF-7 and MDA-MB-231) and the human keratinocyte cell line (HaCaT). The particle sizes of TRZ-SLNs were found to be below 100 nm, and they possessed a negative charge. The high radiolabeling efficiency and good radiolabeling stability in saline and a cell culture medium were obtained in the results of radiolabeling studies. According to the in vitro studies, TRZ-SLNs were found to be biocompatible, and they effectively induced apoptosis in MCF-7 cells. After the parenteral injection of TRZ-SLNs into rats, a sustained release profile in blood circulation was achieved compared with free drug solution by the evaluation of pharmacokinetic parameters. As a conclusion, the study reveals that Technetium-99m ((99m)Tc radiolabeled) TRZ loaded SLN formulations could be promising theranostic agents based on their characterization profiles, in vitro cellular uptake and apoptosis induction capacity, and in vivo pharmacokinetic profiles. American Chemical Society 2022-08-19 /pmc/articles/PMC9435033/ /pubmed/36061662 http://dx.doi.org/10.1021/acsomega.2c03023 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Ozgenc, Emre Karpuz, Merve Arzuk, Ege Gonzalez-Alvarez, Marta Sanz, Marival Bermejo Gundogdu, Evren Gonzalez-Alvarez, Isabel Radiolabeled Trastuzumab Solid Lipid Nanoparticles for Breast Cancer Cell: in Vitro and in Vivo Studies |
title | Radiolabeled Trastuzumab
Solid Lipid Nanoparticles
for Breast Cancer Cell: in Vitro and in Vivo Studies |
title_full | Radiolabeled Trastuzumab
Solid Lipid Nanoparticles
for Breast Cancer Cell: in Vitro and in Vivo Studies |
title_fullStr | Radiolabeled Trastuzumab
Solid Lipid Nanoparticles
for Breast Cancer Cell: in Vitro and in Vivo Studies |
title_full_unstemmed | Radiolabeled Trastuzumab
Solid Lipid Nanoparticles
for Breast Cancer Cell: in Vitro and in Vivo Studies |
title_short | Radiolabeled Trastuzumab
Solid Lipid Nanoparticles
for Breast Cancer Cell: in Vitro and in Vivo Studies |
title_sort | radiolabeled trastuzumab
solid lipid nanoparticles
for breast cancer cell: in vitro and in vivo studies |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9435033/ https://www.ncbi.nlm.nih.gov/pubmed/36061662 http://dx.doi.org/10.1021/acsomega.2c03023 |
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