Preparation and characterization of gadolinium-based thermosensitive liposomes: a potential nanosystem for selective drug delivery to cancer cells
| dc.creator | Ana Luiza Chaves Maia | |
| dc.creator | André Luís Branco de Barros | |
| dc.creator | Daniel Crístian Ferreira Soares | |
| dc.creator | Gilson Andrade Ramaldes | |
| dc.creator | Aline Teixeira Maciel e Silva | |
| dc.creator | Aina Liz Alves Cesar | |
| dc.creator | Fernanda Cristina Gontijo Evangelista | |
| dc.creator | Janaína de Alcântara Lemos | |
| dc.creator | Adriano de Paula Sabino | |
| dc.creator | Ângelo Malachias de Souza | |
| dc.creator | Christian Fernandes | |
| dc.creator | Cristiane dos Santos Giuberti | |
| dc.date.accessioned | 2023-04-26T17:16:04Z | |
| dc.date.accessioned | 2025-09-08T23:17:56Z | |
| dc.date.available | 2023-04-26T17:16:04Z | |
| dc.date.issued | 2021 | |
| dc.description.sponsorship | CNPq - Conselho Nacional de Desenvolvimento Científico e Tecnológico | |
| dc.description.sponsorship | FAPEMIG - Fundação de Amparo à Pesquisa do Estado de Minas Gerais | |
| dc.description.sponsorship | CAPES - Coordenação de Aperfeiçoamento de Pessoal de Nível Superior | |
| dc.identifier.doi | https://doi.org/10.1016/j.jddst.2021.102686 | |
| dc.identifier.issn | 2588-8943 | |
| dc.identifier.uri | https://hdl.handle.net/1843/52518 | |
| dc.language | eng | |
| dc.publisher | Universidade Federal de Minas Gerais | |
| dc.relation.ispartof | Journal of Drug Delivery Science and Technology | |
| dc.rights | Acesso Restrito | |
| dc.subject | Lipossomos | |
| dc.subject | Câncer | |
| dc.subject.other | Gadodiamide | |
| dc.subject.other | Thermosensitive liposomes | |
| dc.subject.other | Liposome characterization | |
| dc.subject.other | Drug delivery | |
| dc.subject.other | Cytotoxic activity | |
| dc.title | Preparation and characterization of gadolinium-based thermosensitive liposomes: a potential nanosystem for selective drug delivery to cancer cells | |
| dc.type | Artigo de periódico | |
| local.citation.epage | 15 | |
| local.citation.spage | 1 | |
| local.citation.volume | 65 | |
| local.description.resumo | Gadodiamide (Gd-DTPA-BMA) is a gadolinium-based complex, used as a contrast agent in magnetic resonance imaging procedures. Recent studies revealed the capacity of this complex of inducing apoptosis in neoplastic cells. However, a great challenge for its use as an anticancer drug is low cellular internalization and drug delivery systems such as thermosensitive liposomes can be a strategy to overcome these limitations and increase anti-tumor efficacy. In this context, this study aimed to develop, characterize, and assess the cytotoxic activity and selectivity index of thermosensitive liposomes containing Gd-DTPA-BMA. Formulations were prepared by the lipid film hydration method and their physicochemical, morphological, and thermal properties were evaluated. Cell viability was performed 4T1/MDA-MB-231 tumor cells and WI-26 VA4 normal cells. Transmission electron microscopy analyses showed high electron density in the inner core of Gd-DTPA-BMA-loaded liposomes that can be attributed to the Gd-DTPA-BMA, since Gd-loaded nanosystems present low light transmittance and high electron density by this technique. The dynamic light scattering, differential scanning calorimetry, small-angle X-ray scattering, and in vitro release results confirm that the lipid composition was suitable since Tc (temperature of the transition Lβ → Lα) values are in accordance with those reported for thermosensitive liposomes used in the treatment of cancer. The cytotoxic studies against breast cancer cell lines demonstrated that the Gd-DTPA-BMA-loaded liposomes have higher cytotoxicity than free Gd-DTPA-BMA. Moreover, these liposomes presented minimal toxicity in a normal cell line when compared to the free Gd-DTPA-BMA. Therefore, the results of this study suggest that thermosensitive liposomes containing Gd-DTPA-BMA might be a new promising nanocarrier system for breast cancer treatment. | |
| local.identifier.orcid | https://orcid.org/0000-0002-7641-6585 | |
| local.identifier.orcid | https://orcid.org/0000-0002-2204-6881 | |
| local.identifier.orcid | https://orcid.org/0000-0002-8067-1810 | |
| local.identifier.orcid | https://orcid.org/0000-0001-8458-0097 | |
| local.identifier.orcid | https://orcid.org/0000-0001-8562-8689 | |
| local.identifier.orcid | https://orcid.org/0000-0002-8703-4283 | |
| local.identifier.orcid | https://orcid.org/0000-0002-3905-3674 | |
| local.identifier.orcid | https://orcid.org/0000-0002-0560-8731 | |
| local.publisher.country | Brasil | |
| local.publisher.department | FAR - DEPARTAMENTO DE ANÁLISES CLÍNICAS E TOXICOLÓGICAS | |
| local.publisher.department | FAR - DEPARTAMENTO DE PRODUTOS FARMACÊUTICOS | |
| local.publisher.department | ICX - DEPARTAMENTO DE FÍSICA | |
| local.publisher.initials | UFMG | |
| local.url.externa | https://www.sciencedirect.com/science/article/pii/S177322472100366X |
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