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In situ drug release measuring in α-TCP cement by electrochemical impedance spectroscopy
The use of drug delivery systems is a good technique to leave the right quantity of medicine in the patient’s body in a suitable dose, because the drug application is delivered directly to the affected region. The current techniques such as HPLC and UV–Vis for the drug delivery calculation has some...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8016803/ https://www.ncbi.nlm.nih.gov/pubmed/33792786 http://dx.doi.org/10.1007/s10856-021-06507-9 |
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author | Pasqual, Júnio Augusto Rodrigues Freisleben, Lucas C. Colpo, Júlio Cesar Egea, Jose Ramón Jurado dos Santos, Luis Alberto Loureiro de Sousa, Vânia Caldas |
author_facet | Pasqual, Júnio Augusto Rodrigues Freisleben, Lucas C. Colpo, Júlio Cesar Egea, Jose Ramón Jurado dos Santos, Luis Alberto Loureiro de Sousa, Vânia Caldas |
author_sort | Pasqual, Júnio Augusto Rodrigues |
collection | PubMed |
description | The use of drug delivery systems is a good technique to leave the right quantity of medicine in the patient’s body in a suitable dose, because the drug application is delivered directly to the affected region. The current techniques such as HPLC and UV–Vis for the drug delivery calculation has some disadvantages, as the accuracy and the loss of the sample after characterization. With the aim of reducing the amount of material used during the characterization and have a non-destructive test with instantaneous results, the present paper shows the possibility of using electrochemical impedance spectroscopy (EIS) to have a drug delivery measurement during the release phenomena for a calcium phosphate cement (CFC) delivery system with gentamicin sulfate (GS) and lidocaine hydrochloride (LH), at a ratio of 1% and 2%, respectively. The equivalent circuit and the chemical mechanism involved during the measurements have been proposed as a tool to determine the drug delivery profile. The method has been compared with the UV–Vis technique. XRD was realized to verify conditions, before and after release. It was possible to verify the potential for using EIS as an instant technique to quantify drug delivery. [Image: see text] |
format | Online Article Text |
id | pubmed-8016803 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-80168032021-04-16 In situ drug release measuring in α-TCP cement by electrochemical impedance spectroscopy Pasqual, Júnio Augusto Rodrigues Freisleben, Lucas C. Colpo, Júlio Cesar Egea, Jose Ramón Jurado dos Santos, Luis Alberto Loureiro de Sousa, Vânia Caldas J Mater Sci Mater Med Delivery Systems The use of drug delivery systems is a good technique to leave the right quantity of medicine in the patient’s body in a suitable dose, because the drug application is delivered directly to the affected region. The current techniques such as HPLC and UV–Vis for the drug delivery calculation has some disadvantages, as the accuracy and the loss of the sample after characterization. With the aim of reducing the amount of material used during the characterization and have a non-destructive test with instantaneous results, the present paper shows the possibility of using electrochemical impedance spectroscopy (EIS) to have a drug delivery measurement during the release phenomena for a calcium phosphate cement (CFC) delivery system with gentamicin sulfate (GS) and lidocaine hydrochloride (LH), at a ratio of 1% and 2%, respectively. The equivalent circuit and the chemical mechanism involved during the measurements have been proposed as a tool to determine the drug delivery profile. The method has been compared with the UV–Vis technique. XRD was realized to verify conditions, before and after release. It was possible to verify the potential for using EIS as an instant technique to quantify drug delivery. [Image: see text] Springer US 2021-04-01 2021 /pmc/articles/PMC8016803/ /pubmed/33792786 http://dx.doi.org/10.1007/s10856-021-06507-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Delivery Systems Pasqual, Júnio Augusto Rodrigues Freisleben, Lucas C. Colpo, Júlio Cesar Egea, Jose Ramón Jurado dos Santos, Luis Alberto Loureiro de Sousa, Vânia Caldas In situ drug release measuring in α-TCP cement by electrochemical impedance spectroscopy |
title | In situ drug release measuring in α-TCP cement by electrochemical impedance spectroscopy |
title_full | In situ drug release measuring in α-TCP cement by electrochemical impedance spectroscopy |
title_fullStr | In situ drug release measuring in α-TCP cement by electrochemical impedance spectroscopy |
title_full_unstemmed | In situ drug release measuring in α-TCP cement by electrochemical impedance spectroscopy |
title_short | In situ drug release measuring in α-TCP cement by electrochemical impedance spectroscopy |
title_sort | in situ drug release measuring in α-tcp cement by electrochemical impedance spectroscopy |
topic | Delivery Systems |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8016803/ https://www.ncbi.nlm.nih.gov/pubmed/33792786 http://dx.doi.org/10.1007/s10856-021-06507-9 |
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