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Personalised 3D Printed Fast-Dissolving Tablets for Managing Hypertensive Crisis: In-Vitro/In-Vivo Studies

Hypertensive crisis (HC) is an emergency health condition which requires an effective management strategy. Over the years, various researchers have developed captopril based fast-dissolving formulations to manage HC; however, primarily, the question of personalisation remains unaddressed. Moreover,...

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Autores principales: Hussain, Amjad, Mahmood, Faisal, Arshad, Muhammad Sohail, Abbas, Nasir, Qamar, Nadia, Mudassir, Jahanzeb, Farhaj, Samia, Nirwan, Jorabar Singh, Ghori, Muhammad Usman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7765967/
https://www.ncbi.nlm.nih.gov/pubmed/33419348
http://dx.doi.org/10.3390/polym12123057
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author Hussain, Amjad
Mahmood, Faisal
Arshad, Muhammad Sohail
Abbas, Nasir
Qamar, Nadia
Mudassir, Jahanzeb
Farhaj, Samia
Nirwan, Jorabar Singh
Ghori, Muhammad Usman
author_facet Hussain, Amjad
Mahmood, Faisal
Arshad, Muhammad Sohail
Abbas, Nasir
Qamar, Nadia
Mudassir, Jahanzeb
Farhaj, Samia
Nirwan, Jorabar Singh
Ghori, Muhammad Usman
author_sort Hussain, Amjad
collection PubMed
description Hypertensive crisis (HC) is an emergency health condition which requires an effective management strategy. Over the years, various researchers have developed captopril based fast-dissolving formulations to manage HC; however, primarily, the question of personalisation remains unaddressed. Moreover, commercially these formulations are available as in fixed-dose combinations or strengths, so the titration of dose according to patient’s prerequisite is challenging to achieve. The recent emergence of 3D printing technologies has given pharmaceutical scientists a way forward to develop personalised medicines keeping in view patients individual needs. The current project, therefore, is aimed at addressing the limitations as mentioned above by developing fast-dissolving captopril tablets using 3D printing approach. Captopril unloaded (F1) and loaded (F2-F4) filaments were successfully produced with an acceptable drug loading and mechanical properties. Various captopril formulations (F2–F4) were successfully printed using fused deposition modelling technique. The results revealed that the formulations (F2 and F3) containing superdisintegrant had a faster extent of dissolution and in-vivo findings were endorsing these results. The present study has successfully exhibited the utilisation of additive manufacturing approach to mend the gap of personalisation and manufacturing fast-dissolving captopril 3D printed tablets. The procedure adopted in the present study may be used for the development of fused deposition modelling (FDM) based fast-dissolving 3D printed tablets.
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spelling pubmed-77659672020-12-28 Personalised 3D Printed Fast-Dissolving Tablets for Managing Hypertensive Crisis: In-Vitro/In-Vivo Studies Hussain, Amjad Mahmood, Faisal Arshad, Muhammad Sohail Abbas, Nasir Qamar, Nadia Mudassir, Jahanzeb Farhaj, Samia Nirwan, Jorabar Singh Ghori, Muhammad Usman Polymers (Basel) Article Hypertensive crisis (HC) is an emergency health condition which requires an effective management strategy. Over the years, various researchers have developed captopril based fast-dissolving formulations to manage HC; however, primarily, the question of personalisation remains unaddressed. Moreover, commercially these formulations are available as in fixed-dose combinations or strengths, so the titration of dose according to patient’s prerequisite is challenging to achieve. The recent emergence of 3D printing technologies has given pharmaceutical scientists a way forward to develop personalised medicines keeping in view patients individual needs. The current project, therefore, is aimed at addressing the limitations as mentioned above by developing fast-dissolving captopril tablets using 3D printing approach. Captopril unloaded (F1) and loaded (F2-F4) filaments were successfully produced with an acceptable drug loading and mechanical properties. Various captopril formulations (F2–F4) were successfully printed using fused deposition modelling technique. The results revealed that the formulations (F2 and F3) containing superdisintegrant had a faster extent of dissolution and in-vivo findings were endorsing these results. The present study has successfully exhibited the utilisation of additive manufacturing approach to mend the gap of personalisation and manufacturing fast-dissolving captopril 3D printed tablets. The procedure adopted in the present study may be used for the development of fused deposition modelling (FDM) based fast-dissolving 3D printed tablets. MDPI 2020-12-20 /pmc/articles/PMC7765967/ /pubmed/33419348 http://dx.doi.org/10.3390/polym12123057 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hussain, Amjad
Mahmood, Faisal
Arshad, Muhammad Sohail
Abbas, Nasir
Qamar, Nadia
Mudassir, Jahanzeb
Farhaj, Samia
Nirwan, Jorabar Singh
Ghori, Muhammad Usman
Personalised 3D Printed Fast-Dissolving Tablets for Managing Hypertensive Crisis: In-Vitro/In-Vivo Studies
title Personalised 3D Printed Fast-Dissolving Tablets for Managing Hypertensive Crisis: In-Vitro/In-Vivo Studies
title_full Personalised 3D Printed Fast-Dissolving Tablets for Managing Hypertensive Crisis: In-Vitro/In-Vivo Studies
title_fullStr Personalised 3D Printed Fast-Dissolving Tablets for Managing Hypertensive Crisis: In-Vitro/In-Vivo Studies
title_full_unstemmed Personalised 3D Printed Fast-Dissolving Tablets for Managing Hypertensive Crisis: In-Vitro/In-Vivo Studies
title_short Personalised 3D Printed Fast-Dissolving Tablets for Managing Hypertensive Crisis: In-Vitro/In-Vivo Studies
title_sort personalised 3d printed fast-dissolving tablets for managing hypertensive crisis: in-vitro/in-vivo studies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7765967/
https://www.ncbi.nlm.nih.gov/pubmed/33419348
http://dx.doi.org/10.3390/polym12123057
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