Cargando…

Development of a Scalable Process of Film-Coated bi-Layer Tablet Containing Sustained-Release Metoprolol Succinate and Immediate-Release Amlodipine Besylate

The development of new drugs that combine active ingredients for the treatment hypertension is critically essential owing to its offering advantages for both patients and manufacturers. In this study, for the first time, detailed development of a scalable process of film-coated bi-layer tablets cont...

Descripción completa

Detalles Bibliográficos
Autores principales: Tuyen, Nguyen Thi Linh, Nghiem, Le Quan, Tuan, Nguyen Duc, Le, Phuoc Huu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8618854/
https://www.ncbi.nlm.nih.gov/pubmed/34834212
http://dx.doi.org/10.3390/pharmaceutics13111797
_version_ 1784604848105193472
author Tuyen, Nguyen Thi Linh
Nghiem, Le Quan
Tuan, Nguyen Duc
Le, Phuoc Huu
author_facet Tuyen, Nguyen Thi Linh
Nghiem, Le Quan
Tuan, Nguyen Duc
Le, Phuoc Huu
author_sort Tuyen, Nguyen Thi Linh
collection PubMed
description The development of new drugs that combine active ingredients for the treatment hypertension is critically essential owing to its offering advantages for both patients and manufacturers. In this study, for the first time, detailed development of a scalable process of film-coated bi-layer tablets containing sustained-release metoprolol succinate and immediate-release amlodipine besylate in a batch size of 10,000 tablets is reported. The processing parameters of the manufacturing process during dry mixing-, drying-, dry mixing- completion stages were systematically investigated, and the evaluation of the film-coated bi-layer tablet properties was well established. The optimal preparation conditions for metoprolol succinate layer were 6 min- dry mixing with a high-speed mixer (120 rpm and 1400 rpm), 30-min drying with a fluid bed dryer, and 5 min- mixing completion at 25 rpm. For the preparation of amlodipine besylate layer, the optimal dry-mixing time using a cube mixer (25 rpm) was found to be 5 min. The average weight of metoprolol succinate layers and bi-layer tablets were controlled at 240–260 mg and 384–416 mg, respectively. Shewhart R chart and [Formula: see text] charts of all three sampling lots were satisfactory, confirming that the present scalable process was stable and successful. This study confirms that the manufacturing process is reproducible, robust; and it yields a consistent product that meets specifications.
format Online
Article
Text
id pubmed-8618854
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-86188542021-11-27 Development of a Scalable Process of Film-Coated bi-Layer Tablet Containing Sustained-Release Metoprolol Succinate and Immediate-Release Amlodipine Besylate Tuyen, Nguyen Thi Linh Nghiem, Le Quan Tuan, Nguyen Duc Le, Phuoc Huu Pharmaceutics Article The development of new drugs that combine active ingredients for the treatment hypertension is critically essential owing to its offering advantages for both patients and manufacturers. In this study, for the first time, detailed development of a scalable process of film-coated bi-layer tablets containing sustained-release metoprolol succinate and immediate-release amlodipine besylate in a batch size of 10,000 tablets is reported. The processing parameters of the manufacturing process during dry mixing-, drying-, dry mixing- completion stages were systematically investigated, and the evaluation of the film-coated bi-layer tablet properties was well established. The optimal preparation conditions for metoprolol succinate layer were 6 min- dry mixing with a high-speed mixer (120 rpm and 1400 rpm), 30-min drying with a fluid bed dryer, and 5 min- mixing completion at 25 rpm. For the preparation of amlodipine besylate layer, the optimal dry-mixing time using a cube mixer (25 rpm) was found to be 5 min. The average weight of metoprolol succinate layers and bi-layer tablets were controlled at 240–260 mg and 384–416 mg, respectively. Shewhart R chart and [Formula: see text] charts of all three sampling lots were satisfactory, confirming that the present scalable process was stable and successful. This study confirms that the manufacturing process is reproducible, robust; and it yields a consistent product that meets specifications. MDPI 2021-10-27 /pmc/articles/PMC8618854/ /pubmed/34834212 http://dx.doi.org/10.3390/pharmaceutics13111797 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tuyen, Nguyen Thi Linh
Nghiem, Le Quan
Tuan, Nguyen Duc
Le, Phuoc Huu
Development of a Scalable Process of Film-Coated bi-Layer Tablet Containing Sustained-Release Metoprolol Succinate and Immediate-Release Amlodipine Besylate
title Development of a Scalable Process of Film-Coated bi-Layer Tablet Containing Sustained-Release Metoprolol Succinate and Immediate-Release Amlodipine Besylate
title_full Development of a Scalable Process of Film-Coated bi-Layer Tablet Containing Sustained-Release Metoprolol Succinate and Immediate-Release Amlodipine Besylate
title_fullStr Development of a Scalable Process of Film-Coated bi-Layer Tablet Containing Sustained-Release Metoprolol Succinate and Immediate-Release Amlodipine Besylate
title_full_unstemmed Development of a Scalable Process of Film-Coated bi-Layer Tablet Containing Sustained-Release Metoprolol Succinate and Immediate-Release Amlodipine Besylate
title_short Development of a Scalable Process of Film-Coated bi-Layer Tablet Containing Sustained-Release Metoprolol Succinate and Immediate-Release Amlodipine Besylate
title_sort development of a scalable process of film-coated bi-layer tablet containing sustained-release metoprolol succinate and immediate-release amlodipine besylate
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8618854/
https://www.ncbi.nlm.nih.gov/pubmed/34834212
http://dx.doi.org/10.3390/pharmaceutics13111797
work_keys_str_mv AT tuyennguyenthilinh developmentofascalableprocessoffilmcoatedbilayertabletcontainingsustainedreleasemetoprololsuccinateandimmediatereleaseamlodipinebesylate
AT nghiemlequan developmentofascalableprocessoffilmcoatedbilayertabletcontainingsustainedreleasemetoprololsuccinateandimmediatereleaseamlodipinebesylate
AT tuannguyenduc developmentofascalableprocessoffilmcoatedbilayertabletcontainingsustainedreleasemetoprololsuccinateandimmediatereleaseamlodipinebesylate
AT lephuochuu developmentofascalableprocessoffilmcoatedbilayertabletcontainingsustainedreleasemetoprololsuccinateandimmediatereleaseamlodipinebesylate