Real-time monitoring of pharmaceutical properties of medical tablets during direct tableting process by hybrid tableting process parameter-time profiles.


Journal

Bio-medical materials and engineering
ISSN: 1878-3619
Titre abrégé: Biomed Mater Eng
Pays: Netherlands
ID NLM: 9104021

Informations de publication

Date de publication:
2020
Historique:
pubmed: 28 11 2019
medline: 28 11 2020
entrez: 28 11 2019
Statut: ppublish

Résumé

Real-time monitoring is required for the pharmaceutical manufacturing process to produce high-quality pharmaceutical products. Changes in the critical tableting process parameters of single-punch tableting machine due to variability in the moisture content of the raw powders were monitored by hybrid tableting pressure-time profiles. After mixing of the raw powders, which consisted of theophylline, anhydrous lactose, potato starch and crystalline cellulose, they were stored at 0%, 45%, or 75% relative humidity (RH) for 24 h, respectively. Continuous tablet productions were carried out using the mixed powder samples at 10%, 45%, or 75% RH, respectively. The critical process parameters, such as upper and lower puncture pressures, die wall pressures, and inter-punch distances were recoded with the tableting machine, and then, tablet hardness (H), weight (W) and disintegration time (DT) of the tablets were measured. Hybrid tableting pressure-time profiles were obtained from various critical process parameters, and calibration models to predict pharmaceutical properties were calculated based on the hybrid profiles using a partial-least-squares regression (PLSR) method. In addition, the consistency of the calibration models were verified by constructing robust calibration models. Informetrical analysis for tablets based on hybrid tableting pressure-time profiles could evaluate the change of tablet properties dependent on the moisture content in the raw powders during the tableting process. The changes of tableting properties and elasticity were caused by agglomeration of powder particles at moisture content.

Sections du résumé

BACKGROUND BACKGROUND
Real-time monitoring is required for the pharmaceutical manufacturing process to produce high-quality pharmaceutical products.
OBJECTIVE OBJECTIVE
Changes in the critical tableting process parameters of single-punch tableting machine due to variability in the moisture content of the raw powders were monitored by hybrid tableting pressure-time profiles.
METHODS METHODS
After mixing of the raw powders, which consisted of theophylline, anhydrous lactose, potato starch and crystalline cellulose, they were stored at 0%, 45%, or 75% relative humidity (RH) for 24 h, respectively. Continuous tablet productions were carried out using the mixed powder samples at 10%, 45%, or 75% RH, respectively. The critical process parameters, such as upper and lower puncture pressures, die wall pressures, and inter-punch distances were recoded with the tableting machine, and then, tablet hardness (H), weight (W) and disintegration time (DT) of the tablets were measured.
RESULTS RESULTS
Hybrid tableting pressure-time profiles were obtained from various critical process parameters, and calibration models to predict pharmaceutical properties were calculated based on the hybrid profiles using a partial-least-squares regression (PLSR) method. In addition, the consistency of the calibration models were verified by constructing robust calibration models.
CONCLUSION CONCLUSIONS
Informetrical analysis for tablets based on hybrid tableting pressure-time profiles could evaluate the change of tablet properties dependent on the moisture content in the raw powders during the tableting process. The changes of tableting properties and elasticity were caused by agglomeration of powder particles at moisture content.

Identifiants

pubmed: 31771033
pii: BME191071
doi: 10.3233/BME-191071
doi:

Substances chimiques

Powders 0
Tablets 0
Cellulose 9004-34-6
Starch 9005-25-8
Theophylline C137DTR5RG

Types de publication

Evaluation Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

509-524

Auteurs

Shuji Saito (S)

Graduate School of Pharmaceutical Sciences, Musashino University, Nishi-Tokyo, Tokyo, Japan.

Yusuke Hattori (Y)

Graduate School of Pharmaceutical Sciences, Musashino University, Nishi-Tokyo, Tokyo, Japan.

Tomoaki Sakamoto (T)

Division of Drugs, National Institute of Health Sciences, Kawasaki-ku, Kawasaki City, Kanagawa, Japan.

Makoto Otsuka (M)

Graduate School of Pharmaceutical Sciences, Musashino University, Nishi-Tokyo, Tokyo, Japan.

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Classifications MeSH