Formulation and In Vitro Evaluation of Paracetamol Sustained Release 1000 mg Tablets using Banana Starch As Dual-Action Control

This study aimed to develop and evaluate sustained release (SR) paracetamol 1000 mg tablets for 12-hour drug release, integrating immediate release (IR) and controlled release (CR) layers. IR layers (300 mg paracetamol) were formulated using banana starch (BS), polyvinyl alcohol (PVA), and hydroxypropyl methylcellulose (HPMC) as release rate retardants. Selected IR and CR layers were combined into 15 SR tablet formulations (SR1-SR15) prepared by direct compression. Evaluation of post-compression parameters and in vitro dissolution in pH 6.8 phosphate buffer showed ten formulations achieved over 90% drug release by 12 hours. Notably, SR1 and SR3, incorporating BS in both IR and CR layers, achieved 97.12% and 95.56% release, respectively. BS demonstrated superior functionality as a disintegrating agent and rate release retardant, with direct compression providing optimal SR tablet performance for sustained therapeutic efficacy.

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Publication Details

Journal
Journal of Neonatal Surgery
Published
2025-03-17
DOI
https://doi.org/10.52783/jns.v14.2224
Primary Topic
Food Science and Nutritional Studies
Type
article
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article

Formulation and In Vitro Evaluation of Paracetamol Sustained Release 1000 mg Tablets using Banana Starch As Dual-Action Control

C. Kumar, Ramakurthi Kundharaju
Journal of Neonatal Surgery
Food Science and Nutritional Studies
article

Formulation and In Vitro Evaluation of Paracetamol Sustained Release 1000 mg Tablets using Banana Starch As Dual-Action Control

C. Kumar, Ramakurthi Kundharaju
article en

Abstract

This study aimed to develop and evaluate sustained release (SR) paracetamol 1000 mg tablets for 12-hour drug release, integrating immediate release (IR) and controlled release (CR) layers. IR layers (300 mg paracetamol) were formulated using banana starch (BS), polyvinyl alcohol (PVA), and hydroxypropyl methylcellulose (HPMC) as release rate retardants. Selected IR and CR layers were combined into 15 SR tablet formulations (SR1-SR15) prepared by direct compression. Evaluation of post-compression parameters and in vitro dissolution in pH 6.8 phosphate buffer showed ten formulations achieved over 90% drug release by 12 hours. Notably, SR1 and SR3, incorporating BS in both IR and CR layers, achieved 97.12% and 95.56% release, respectively. BS demonstrated superior functionality as a disintegrating agent and rate release retardant, with direct compression providing optimal SR tablet performance for sustained therapeutic efficacy.

Journal of Neonatal SurgeryVol. 14(6S)
Openalex Percentile: Top 94%
Food Science and Nutritional Studies
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