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ArticlePeer ReviewedOpen AccessPlagiarism Passed
Paper ID:IJSREM53291

Development and Characterization of Mucoadhesive Buccal Tablets for Pravastatin Sodium Delivery: A DoE-Based Formulation Strategy

Stream/Area:

-

Subject:

-

Paper ID:

IJSREM53291

Volume:

9 |

10 |

Oct 2025

Pages:

Publication Frequency:

Monthly (12 issues per year)

DOI
Digital Object Identifier
10.55041/IJSREM53291

License:International Journal of Scientific Research in Engineering and Management follows the Creative Commons Attribution 4.0 (CC BY 4.0) License, allowing free use and distribution with proper attribution.

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Authors

1P2KP

1Akanksha Pathak 2Mr. Kamlesh Patel

3BKT

3Dr. Brajesh Kumar Tiwari

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Abstract

This study aimed to develop, optimize, and evaluate mucoadhesive buccal tablets of Pravastatin Sodium (PVS) using a systematic Design of Experiments (DoE) approach. Pravastatin Sodium, a lipid-lowering agent, suffers from low bioavailability due to extensive first-pass metabolism. A buccal drug delivery system offers an effective way to bypass the first-pass metabolism and improve bioavailability. The study employed Box-Behnken Design (BBD) to optimize formulation parameters like polymer concentrations, excipients, and processing conditions. The tablets were evaluated for various physicochemical parameters, in vitro release, mucoadhesion, and stability. The optimized formulation showed satisfactory drug release, mucoadhesive strength, and stability, making it a promising candidate for improving the therapeutic efficacy of Pravastatin Sodium.

KEYWORDS

Mucoadhesive buccal tablets Pravastatin Sodium Design of Experiments (DoE) Box-Behnken Design Bioavailability Drug Delivery System

Cite This Article

1Akanksha Pathak 2Mr. Kamlesh Patel, 3Dr. Brajesh Kumar Tiwari, "Development and Characterization of Mucoadhesive Buccal Tablets for Pravastatin Sodium Delivery: A DoE-Based Formulation Strategy," International Journal of Scientific Research in Engineering and Management, vol. 9, no. 10, Oct 2025. https://doi.org/10.55041/IJSREM53291

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Publication Date

10/29/2025

Peer Review Type

Double-Blind Peer Review

Review Rounds: 2

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The authors declare no conflict of interest related to this research work.

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