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Taste Masking of Prednisolone by Adsorption Method Ali, Hiba Muhammed Suza; Al-Khedairy, Eman Bekir
Academia Open Vol. 10 No. 2 (2025): December
Publisher : Universitas Muhammadiyah Sidoarjo

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.21070/acopen.10.2025.12834

Abstract

General Background: Prednisolone, a synthetic glucocorticoid with potent anti-inflammatory and immunosuppressive properties, is widely used to treat conditions such as asthma, allergies, and rheumatoid arthritis. Specific Background: Despite its therapeutic benefits, prednisolone’s intensely bitter taste negatively affects patient compliance, particularly in pediatric and geriatric populations. Knowledge Gap: Conventional taste-masking techniques often alter drug stability or release profiles, creating a need for simple, effective, and non-chemical masking approaches. Aims: This study aimed to mask the bitter taste of prednisolone using a physical adsorption method with Veegum® and Bentonite as adsorbents at varying concentrations. Results: Eight formulations were prepared and assessed for percentage yield, drug content, and in vitro taste masking. The optimal formula (F5, 1:5 drug-to-Veegum® ratio) achieved an 89% yield, 108.3% drug content, and reduced drug release in simulated saliva (pH 6.8) from 55% to 16.6% within one minute, without any detectable drug–excipient interaction by FTIR analysis. Novelty: This study demonstrates a successful use of physical adsorption as a straightforward and non-chemical method for prednisolone taste masking. Implications: The Veegum®-based adsorption approach offers a promising foundation for developing patient-friendly oral formulations of bitter drugs.Highlight : The study aimed to mask the bitter taste of prednisolone using the adsorption method. Veegum® at a 1:5 drug-to-adsorbent ratio showed the best taste masking result. FTIR analysis confirmed no chemical interaction between prednisolone and the adsorbents. Keywords : Prednisolone, Taste Masking, Adsorption Method, Veegum®, Bentonite
A Review on Manufacturing and Characterization Oro-Dispersible Tablet Ali, Hiba Muhammed Suza; Al-Khedairy, Eman Bekir
House of Wisdom: Journal on Library and Information Sciences Vol. 2 No. 4: Desember
Publisher : Universitas Muhammadiyah Sidoarjo

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.21070/how.v2i4.270

Abstract

General Background: Oro-dispersible tablets have emerged as an important advancement in oral solid dosage forms due to their ability to rapidly disintegrate in the oral cavity without water. Specific Background: Their development is driven by patient demand for convenient medication, especially for pediatric, geriatric, and dysphagic populations who experience difficulty swallowing conventional tablets. Knowledge Gap: Despite wide application, comprehensive evaluation of fabrication methods, excipient functions, and characterization parameters across traditional and modern manufacturing technologies remains limited. Aims: This review analyzes the terminology, advantages, limitations, commonly used excipients, manufacturing techniques, and critical quality assessments of ODTs. Results: The study highlights diverse preparation approaches including lyophilization, sublimation, wet granulation, direct compression, mass extrusion, and emerging three-dimensional printing, each offering unique benefits related to disintegration behavior, mechanical strength, and processing efficiency. Novelty: The article synthesizes conventional pharmaceutics knowledge with recent technological innovations such as selective laser sintering and fused deposition modeling, demonstrating how modern techniques enhance precision and personalization of dosage forms. Implications: Findings underscore that optimized excipient selection and manufacturing strategies are fundamental to ensuring rapid disintegration, mechanical stability, acceptable taste, and enhanced bioavailability, reinforcing ODTs as a growing platform for patient-centered drug delivery.Highlight : Oro-dispersible tablets dissolve rapidly on the tongue, improving convenience for patients with swallowing difficulties. Formulation uses specific excipients—especially superdisintegrants—to achieve fast disintegration and effective performance. Can be produced using various traditional and modern manufacturing methods such as direct compression, sublimation, and 3D printing. Keywords : Disintegration, Oral solid dosage form, Oro-dispersible tablet, Patients’ compliance, Manufacturing techniques