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Sodium Starch Glycolate
From Oral to Sublingual: A Redefined Avanafil Tablet with a Breakthrough in Bioavailability and…
Abstract
Introduction
Avanafil (AVA) is a very efficient phosphodiesterase type 5 inhibitor for the treatment of erectile dysfunction. However, it has limited bioavailability when taken orally and considerable first-pass metabolism. Enhancing its solubility and choosing an alternative delivery…
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In Vitro-In Vivo Correlation Of Amorphous Solid Dispersion Enabled Itraconazole Tablets
Purpose
There are scarce reports on in vitro-in vivo correlation (IVIVC) model development of immediate-release (IR) formulations, and few investigations of the impacts of formulation and process of spray-dried solid dispersions (SDD)-based tablets on human pharmacokinetics (PK), despite commercial…
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Development of tablet formulations containing genistein solid dispersion optimized using Box-Behnken…
Abstract
Genistein, a bioactive isoflavone, offers therapeutic potential but is hindered by poor water solubility, limiting its oral bioavailability. This study aimed to enhance genistein’s solubility by developing solid dispersion (SD) and formulating them into tablets. The SDs were prepared using…
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Evaluating Swellable Cross-Linked Biopolymer Impact on Ink Rheology and Mechanical Properties of…
Abstract
Background/Objectives: Interest in 3D printing oral thin films (OTFs) has increased substantially. The challenge of 3D printing is film printability, which is strongly affected by the rheological properties of the ink and having suitable mechanical properties. This research assesses the…
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The compaction effects of different disintegrants in a formulation of oral mefenamic tablets
Introduction
Super disintegrants are chemically modified version of traditional disintegrants used within tablets to improve the speed of release. The investigation looked at taking three commonly used super disintegrants (SSG, CCS and PVP) and incorporating into an Immediate release formulation.…
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Advances in Taste-Masking Strategies for Pediatric Brain-Related Disease Treatments: Focus on…
Abstract
Pediatric treatment of brain-related diseases often requires oral medications, where palatability is crucial for patient adherence and therapeutic success. The unpleasant taste of many drugs, especially those used in neurological or psychiatric conditions, can reduce compliance in…
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Particle-based investigation of excipients stability: the effect of storage conditions on moisture…
Abstract
Moisture sensitivity poses a challenge in formulating oral dosage forms, particularly when considering disintegrants’ swelling due to prior moisture exposure, impacting performance and physical stability. This study utilises dynamic vapour sorption to simulate real-world storage scenarios,…
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Impact of disintegrants on rheological properties and printability in SSE 3D printing of…
Abstract
This study investigates the effects of disintegrants sodium starch glycolate (SSG) and crospovidone (CP) on the printability, rheological properties, and disintegration time of agar and hydroxypropyl methylcellulose (HPMC)-based formulations designed for semi-solid extrusion. Printability…
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Use of Liquid Solid Technique for Development and Evaluation Study of Nifedipine Tablets to Enhance…
Abstract
Objectives: The current research finding suggests dissolution enhancement of nifedipine tablets using Liquid solid technique.
Materials and Methods: The drug's solubility in various liquid carriers has been examined, out of which drug shows maximum solubility in PEG 400 which acts…
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Implementing Quality by Design for Development and Optimization of Sublingual Tablet of Valsartan
Abstract
Purpose
Heart failure, a progressive cardiovascular disorder, significantly affects patient morbidity and mortality. Valsartan, an angiotensin II receptor antagonist, is widely used to mitigate the effects of heart failure, but its oral administration faces challenges such as poor…
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