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Quercetin-Eudragit® polymer complexes with enhanced loading, solubility, stability, and…
Abstract
Aim
Quercetin is a natural dietary compound known for its potential to prevent chronic diseases. However, the translation of this success to humans is hindered due to quercetin’s poor oral bioavailability, attributed to its extremely low water solubility and permeability. These…
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Solid lipid discs from water-in-oil emulsion as controlled release delivery systems of highly…
Abstract
Solid lipid systems (SLSs) are widely employed to control the release of highly hydrophilic drugs, and they are, in general, obtained by solubilizing or suspending the drug within melted lipid excipients. This work proposes an advantageous strategy to modulate the drug release of a…
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Enzymatic absorption promoters for non-invasive peptide delivery
Abstract
Peptide drugs offer considerable potential for treating a diverse range of diseases. Yet, their clinical application is generally restricted to injectable therapies. The main challenge hindering their broader use through globally accessible, patient-friendly, and non-invasive delivery…
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Impact of antioxidant addition on drug dissolution: Implications for NDSRI mitigation biowaivers
Abstract
Nitrosamine impurities have garnered recent attention due to their presence in pharmaceuticals and their mutagenic risks. Recent studies have emphasized controlling impurities and suggest ways to mitigate the further formation of nitrosamines by the addition of antioxidants to tablets and…
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Revolutionizing White Coatings: A Titanium-Free Approach
Reimagining the future of coatings without TiO₂.
Titanium dioxide (TiO₂) has long been the go-to for perfectly white tablet coatings. But with growing regulatory scrutiny and consumer demand for cleaner labels, drug manufacturers could use a reliable alternative. Scientists at Roquette set out to…
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Modified starch as a new co-excipient in hydrophilic gels for prolonged drug delivery
Abstract
The hydrogels with methylene blue (MB), based on selected synthetic and semisynthetic polymers (SP), doped with citrate starch (CS), was evaluated successfully in the terms of MB release from polymeric matrix with prolonged release effect. The hydrophilic matrix in the hydrogel systems…
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Development and Evaluation of Sublingual Tablet of Lercanidipine by Solid Dispersion Method
Abstract
The purpose of this study was to develop and evaluate a sublingual tablet of lercanidipine hydrochloride for the direct compression method of treating hypertension by using a solid dispersion technique. The dihydropyridine calcium-channel blocker lercanidipine Hydrochloride is used to…
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Bioadhesive Eudragit RL®100 Nanocapsules for Melanoma Therapy: A Repurposing Strategy for…
Abstract
Background/Objectives: Cutaneous melanoma is a potent neoplasm whose advancement is linked to catecholamine-induced angiogenesis through β-adrenergic receptors. Propranolol (PROP), a non-selective β-blocker, holds potential in oncology, but its systemic side effects restrict its viability.…
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Application of Lactose Co-Processed Excipients as an Alternative for Bridging Pharmaceutical Unit…
Abstract
Improving the manufacturability of drug formulations via direct compression has been of great interest for the pharmaceutical industry. Selecting excipients plays a vital role in obtaining a high-quality product without the wet granulation processing step. In particular, for diluents which…
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Development and Characterization of α-Lipoic Acid Amorphous Solid Dispersion for Improved Oral…
Abstract
α-Lipoic acid (LA), a naturally occurring antioxidant and anti-inflammatory agent, has limited aqueous solubility and bioavailability which hinders its clinical application. To overcome these limitations, in this study, we have developed LA solid dispersion (LASD) using soluplus (SOL) to…
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