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Cyclodextrin
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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A recent update of water-soluble polymers in cyclodextrin-based formulations for mucosal drug…
Abstract
Cyclodextrins (CDs) play a crucial role in pharmaceutical formulations due to their unique ability to form inclusion complexes with a wide range of lipophilic drugs. Ternary complexes comprising CD, water-soluble polymer, and drug molecule have emerged as promising multicomponent to the…
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Deep Eutectic Solvents: An Eco-friendly Design for Drug Engineering
Abstract
In the spirit of circular economy and sustainable chemistry, the use of environmentally friendly chemical products in pharmacy has become a hot topic. In recent years, organic solvents have been the subject of a great range of restriction policies due to their harmful effects on the…
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An Experimental Design Approach for Producing Curcumin-Loaded Solid Lipid Nanoparticles
Abstract
Background/Objectives: Curcumin has well-established efficacy in a variety of disorders due to its prominent antioxidant, antiaging, anti-inflammatory, chemosensitizing, and anticancer activities. Despite its numerous benefits, curcumin exhibits low bioavailability mainly due to its poor…
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Exploring the potential of mucoadhesive buccal films in geriatric medicine
Abstract
As the global demographic shifts toward an aging society, the geriatric patient population is steadily increasing. These patients often suffer from comorbidities and require numerous oral medications, which can be especially challenging for dysphagic geriatric patients. Mucoadhesive buccal…
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New product – Kleptose F 7% – BETA CYCLODEXTRIN
Roquette presents a new product:
KLEPTOSE® F 7% - EXP β-cyclodextrin for oral dosage forms contains less than 7% of water. It is well suited for dry processing techniques, such as direct compression, where its low water content benefits moisture-sensitive APIs and formulations (e.g., ODTs,…
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Cyclodextrin-mediated enhancement of gastrointestinal drug delivery: unveiling mucoadhesive and…
This study evaluates the in vivo mucoadhesive properties of thiolated cyclodextrins (CDs) with varying S-protection using polyethylene glycol (PEG) of different chain lengths. Free thiol groups of thiolated β-CDs (CD-SH) were S-protected with 1 kDa and 2 kDa PEG bearing a terminal thiol group,…
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Formulation and Evaluation of Orodispersible Tablet of Piroxicam by using Natural Polymers
ABSTRACT:
Piroxicam is an oxicam class of NSAID which is a drug of choice in the treatment of severe pains occurs in chronic diseases like osteoarthritis, rheumatoid arthritis, ankylosing spondylitis and many more severe conditions. The solid dispersion method with piroxicam were prepared by…
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Quantification of Antibiotics in Multicomponent Drug Formulations using UV-Vis Spectrometer with PLS…
Abstract
This study explores the potential of spectroscopic analysis combined with Partial Least Squares Regression (PLS) and Multivariate Curve Resolution-Alternating Least Squares (MCR-ALS) for the simultaneous quantification of antibiotics in multicomponent drug formulations, specifically…
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Recent progress in pharmaceutical excipients as P-glycoprotein inhibitors for potential improvement…
Abstract
Pharmaceutical excipients such as P-glycoprotein inhibitors can also increase the solubility and affinity of drugs to the intestinal membrane, enhance paracellular pathways and endocyte uptake, and activate lymph transport pathways, thereby increasing the bioavailability of oral drugs.…
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