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Poloxamer
Bespoke hydroxypropyl methylcellulose-based solid foams loaded with poorly soluble drugs by tunable…
Abstract
A tunable modular design (TMD) as a new approach was proposed to tailor the dose and drug release profile of poorly water-soluble drugs from hydroxypropyl methylcellulose (HPMC)-based solid foams by combining two manufacturing principles:
(1) freeze-drying aqueous HPMC-based gels to…
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Autoclaving behavior of trimyristin nanoemulsions stabilized with different poloxamers
Abstract
Lipid nanoemulsions are being investigated as carrier systems for the parenteral administration of poorly soluble drugs. Defined particle sizes, narrow particle size distributions, and sterility are prerequisites for the safe administration of such formulations to patients. In the current…
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Soluplus®-Based Pharmaceutical Formulations: Recent Advances in Drug Delivery and Biomedical…
Abstract
Poor water solubility remains a significant challenge in the pharmaceutical industry that limits the therapeutic efficacy and bioavailability of many active pharmaceuticals. Soluplus® (SLP), an amphiphilic graft copolymer made of polyethylene glycol, polyvinyl caprolactam, and polyvinyl…
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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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Topical drug formulation for enhanced permeation: A comparison of Bayesian optimisation and response…
Abstract
Topical skin products aim to address aesthetic, protective, and/or therapeutic needs through interaction with the human epidermal system. Traditionally, formulation development relies on empirical knowledge and trial-and-error experiments. In this paper, we introduced the Bayesian…
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3D printed gastroretentive floating-hollow capsular device (GRF-HCD) for levofloxacin oral delivery…
Abstract
The development of gastroretentive drug delivery systems is one such instance, which was developed to improve the oral bioavailability and effectiveness of drugs, which has a poor absorption window in the upper GIT and/or triggers local activity such as duodenal and stomach activity. In…
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In Situ Gels for Nasal Delivery: Formulation, Characterization and Applications
Abstract
The nasal route offers many advantages for drug delivery: quick onset of action, better patient compliance, avoidance of first-pass metabolism and bypassing the blood-brain barrier. Despite the potential of this route, several challenges exist, such as the short drug retention time…
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Excipients in drug delivery systems: A comprehensive review of approved inactive ingredients for…
Abstract
Pharmaceutical excipients, commonly known as inactive ingredients, encompass any substance aside from the active ingredient that fulfills a distinct and vital role in a formulation. Their purpose is to enhance specific characteristics, whether associated with the performance of the…
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Patches containing quercetin microcapsules to ameliorate dermal herpes simplex virus injuries in…
Abstract
This study aimed to develop patches containing quercetin-loaded microcapsules and to evaluate their in vitro and in vivo safety and efficacy in preclinical surveys. A set of in vitro experiments evidenced the virucidal activity of quercetin against the HSV-1-KOS (sensitive to acyclovir)…
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Understanding Microemulsions and Nanoemulsions in (Trans)Dermal Delivery
Abstract
Continuously explored in pharmaceuticals, microemulsions and nanoemulsions offer drug delivery opportunities that are too significant to ignore, namely safe delivery of clinically relevant drug doses across biological membranes. Their effectiveness as drug vehicles in mucosal and…
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