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Mucosal Applications of Poloxamer 407-Based Hydrogels: An Overview.

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TLDR
This review focuses on the application of poloxamer 407-based hydrogels for mucosal drug delivery with particular attention being paid to the latest published works.
Abstract
Poloxamer 407, also known by the trademark Pluronic® F127, is a water-soluble, non-ionic triblock copolymer that is made up of a hydrophobic residue of polyoxypropylene (POP) between the two hydrophilic units of polyoxyethylene (POE). Poloxamer 407-based hydrogels exhibit an interesting reversible thermal characteristic. That is, they are liquid at room temperature, but they assume a gel form when administered at body temperature, which makes them attractive candidates as pharmaceutical drug carriers. These systems have been widely investigated in the development of mucoadhesive formulations because they do not irritate the mucosal membranes. Based on these mucoadhesive properties, a simple administration into a specific compartment should maintain the required drug concentration in situ for a prolonged period of time, decreasing the necessary dosages and side effects. Their main limitations are their modest mechanical strength and, notwithstanding their bioadhesive properties, their tendency to succumb to rapid elimination in physiological media. Various technological approaches have been investigated in the attempt to modulate these properties. This review focuses on the application of poloxamer 407-based hydrogels for mucosal drug delivery with particular attention being paid to the latest published works.

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Pharmaceutical assessment of polyvinylpyrrolidone (PVP): As excipient from conventional to controlled delivery systems with a spotlight on COVID-19 inhibition.

TL;DR: Polyvinylpyrrolidone (PVP) is a water-soluble polymer obtained by polymerization of monomer N-vinyl pyrrolide as discussed by the authors, which can be used as a brace component for gene delivery, orthopedic implants, and tissue engineering applications.
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Biodegradable Polymeric Nanoparticles for Drug Delivery to Solid Tumors.

TL;DR: In this paper, the use of polymeric nanoparticles as drug delivery systems of anticancer compounds, their physico-chemical properties and their ability to be efficiently localized in specific tumor tissues have been described.
Journal ArticleDOI

Drug-Loaded Biocompatible Nanocarriers Embedded in Poloxamer 407 Hydrogels as Therapeutic Formulations.

TL;DR: The state of the art of the most important mixed systems made up of colloidal carriers localized within a P407 hydrogel will be provided in order to illustrate the possibility of obtaining a controlled release of the entrapped drugs and an increase in their therapeutic efficacy as a function of the biomaterial used.
Journal ArticleDOI

Formulation Strategies to Improve Nose-to-Brain Delivery of Donepezil

TL;DR: The permeation and prediction parameters were significantly higher for DPZ-PNE, suggesting the use of polymers to be an effective strategy to improve the bioadhesion and penetration of the drug through nasal mucosa, which consequently increase its bioavailability.
References
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Reference BookDOI

Polymer Interface and Adhesion

Souheng Wu
TL;DR: In this paper, the surface tension and surface tension of polymers were calculated from contact angles by the Harmonic-Mean and Geometric-means methods. But the results of the analysis of the contact angles were limited.
Journal ArticleDOI

Micellization of poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) triblock copolymers in aqueous solutions: Thermodynamics of copolymer association

TL;DR: In this article, a closed association model was used to describe the copolymer micellization process for the majority of the Pluronics and used to obtain the standard free energies, enthalpies, and entropies of micellisation.
Journal ArticleDOI

Poly(ethylene oxide)-poly(propylene oxide )-poly (ethylene oxide) block copolymer surfactants in aqueous solutions and at interfaces: thermodynamics, structure, dynamics, and modeling

TL;DR: In this article, the association properties of poly(ethylene oxide)-block-poly(propyleneoxide)-blockpoly(methylene oxide) (PEO) copolymers in aqueous solutions, and the adsorption at interfaces are reviewed.
Journal ArticleDOI

In situ-forming hydrogels--review of temperature-sensitive systems.

TL;DR: This manuscript focuses on aqueous polymeric solutions that form implants in situ in response to temperature change, generally from ambient to body temperature, and mainly reviews the characterization and use of polysaccharides, N-isopropylacrylamide copolymers, poly(ethylene oxide) (poloxamer) and itsCopolymers.
Journal ArticleDOI

Pluronic block copolymers: evolution of drug delivery concept from inert nanocarriers to biological response modifiers.

TL;DR: These studies suggest that Pluronics have a broad spectrum of biological response modifying activities which make it one of the most potent drug targeting systems available, resulting in a remarkable impact on the emergent field of nanomedicine.
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