Publications by authors named "Phuong H-L Tran"

Article Synopsis
  • This study explores the release behaviors of Hydroxypropyl Methylcellulose (HPMC) and paracetamol from hydrophilic matrix tablets, highlighting the difference in kinetics between high and low viscosity HPMC.
  • Different HPMC viscosity grades and drug-to-HPMC ratios were utilized to assess how these factors influence drug release, utilizing methods like HPLC and NMR for analysis.
  • Results show that high viscosity HPMC leads to slower release and distinct hydration behaviors, with varying release kinetics models for both HPMC and paracetamol, offering insights into their release mechanisms in tablet formulations.
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Clays have been used in various health care products, including drug delivery systems. Advanced formulations have been investigated to take full advantage of clays or clay-based materials. The remarkable properties of clays, such as high adsorption, high surface area and high ion exchange capacities, provide an ideal system for the delivery of poorly water-soluble drugs.

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Extracellular vesicles (EVs) are important intercellular communication messengers. Half of the published studies in the field are in vitro cell culture based in which bovine serum in various concentrations and forms is used to facilitate the production of extracellular vesicles. 'Exosome depleted serum' is the type of bovine serum most widely used in the production of human EVs.

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Two ATP-binding cassette transporters, ABCB1/MDR1 and ABCG2/BCRP, are considered the most critical determinants for chemoresistance in hepatocellular carcinoma. However, their roles in the chemoresistance in liver cancer stem cells remain elusive. Here we explored the role of inhibition of MDR1 or ABCG2 in sensitizing liver cancer stem cells to doxorubicin, the most frequently used chemotherapeutic agent in treating liver cancer.

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  • The study developed a method to encapsulate volatile perfume in microcapsules using eco-friendly biopolymers, chitosan and Eudragit S100, achieving high encapsulation efficiency.
  • The process involved emulsifying limonene in ethyl acetate with specific polymers, which formed a stable emulsion that solidified after freeze-drying.
  • Results showed that the encapsulation efficiency exceeded 94%, with optimal performance at a 1:1 polymer ratio, allowing sustained release of the perfume for up to 120 hours.
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  • The study investigates how different solvents affect the formation of self-assembled nanoparticles from albumin-oleic acid conjugates (AOCs) for developing in situ forming implants.
  • A poorly soluble drug, paliperidone palmitate (PPP), is used as a model to evaluate the AOCs synthesized through a specific chemical reaction, with various organic solvents examined for their role in nanoparticle formation.
  • Results show that more polar solvents lead to smaller, spherical nanoparticles and that a combination of AOC and PLGA effectively regulates the drug release rate over 14 days, especially controlling the initial burst of the drug.
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Industrial-scale pharmaceutical applications still face many challenges in overcoming the low absorption and bioavailability of poorly water-soluble drugs. Hot-melt extrusion has emerged as a promising approach with continuous processing on an industrial scale for the preparation of drug delivery systems. Many reviews have mentioned the potential applications, processes, principles and advantages and disadvantages of hot-melt extrusion in the pharmaceutical industry.

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Lipid-based formulations have recently been investigated as a promising approach to enhance the bioavailability of drugs, especially poorly water-soluble drugs. The encapsulation of lipid-based formulations in porous materials can result in a transformation of liquids or semisolid forms to solid dosage forms. Moreover, the specific structure of porous carriers could offer an enhanced ability to load and control active pharmaceutical ingredients.

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Fucoidan is well known to have various biological functions and is often investigated for pharmaceutical applications. Several studies have been conducted on clinical applications of fucoidan in recent years, especially regarding its oral drug delivery. Although fucoidan has shown promising results in various dosage forms, its potential applications as a dietary supplement have been demonstrated, and recent studies show that oral administration of fucoidan is preferred.

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The freeze-drying process has been particularly attractive for preparing tablets for controlled drug release. Although traditional methods, such as granulation or direct compression methods, have been used in various studies to produce tablets with controlled release, freeze-drying processes have been utilized in certain circumstances due to their distinct advantages. However, overall, further development of these strategies, which started with early studies on orally disintegrating tablets, is still necessary.

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Blueberries are consumed as healthy fruits that provide a variety of benefits to the nervous system. Scientists have found that blueberries can be used as a daily edible source for supplementation to prevent and minimize complexities of age-related diseases as well as to improve learning and memory in children. Anthocyanins are the most mentioned compounds among the components in blueberries, as they play a major role in providing the health benefits of this fruit.

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Background: This study aimed to evaluate the effects of hydrophobic and hydrophilic Film-Forming Gels (FFGs) on the controlled delivery of drugs with different levels of hydrophobicity.

Methods: This evaluation was carried out by employing zein and polyvinylpyrrolidone as hydrophobic and hydrophilic film-forming agents, respectively, in combination with hydroxypropyl methylcellulose functionalized as a hydrogel basement at a ratio that had been optimized to achieve the fastest drying time. Free curcumin or terbinafine hydrochloride was subsequently dispersed into blank FFGs to produce the final FFG formulations.

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Background: Mucoadhesive polymers play a critical role in controlled-release tablets for buccal drug delivery.

Objective: This research aimed to investigate the characterization and mechanisms of solid lipid particle-based tablets with different mucoadhesive polymers for buccal delivery.

Methods: Prednisolone (PSL)-loaded Solid Lipid Particles (SLPs) were conventionally prepared by ultrasonication.

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Aspirin has emerged as a promising intervention in cancer in the past decade. However, there are existing controversies regarding the anticancer properties of aspirin as its mechanism of action has not been clearly defined. In addition, the risk of bleeding in the gastrointestinal tract from aspirin is another consideration that requires medical and pharmaceutical scientists to work together to develop more potent and safe aspirin therapy in cancer.

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Article Synopsis
  • Solid dispersions enhance oral drug delivery of poorly water-soluble drugs by increasing solubility and dissolution, leading to improved absorption and higher bioavailability.
  • Fast-dissolving solid dispersions are particularly beneficial for achieving rapid pharmacological effects when needed.
  • The report will cover current studies, applications, pharmaceutical strategies, and the role of polymers in developing fast-dissolving solid dispersions for controlled drug release.
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  • Mucoadhesive formulations enhance drug delivery by promoting local retention and sustained release through adhesion to mucosal tissues.
  • Recent studies focus on colon-targeted oral drugs using mucoadhesive systems, leading to innovative designs of drug carriers.
  • This review covers strategies for creating effective mucoadhesive systems for controlled drug release in the colon, aiming to improve treatment for various diseases.
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Physicochemical characterization is a crucial step for the successful development of solid dispersions, including the determination of drug crystallinity and molecular interactions. Typically, the detection of molecular interactions will assist in the explanation of different drug performances (e.g.

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Studies of small extracellular vesicles (sEVs), known as exosomes, have been flourishing in the last decade with several achievements, from advancing biochemical knowledge to use in biomedical applications. Physiological changes of sEVs due to the variety of cargos they carry undoubtedly leave an impression that affects the understanding of the mechanism underlying disease and the development of sEV-based shuttles used for treatments and non-invasive diagnostic tools. Indeed, the remarkable properties of sEVs are based on their nature, which helps shield them from recognition by the immune system, protects their payload from biochemical degradation, and contributes to their ability to translocate and convey information between cells and their inherent ability to target disease sites such as tumors that is valid for sEVs derived from cancer cells.

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In recent decades, solid dispersions have been demonstrated as an effective approach for improving the bioavailability of poorly water-soluble drugs, as have solid dispersion techniques that include the application of nanotechnology. Many studies have reported on the ability to change drug crystallinity and molecular interactions to enhance the dissolution rate of solid dispersions using hydrophilic carriers. However, numerous studies have indicated that insoluble carriers are also promising excipients in solid dispersions.

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Article Synopsis
  • This study examines how mucoadhesive polymers can enhance the controlled release of poorly water-soluble drugs in tablet form.
  • The researchers used prednisolone and zein in the core tablets, testing Carbopol 940 and hydroxypropyl methylcellulose (HPMC) as the mucoadhesive polymers for sustained release.
  • Results show that HPMC is effective for drug release control due to its ability to absorb water and create pores in the coating, facilitating a gradual drug release suitable for targeting the colon.
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Background: Although curcumin has been demonstrated to be beneficial in treating various diseases, its low solubility, chemical stability and bioavailability limit its application, especially in cancer therapy.

Methods: Solid dispersions have been utilized in the last few decades to improve the bioavailability and stability of curcumin.

Results: However, there is a lack of summaries and classifications of the methods for preparing curcumin with this technology.

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It has been well established that solid dispersions have a high potential to increase the release rate of poorly water-soluble drugs, resulting in high drug bioavailability. Solid dispersions have been vigorously investigated with various practical approaches in recent decades. Improvements in wettability, molecular interactions and drugs being held in an amorphous state in solid dispersions are the main mechanisms underlying the high drug release rate.

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Cellular properties and microenvironments, as well as the characteristics of nanoparticles (NPs), affect the cellular uptake and cytotoxic effects of drug-loaded NPs. Since there is fluid flow in the human blood system, fluid flow also affects the drug delivery efficiency of NPs. This study aimed to evaluate the cellular behaviors of drug-loaded soft NPs on A549 cancer cells under different levels of shear stress (0.

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Colon-targeted oral delivery has recently attracted a substantial number of studies on both systemic and local treatments. Among approaches for colonic delivery, film coatings have been demonstrated as effective elements of the drug delivery systems because they can integrate multiple release strategies, such as pH-controlled release, time-controlled release and enzyme-triggered release. Moreover, coating layer modulations, natural film materials and nanoparticle coatings have been vigorously investigated with promising applications.

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Article Synopsis
  • Film-forming hydrogels combine the benefits of traditional films and hydrogels but still have some limitations.
  • This study focuses on how film-forming hydrogels, in combination with nanocarriers, can improve the sustained release of curcumin, a poorly water-soluble drug.
  • Results indicated that using gelatine nanoparticles with zein film-forming nanogels significantly enhances curcumin's permeability, making this approach a promising strategy for delivering hydrophobic drugs effectively.
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