Publications by authors named "Pakorn Kraisit"

Article Synopsis
  • Androgenetic alopecia (AGA) is a hair loss condition linked to the hormone dihydrotestosterone (DHT), and the study focuses on enhancing caffeine delivery to hair follicles to counteract its effects.
  • Researchers developed a new drug delivery system using caffeine-loaded hollow mesoporous silica nanoparticles coated with ultradeformable liposomes (ULp-Caf@HMSNs), which improve caffeine's ability to penetrate skin and reduce hair loss.
  • Results showed that this new system is non-toxic to hair follicle cells, increases cell viability, and effectively reduces harmful oxidative stress in cells affected by DHT, making it a promising alternative to existing treatments like minoxidil.
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  • * Machine learning and data analytics are being used to speed up drug discovery, improve formulation development, and ensure quality control.
  • * The review highlights both the advancements and challenges of using AI technologies in pharmaceuticals, providing insights into future trends in drug development and regulation.
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The aqueous solution of binary mixtures of amphiphilic copolymers is a potential platform for fabricating mixed polymeric micelles for pharmaceutical applications, particularly in developing drug delivery depots for a poorly water-soluble compound. This study fabricated and investigated binary mixtures of poloxamer 403 (P403) and poloxamer 407 (P407) at varying P403:P407 molar ratios to develop a vehicle for the poorly water-soluble compound, using ibuprofen as a model drug. The cooperative formation of mixed micelles was obtained, and the solubility of ibuprofen in the binary mixtures was enhanced compared to the solubility in pure water and an aqueous single P407 solution.

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  • This study focused on creating H-K4M hydroxypropyl methylcellulose (HPMC) films with nanostructured lipid carriers (NLCs) that are loaded with the drug furosemide, using techniques like hot homogenization and ultrasonic probes to manufacture and size the NLCs.
  • A Box-Behnken design was used to explore how three factors—H-K4M concentration, surfactant concentration, and mixing speed—affected the physical and chemical properties of both the NLCs and the resulting films.
  • Results indicated that the furosemide-loaded NLCs had small particle sizes and a varied polydispersity index, while the films showed good thickness, weight,
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Fluconazole (FZ) is a potential antifungal compound for treating superficial and systemic candidiasis. However, the use of conventional oral drug products has some limitations. The development of buccal film may be a potential alternative to oral formulations for FZ delivery.

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A pullulan (Pul)-derivative hydrogel was developed by introducing methacrylate (MA) groups and β-cyclodextrin (βCD) to form a Pul-βCD-MA hydrogel by UV cross-linking. The MA was expected to improve the hydrogel's mechanical properties and the βCD to increase the solubility of curcumin. Pul-βCD-MA was successfully synthesized, as confirmed by the H NMR and FTIR spectra.

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The combination of the thermoresponsive polymer and protein has demonstrated great promise in its applications in drug delivery and tissue engineering fields. This study described the impact of bovine serum albumin (BSA) on the micellization and sol-gel transition behaviors of poloxamer 407 (PX). The micellization of aqueous PX solutions with and without BSA was examined using isothermal titration calorimetry.

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  • The study developed a 3D-printed bento box model (BB) designed to release the drug propranolol hydrochloride (PNL) in a controlled manner using USP dissolution guidelines.
  • The BBs were created with polyvinyl alcohol and varied in infill percentages and wall thickness, impacting their physical properties and drug release capabilities.
  • Results indicated that some formulations of the 3D-printed BBs successfully met the drug release standards set by USP, suggesting a promising application for improved drug delivery in the pharmaceutical field.
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  • The research examined how different hydroxypropyl methylcellulose (HPMC) types in matrix tablets influence the release of propranolol hydrochloride (PNL), a drug ideal for studying extended-release formulations.
  • Using methods like FTIR, PXRD, and DSC, the study confirmed the compatibility of PNL with the excipients.
  • Results showed that HPMC tablets sustained PNL release for over 12 hours, with release mechanisms indicated by values between 0.476 and 0.497, suggesting an anomalous transport process.
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Herein, thermosensitive blends of poloxamer 407 (P407)/poloxamer 188 (P188)/polycarbophil (PCB) were developed in terms of maximized content of PCB (a mucoadhesive polymer) and desired temperature-dependent rheological properties of the blends as in situ gelling matrices. Maximizing PCB content while achieving the preferable rheological characteristics was accomplished through the Box-Behnken design. The quantitative effect of the polymer composition in the blends on the thermosensitive characteristics was evaluated using the fitted design model and the corresponding surface plots.

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The aim of this study was to combine fluconazole (FZ)-loaded solid lipid nanoparticles (FZ-SLNs) and chitosan films (C-films) for the potential administration of FZ across the buccal mucosa using a Box-Behnken design. The chitosan films containing FZ-SLNs (C-FS-films) and C-films were prepared using a film casting method. The ATR-FTIR analysis confirmed the presence of hydrogen bonds between the NH groups of chitosan and the OH or COO groups of glyceryl monostearate in the films.

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The objective of this study was focused on the optimization of the pharmaceutical excipients and banana extract in the preparation of orally disintegrating banana extract tablets (OD-BET) and conventional banana extract tablets (CO-BET) using a simplex lattice design. Various ratios of banana extract (BE), dibasic calcium phosphate (DCP) and microcrystalline cellulose (MCC) were used to prepare banana extract tablets (BET). The results indicated that the optimal OD-BET and CO-BET consisted of BE: DCP: MCC at 10.

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The aim of this present work was to prepare triamcinolone acetonide (TA)-loaded nanostructured lipid carriers (TA-loaded NLCs) for buccal drug delivery systems using the Box-Behnken design. A hot homogenization method was used to prepare the TA-loaded NLCs. Spermaceti (X₁), soybean oil (X₂), and Tween 80 (X₃) were used as solid lipid, liquid lipid, and stabilizer, respectively.

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The aims of this study were to prepare and characterize hydroxypropyl methylcellulose (HPMC)/polycarbophil (PC) mucoadhesive blend films saturated with propranolol hydrochloride (PNL)-loaded nanoparticles to improve permeability of drugs that undergo first-pass metabolism. An ionic cross-linking method and film casting technique was used to prepare nanoparticles and mucoadhesive blend films, respectively. Increasing concentrations of PNL (70, 80, 90 mg/film) in HPMC/PC blend films containing PNL-loaded nanoparticles (PN-films) and HPMC/PC blend films containing PNL (80 mg/film) without nanoparticles (PP-films) were prepared to test swelling, mucoadhesiveness, release, permeation and physicochemical properties.

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The objectives of this study were to prepare the hydroxypropyl methylcellulose (HPMC)/polycarbophil (PC) mucoadhesive blend film and to investigate the main and interaction effect of HPMC and PC mixtures on the physicochemical and mechanical properties of blend films using a simplex lattice mixture design approach. The cubic and quadratic models were selected to analyze mucoadhesive properties in terms of work of adhesion and maximum detachment force, respectively. It was shown that HPMC/PC blend film had higher mucoadhesive properties than pure HPMC film.

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The potential of using two natural polymers (chitosan and shellac) for the formation of nanoparticles by the process of ionic cross-linking to encapsulate bovine serum albumin, a model protein was investigated. Depending on the concentrations of chitosan, shellac and bovine serum albumin, three physical states - nanoparticle, aggregation, and solution could be observed as a result of the electrostatic force. The formation of nanoparticles was due to the balance between the repulsion force and attractive force while the imbalance between both forces resulted in the formation of aggregation and solution.

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