This study used polymeric micelles to improve quality by increasing drug solubility, extending mucosal drug retention time, enhancing mucoadhesiveness, and promoting drug permeation and deposition. Fluocinolone acetonide (FA) was loaded into polymeric micelles (FPM), which were composed of poloxamer 407 (P407), sodium polyacrylate (SPA), and polyethylene glycol 400, and their physicochemical properties were examined. Small-angle X-ray scattering (SAXS) revealed a hexagonal micellar structure at all temperatures, and the concentrations of P407 and SPA were shown to significantly affect the solubility, mucoadhesion, release, and permeation of FPMs. The proportion of P407 to PEG at a ratio of 7.5:15 with or without 0.1% w/v of SPA provided suitable FPM formulations. Moreover, the characteristics of FPMs revealed crystalline states inside the micelles, which was consistent with the morphology and nano-hexagonal structure. The results of ex vivo experiments using focal plane array (FPA)-based Fourier transform infrared (FTIR) imaging showed that the FPM with SPA penetrated quickly through the epithelium, lamina propria, and submucosa, and remained in all layers from 5–30 min following administration. In contrast, the FPM without SPA penetrated and passed through all layers. The FPM with extended mucoadhesion, improved drug–mucosal retention time, and increased FA permeation and deposition were successfully developed, and could be a promising innovation for increasing the efficiency of mouth rinses, as well as other topical pharmaceutical and dental applications.

This study developed a sustainable super-disintegrant derived from Dioscorea hispida Dennst. var. hispida starch for use in immediate-release pharmaceutical tablets. Native starch (NS) was extracted and chemically modified via carboxymethylation to obtain carboxymethyl starch (CMS), followed by phosphate cross-linked to yield modified starch (MS). Physicochemical properties demonstrated that MS exhibited superior water uptake, swelling, and viscosity compared to NS and CMS. Scanning Electron Microscopy (SEM) revealed smaller and more uniform granules in MS, confirming enhanced structural modification. Preliminary tablet trials with dicalcium phosphate showed that 4% w/w MS achieved the fastest disintegration (16.5 s). In paracetamol tablets prepared by wet granulation, MS significantly improved hydration and disintegration performance relative to NS and CMS. Although commercial sodium starch glycolate (SSG) provided slightly faster disintegration, dissolution profiles of tablets containing MS and SSG were statistically equivalent (f₁ = 7, f₂ = 63), confirming comparable efficacy. Porosity analysis using synchrotron radiation X-ray tomography (SR-XTM) indicated that wet-granulated tablets possessed higher intra- and inter-granular porosity than direct compression tablets, facilitating rapid water penetration and disintegration. In contrast, denser direct compression tablets exhibited greater friability and lower mechanical integrity. Modified Dioscorea hispida starch demonstrated excellent disintegration efficiency, eco-friendliness, and local availability, presenting a promising natural alternative to synthetic super-disintegrants in immediate-release tablet formulations.

The translation of underutilized botanical resources into advanced therapeutic dosage forms represents a critical frontier in pharmaceutical sciences. This study systematically characterizes the phytochemical and biological profiles of three Acanthus species (Acanthus ebracteatus, Acanthus ilicifolius, and Acanthus montanus) to develop a functional, rapid-release effervescent mouthwash tablet for oral mucosal repair. Phytochemical screening demonstrated that ethanolic extraction selectively concentrated bioactive phenolics and saponins compared to conventional aqueous methods. The ethanolic A. montanus extract emerged as the premier candidate, exhibiting the highest total phenolic content, excellent biocompatibility with human gingival fibroblasts, and significant promotion of in vitro cellular migration. Furthermore, it demonstrated robust, broad-spectrum antimicrobial efficacy against key cariogenic (Streptococcus mutans) and opportunistic (Candida albicans) oral pathogens. To transition this botanical discovery into a viable delivery system, the optimized extract was integrated into an effervescent base via wet granulation utilizing absolute ethanol, followed by blending with extragranular excipients and single-stroke compression. The resulting optimized matrix, incorporating 10% sodium starch glycolate, achieved an ideal mechanical-kinetic balance, yielding exceptional structural toughness (0.23% friability) and rapid disintegration (2.02 min). Advanced 3D synchrotron X-ray tomographic microscopy revealed that this specific super-disintegrant ratio generates a highly interconnected, porous internal architecture driving accelerated capillary-mediated breakdown. Ultimately, this study successfully translates a botanical extract into a mechanistically optimized, functionally validated dosage form for targeted oral therapies.