RESUMO
The Rayleigh-Plateau instability, a phenomenon of paramount significance in fluid dynamics, finds widespread application in the Continuous InkJet (CIJ) printing process. This study presents a comprehensive dataset comprising experimental investigations of fluid jet breakup phenomena under large-amplitude stimulation conditions using an industrial CIJ print-head from Markem-Imaje. Unlike previous studies, this dataset encompasses a diverse range of experimental conditions, including nine different Newtonian fluids with meticulously measured rheological properties (viscosities, surface tensions and densities). The applied stimulation amplitudes vary from 5V to 45V, representing a substantial span of excitation levels. The experimental setup captures the intricate dynamics of fluid jets subjected to these varying conditions, producing a rich collection of over 5,000 high-resolution images depicting the breakup phenomena. Each amplitude of stimulation and fluid type yields more than 55 distinct images, providing detailed insights into the evolving jet morphologies. To ensure the accuracy and relevance of the dataset, all ejection parameters are rigorously documented and included. The dataset thus serves as a valuable resource for researchers seeking to explore the dynamics of large-amplitude Rayleigh-Plateau instability in CIJ printing. Its comprehensiveness and diversity make it particularly suitable for the application of novel machine learning and deep-learning approaches, enabling the study of jet morphological evolution beyond the confines of classical Rayleigh's theory. This dataset holds promise for advancing our understanding of fluid jet dynamics and enhancing the efficiency and quality of CIJ printing processes.
RESUMO
We previously developed two optimized formulations of dexamethasone acetate (DXMa) hydrogels by means of special cubic mixture designs for topical ocular administration. These gels were elaborated with hydroxypropyl-ß-CD (HPßCD) and hydroxypropyl-γ-CD (HPγCD) and commercial hydrogels in order to enhance DXMa water solubility and finally DXMa's ocular bioavailability and transcorneal penetration. The main objective of this study was to characterize them and to evaluate in vitro, ex vivo, and in vivo their safety, biopermanence, and transcorneal permeation. Gels A and B are Newtonian fluids and display a viscosity of 13.2 mPa.s and 18.6 mPa.s, respectively, which increases their ocular retention, according to the in vivo biopermanence study by PET/CT. These hydrogels could act as corneal absorption promoters as they allow a higher transcorneal permeation of DXMa through porcine excised cornea, compared to DEXAFREE® and MAXIDEX®. Cytotoxicity assays showed no cytotoxic effects on human primary corneal epithelial cells (HCE). Furthermore, Gel B is clearly safe for the eye, but the effect of Gel A on the human eye cannot be predicted. Both gels were also stable 12 months at 25 °C after sterilization by filtration. These results demonstrate that the developed formulations present a high potential for the topical ocular administration of dexamethasone acetate.
