We report a mathematical model for the uptake of lipophilic agrochemicals from dispersed spherical particles within a formulation droplet across the leaf cuticle. Two potential uptake pathways are identified: direct uptake via physical contact between the cuticle and particle and indirect uptake via initial release of material into the formulation droplet followed by partition across the cuticle-formulation interface. Numerical simulation is performed to investigate the relevance of the particle-cuticle contact angle, the release kinetics of the particle, and the particle size relative to the cuticle thickness. Limiting cases for each pathway are identified and investigated. The input of typical physicochemical parameters suggests that the indirect pathway is generally dominant unless pesticide release is under strict kinetic control. Evidence is presented for a hitherto unrecognized "leaching effect" and the mutual exclusivity of the two pathways.
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http://dx.doi.org/10.1021/acsagscitech.2c00029 | DOI Listing |
J Control Release
January 2025
Department of Pharmacy, University of Copenhagen, Universitetsparken 2, Copenhagen 2100, Denmark; Bioneer A/S, Kogle Allé 2, Hørsholm 2970, Denmark. Electronic address:
The ability to predict the absorption of exenatide (Ex), a GLP-1 analogue, after oral dosing to rats in self-nanoemulsifying drug delivery systems (SNEDDS), using in vitro methods, was assessed. Ex was complexed with soybean phosphatidylcholine (SPC) prior to loading into SNEDDS. A design of experiments (DoE) approach was employed to develop SNEDDS incorporating medium-chain triglycerides (MCT), medium-chain mono- and diglycerides (MGDG), Kolliphor® RH40, and monoacyl phosphatidylcholine.
View Article and Find Full Text PDFInt J Nanomedicine
January 2025
Department of Pharmaceutics, Faculty of Pharmacy, Northern Border University, Arar, Saudi Arabia.
Introduction: Rhein, a natural bioactive lipophilic compound with numerous pharmacological activities, faces limitations in clinical application due to poor aqueous solubility and low bioavailability. Thus, this study aimed to develop a rhein-loaded self-nano emulsifying drug delivery system (RL-SNEDDS) to improve solubility and bioavailability.
Methods: The RL-SNEDDS was prepared by aqueous titration method with eucalyptus oil (oil phase), tween 80 (surfactant), and PEG 400 (co-surfactant) and optimization was performed by 3 factorial design.
Int J Pharm
January 2025
School of Pharmacy, Guilin Medical University, Guilin, Guangxi 541199, China. Electronic address:
Alprazolam (Alp), a triazolobenzodiazepine, is widely prescribed for the treatment of sleep disorders, anxiety, and panic disorder. While oral administration remains the standard route, its slow onset of action has prompted interest in intranasal delivery as an alternative, offers the potential for direct drug delivery to the brain. This study aims to develop a fast-acting intranasal formulation of Alp (Alp-nd).
View Article and Find Full Text PDFPolymers (Basel)
December 2024
Department of Wood Science and Technology, Biotechnical Faculty, University of Ljubljana, Jamnikarjeva 101, 1000 Ljubljana, Slovenia.
This study compared the use of cellulose nanofibrils (CNF) and lignocellulose nanofibrils (LCNF) in different concentrations to reinforce the poly(vinyl alcohol) (PVA) matrix. Both nanofillers significantly improved the elastic modulus and tensile strength of PVA biocomposite films. The optimum concentration of CNF and LCNF was 6% relative to PVA, which improved the tensile strength of the final PVA biocomposite with CNF and LCNF by 53% and 39%, respectively, compared to the neat PVA film.
View Article and Find Full Text PDFAAPS PharmSciTech
January 2025
Consulting, Fort Collins, Colorado, USA.
Continuously explored in pharmaceuticals, microemulsions and nanoemulsions offer drug delivery opportunities that are too significant to ignore, namely safe delivery of clinically relevant drug doses across biological membranes. Their effectiveness as drug vehicles in mucosal and (trans)dermal delivery is evident from the volume of published literature. Commonly, their ability to enhance skin permeation is attributed to dispersion size, a characteristic closely related to solubilization capacity.
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