A5001887992- Advancements in Transdermal Drug Delivery
- Advanced Drug Delivery Systems
- Drug Solubulity and Delivery Systems
- Surfactants and Colloidal Systems
- Essential Oils and Antimicrobial Activity
- Nanoparticle-Based Drug Delivery
- Bee Products Chemical Analysis
- RNA Interference and Gene Delivery
- Polymer Surface Interaction Studies
- Microencapsulation and Drying Processes
- Proteins in Food Systems
- biodegradable polymer synthesis and properties
- Food Chemistry and Fat Analysis
- Drug Transport and Resistance Mechanisms
- Advanced Polymer Synthesis and Characterization
- Contact Dermatitis and Allergies
- Protein purification and stability
- Pharmacological Effects of Natural Compounds
- Natural product bioactivities and synthesis
- Dendrimers and Hyperbranched Polymers
- Dermatology and Skin Diseases
- Graphene and Nanomaterials Applications
- Electrospun Nanofibers in Biomedical Applications
- Coccidia and coccidiosis research
- Hydrogels: synthesis, properties, applications
Mahidol University
2016-2025
Nanocrystals, a carrier-free colloidal delivery system in nano-sized range, is an interesting approach for poorly soluble drugs. Nanocrystals provide special features including enhancement of saturation solubility, dissolution velocity and adhesiveness to surface/cell membranes. Several strategies are applied nanocrystals production precipitation, milling, high pressure homogenization combination methods such as NanoEdge™, SmartCrystal Precipitation-lyophilization-homogenization (PLH)...
The aim of this study was to encapsulate cannabidiol (CBD) extract in nanostructured lipid carriers (NLCs) improve the chemical stability and anti-inflammatory activity CBD for dermal delivery. CBD-loaded NLCs (CBD-NLCs) were prepared using cetyl palmitate (CP) as a solid stabilized with Tego® Care 450 (TG450) or poloxamer 188 (P188) by high-pressure homogenization (HPH). loaded at 1% w/w. Three different oils employed produce CBD-NLCs, including Transcutol® P, medium-chain triglycerides...
Microcapsules of vitamin A palmitate were prepared by gelatin-acacia complex coacervation. The effects colloid mixing ratio, core-to-wall hardening agent, concentration core solution, and drying method on the coacervation process properties microcapsules investigated. using different weight ratios gelatin acacia, that is, 2:3, 1:1, 3:2 under controlled conditions. other factors studied 1:2, 1:3 ratios; 30, 60, 120 min time; 2, 5, 10 ml formaldehyde per 280 g system as a agent; 30%, 40%, 50%...
Abstract Self-nanoemulsifying drug delivery systems (SNEDDS) have been used to improve the oral bioavailability of various drugs. In current study, apigenin was developed as SNEDDS solve its dissolution problem and enhance antioxidant potential. were prepared by mixing Gelucire 44/14, Tween 80, PEG 400 under controlled conditions. The droplet diluted demonstrated a spherical shape with size less than 100 nm neutral charge. very fast self-emulsification obtained within 32 s, transmittance...