The midterm exam for the "Entrepreneurship" course (Semester 10) for Clinical Pharmacy Program students will take place on Thursday, March 13, 2025, starting at 12:00 PM in Hall (1) beneath the lecture halls.

Metformin hydrochloride (MTF) has pharmacological properties for managing inflammatory skin conditions. MTF is a hydrophilic medication. Accordingly, embedding MTF into lipid carriers for enhancing skin penetration presents a challenge. The study aims to optimize the loading of MTF into nanostructured lipid carriers (NLCs) using a 22 full factorial design, employing the solvent injection technique. The NLCs were evaluated for encapsulation efficiency, hydrodynamic diameter, zeta potential, and polydispersity index. Alkalinization of the aqueous phase (pH = 12.5) resulted in maximizing the entrapment of MTF within NLCs. Furthermore, the tested solid lipids impacted the encapsulation of MTF based on their hydrophilic-lipophilic balance. The optimized formulation is composed of a lipid phase incorporating beeswax (75 mg), oleic acid (25 mg), and Span 60 (1% w/w), and an aqueous phase comprised of 1% w/w Tween 80, pH 12.5. The selected formula attained an entrapment efficiency of 53.68 ± 0.27%, a particle size of 333.0 ± 6.4 nm, and a negative surface charge, indicating adequate particles` stability. DSC and Molecular docking analyses confirmed the MTF incorporation within the lipid phase. The outcomes emphasize the importance of optimizing investigations in developing a viable delivery system for MTF to boost its permeation across the skin layers

Rosuvastatin (ROS), a statin drug with promising anticancer properties has a low bioavailability of approximately 20% due to lipophilicity and first-pass metabolism. This study aimed to enhance ROS anticancer efficacy through loading into flexible chitosomes. The chitosomes were prepared starting from negatively charged liposomes through electrostatic interactions with chitosan. The conversion of zeta potential from negative to positive confirmed the successful formation of chitosomes. The chitosan coating increased the particle size and zeta potential, which ranged from 202.0 ± 1.7 nm to 504.7 ± 25.0 nm and from − 44.9 ± 3.0 mV to 50.1 ± 2.6 mV, respectively. Chitosan and drug concentrations had an important influence on the chitosome properties. The optimum chitosome formulation was used to prepare ROS-loaded flexible chitosomes using different concentrations of four edge activators. The type and concentration of edge activator influenced the particle size, drug entrapment efficiency, and drug release rate of the flexible chitosomes. Flexible chitosomes significantly increased drug permeation through rat abdominal skin compared to control transferosomes and drug solution. The optimal ROS flexible chitosomes containing sodium deoxycholate as an edge activator had a 2.23-fold increase in ROS cytotoxic efficacy against MCF7 cells and a 1.84-fold increase against HepG2 cells. These results underscore the potential of flexible chitosomes for enhancing ROS anticancer efficacy.

Uric acid (UA) is a crucial biomarker for various metabolic and renal disorders, making its accurate determination essential for clinical diagnostics and disease management. This study presents a novel fluorometric method for UA detection using a glutathione@cadmium/carbon dots/uricase system (GSH@Cd/CDs/uricase system), which offers enhanced sensitivity and selectivity compared to existing techniques. The method employs a cascade reaction mechanism initiated by uricase-catalyzed oxidation of UA to produce H₂O₂. This H₂O₂ subsequently oxidizes GSH to oxidized glutathione (GSSG), releasing cadmium ions from GSH complexes. The liberated Cd²⁺ ions interact with two types of carbon dots (CDs) in the system: blue-emitting CDs (BCDs) and red-emitting CDs (RCDs). This interaction triggers a dual fluorescence response, characterized by a decrease in fluorescence intensity at 400 nm (BCDs) and an increase at 610 nm (RCDs), enabling ratiometric detection of UA levels. Comprehensive characterization and mechanistic investigations were conducted using various optical and morphological techniques, including transmission electron microscopy, X-ray diffraction, Fourier transform infrared spectroscopy, and fluorescence spectroscopy. The method exhibits outstanding analytical performance, characterized by strong linearity (R² = 0.9932), a broad detection range (0.05–7.0 μM), and a low detection limit of 0.015 μM. The method demonstrated excellent selectivity against common interfering substances and was successfully applied to human serum and urine samples with high recovery values (97.65 % to 99.20 %), highlighting its potential for clinical applications. This innovative approach combines the specificity of enzymatic recognition with the sensitivity of dual-emission fluorescence, offering a promising tool for accurate UA quantification in complex biological matrices.

A new ratiometric fluorescence strategy for sensitive and selective detection of cobalt ions (Co²⁺) and topotecan (TOP) is proposed. The dual-probe system consists of red-emissive nitrogen and sulphur doped carbon dots (R-NS@CDs) and TOP. For Co²⁺ detection, the fluorescence of R-NS@CDs at 680 nm is enhanced upon addition of Co²⁺, while complexed TOP emission peak at 545 nm remains constant. This enables ratiometric detection of Co²⁺ over a range of 5.0–160.0 ng mL⁻¹. The mechanism of R-NS@CDs fluorescence enhancement by Co²⁺ is elucidated using FTIR, fluorescence spectroscopy, zeta potential measurements, and TEM imaging. For the detection of TOP, a ratiometric probe system comprising R-NS@CDs and Co²⁺ was utilized. TOP forms a complex with Co²⁺ bounded to R-NS@CDs, quenching the R-NS@CDs-Co²⁺ fluorescence and simultaneously the native TOP fluorescence is enhanced. This allows ratiometric quantification of TOP from 1.0-90.0 ng mL⁻¹. The method provides high selectivity and low detection limits of 1.51 ng mL⁻¹ for Co²⁺ and 0.37 ng mL⁻¹ for TOP. Practical applicability is demonstrated through selective detection of Co²⁺ in environmental water samples and TOP in real plasma samples. The built-in self-calibration enabled by dual analyte modulation of R-NS@CDs makes this a simple and powerful analytical approach.