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God willing, The Pharmaceutical Analytical Chemistry Department Council will hold its regular monthly meeting number (524) This will take place on Monday, April 7, 2025, at 12:00 PM.
By the will of God, the Scientific Conference of the Department of Pharmaceutical Analytical Chemistry will be held on Monday, April 7, 2025, at 11:00 AM. The conference will take place in the meeting hall on the fifth floor of Building (B) at the Faculty.
The Department of Pharmacognosy has the honor to invite you to attend the scientific conference (faculty member, assistant staff and students) of the department
This will take place at 10:00 AM on Monday, April 7, 2025.
The meeting room of the department.
Head of the Department Council
(Professor Dr. Soad Abdel Latif Hassan
The Faculty of Pharmacy family extends heartfelt congratulations to
Professor Dr. Hassan Refaat Hassan
for his reappointment as Vice Dean for Education and Student Affairs.

Introduction: Tick-borne diseases represent a major threat to both
animal and human health globally. This study explores the prevalence of
tick infestation and associated piroplasm infections specifically Theileria
and Babesia species in cattle, in addition to evaluating the acaricidal
effectiveness of Chrysanthemum extract (Dendranthema grandiflora) and
neem oil emulsion (Azadirachta indica).
Methods: Among 130 cattle examined, 61 were infested with ticks and
subsequently screened for piroplasm infections. Molecular analysis identified
infections caused by Theileria annulata and Babesia bigemina.
Results: A strong association was found between tick infestation and Babesia
species, while T. annulata infection showed a slight correlation. Hemolymph
examination confirmed the critical role of ticks in the life cycle of piroplasm
infection. Chrysanthemum extract and neem oil were tested for their acaricidal
properties against adult ticks (Rhipicephalus annulatus). Chrysanthemum extract
(0.5 mg/mL) caused tick mortality within 24 h. However, neem oil induced
rapid and significant tick mortality at (20 mg/L) and (15 mg/L), achieving 100%
mortality within the same time frame. Both treatments demonstrated high
effectiveness, with results indicating strong dose-and time-dependent effects
compared to controls. Scanning electron microscopy (SEM) revealed extensive
morphological damage to treated ticks. This damage included destruction of
the hypostome, loss of surface striations, wrinkling with pore formation, and
cracking following exposure to neem oil and Chrysanthemum extract.
Discussion: These findings highlight the potential of D. grandiflora extract and
neem oil emulsion as effective natural acaricides for controlling tick infestations
and reducing tick-borne diseases.
Silver-based metal organic frameworks (MOFs) have recently acquired considerable interest due to their potential applications in sensing and detection, bioimaging, and light-emitting devices. Incorporating specific linkers or functional groups into the MOF structure can tailor their fluorescence characteristics and thus can selectively respond to target analytes. Herein, we report the synthesis of a novel luminescent silver-based MOFs (SOF1) derived from 2,3-dihydroxyterephthalic acid (2,3-DHBDC). The formation of SOF1 was established via Fourier transform infrared spectroscopy (FTIR), powder X-ray diffraction (PXRD), thermogravimetric analysis (TGA), X-ray photoelectron spectroscopy (XPS) and elemental analysis. The synthesis conditions i.e. molar ratio of Ag to 2,3-DHBDC and temperature played a crucial role in the formation of clean SOF with no formation of silver nanoparticles (NPs). High-resolution transmission electron microscopy (HRTEM) revealed various shapes depending on the synthesis conditions. Mostly, octahedrons and hexagons were observed for SOFs obtained utilizing molar ratio of 1:1 and 1:2, respectively. Furthermore, the selected area electron diffraction (SAED) revealed its high crystallinity. The synthesized SOF1 showed a distinct and strong fluorescent signal that is much higher than that produced from SOF2 based on the isomeric ligand; 2,5-dihydroxyterephthalic acid (2,5-DHBDC). The designed sensor was utilized for the sensitive detection of trifluralin (TRF) pesticide in river water samples. The achieved limit of detection of TRF was found to be 8 μg/L. The fluorescence quenching was experimentally and mathematically confirmed to primarily occur through the mechanisms of inner-filter effect (IFE), static quenching (SQ) and photoinduced electron transfer (PET). Moreover, a thin film of SOF1 was synthesized for selective visualization of TRF.
A novel and selective analytical method has been developed for doxycycline (DOX) determination, addressing the critical need for monitoring this widely used antibiotic in environmental samples. The method employs a hybrid sensing system combining orange-emitting carbon dots (O-CDs) with a calcium-murexide (Ca@Mu) complex, offering a unique dual-mode detection approach. Unlike conventional methods that rely on direct fluorescence quenching by DOX, which often suffer from poor selectivity, this system utilizes the competitive binding between DOX and murexide for Ca2+ ions. Initially, the pink-colored Ca@Mu complex formed under alkaline conditions causes fluorescence quenching of O-CDs at 552 nm. Upon introduction of DOX, its stronger Ca2+-binding affinity leads to the formation of a calcium-DOX complex, liberating free Mu and triggering both colorimetric (pink to orange) and fluorometric (restoration of O-CDs emission) responses. Comprehensive characterization and mechanistic investigations employing different spectroscopic techniques confirmed the sensing mechanism. The method demonstrates excellent selectivity for DOX among other tetracyclines and potential interferents, along with impressive analytical performance including good linearity (1.0-35.0 μM), low detection limit (325 nM), and high precision. Additionally, a smartphone-based colorimetric platform was developed for convenient on-site analysis. The practical utility of this method was validated through successful determination of DOX in environmental water samples with excellent recovery rates, offering a reliable and user-friendly approach for environmental monitoring of this important antibiotic.