PhD in Pharmaceutical Technology – Universiti Sains Malaysia (USM), Penang, Malaysia — 2019 Research focus: Drug delivery systems, nanotechnology, and polymeric pharmaceutical formulations.
MSc in Pharmaceutical Technology – Jordan University of Science and Technology, Irbid, Jordan — 2011
BSc in Pharmacy – Kufa University, Najaf, Iraq — 2006
Teaching and supervising undergraduate students in pharmaceutical sciences and technology.
Conducting scientific research in drug delivery systems, nanotechnology, and pharmaceutical formulation development.
Designing and implementing laboratory experiments related to pharmaceutics and pharmaceutical technology.
Contributing to curriculum development and continuous improvement of pharmacy education.
Participating in academic committees, departmental meetings, and institutional activities.
Guiding students in research projects, publications, and scientific presentations.
Organizing and participating in scientific conferences, workshops, and seminars.
Promoting collaboration and innovation in pharmaceutical education and research
Memberships
Member, Iraqi Pharmaceutical Syndicate – Baghdad, Iraq
Awards and Recognitions
PhD Scholarship Award, Universiti Sains Malaysia (USM), Penang, Malaysia – for doctoral studies in Pharmaceutical Technology (2015–2019)
Participation Certificates from multiple international scientific conferences, including the 4th Annual International Conference on Pharmacology and Pharmaceutical Sciences (PHARMA 2016), Singapore
Recognized for contributions to organizing scientific conferences and workshops in the field of Pharmaceutical Sciences
Drug delivery systems and controlled-release formulations
Nanotechnology and nanoparticle-based pharmaceutical delivery
Polymeric and co-processed excipient systems for drug formulation
Solid dispersion techniques for poorly soluble drugs
Formulation optimization and characterization of novel dosage forms
Pharmaceutical technology and process development
Biopharmaceutics and drug dissolution enhancement strategies
Quality control and analytical method development in pharmaceutics
Pharmaceutical Technology
Drug Delivery Systems
Nanotechnology in Pharmacy
Formulation and Industrial Pharmacy
Biopharmaceutics and Physical Pharmacy
Lecturer in Physical Pharmacy for Stage 2 undergraduate students, focusing on the physical and chemical principles underlying drug formulation and delivery.
Lecturer in Industrial Pharmacy for Stage 4 and Stage 5 students, emphasizing pharmaceutical manufacturing processes, quality control, and formulation development.
It was aimed to investigate the compressibility, compactibility, powder flow and tablet disintegration of a new excipient comprising magnesium (Mg) silicate co-processed (5%–85% w/w) onto chitin, microcrystalline cellulose (MCC) and starch as the hydrophilic polymers of interest. Initially, the mechanism of tablet disintegration was studied by measuring water infiltration rate, moisture sorption, swelling capacity and hydration ability. Moreover, the powders compression behavior was carried out by applying Kawakita model of compression analysis in addition to porosity and radial tensile strength measurements. In vitro drug release of compacts made of 400 mg ibuprofen and 300 mg of the hydrophilic polymers containing 30% w/w Mg silicat
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Solid dispersion (SD) formulation has attracted much attention due to its potential in enhancing dissolution performances of poorly soluble active pharmaceutical ingredients (API). Recently, a review on dissolution performances of SDs classifies the improvement into 3 categories, where 82 % of the studies showed improved bioavailability, 8 % showed reduced bioavailability and 10 % revealed similar bioavailability as compared to pure APIs. This indicates the inconsistent degrees of dissolution improvement of poorly soluble APIs in SD. Although a few factors related to the choice of carriers have been suggested to contribute to the dissolution improvement, however, the underlying factor determining the discrepancy in the degree of dissolution
... Show MoreA simple, economic, rapid, reliable, and stability-indicating high-performance liquid chromatography (HPLC) method has been developed and validated for the simultaneous determination of paracetamol (PCM) and caffeine (CF) in solid dosage form. The chromatographic separations were achieved with a Waters Symmetry® C18 column (5 μm, 4.6 × 150 mm), using a mixture of methanol and water (40:60, v/v) as a mobile phase, under isocratic elution mode with a flow rate of 0.8 mL/min, and ultraviolet (UV) detection was set at 264 nm. The oven temperature for the column was set and maintained at 35 °C. The method was validated according to International Conference on Harmonization (ICH) guidelines, and it demonstrated excellent linearity, wi
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