Abdullah Al Masud, Ph.D.

Postdoctoral Scholar at University of Kentucky College of Pharmacy
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Contact Information
us****@****om
(386) 825-5501
Location
United States, US

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Experience

    • United States
    • Higher Education
    • 1 - 100 Employee
    • Postdoctoral Scholar
      • Jul 2021 - Present

      • Liposomal formulation development, primarily for small molecules but quite familiar with macromolecules such as DNA, RNA and protein based liposomal formulations. • Liposome preparation using microfluidics and thin film hydration • Purifying liposomes using diverse methods such as Dialysis, column separation, ultrafiltration, ultracentrifugation • Testing physical characteristics of liposomes like size, PDI and surface charge using DLS • Determining the encapsulation capacity of the liposomes utilizing HPLC or plate reader • Evaluating drug leakage profile, cellular accumulation and distribution • Testing in-vitro efficacy and toxicity of the formulations • Stability testing Show less

    • United States
    • Higher Education
    • 700 & Above Employee
    • Graduate Research And Teaching Assistant
      • Aug 2015 - May 2021

      ∙ Fabricating plasmonic nanostructures " Zero Mode Waveguides (ZMWs) utilizing e-beam lithography and photo-lithography ∙ Understanding plasmon induced single molecule fluorescence characteristics such Fl intensity, photostability, Fl lifetime and photon anti-bunching. ∙ Fabricating PDMS based microfluidics for real time imaging of the processes associated with cancer cell migration during metastasis ∙Aligning lasers (CW and pulsed) and optics for single molecule imaging and characterization ∙ Generating macrophage derived nanovesicles for target oriented therapeutic delivery and immunomodulation ∙ Teaching laboratory courses CHE 111 and CHE 113 ∙ Assisiting new TAs as Lead TA Show less

    • Bangladesh
    • Education Administration Programs
    • 300 - 400 Employee
    • Lecturer
      • May 2013 - Jul 2015

      ∙ Teaching undergraduate level pharmaceutical science courses ∙ Responsible for both lecture and lab courses ∙ Supervising undergraduate level research projects ∙ Teaching undergraduate level pharmaceutical science courses ∙ Responsible for both lecture and lab courses ∙ Supervising undergraduate level research projects

    • Bangladesh
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Sr. Executive, Product Development
      • Nov 2011 - May 2013

      ∙ Formulation development for oral solids (Tablets and capsules) ∙ Conducting pre-formulation studies ∙ Preparing small scale batches and evaluating the primary parameters such as disintegration time, weight variation, friability etc. ∙ Scaling up from pilot scale batch to development batches ∙ Developing manufacturing processes ∙ Preparing product specification, batch manufacturing record (BMR) and batch packaging record (BPR) ∙ Formulation development for oral solids (Tablets and capsules) ∙ Conducting pre-formulation studies ∙ Preparing small scale batches and evaluating the primary parameters such as disintegration time, weight variation, friability etc. ∙ Scaling up from pilot scale batch to development batches ∙ Developing manufacturing processes ∙ Preparing product specification, batch manufacturing record (BMR) and batch packaging record (BPR)

    • Bangladesh
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Product Development Officer
      • Jun 2008 - Oct 2011

      ∙ Analytical method development and validation for drug products with diverge dosage range such as solids, liquids and semi-solids ∙ Stability testing of the development batches stored at accelerated and ambient condition. ∙ Analyzing drug product's potency, dissolution properties and other physico-chemical characteristics using numerous analytical tools such as HPLC, GC, UV, IR, dissolution tester, DT tester, friability, Karl fisher titrator, LOD etc. ∙ Reporting and record keeping ∙ Analytical method development and validation for drug products with diverge dosage range such as solids, liquids and semi-solids ∙ Stability testing of the development batches stored at accelerated and ambient condition. ∙ Analyzing drug product's potency, dissolution properties and other physico-chemical characteristics using numerous analytical tools such as HPLC, GC, UV, IR, dissolution tester, DT tester, friability, Karl fisher titrator, LOD etc. ∙ Reporting and record keeping

Education

  • University of Kentucky
    Doctor of Philosophy - PhD, Analytical and Biophysical chemistry
    2015 - 2021
  • University of Dhaka
    Master of Pharmacy (Mpharm), Pharmaceutical Sciences
    2008 - 2010
  • University of Dhaka
    Bachelor of Pharmacy - BPharm, Pharmaceutical Sciences
    2003 - 2008

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