CURRICULUM VITAE
Sayed Ibrahim Abdel-Rahman Hassan
Professor
Pharmaceutical Technology & Pharmaceutics
Born January 5, 1951, married, Egyptian	
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Head, Department of  Industrial Pharmacy, Faculty of Pharmacy,  Assiut, Egypt  
Mobile: +2010 1484015, Residence: (+2088) 2311873, (+202) 37408764
Office: (+2088) 2411273  		e-mail: <sayedia@lycos.com> 
Current Address   Department of Industrial Pharmacy, Faculty of Pharmacy,  Assiut University,  Assiut, Egypt. 
Education:
Degree of Doctor of Philosophy (Ph.D.) in Pharmaceutical Sciences (Industrial Pharmacy), thesis, entitled "A study on solubilization of some diuretics by nonionic surfactants", Assiut University, Egypt, and West Wilhelems University, Munster, Germany, 1979-1984.  The practical work and the literature reviews of the Ph.D. have been carried out in Germany, 1981-1983. 
Master Degree (M.Sc.) in Pharmaceutical Sciences, (Industrial Pharmacy), thesis, entitled "A study of the interaction between certain pharmaceuticals and certain macromolecules". To fulfill the requirements of the Master Degree, advanced courses in Industrial Pharmacy and Pharmaceutics, Solution Technology, Tablet Technology, Instrumental Analysis, Physical Chemistry and Statistics were studied in one year.  The Master Degree has been granted from Assiut University, Egypt, 1975-1978.
Bachelor Degree (B.Sc.) in Pharmaceutical Sciences, one preparatory year in the Faculty of Sciences and four years in the Faculty of Pharmacy.  General Grade: Very Good, Assiut University, Egypt, 1969-1974. 
Employment, Teaching and Research Experiences: 
Current Job: Department Head, Industrial Pharmacy, Assiut University, Egypt
Previous Jobs:
Professor of Pharmaceutical Technology & Pharmaceutics,  King Sauid University, Riyadh, Saudi Arabia,  January 2008-July 2009.
Professor of Pharmaceutical Technology & Pharmaceutics, Vice Dean for Society Service & Environment Development, Faculty of Pharmacy, Assiut University.
Director of the Drug Research Center, Assiut University. This center contributes to research in pharmaceutical technology fields. It also manufactures pharmaceutical products for Assiut University Hospitals of about one million Egyptian pounds per year.    
Vice Director of Pharmaceutical Services Center, Faculty of Pharmacy, Assiut University. This serves as drug information center and is about to be licensed to carryout bioequivalence studies for generic and innovated drug products on the behalf of the pharmaceutical industry as a part of the marketing authorization of these products.     
Professor of Pharmaceutical Technology and Pharmaceutics, Department Head, Assiut University. 
Professor, teaching under-graduate and graduate students, supervising M.Sc. students. Addis Ababa University School of Pharmacy, under the auspices of the Egyptian Ministry of Foreign Affairs, 1999-Aug.2004. 
Professor and  Department Head, teaching Pharmaceutical Tech. and Pharmaceutics, doing independent and collaborative research work, member of the committees supervising Ph.D. and M.Sc. works of graduate students and teaching Industrial Pharmacy and Pharmaceutics, Assiut University, Egypt and The University of Cincinnati, USA, 1995-1999. 
Associate Professor, research and teaching activities in Industrial Pharmacy and Pharmaceutics, Assiut University and the Ohio State University, Columbus, USA, 1989-1995. Establishment of Pharmaceutics Department and teaching Pharmaceutics   in The Arab Medical University, Benghazi, Libya, 1990-1992.
Assistant Professor, teaching and research activities of Pharmaceutics and Pharmaceutical Technology, Assiut University and The University of Georgia, Athens, 
USA, 1984-1989.
Research Associate and Lecturer, Industrial Pharmacy, Assiut University and The 
West  Wilhelms University , Munster, Germany,1975-1984.
Courses Taught
General pharmaceutics, biopharmaceutics & pharmacokinetics, pharmacy orientation & history of pharmacy, pharmaceutical technology (unit operations, manufacture of dosage forms, cGMP & process validation, super critical fluids, nanotechnology,etc), preformulation, drug development and innovation, drug delivery systems, drug supply management
Books Editing: 
The applicant has been a senior or co-editor of books for post- and under-graduate levels on practical and theoretical pharmaceutical technology subjects. Assuit  and Al-Azhar  Universities !993-1998. In King Saud University, a book entitled "Stability of Pharmaceuticals" is to be published in about six months period.
Scholarships and Fellowships:        
Visiting Research Professor, in the University of Cincinnati College of Pharmacy, Cincinnati, Ohio, USA. The applicant has been a team leader to develop innovated and generic solid dosage forms (tablets and capsules) for some drugs under cGMP, eventually, for marketing approval after submission to the FDA, 1998.  
Fulbright Grant: Visiting Professor in the Ohio State University, Columbus, Ohio, USA. A research project has been designed by the applicant and has won this grant to perform collaborative work in the USA institution. The work has concerned with the 
optimization of drug release from dosage forms using different   excipients and techniques, February- July, 1994.
Post-doctoral Fellowship: College of Pharmacy, the University of Georgia, Athens, USA. These studies have dealt with enhancing the dissolution of some poorly soluble drugs by recrystallization in hydrophilic media and formulation in dispersions of soluble macromolecules, one year, 1986.
Scholarship for Ph.D.: for laboratory work and literature reviewing, Institute of Pharmaceutics, the Western Wilhelms University, Munster, Germany. This work has dealt with the solubilization, binding and stability of benzothiadiazine diuretics with nonionic surfactants and other macromolecules, 1981-1983.
Experimental Techniques:  
Many techniques have been employed in order to study the physicochemical properties of drugs and excipients and to prepare   dosage forms of improved  pharmaceutical characteristics. Examples of these techniques are: freeze drying, solid dispersion, tablet 
manufacturing and quality control, complexation in the solid state,  solubility and complexation in the liquid state, crystal modification and controlled release dosage forms  . The research has covered in vitro  and in vivo  studies of solid, semi-solid and liquid dosage  forms. Dialysis, ultrafiltration, molecular sieving, vapor pressure osmometry, electron microscopy, surface area measurements, dissolution and solubility techniques, thermal analysis, chromatography, NMR, IR and mass spectroscopy are among the   methods which have been used  to analyze and interpret the results.  
Training Courses and Seminars:
Since 1975-present, many such courses and seminars have been joined in Assiut University and abroad. For example, in vitro/in vivo correlation trials, FDA regulatory
affairs and guidelines,  the principles and means for  teaching undergraduate and
postgraduate students, high performance liquid chromatography, 
electron microscopy .The theoretical and practical aspects of many analytical methods, 
e.g., NMR,  IR and Mass spectroscopy, high performance thin layer chromatography, thermal analysis and X-ray diffractometry have been studied and utilized  in the 
applicants research work. 
The work under the sponsorship of generic and innovation drug companies in USA  has given the applicant chances to attend and practice  courses, workshops and seminars on cGMP, drug regulation affairs, in vivo / in vitro availability studies.
Recently, the applicant has attended workshops in biotechnology, nanotechnology and has lectured in solid dosage form stability protocols and regulatory aspects.
He effectively participated in implementing the quality programs for the undergraduate and graduate teaching, learning and research during his vice deanship. 
Published Research Work:
The applicant has published and presented papers in National and International periodicals and conferences. These articles have dealt with many areas in Pharmaceutics and Pharmaceutical Technology, e.g., enhancement of dissolution and bioavailability   of poorly soluble drugs by, for example, solubilization and complexation, binding phenomena of drugs to macromolecules, sustained release formulation using different polymeric matrices, in vitro/in vivo availability of many drugs form different dosage forms, physical and chemical stability studies of many drugs in different formulations,....etc. Please refer to the list of publications and current research work.
Languages:
Arabic: Native language	 English: First foreign language
German: Second foreign language 

Scientific Memberships: 
 Member of t the Egyptian Society of Pharmaceutical Sciences, the American Association of Pharmaceutical Scientists (AAPS), Controlled Release Society, and the Egyptian Syndicate of Pharmacists.                     

List of Publications and Current Research
 
Scientific Reports Delivered at Meetings:
1. Interaction of free medicament concentration in surfactant solution using   
      vapor pressure osmometry_ S.I. Abdel-Rahman, P. Rohdewald and A.E. 
     Aboutaleb. Erester  Gesamt Kongress der Pharmazeutischen Wissenschaften,   
     Munich, Germany,  April 17-20, 1983, Cong. Abs. Book p. 182.
 2. "Dissolution profiles of salicylamide recrystallized from solutions containing 
     various surfactants or macromolecules",  S.I. Abdel-Rahman and  J.C. Price.
     First National Meeting of the American Association of Pharmaceutical Scientists
     (AAPS), Washington DC, USA, November 2-6, 1986.Pharm.Research, 3, 42(1986).
3. "Dissolution behavior of propylthiouracil-polyvinylpyrrolidone solid dispersions",
    S.I. Abdel-Rahman, A.M.El-sayed and A.E. Aboutaleb. Feder.Internat.Pharm. 47th 
   (FIB), Amsterdam, the Netherlands, August 31-September 4, 1987.FIP 87 Abstract    
    No 236.
4. " Accelerating dissolution rates of benzothiadiazines", A.M.El-Sayed,
     S.I. Abdel-Rahman, H.A.Sayed and S.A. Ibrahim. The same previous conference, 
     FIP 87 Abstract No 310.
5. "Solid dispersions of propylthiouracil-polyethylene glycols: dissolution and 
     differential scanning calorimetric studies", S.I.Abdel-Rahman and  J.C. Price.
     XX conference of Pharm.Sci, Cairo, Egypt, Feb.23,1988, Abs.P.16.
6. "Stability behavior of vitamin C tablets prepared employing readily compressible  
     L-ascorbic acid granular forms", S.I. Selah, S.I. Abdel-Rahman and A. Stamm.
    The same previous conference, Abstracts Book p. 14.
7.  "Preparation and release characteristics of directly compressed sustained release  
      tablets containing nitrofurantoin or phenazopyridine hydrochloride". 
      S.I. Abdel-Rahman, S.I. Saleh, S.M. Ahmed, A.E. Aboutaleb and A. M. Aly. 2nd    
     Anglo-Egyptian of Pharm. Sci., Alexandria, Egypt, November 9-12, 1991.
8.  "Formulation and release characteristics of some sustained release formulations of 
      nitrofuratoin". S.I. Saleh, S.M. Ahmed, S.I. Abdel- Rahman, A.E. Aboutaleb and
      A.M. Aly. 2nd Anglo-Egyptian Conference of Pharm. Sci., Alexandria, Egypt,  
      November 9-12, 1991.
 9. "Bioavailability of sustained release nitrofuratoin tablets prepared by two different
      methods" S.I. Abdel-Rahman, S.I. Saleh, S.M. Ahmed, A.E. Aboutaleb and A. M.
     Aly. 2nd Anglo-Egyptian Conference of Pharm. Sci., Alexandria, Egypt, 1991.
10. "Evaluation of ibuprofen-cellulose polymers sustained release tablets" A.A. 
      Abdel-Rahman, S.I. Abdel-Rahman, A.E. Aboutaleb and A. Stamm. 11th
      Conference of Arab Pharmacists Union, Tripoli, Libya, 1991.
11. " Sustained release formulations of phenazopyridine hydrochloride with cellulose
     acetate phthalate" A.M. Aly, Ahmed S.M., S.I. Abdel-Rahman, S.I. Saleh and A.E.       
    Aboutaleb" 1st Egyptian-Italian Symposium on Biotechnology, Assiut, Egypt,1992.
12. "Compexing behavior of 2-hydroxypropyl--cyclodextrin with local
      anesthetics" S.I. Abdel-Rahman and S.G. Frank, 9th Annual Meeting Amer.  
      Assoc. Pharm. Scientists (AAPS), San Diego, CA, USA, 1994.
13. "Preparation and evaluation of sustained release systems of vitamin B1”
       S.I.   Abdel-Rahman, M.O. Ahmed and E.M. Samy, 24th Conf. Pharm. Sci., Cairo, 
       Egypt, 1994.
14. "Complexation of hydrochlorothiazide and bendrofluazide with -cyclodextrin in 
      solution and in ground mixtures" M.O. Ahmed, S. M. Ahmed, S.I. Saleh and
      S.I.  Abdel-Rahman, 24th Con. Pharm. Sci., Cairo, Egypt, 1994.
 15. "Improvement of solubility and dissolution of acetazolamide by inclusion 
       complexation with different cyclodextrins" S.I. Abdel-Rahman, S.M. Ahmed and
       M.O. Ahmed. XXV Conference of Pharm. Sci., Cairo, Egypt, 1996
16 Techniques and mechanisms of enhancing the dissolution of loratadine using  
       inclusion complexation  Sayed I. Abdel-Rahman, Sayed M. Ahmad, E.M. Samy 
       and A.M.M. Badawy, 3rd Assiut Univ. Pharm. Sci. Conf., Egypt, Assiut, Abs.
       Book, No. PHT 5, p 15, March 5-6, 2002.
18. "View on tablet stability" plenary lecture, Sayed  I. Abdel-Rahman, workshop on
      Theory and Practice in Tablet Technology". Sponsored by Pharmaceutical
      Technology Center, KSU, Riyadh, KSA,  Feb. 26-27, 2008. 
19. Formulation and evaluation of isoxsuprine hydrochloride    sustained release tablets 
      prepared by wet granulation" A. Aboutaleb, Sayed I. Abdel-Rahman and Jelan A.
      Razic,  31st International Conf. Pharm.  Sci, Cairo, December 23-25,  2008
 20. Plenary  lectures on different topics in workshops and conferences, e.g., American
       Association of Pharmaceutical Scientists (AAPS) Conference, Washington DC, 
     1999, Saudi Pharmaceutical Association Conference, Riyadh, 2008, Future University
      workshop 2011, Egyptian Pharmaceutical Conference, Cairo, December 2011. 

 List of Publications:
17. "Application of ultrafiltration technique for studying solubilized systems",
      A.E.Aboutaleb, A.Sakr and  S.I. Abdel-Rahman. Arch. Pharm.Chem., Sci.
      Ed.,5, 105 (1977).
18. "Investigation of salicylamide solubilized systems by molecular sieve and
      ultrafiltration techniques", A.E.Aboutaleb, A.Sakr and S.I. Abdel-Rahman.
      Pharm.Ind.42, 24(1980).
19. "Interaction of phenacetin with nonionic surfactants", A.E.Aboutaleb,
     A. Sakr and S.I. Abdel-Rahman.  Pharmazie, 35, 99 (1980).
20. "Evaluation of encapsulated aspirin tablets", S.I. Abdel-Rahman, H.A. Sayed,
       A.M. El-Sayed, E.Hafez and S.A. Ibrahim.
       Full paper published in the proceedings of the 15th International Symposium on
       controlled Release of Bioactive Materials, Basel, Switzerland, Aug.15-19,1988.
21. "Interaction of some insoluble diuretics with silica and silicate carriers",
       A.M.El-Sayed and S.I. Abdel-Rahman.
       Full paper published in the proceedings of the previous symposium.
22. "Dissolution behavior of propylthiouracil- polyvinyl- pyrrolidone solid 
       dispersions" S.I. Abdel-Rahman, A.M.El-Sayed and A.E.Aboutaleb,
       Bull. Pharm.Sci. the Egyptian Society of Pharmaceutical Sciences Assiut Univ., 11(2), 261 (1988).
23. "Accelerating dissolution rates of benzothiadiazine diuretics" A.M. El-Sayed,	
        S.I.Abdel-Rahman and S.A. Ibrahim, S.T.P.Pharma 5(3), 160 (1989).
24 ."Preformulation and evaluation of furazolidone ointments "A.M. El-Sayed
        and S.I. Abdel-Rahman, 5th International conference on Pharmaceutical 
        Technology proceedings, pp.117-126 (1989).
25. "Effect of formulation variables on the release behavior of  allopurinol from 
       suppositories" S.I. Abdel-Rahman, S.Shawky and A.M. El-Sayed, previous 
       conference, proceedings pp. 134-143 (1989).
26. " Interaction of some benzothiadiazines with - cyclodextrin" S.I.Abdel-Rahman
and A.M.El-Sayed, 1st Anglo-Egyptian conference of Pharm. Sci., Alexandria,          Egypt 91988). Acta Pharm. Hungarica, 60(2-3),69-75 (1990).
27. "Preparation and release kinetics of ethylcellulose-walled microcapsules  
       containing phenazopyridine in polymethyl-methacrylate matrices" S.M. Ahmed, 
       S.I.Saleh, S.I. Abdel-Rahman, S.H. Khidr and A.M. Ali, S.T.P. Pharm. Sci., 2(2), 
       205- 209(1992).
28. "Evaluation of ibuprofen controlled release tablets:1- Eduragit matrix controlled   
       tablets" A.A. Abdel-Rahman, E.M. Samy, S.I. Abdel-Rahman, A.E. Aboutaleb 
       and A. Stamm, Eur.J.Pharm. Biopharm. 38 (2), 71-77 (1992).
29."Optimization of Eudragit or cellulsic polymers- ibuprofen sustained release
       systems using principal component analysis" A.A. Abdel-Rahman, A.E.
      Aboutaleb, S.I. Abdel-Rahman and E.M. Samy, Bull.Pharm. Sci. Assiut
       Univ., 15, 63-82 (1992).
30. "Effect of cellulosic polymers on the physical properties and dissolution of 
       ibuprofen granules" A.A.Abdel-Rahman, A.E.Aboutaleb, A. Stamm,       
       S.I. Abdel-Rahman and  E.M.Samy Bull. Pharm. Sci. Assiut Univ., 15,89-
       99(1992).
31. "Bioavailability and in vivo/in vitro correlation of two sustained release
       nitrofurantoin tablets prepared by different methods" S.I.Abdel Rahman,
       S.M.Ahmed, S.I. Saleh, A.E.Aboutaleb and A. M.Al y, S.T.P.Pharm. Sci., 394,
       294-299 (1993).
32. " Preparation and release characteristics of some sustained release formulations
        of nitrofurantoin" S.I.Saleh, S.M.Ahmed, S.I. Abdel-Rahman, S.H.Khidr and
        A.M.Aly, S.T.P.Pharm.Sci., 3,(5),379-385 (1993). 
33. "Preparation and release characteristics of directly compressed sustained
       release tablets containing nitrofurantoin or phenazopyridine hydrochloride"
       S.I.Abdel-Rahman, S.I.Saleh, S.M.Ahmed and A.M.Ali, S.T.P.Pharm. Sci., 3(5),
       386-390 (1993).
34. "Accelerated stability of ibuprofen-Eudragit RSPM sustained release tablets, IR 
       and DSC solid stability testing" A.A. Abdel-Rahman, A.E. Aboutaleb, A. Stamm, 
       E.M Samy and S.I. Abdel-Rahman, J. Pharm. Belg. 48(6), (463-470 1993).
35. "Accelerated stability testing of ibuprofen-Eudragit RSPM sustained release
       tablets using  H -NMR, HPLC and TLC" A.A. Abdel-Rahman,  
       S.I..Abdel-Rahman,  E.M. Samy, A.E.Aboutaleb and A Staamm, Bull. Pharm.,
        Sci. Assiut Univ.,16 (1), 1-11 (1993).
 36. "Solid stability testing of ibuprofen-Eudragit RESPM sustained release tablets"
       A.A.Abdel -Rahman, A.E.Aboutaleb, A.Stamm, S.I.Abdel-Rahman and
       E.M.Samy, Bull. Pharm. Sci.Assiut Univ., 16 (1), 12-24 (1993).
37."Evaluation of ibuprofen cellulosic polymers sustained release tablets "A.A.
        Abdel -Rahman  A.E.Aboutaleb, A.Stamm and S.I.Abdel-Rahman, Bull,
        Pharm.Sci. Assiut Univ., 16(1), 25-35 (1993).
38. " Sustained release formulations of phenazopyridine hydrochloride with cellulose
        acetate phthalate" A.M.Aly, S.M.Ahmed, S.I. Abdel-Rahman, S.I. Saleh and  
       A.E.Aboutaleb, Bull.Pharm. Sci. Assiut Univ. 16 (1) 63-72 -72 (1993).
39. "Microencapsulation of nitrofurantoin by coacervation using certain polymeric 
        materials" A.M. Aly, S.I.Saleh,  S.M. Ahmed, S.I.Abdel -Rhaman and
       A.E.Aboutaleb, Bull. Pharm.Sci. Assiut Univ., 16 (1), 73-87 (1993)
40."Interaction of benzocaine with cyclodextrins" S.I. Abdel-Rahman,
       Egypt. J. Anaeth., 10(2), 381-390 (1994).
41. "Enhancing the dissolution rates of dibucaine and lidocaine", S.I. Abdel-Rahman,
       Egypt. J. Anaeth., 10(2), 369-379 (1994).
42."Complexation of hydrochlorothiazide and bendrofluazide with -cyclodextrin in
      solution and in ground mixtures" M.O.Ahmed, S.M. Ahmed, S.I. Saleh and
      S.I. Abdel-Rahman, Saudi Pharm. J.4(1), 23 (1996).
 43. Interaction of loratadine with cyclodextrins_ Sayed I. Abdel-Rahman, Sayed M.
       Ahmad, Iman M.Samy and Ahmad M. Badawy, Ethiop. Pharm. J. 17, 1-19
      (1999).
44. Preparation and in vitro evaluation of floating sustained release captopril tablets
      and capsules_ S.H. kidr, S.I. Abdel-RAHMAN, E.M. Fettoh and O Abd-EL-
       Hakeem, Bull. Pharm. Sci. Assiut Univ. 23(1), 86-90 (2000).	
45.  Local gum of Acacia polyacantha as a binder in tablet formulation, I: Effects on 
       granule properties , Tegegne Aklilu, Sayed I. Abdel-Rahman and Tsige Gebre-
       Mariam, Ethiop. Pharm. J. 20, 1-14 (2002).
46. Local gum of Acacia polyacantha as a binder in tablet formulation, II:
      Effects on  tablet  properties , Tegegne Aklilu, Sayed I. Abdel-Rahman and  
      Tsige Gebre-Mariam, Ethiop. Pharm. J. 20, 15-30 (2002).
47. Preparation and comparative evaluation of metclorpramide sustained release matrix 
tablets, Sayed I. Abdel-Rahman, Jamal Mahrous and M. El-Badry,  Saudi Pharmaceutical Journal, 17(4), 295-303 (2009)

Supervision on Research Work:
The applicant has supervised (as a senior supervisor or a member of a committee) 32 research work for Ph.D. and M.Sc. degrees since 1987, some of which are:
"Formulation of some sustained release anti-inflammatory dosage forms"Ph.D.(1991).
"Preparation and evaluation of controlled release tablets of some diuretics"
  Ph.D. (1992).
"Solubility and stability enhancement of some model drugs by solubilization and        
  Complexation techniques" M.Sc.(1994). 
"Formulation of captopril controlled-release floating and bioadhesive delivery 
   systems,  M.Sc. (1996).
 “Evaluation of tablet process validation in the Ethiopian Pharmaceutical Factory”
 M.Sc. (2001).
"Formulation and evaluation of sustained release solid dosage forms containing 
 isoxsuprine hydrochloride" Ph.D. (2009).

Other Activities:
1.	Member of committees for promotion of staff to associate professor and professorship ranks.
2.	Reviewing and examining  Ph.D. / M.Sc. thesis  on different disciplines of 
pharmaceutics and pharmaceutical technology.
3.	Referring articles to be published in some pharmaceutical journals.
4.	Participating in editorial and correspondence work for conferences and workshops.
5.	Head/member of the committees approving M.Sc. /Ph.D. proposals.
6.	Head/member of the committees of higher studies , environmental affairs, student affairs, libraries and laboratories. Member of the College Council.  
7.	Supervising directed studies of final-year undergraduate students as well as the seminars of the postgraduates.
8.	Head of the Leadership & Governing Committee in the project of the Faculty of Pharmacy, AssiutUniversity for Contentious Development and Qualification for Accreditation from 2008 until the Faculty obtained the Accreditation in 2011. This is about how the organization is managed, the idealization of selecting the Faculty dean, vice deans and department heads. Also, it concerns the follow-up and assessment of their work and the corrective measures that could be taken to improve their performances. 
9.	Head of Management Skeleton Development of the Faculty as a part of the project mentioned in item 8 for the same period. This involves all about the employees and workers; work place, motivation, personnel qualification, training relevant for each job, assessment and promotion measures.
10.	Trainer in different aspects of Pharmaceutical Technology(QA, GMP, QC, Process Validation, R&D .etc.) for pharmacists in the Pharmaceutical Industry.

Current Research :
Working in the flowing scopes is currently performed as thesis supervised by the applicant or designed to be published as articles.  
" Micro-environmental  buffering as means for  modifying release and stabilizing solid 
  dosage forms"
 " Microemulsions as transdermal drug delivery systems" 	
 “Nano-particles as a new trend for targeting and improved efficiency of certain drugs.”
 “Effective preservation of solution dosage forms containing complexing and solubilizing  
   Agents”
"Gastro-retentive dosage forms; bioadhesion and flotation: formulation and evaluation"

I certify that the aforementioned statements are true and complete.

Sayed Ibrahim Abdel-Rahman Hassan, Ph.D.

Professor,
Pharmaceutical Technology & Pharmaceutics