DR ANTHONY MELVIN CRASTO,WorldDrugTracker, helping millions, A 90 % paralysed man in action for you, I am suffering from transverse mylitis and bound to a wheel chair,With death on the horizon, This will not stop me, Gods call only..........
DR ANTHONY MELVIN CRASTO Ph.D ( ICT, Mumbai) , INDIA 29Yrs Exp. in the feld of Organic Chemistry,Working for GLENMARK PHARMA at Navi Mumbai, INDIA. Serving chemists around the world. Helping them with websites on Chemistry.Million hits on google, world acclamation from industry, academia, drug authorities for websites, blogs and educational contributio
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Thursday, 14 July 2016

Simi Gunaseelan

Simi Gunaseelan, PhD
Simi Gunaseelan, Ph.D.
Assistant Professor of Pharmaceutical Sciences, The University of Texas at Tyler, TEXAS, USA
links




Title: Assistant Professor of Pharmaceutical Sciences
Department: Pharmaceutical Sciences - Pharmacy
Building: WTB 346
Email: sgunaseelan@uttyler.edu
Phone: 903.565.5783

Experience





Assistant Professor of Pharmaceutical Sciences, The University of Texas at Tyler College of Pharmacy

Assistant Professor of Pharmaceutical Sciences, The University of Texas at Tyler, Tyler, TEXAS, USA
 – Present (2 years)Tyler, Texas
A. Responsibilities / Committee Appointments as ‘Founding Faculty’ at University of Texas at Tyler, Ben and Maytee Fisch College of Pharmacy, Tyler, Texas, USA (2014-Present):
• Curricular Development (Team-Based Learning Course Content, Curricular Sequencing & Integration), Curricular Mapping (2016 Standards, Appendix B, Cape Outcomes, etc.) and Programmatic & Curricular Assessment Plans
• Chair, Assessment Committee
• Member, Library Advisory Committee at University Level

B. Teaching Responsibilities at University of Texas at Tyler, Ben and Maytee Fisch College of Pharmacy, Tyler, Texas, USA (2014-Present):
• Pharmaceutical Calculations
• Pharmaceutics (Physical Pharmacy and Dosage Forms)
• Compounding Lab
• Biopharmaceutics and Advanced Drug Delivery Systems
• Elective Courses on Introduction to Nuclear Pharmacy and Advanced Drug Delivery Systems

C. Scholarly Work at University of Texas at Tyler, Ben and Maytee Fisch College of Pharmacy, Tyler, Texas, USA (2014-Present):
• Scientific research on HIV Prevention
• Development of Drug Formulations
• Pharmacy Educational Research
This scholarly work led to 2 publications in peer-reviewed journals.
(Open)2 honors and awards




Assistant Professor of Pharmaceutical Sciences, West Coast University School of Pharmacy

Assistant Professor of Pharmaceutical Sciences, West Coast University, Los Angeles, CALIFORNIA, USA
 –  (2 years)Los Angeles, California
A. Responsibilities / Committee Appointments as ‘Founding Faculty’ at West Coast University, School of Pharmacy, Los Angeles, California, USA (2012 – 2014):
• Development of School’s Vision, Mission, Values, Long & Short-term Strategic Planning of Goals, Curricular Philosophy, Programmatic Learning Outcomes, Curricular Development (Course Content, Course Credit Allocation, Curricular Sequencing & Integration), Curricular Mapping (Appendix B, Cape Outcomes, etc.) and Programmatic & Curricular Assessment Plans
• Accreditation Council for Pharmacy Education (ACPE) Application Preparation for Pre-Candidate Status
• Chair, Writing ACPE Curriculum Standards 9-15
• Chair, Admissions Committee
• Member, Faculty Search Committee
• Member, Bylaws Committee
• Member, Assessment Committee
• Member, Academic Standing Committee

B. Teaching Responsibilities at West Coast University, School of Pharmacy, Los Angeles, California, USA (2012 – 2014):
• Pharmaceutical Calculations
• Pharmaceutics I (Physical Pharmacy and Dosage Forms)
• Compounding Lab
• Pharmaceutics II (Biopharmaceutics and Advanced Drug Delivery Systems)
• Contemporary Biotechnology
• Medicinal Chemistry
• Elective Courses on Introduction to Nuclear Pharmacy and Clinical Toxicology

C. Teaching Responsibilities at West Coast University, College of Nursing, California, USA (2012 – 2014):
• Biochemistry, Fall Term 2013 (North Hollywood Campus, 40 hours of teaching) & Winter Term 2013 (Ontario Campus, 24 hours of teaching) (Total of 64 hours of teaching to nursing students).

D. Scholarly Work at West Coast University, School of Pharmacy, California, USA (2012 – 2014):
• Pharmacy curricular development
• Global trends in introducing clinical and patient-centered pharmaceutical care aspects of pharmacy education in the pharmacy curriculum.
• Review of cardiovascular effects on natural products.
This scholarly work led to 3 publications in peer-reviewed journals.

Degrees

  • 2002
    Doctor of Philosophy, Ph.D. (Physical Organic Chemistry), Dept. of Chemistry, North-Eastern Hill University, Shillong, India.
  • 1996
    Master of Science, M.Sc.(Organic Chemistry), Dept. of Chemistry, North-Eastern Hill University, Shillong, India.
  • 1994
    Bachelor of Science, B.Sc.(Chemistry), North-Eastern Hill University, Shillong, India

Education





Loma Linda University School of Pharmacy, Dept. of Pharmaceutical Sciences, CALIFORNIA, USA

Subliming Solid-Based Intravaginal Microbicide Delivery Technology for HIV Prevention

A. Research Work at Loma Linda University, School of Pharmacy, California, USA (Collaboration with Scripps Research Institute, California and University of Pittsburgh, Pennsylvania) (2010 – 2012):
Research included the development of ‘Universal Subliming Solid-based Drug Delivery Systems’ for achieving steady-state durations of intravaginal HIV microbicide delivery ranging from weeks to several months.

This research work led to 2 publications in highly reputed journals.

B. Teaching Responsibilities at Loma Linda University, School of Pharmacy, California, USA (2010 – 2012):
• Pharmaceutics II (Physical Pharmacy), PY1, Winter Quarter 2012




Rutgers University School of Pharmacy, Dept. of Pharmaceutical Sciences, NEW JERSEY, USA

Polymer-Based Drug Delivery Technology for Cancer and HIV Therapeutics

Research Work at Rutgers University, School of Pharmacy, New Jersey, USA (2002 – 2010): Research included the development of an anti-cancer drug delivery system using novel hydrogel formulation for cancer therapy by releasing drug or modified version of that drug (nanocarriers using PEGs/polymers, peptidic carriers and targeting agents) at a relatively constant rate for a period ranging from days to weeks. Research also included the development of an anti-HIV drug delivery system using novel prodrugs/nanocarriers of HIV protease inhibitors and peptides and peptide mimetics involving PEGs/polymers, peptidic carriers and targeting agents with a potential for development into new types of AIDS therapeutics.

This research work led to 3 ‘Issued’ United States Patents, 2 United States Patent Applications and 8 publications in highly reputed journals.





North-Eastern Hill University, Dept. of Chemistry, Shillong, INDIA

Doctor of Philosophy (Ph.D.), Physical Organic Chemistry

PhD Research Work at North-Eastern Hill University, Dept. of Chemistry, Shillong, India (1997 – 2002):
• Oxidation of different types of aldehydes, ketones and acids using inorganic oxidizing agent, quinolinium dichromate (QDC). Chemical characterization of oxidized products.
• Kinetics and Mechanism of Oxidation Reactions – Extensive kinetic studies on oxidation reactions of aldehydes, ketones and acids spectrophotometrically. Evaluating mechanistic pathway of these oxidation reactions based on their kinetic profile.

This research work led to 10 publications in journals of repute.

Summary

Dr. Gunaseelan is currently an Assistant Professor at the University of Texas at Tyler College of Pharmacy for the past 2 years. She moved from West Coast University School of Pharmacy, California where she served as an Assistant Professor for 2 years. She possesses 8 extensive years of research experience from Rutgers University School of Pharmacy, New Jersey. She also gained 2 years of research and teaching experience from Loma Linda University School of Pharmacy, California. For the past 14 years she has been working on `Novel Drug Delivery Systems' for HIV Prevention & HIV and Cancer Therapeutics. At Rutgers University, New Jersey, she worked on NIH RO1 grant projects where her main focus was on `Polymer-Based Drug Delivery Technology for HIV & Cancer Therapeutics' while at Loma Linda University, California, she worked on NIH RO1 grant project specific to `Subliming Solid-Based Intravaginal Microbicide Delivery Technology for HIV Prevention'. Her research work resulted in 5 patents, 25 publications in high-impact journals and 27 presentations at national and international level. Her dedication towards research work at Rutgers University, New Jersey, led her to be a recipient of Merit Award for 3 consecutive years. She has been honored with a 'Certificate of Recognition' for her research presentation (podium) on "Novel Intravaginal Delivery of Antiretroviral-based Microbicides for HIV Prevention" at the 2015 World Drug Delivery Summit, Houston where she was an Invited Speaker. She received the 2016-2017 University of Texas at Tyler Research Award for her research "Elimination of Bitterness in Pediatric Oral Suspension using Novel Formulation". She is currently a reviewer for Advanced Drug Delivery Reviews, Pharmaceutical Research and Controlled Release Society Meetings.

http://www.uttyler.edu/directory/pharmacy-pharmaceuticalsciences/gunaseelan.php

http://drugdelivery.pharmaceuticalconferences.com/speaker/2015/simi-gunaseelan-university-of-texas-usa
Teaching Appointments

2014 – Present
Founding Faculty (Assistant Professor), Dept. of Pharmaceutical Sciences, Ben and Maytee Fisch College of Pharmacy, The University of Texas at Tyler, Texas, USA.
2012 – 2014
Founding Faculty (Assistant Professor), Dept. of Pharmaceutical Sciences, School of Pharmacy, West Coast University, California, USA.
2010 -2012
Senior Research Associate (NIH project - “Subliming Solid - Based Intravaginal Microbicide Delivery Technology for HIV Prevention”), Dept. of Pharmaceutical Sciences, School of Pharmacy, Loma Linda University, California, USA.
2002 - 2009
Postdoctoral Associate, Research Associate, Senior Research Associate(NIH projects-“Polymer-Based Drug Delivery Technology for Cancer& AIDS Therapeutics”), Dept. of Pharmaceutical Sciences, School of Pharmacy, Rutgers University, New Jersey, USA.

Complete Curriculum Vitae







Biography

Gunaseelan’s research expertise is in drug delivery. For the past 10 years she has been working towards developing ‘Novel Drug Delivery Systems’ for HIV Prevention & HIV and Cancer Therapeutics. Her research works resulted in 5 patents, more than 20 publications in high-impact journals and presentations in 20 national and international conferences. Her dedication towards research work at Rutgers University School of Pharmacy New Jersey, led her to be a recipient of Merit Award for 3 consecutive years. She is currently a journal reviewer for Advanced Drug Delivery Reviews, Pharmaceutical Research, and Controlled Release Society Meeting Abstracts

Abstract

Objectives: Microbicides, products applied vaginally or rectally, are effective at preventing HIV transmission. However, many products (e.g., peptides, antiretroviral drugs) are reactive or incompatible in the existing diffusion/hydrolysis/dissolution based delivery systems. To overcome the issues of extended delivery and product compatibility, the use of a novel subliming solid matrix-based delivery system is described here. Methods: The microbicides C5A, tenofovir fumarate, emtricitabine, dapivarine, UC-781 and IQP0528 were employed as representatives of a range of molecular structures and physicochemical properties. Hydrophobic, chemically inert subliming solid matrices, utilized for microbicide formulations and achieving a defined range of sustained release rates, included norbornane, hexamethylcyclotrisiloxane, perfluoroundecane, perfluorododecane and cyclododecane. Rates of matrix sublimation and concomitant microbicide release were determined in vitro. Formulations were tested for cellular toxicity, and durations of anti-HIV-1 activity by constant release of microbicides from the sublimable matrices. Results: Subliming solid matrices release microbicides by surface erosion achieved through sublimation. Zero order sustained microbicide release was achieved in vitro, at rates independent of microbicide structures and properties, and controlled exclusively by sublimation enthalpies of each hydrophobic matrix material. The matrices provided prolongation of anti-HIV-1 activity relative to bolus microbicide administration, when evaluated in cultured human ectocervical tissue, macrophages, and TZM reporter cells. No evidence of matrix toxicity was observed after continuous exposure to macrophages, T-lymphocytes, PBMC cells and ectocervical explants. Implications: Subliming matrices offer unique attributes that will allow steady-state delivery of any microbicide, over durations ranging from weeks to months, by employing, simple, stable, and readily available matrix materials, suggesting novel delivery capabilities.

As a Faculty all geared up in my PhD gown to honor the University of Texas Students at the Phi Kappa Phi Honors Society_Tyler, Texas April 2016— at University of Texas at Tyler.



With my favorite Pharmacy Doctorate Students @ West Coast University, Los Angeles, California - November 2014

STR1
See ppt at

Biography

Gunaseelan’s research expertise is in drug delivery. For the past 10 years she has been working towards developing ‘Novel Drug Delivery Systems’ for HIV Prevention & HIV and Cancer Therapeutics. Her research works resulted in 5 patents, more than 20 publications in high-impact journals and presentations in 20 national and international conferences. Her dedication towards research work at Rutgers University School of Pharmacy New Jersey, led her to be a recipient of Merit Award for 3 consecutive years. She is currently a journal reviewer for Advanced Drug Delivery Reviews, Pharmaceutical Research, and Controlled Release Society Meeting Abstracts

Abstract

Objectives: Microbicides, products applied vaginally or rectally, are effective at preventing HIV transmission. However, many products (e.g., peptides, antiretroviral drugs) are reactive or incompatible in the existing diffusion/hydrolysis/dissolution based delivery systems. To overcome the issues of extended delivery and product compatibility, the use of a novel subliming solid matrix-based delivery system is described here. Methods: The microbicides C5A, tenofovir fumarate, emtricitabine, dapivarine, UC-781 and IQP0528 were employed as representatives of a range of molecular structures and physicochemical properties. Hydrophobic, chemically inert subliming solid matrices, utilized for microbicide formulations and achieving a defined range of sustained release rates, included norbornane, hexamethylcyclotrisiloxane, perfluoroundecane, perfluorododecane and cyclododecane. Rates of matrix sublimation and concomitant microbicide release were determined in vitro. Formulations were tested for cellular toxicity, and durations of anti-HIV-1 activity by constant release of microbicides from the sublimable matrices. Results: Subliming solid matrices release microbicides by surface erosion achieved through sublimation. Zero order sustained microbicide release was achieved in vitro, at rates independent of microbicide structures and properties, and controlled exclusively by sublimation enthalpies of each hydrophobic matrix material. The matrices provided prolongation of anti-HIV-1 activity relative to bolus microbicide administration, when evaluated in cultured human ectocervical tissue, macrophages, and TZM reporter cells. No evidence of matrix toxicity was observed after continuous exposure to macrophages, T-lymphocytes, PBMC cells and ectocervical explants. Implications: Subliming matrices offer unique attributes that will allow steady-state delivery of any microbicide, over durations ranging from weeks to months, by employing, simple, stable, and readily available matrix materials, suggesting novel delivery capabilities.

Speaker Presentations




 
Simi Gunaseelan
 Presentations at the 2016 AACP (American Association of Colleges of Pharmacy) Meeting : A 5-Day Annual Pharmacy Conference_July 2016_Anaheim Convention Center, California — at Anaheim Convention Center.

 


 


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Wednesday, 13 July 2016

Marcep Inc. Organises Pharma Quality Metrics Conclave, 26-27 July 2016, Mumbai, India

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Pharma Quality Metrics Training Brochure


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Phone022 6707 6707






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Head Research

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Email:   abadu@marcepinc.com
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Mosad Ghareeb

DrMosad Ghareeb's Profile Photo



Mosad Ghareeb
Lecturer at Theodor Bilharz Research Institute (TBRI)


Dr. Mosad Ahmed Ghareeb, Ph.D.
Lecturer (Medicinal Chemistry).
Biochemistry& Molecular Biology and Medicinal Chemistry Department.
Theodor Bilharz Research Institute (TBRI).
Warrak El-Hadar-12411, P.O Box 30 Imbaba, Giza, Egypt.

Web Site: http://www.tbri.sci.eg.Tel. 002-0235401019; Fax 002-0235408125.
Home  Tel. 00201122034012.

E. Mails: mosad_tbri@hotmail.com/ m.ghareeb@tbri.gov.eg
                 mosad.tbri@gamilcom/ mosad_tbri@yahoo.com

Home Address: 7 El-Nozha St., Gezert El-Nagdi, Kaluib City, El-Kaluibia, Governorate, Egypt





Summary

I am interested in the field of natural products. My research includes: Medicinal Chemistry, Chemistry of natural product, phytochemistry including isolation, purification and structural elucidation of the different classes of natural products which isolated from medicinal plants. Biological evaluation of the different extracts as well as fractions and the isolated compounds as anti-tumor (Cell Lines), anti-HIV, antimicrobial, antioxidant and hepatoprotective activities. Study of the structure activity relationship (SAR) of the isolated compounds as well as nanoparticles technology. In details, my research interests focus on finding out novel bioactive antioxidant and anticancer chemo-preventive agents from the medicinal plants by subjecting the plants under investigation to comprehensive bioassay-guided investigation to isolate and evaluate the anticancer related activities of the known and novel secondary metabolites that might be present in these plants. Isolation and identification of the potent anti-tumor lead compounds based on various chromatographic methods, and spectroscopic NMR and MS analysis. Study the mechanism of action and evaluating the cytotoxicity, antioxidant and antitumor in vitro activities of the obtained extracts, fractions, sub-fractions, and the isolated secondary metabolites in a close collaboration with the biologists and pharmacologists.

Experience

Lecturer

Theodor Bilharz Research Institute (TBRI)
 – Present (5 years 5 months)Biochemistry& Molecular Biology and Medicinal Chemistry Department

Dr

Self-employed
 – Present (12 years 8 months)

Publications

Antioxidant and Cytotoxic Activities of Gmelina arborea ROXB. Leaves(Link)

British Journal of Pharmaceutical Research
October 5, 2013
Aims: The leaves of Gmelina arborea (ROXB.) (Family Verbenaceae) are widely used in
the folklore to treat various types of diseases. In this study, the antioxidant and cytotoxic
activities of different methanolic extracts and the derived subfractions of 90% methanolic
extract of this plant were evaluated.
Methodology: The antioxidant activity was carried out via three different quantitative

Radical scavenging potential and cytotoxic activity of phenolic compounds from Tectona grandis (Linn.)

Global Journal of Pharmacology
November 10, 2013
Ten compounds including two phenolic acids and eight flavonoids were isolated from n-butanol and
ethyl acetate fractions of Tectona grandis leaves part (Family Verbenaceae). All of the compounds were
isolated and purified via different column chromatography. Their structures were elucidated via UV, IR
and NMR spectral techniques as well as (Co-PC, Co-TLC and Co-m.p.) and acid hydrolysis to be...more

Antioxidant and cytotoxic activities of Tectona grandis Linn leaves

International Journal of Phytopharmacology
January 15, 2014
Cancer prevention and treatment have attracted increasing interest. Leaves of Tectona grandis Linn. (Verbenaceae) are widely used in the folklore to treat various types of diseases. This study characterizes the antioxidant activity, total phenolic content (TPC) and cytotoxic activity of different methanolic extracts as well as the derived subfractions (Pet. ether; CHCl3, EtOAc and n-BuOH) from the...more

Antioxidant and cytotoxic activities of flavonoidal compounds from Gmelina arborea (Roxb.)

Global Journal of Pharmacology
January 10, 2014
A bioassay-guided fractionation and chemical investigation of the Gmelina arborea leaves
(Verbenaceae) resulted in the isolation and characterization of six known flavonoids (1, 3-7) along with new
flavone glycoside (2), identified as; luteolin (1), luteolin-4'-O- -D-4C -galactoside (2), kaempferol (3), quercetin -
1
3 - O - - D - 4C -glucopyranoside (isoquercitrin) (4), quercetin - 3 - O - -...more

Antioxidant Activity of Heterocyclic Compounds Derived from 4-(4-Acetamidophenyl)-4-oxobut-2-enoic Acid

International Journal of Science and Research
May 10, 2014
4-(4-Acetamidophenyl)-4-oxobut-2-enoic acid 1 and / or its aza Michael adduct 2 were efficiently utilized to construct novel
various heterocycles including derivatives of furanones (3a-c & 14), pyridazinones (4-6), diazepine (7), piperazine (8), oxazine (9),
oxazole (10a), thiazole (10b), benzo-, [-diazin, -oxazin, -thiaz-]-ones (11a-c). Conduct (11c) with NH2-NH2..H2O in boiling ethanol and...more

TOTAL PHENOLIC CONTENTS AND ANTIOXDANT ACTIVITIES OF FICUS SYCOMORUS AND AZADIRACHTA INDICA

Pharmacologyonline 3: 590-602 (2009)
February 10, 2009
In this study, the total phenolic content of the methanol, methanol-water mixtures and
water extracts of the leaves of two plants growing in Egypt; Ficus sycomorus and
Azadirachta indica were determined by using Folin-Ciocalteu reagent. Also, the
antioxidant activity of these extracts was evaluated by using two methods including
DPPH radical scavenging activity assay and total antioxidant...more

BIO-GUIDED ISOLATION AND STRUCTURE ELUCIDATION OF ANTIOXIDANT COMPOUNDS FROM THE LEAVES OF FICUS SYCOMORUS

Pharmacologyonline 3: 317-332 (2010)
March 15, 2010
This study was performed to investigate the antioxidant activity of the defatted
70% methanol extract of Ficus sycomorus leaves using DPPH radical scavenging
assay-guided isolation. This extract was fractionated using CHCl3, EtOAc and n-
BuOH. The results revealed that EtOAc and n-BuOH have strong DPPH radical
scavenging (SC50 =13.48 and 8.47 μg/ml). Therefore, each EtOAc and n-BuOH was
...more

EFFECT OF FICUS SYCOMORUS AND AZADIRACHTA INDICA EXTRACTS ON LIVER STATE OF MICE INFECTED WITH SCHISTOSOMA MANSONI

J. Egypt. Soc. Parasitol., 41 (1), 2011: 77 - 88
March 20, 2011
The potential role of hepatoprotective and antipathological effect of Ficus
sycomorus and Azadirachta indica extracts was evaluated for scavenging the
reactive oxygen species (ROS) and reduced the oxidative damage and pathological
changes in the liver of S. mansoni infected mice. The levels of alanine
aminotransferase (ALT), asparate aminotransferase (AST) and gamma glutamyl
transferase (GGT)...more

Chemical constituents, antischistosomal and antioxidant activity of methanol extract of Azadirachta indica

Egyptian Journal of Chemistry 54, 105-119, 2011
June 15, 2011

In vitro Antimicrobial Activity of Five Egyptian Plant Species

Journal of Applied Pharmaceutical Science
September 4, 2015
In this study, five Egyptian species were tested for their In vitro antimicrobial activities. The antimicrobial
screening was carried out via disc diffusion method toward four strains of the clinical antibiotic resistant
pathogens including Escherichia coli, Staphylococcus aureus, Candida albicans and Aspergillus niger. Among
the methanolic extracts screened, Azadirachta indica, Tectona grandis...more

CYTOTOXIC SCREENING OF THREE EGYPTIAN PLANTS USING BRINE SHRIMP LETHALITY TEST

International Journal of Pharmacy and Pharmaceutical Sciences
August 25, 2015
Objective: Brine shrimp (Artemia salina L.) bioassay is considered as a preliminary screening for the presence of antitumor compounds and used to determine the toxicity of plant extracts. Different extracts of three Egyptian plants, philodendron selloum (Araceae), Bougainvillea alba (Nyctaginaceae) and Ulmus parvifolia (Ulmaceae) 

Additional Info

  • Advice for Contacting Mosad

    E-mail addresses: mosad_tbri@hotmail.com.
    mosad_tbri@yahoo.com.





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