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Manager Development

Location:
500062, India
Posted:
June 08, 2011

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Resume:

CURRICULUM VITAE

Dr.Devendra Narayanrao Ridhurkar

M.Pharm., Ph.D. (P'ceutics)

Flat No 101, Jyoti Pearl Apartment,

Srinivas Nagar Colony, Dr.A.S. Rao Nagar

Kapra, Hyderabad (A.P), India

Contact No.080********, 093********

E-mail: *******@*****.**.**

[pic]

Career Objective:

To become an essential intellectual asset to the company, by contributing

my proficiency comprehension and management skills.

About Me:

An upbeat, self-assured and ambitious young man. Assertive in nature,

clarity in thoughts with strongly inquisitive and research oriented mind.

Excellent outlook to work in a group having problem solving approach in

work and ability to plan and implement novel ideas. Well informed and can

put forth my ideas and arguments very lucidly and succinctly and having

excellent theoretical background with a good practical hand. Ambition in

life is to reach the heights in the field I am working, for which

prerequisites would be, honesty, hardworking and determination to success.

Personal Profile:

Name : Devendra N.Ridhurkar

Father's Name : Narayanrao M. Ridhurkar

Mother's Name : Maltitai N.

Ridhurkar

Present address : Devendra N. Ridhurkar

Flat No 101, Jyoti Pearl Apartment,

Srinivas Nagar Colony, Dr.A.S. Rao Nagar

Kapra, Hyderabad (A.P), India

*****************@*****.***

Date of Birth : 22nd November1977

Sex : Male

Nationality : Indian

Languages known : Hindi, English, Marathi and French

Marital status : Married

Educational Qualification:

Sr.N Exam Passed Board/University Year of % of Marks/

o. Passing CGPA

1 Ph.D.(Pharmaceutics) I.T.,B.H.U., Varanasi June 2007 Degree

awarded

2 M.Pharm.(Pharmaceutics I.T.,B.H.U., Varanasi May 2003 7.89 (CGPA)

)

3 B.Pharm Nagpur University July 2001 60.10

4 D.Pharm. B.T.E. Mumbai June 1997 60.10

5 S.S.C. Nagpur April 1993 68.0

6 Diploma in French B.H.U., Varanasi April 2007 57.2

Research Interests:

> Formulation and development of oral solid, Parenteral and liquid drug

delivery systems.

> Extended, modified and controlled drug delivery system.

> NDDS and targeted drug delivery systems.

> Pharmacokinetics and Bioavailability studies.

> Intellectual Property Rights (IPR), ANDA, formulation and development

of NCE and NDA for regulatory markets.

Projects:

Title of M.Pharm Dissertation:

"Formulation, characterization and in-vitro evaluation of floating

microspheres of cimetidine"under A .K.Srivastava, Department of

Pharmaceutics, I.T., B.H.U, Varanasi.(Abstract attached - Annexure I)

Title of Ph.D. Thesis:

"Hydrophilic swellable polymer based gastric floating systems for oral

controlled delivery of cinnarizine hydrochloride" under Prof J.K.Pandit,

Department of Pharmaceutics, I.T.B.H.U.,Varanasi. (Abstract attached -

Annexure II)

Present Position:

Working as Deputy Manager in Center of Excellence (Formulation and

Technology) Dr. Reddy's Laboratories, Hyderabad from December 2010 to till

date.

Membership in Professional Bodies:

Life member of Indian Pharmaceutical Graduate Association (IPGA).

Extracurricular Activities and Hobbies:

o Played Cricket and volleyball at College level.

o Volunteer for organizing "PTFD-2004"Pharmaceutical conference

organized by Society of department of Pharmaceutics held at BHU-

2004".

o Swimming, traveling and reading tabloids.

Working Experience:

Total working experience -5.0 years.

A) Presently Working as a Deputy Manager in Center of Excellence

(Formulation and Technology Dr. Reddy's Laboratories, Hyderabad from

December 2010 to till date.

Handling NDA and Platform Technology based Projects for US/EU Market like

lyophilisation, nanotechnology, cyclodextrin complexation and hot melt

extrudation.

B) Worked as an Assistant Manager in formulation and development department

in IPCA Laboratories, Mumbai in Formulation and Development division from

July 2009 to November 2010.

*successfully completed projects while working with IPCA Laboratories.

Handling sustained release and extended release projects based on

Reservoir, Matrix and MUPS Technology to be developed for US and Europe

Market like.

1. Development of extended release tablets based on matrix approach for

higher dose BCS class I drug used as oral antihyperglycemic

agent.(With PARA-IV Approach)

2. Development of extended release tablets based on Floating Bilayer and

monolithic matrix approach for class -I molecule which is light and

moisture sensitive. Also the molecule is having stomach specific

absorption and used in the treatment of benign prostate hyperplasia

(with PARA-IV Approach).

3. Development of extended release tablets for 24 hours, based on

Reservoir approach for class-I molecule generally used as an

antidepressant. (With PARA-IV Approach).

4. Development of sustained release tablets for 12 hours, based on Matrix

approach for highly unstable molecule generally used as an

antidepressant and seasonal affective disorder. (With PARA-III

Approach).

5. Development of extended release tablets for 24 hours, based on Matrix

approach for class II molecule generally used as an anti-inflammatory

(With PARA-III Approach).

6. Development of extended release tablets for 24 hours based on

Reservoir approach for class I molecule generally used as an anti-

inflammatory/analgesic using water insoluble polymers like ethyl

cellulose. (With PARA-III Approach).

7. Development of trilayer, bilayer tablets for combination of Sustained

and Immediate release layers containing 3-4 drugs using various

solubilising techniques to solubilise the class II and IV drugs

present in formulation.

C) Worked as a Research Scientist with Macleods Research Center, Andheri,

Mumbai in Formulation and Development division from June 2007 to July 2009.

*successfully completed projects while working with Macleods Research

Center.

1. Extended release tablets for BCS class I Drugs like beta blockers.

2. Sustained release capsules for poorly soluble drugs having dosage in

microgram used for benign prostate hyperplasia.

3. Developed delayed release tablets for acid sensitive proton pump

inhibitor used as an antiulcer agent for ANDA filing with

noninfringement strategy.

4. Recently filled two patent applications for Development of D.R.

Tablets for acid sensitive drug like PPI and extended release bilayer

tablet containing antipyretic drugs.

5. Two pilot bioequivalence for ANDA (with PARA-IV approach) was conceded

for two of my project handling in Macleods.

a) For delayed release tablets of acid sensitive Benzimidazole

derivative used as a proton pump inhibitor using enteric coated

polymer like Eudragit.

b) For film coated IR tablets for drug used for Alzheimer disease.

6. Knowledge about international GMP guidelines and experience in

a GMP environment in

Pharmaceutical sector.

C) Worked as a Principal for 3 months at IDIOP Digras, Maharashtra during

February 2004 to May 2004.

D) Worked as an R&D officer in F&D division in Indchemie (Alkem group) for

8 months at Daman during May 2003 to December 2003.

*successfully completed projects while working with Indchemie (Alkem group)

1) Development of antiviral drugs (Saquinavir and Lopinavir) and

2) Antiallergics and Antitussives in soft gelatin during working with

Indchemie.

Practical Skills:

< Formulation of novel drug delivery systems, formulation and

development of soft gelatin capsules and tablets.

< Sound knowledge of development of formulation for regulatory market

like USA, Europe, Japan and Australia, Intellectual Property Rights

(IPR),

< Sound knowledge of Quality by design and Design of experiment.

< Documentation and validation of formulations prepared on pilot plant

and commercial scale.

< Stability studies according to ICH guidelines.

< Handling of instruments viz.U.V. Spectrophotometer, HPLC, and

fluorometer and also having exposure to XRD, NMR, DSC, SEM and FT-IR

during M.Pharm.and Ph.D. projects.

< Handled critical projects like benzimidazole and statin derivatives,

and successfully developed the formulations up to Exhibit batch for

US/EU with Para IV filling.

< Knowledge about SOP,cGMP,SUPCA-IR/MR and instrument qualifications.

< Documentations required for scale up like MMF, Process optimizations

report, patent write up, and ANDA filling like product development

report as per CTD format

Awards and achievements:

* Recipient of Suresh Kare Indoco foundation scholarship from December

2004 to June 2005 and University Grant Commission, New Delhi granted

Junior Research Fellowship (JRF) for Ph.D. from July 2005 till June

2006. Banaras Hindu University granted Senior Research Fellowship

(SRF) for Ph.D. from July 2006 up to June 2007.

Publications:

a) Published: International -4, National-1 b) Under Review: 1 c)

International and National Conferences: 9 and patent application-2 ((List

attached - annexure III)

Computer literacy:

Windows, M.S. word, Microsoft excel, Power Point, Outlook express, Sigma

plot -5 and origin-6

Reference:

Prof.J.K.Pandit

Professor of Pharmaceutics

Department of Pharmaceutics, I.T.,B.H.U.Varanasi - 221 005

Tel.: (054*-*******, 49 (O) 098********

Declaration:

I here by declare that the information furnished above is true to the

best of my knowledge.

Date: / /2011

Place: Hyderabad

Dr.Devendra N. Ridhurkar

ANNEXURE-I

M.Pharm Project: Formulation, characterization and in-vitro evaluation of

floating microspheres of cimetidine.

Project Abstract: The present study involves preparation and evaluation of

floating microspheres of cimetidine for prolongation of gastric residence

time. Cimetidine is a H2 receptor antagonist having an antiulcer activity.

The choice of cimetidine is because of its poor absorption in lower

gastrointestinal tract; short half life and pH dependent solubility. The

microspheres were prepared by the solvent evaporation method using polymers

hydroxypropylmethyl cellulose and ethyl cellulose. The shape and surface

morphology of prepared microspheres were characterized by optical and

scanning electron microscopy, respectively. In vitro drug release studies

were performed and drug release kinetics was evaluated using the linear

regression method. The prepared microspheres exhibited prolonged drug

release (8 h) and remained buoyant for > 10 h. In vitro studies

demonstrated diffusion-controlled drug release from the microspheres.It is

also observed that there is decrease in release in pH 7.4 as compared to

pH1.2.

ANNEXURE-II

Ph.D. Project: Hydrophilic swellable polymer based gastric floating systems

for oral Controlled delivery of Cinnarizine

hydrochloride.

Project Abstract:

The present work is designed to develop monolithic and bilayer

floating matrix tablets of Cinnarizine HCl, which on oral administration

would be retained in gastric environment for prolonged times and thereby

increase its bioavailability and diminished side effects. Cinnarizine HCl

has a half-life of 3- 6 hr, pH dependent solubility and is better absorbed

in the upper part of gastrointestinal tract (Martindale 1993).

The major objectives of the present work were I) To develop a single unit

and bilayer gastroretentive drug delivery system employing swellable

polymers. II) To find out the relationship of swelling, erosion properties

of hydrophilic polymers with kinetics, mechanism of drug release and

floating behavior. III) In vivo evaluation of pharmacokinetics properties

(Bioavailability study) on animals.

Matrix tablets were comprised of an active ingredient, 0-80% by weight

inert materials and 20-75% by weight of one or more polymers along with

tablet excipients. All fabricated systems were evaluated for hardness,

thickness, drug content uniformity, friability, density of tablets,

resultant weight kinetics, swelling kinetics, measurement of matrix erosion

and in-vitro drug release. Compatibility study was performed on DSC and FT-

IR in order to find out drug -excipients interaction. Stability studies

were also conducted for selected formulations at room temp (27 10C) and at

50 10C for a period of 6 months. Selected formulation was also evaluated

for in vivo bioequivalence study on animals.

ANNEXURE -III

Publications:

A) Patent applications-

1) D.N.Ridhurkar, Rajendra Agarwal and Hitesh Maheshwari, Application no-

534/MUM/2009, "Extended Release Formulation Of Cyclobenzaprine".

2) D.N.Ridhurkar, Rajendra Agarwal and Hitesh Maheshwari, Application no-

2741/MUM/2008, "Paracetamol Extended Release Tablet Formulation".

B) Research papers published in international journals.

1) D. N.Ridhurkar, R. Nagarwal and J.K.Pandit "In-vitro Release Kinetics

and Bioavailability of Gastroretentive Cinnarizine Hydrochloride

Tablet".AAPS PharmSciTech, Vol.II, No.1, 294-303, 2010.

2) D.N. Ridhurkar, J. K. Pandit, Romi Barat, Neelam Mittal, D. N. Mishra,

A. Srinatha and J. Balasubramaniam "Niridazole biodegradable inserts

for local long-term treatment of periodontitis: possible new life for

an orphan drug". Drug Delivery, 13:365-373, 2006.

3) D. N. Ridhurkar, A. K. Srivastava and S. Wadhwa. Floating microspheres

of cimetidine: Formulation, characterization and in-vitro evaluation.

Acta Pharm. 55,277-285, 2005.

4) D.N. Ridhurkar, A. K. Srivastava, Saurabh Wadhwa and B. Mishra "Oral

sustained delivery of atenolol from floating matrix tablets-

formulation and in-vitro evaluation". Drug Dev. Ind. Pharm.31, 377-

384, 2005.

C) Research papers published in national journals.

1) D.N. Ridhurkar, J.K.Pandit, D Bharathi, A Srinatha and S. Singh "Long

acting ophthalmic formulation of indomethacin: Evaluation of alginate

gel systems". Indian Journal Of Pharmaceutical Sciences 69(1), 37-40,

2007.

Papers Abstracted in Congress/Seminars/Symposia

1. D. N. Ridhurkar and J. K. Pandit, "Swellable polymer based

gastroretentive matrix tablets of cinnarizine HCL: relationship

between swelling, erosion, floating and in-vitro drug release". 59th

IPC, BHU, Varanasi, December 2007.

2. D. N. Ridhurkar, A.Srinatha, R.Nagarwal, and J. K. Pandit.

"Gastroretentive insitu gelling systems of metformine: A novel

platform for redesigning liquid formulations". 58th IPC, Mumbai,

December 2006.

3. D. N. Ridhurkar, M.Thilek Kumar and J. K. Pandit. "Gastroretentive

insitu gelling systems of amoxicillin". 57th IPC, Hyderabad, December

2005.

4. D. N. Ridhurkar, M.Thilek Kumar, A.Srinatha, R.Nagarwal, M.K.Senapati

and J. K. Pandit. "Formulation and invitro evaluation of matrix

tablets containing natural polysaccharides as release modulators".

57th IPC, Hyderabad, December 2005.

5. D. N. Ridhurkar, M.Thilek Kumar, A.Srinatha, S.Chakraborty,

M.K.Senapati and J.K.Pandit "Amoxicillin -Gellan gum based matrix

tablets: Fabrication and in-vitro evaluation". 56th IPC, Kolkatta,

December 2004.

6. D.N.Ridhurkar, M.Thilek Kumar, A.Srinatha, S.Chakraborty, M.K.Senapati

and J.K.Pandit "In situ gelling system of amoxicillin for sustained

delivery". 56th IPC, Kolkatta, December 2004.

7. D.N.Ridhurkar, S.Kaushik, A.K. Srivastava, S. Wadhwa, and B.Mishra.

"Swelling modulated osmotically controlled oral drug delivery systems

of Diltiazem Hydrochloride: development and evaluation". 56th IPC,

Kolkatta, December 2004.

8. D. N. Ridhurkar, A.K. Srivastava, J. Singh, S.Singh, S. Wadhwa and

B.Mishra. "Floating microspheres of cimetidine: Formulation,

characterization and invitro evaluation". 56th IPC, Kolkatta, December

2004.

9. D.N.Ridhurkar, M.Thilek Kumar, A.Srinatha, S.Chakraborty, M.K.Senapati

and J.K.Pandit "Floating beads of Amoxicillin for prolonged oral

delivery". 56th IPC, Kolkatta, December 2004.



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