Tuesday, 31 July 2012


Completion and validation of a Graduation Research Project is an essential requirement for obtaining the degree of B. Pharm. The Project is required to be prepared as per the following rules and conditions:
The students in the fourth year of B. Pharm. shall present a project based on all round knowledge they have acquired in the five main subjects viz., pharmacy practice, pharmaceutics & pharmaceutical technology, pharmaceutical & medicinal chemistry, pharmacognosy, & phytochemistry and pharmacology & toxicology. This project also includes a research work, which the students carry out on recent developments in pharmaceutical sciences.
Objectives of the Graduation Research Project
  • To ensure that the sum total of the academic achievement of the student is in consonance with the goals of the College.
  • To ensure that the student is sufficiently trained to extract necessary pharmaceutical information directly from different sources like Internet, Journals etc.
  • To have sufficient training to compile, classify and organize matters relating to pharmacy.
  • To train the student in presenting coherently the information collected by her.
  • To make the student aware of the latest aspects of pharmaceutical science.
  • To develop keenness in student for acquiring more and more knowledge about pharmaceutical sciences.
  • To create an ability among students in carrying out applied academic research on matters connected with latest development in pharmaceutical sciences.
Completion of the Graduation Research Project
The dissertation project shall be completed within one year starting in one September and finishing in the next September. Completion of the Graduation project, involves the following steps.
Presentation Procedure
  • Each member of the Pharmacy College staff or of the teaching panel from the Medical College shall suggest a few topics in right proportion to the number of students.
  • The selected topics shall be notified to the students at the end of the 2nd semester of the 3rd year.
  • Each student shall select six essays and one research topic by the end of June.
Procedure for selection and registration of topics for Graduation Research Project
  • Each staff member teaching in B. Pharm. gives a list of six essay topics and two research topics in his/her area of specialization to the Dean. 
  • All essay and research Project topics shall be notified to the students at the end of the 2nd semester of the 3rd year. 
  • Each group of two students selects from this list six essay topics and one research topic latest by 30th June. 
  • These essay and research topics shall be registered with the Supervisors latest by 10th July. 
  • The College Council shall approve research and essay topics and appoint the Supervisors.
Collection of data for Graduation Research Project
Dubai Pharmacy College provides sufficient facilities to the students for conducting the research and writing the Project.
Facilities for Project writing
  • Drug Information Center of Dubai Pharmacy College.
  • Central Library of Dubai Pharmacy College.
  • Internet facility provided by Dubai Pharmacy College.
  • Computers available in the College.
  • Library of Dubai Hospital.
Facilities for Research work of Project
  • Science Laboratories of Dubai Pharmacy College.
  • Science Laboratories of Dubai Medical College for Girls.
  • Instrumentation facilities of Central Laboratory of the Foundation.
  • Dubai Government hospitals under the Ministry of Health.
  • Pharmaceutical Companies.
  • Some general pharmacies.
Typing and designing of the Project’s dissertation
  • The typing and designing of the Project’s dissertation should be done as per the following guidelines.
  • The design of the cover page of the Project’s dissertation should be as given below:

  • The second page should have the contents of the Project’s dissertation.
  • The third page should have Part-I of Project essay topic number-I.
  • The fourth page should have the design as shown below

  • Pages following the one containing the Project topic I, should have the following:
    • Synopsis of the study.
    • The data given in support of the topic should be systematic, with reference numbers.
    • The tables or figures given at the end of each project should be numbered properly.
    • All lists and figures must be numbered.
  • After finishing the Project topic I the same pattern should be followed in writing the other Project essays.
  • After this , in the stage of writing the research work follow the pattern given below:

  • All the above mentioned points should be discussed with the concerned Supervisor. Rough copy should be got checked and approved from the Supervisor before the final copy is made.

project topics in chemistry and pharmaceutics

Method Development of Capecitabine HCl by HPLC

Method Development of  Resveratrol by HPLC

Method Development of Ropinarole by HPLC

Method Development of  Gefitinib by HPLC

Method Development of  Dorzolamide by HPLC

Estimation of Esomeprazole Magnesium in Pharma Dosage Forms  by HPLC

Estimation of  Fluconazole in Pharma Dosage Forms  by HPLC

Estimation of  Loratadine in Pharma Dosage Forms  by HPLC

Estimation of  Quetiapine Femarate in Pharma Dosage Forms  by HPLC

Estimation of  Gabapentin in Pharma Dosage Forms  by HPLC

UV Visible Method For Estimation Of Rebaprazole Sodium in the Dosage Forms

UV Visible Method For Estimation Of  Pentoprazole Sodium in the Dosage Forms

UV Visible Method For Estimation Of  Tadalafil in the Dosage Forms

UV Visible Method For Estimation Of  Sertraline HCl in the Dosage Forms

UV Visible Method For Estimation Of  Irbesatran HCl in the Dosage Forms

Simultaneous Estimation of Omeprazole and Domperidone by HPLC

Simultaneous Estimation of Metformine HCl and Pioglitazole by HPLC

Simultaneous Estimation of Rabeprazole and Domperidone by HPLC

Simultaneous Estimation of Nebivolol and Hydrochlorothiazide by HPLC

Simultaneous Estimation of Cefixime and Ornidazole by HPLC

RP- HPLC Method Development of Ofloxacin and Ornidazole by HPLC

RP- HPLC Method Development of Montelukaust Sodium and Cetrizine by HPLC

RP- HPLC Method Development of Amlodipine and Atorvostatine by HPLC

RP- HPLC Method Development of Lamividine and Zodovidine by HPLC

RP- HPLC Method Development of Losartan Potassium and Rosuvastatine by HPLC

Dissolution Studies of  Metformine Sustain Release Pellets

Dissolution Studies of Diclofenac Sodium Sustain Release Pellets

Dissolution Studies of Indomethacin Sustain Release Pellets

Dissolution Studies of Cefixime Immediate Release Pellets

Dissolution Studies of  Pentoprazole Sodium Enteric Coated Release Pellets

Saturday, 21 July 2012

format for m.pharm and b. pharm synopsis


“DESIGN AND DEVELOPMENT OF ---------------------------------- FOR ------------- DELIVERY”

Synopsis for M.Pharm Dissertation submitted to the
------------------------- Universit ,  District , STATE.

By




Name of Student
M.Pharm. SEM-I/II/III/IV
Or
B.Pharm. Sem-I/II/III/IV/V/VI/VII/VIII


 SHAPE  \* MERGEFORMAT
Mono of the university




Under the guidance of


Name of Guide,  M.Pharm, Ph.D. (Qualification)


Department of Pharmaceutics,/Pharmacognosy/Pharmacology…..(As correct)
Name and address of college
Year (e.g. 2012-2013)


RAJIV GANDHI UNIVERSITY OF HEALTH SCIENCES,

 KARNATAKA, BANGALORE.

ANNEXURE II

PROFORMA FOR REGISTRATION OF SUBJECTS FOR DISSERTATION


 1.
NAME OF THE CANDIDATE
AND ADDRESS (IN BLOCK LETTERS)

 2.

NAME OF THE INSTITUTION


 3.

COURSE OF STUDY AND SUBJECT


 4.
DATE OF ADMISSION OF COURSE

 5.
TITLE OF TOPIC

 6.
BRIEF RESUME OF THE
INTENDED WORK
6.1 Need for the study
6.2 Review of the literature
6.3 Objectives of the study

                      
ENCLOSURE - I
ENCLOSURE - II
                   ENCLOSURE – III
7.                    

MATERIALS AND METHODS

7.1 Source of data   

7.2 Method of collection of data

7.3Does studies require any investigations or interventions to be conducted on patients or other human or animal? If so, please describe briefly.

7.4 Has ethical clearance been obtained from your institution in case of 7.3

                    ENCLOSURE – IV
 ENCLOSURE -  V
                    ENCLOSURE – VI




                    
                    ENCLOSURE – VI

 8.

LIST OF REFERENCES

ENCLOSURE – VII

  9.

SIGNATURE OF CANDIDATE


                  

10.

REMARKS OF GUIDE

RECOMMENDED

11.






























NAME AND DESIGNATION OF

11.1 Guide







11.2 Signature


11.3 Co guide (if any)


11.4 Signature



11.5 Head of department






11.6 Signature











Not applicable.


Not applicable.









12.1 Remarks of the   
        Chairman and Principal

12.2 Name and designation of principal





12.3 Signature





       RECOMMENDED & FORWARDED


.


6.0



























































































































  BRIEF RESUME OF THE INTENDED WORK

ENCLOSURE - I

6.1 Need for the study 
                                                
ENCLOSURE - II
6.2 Review of the literature 

ENCLOSURE – III

6.3 Objectives of the study
1.                   To prepare the -------- loaded with
2.                   To carry out the evaluation  for the prepared -----------------.
3.                   To study the drug polymer compatability and surface morphology of the prepared
4.                   To carry out the in vitro release studies and stability studies of the prepared

MATERIALS AND METHODS:
DRUG           :  
POLYMERS :
SOLVENTS  : 

Methods
  • Preparation of --------- by
·        Evaluation
     
                

ENCLOSURE – IV

7.1. Source of data

a.       Library: College of Pharmacy. 

b.      E-library: College of Pharmacy.

ENCLOSURE-V
7.2. Method of collection of data
       1.Literature search.
       2.Laboratory experiments.
       3.--- -------------------other studies
          

A) Preparation
       
B) Characterization:
     



ENCLOSURE – VI


7.3. Does the study require any investigation or intervention to be conducted on patients or other humans or animals? If so, please mention briefly.

                                                                 -YES-

7.4. Has ethical clearance been obtained from your institution in case of 7.3?
                                                                   -IN PROCESS-


                                                                                         
                                                     

                                                       
                                                ENCLOSURE – VII

LIST OF REFERENCES:

1.       
2.      Maheshwari RK, Singh AK, Gaddipati J, Srimal RC. Multiple biological activities of curcumin:a short review. Life Sci 2006;78;2081–2087. 
3.      Arvind Sharma, Subheet jain, Manu modi , Vikrant Vashisht, Harpreet singh. Chitosan based biodegradable nanoparticles. Rjpbcs 2010;1;78-88.
4.      Hiroki Sasaki, Yoichi Sunagawa, Kenji Takahashi, Atsushi Imaizumi, Hiroyuki Fukuda, Tadashi Hashimoto, Hiromichi Wada, Yasufumi Katanasaka, Hideaki Kakeya,Masatoshi Fujita, Koji Hasegawa  and Tatsuya Morimoto. Innovative Preparation of Curcumin for Improved Oral Bioavailability Biol. Pham 2011;34; 660-665.

  

http://www.csvtu.ac.in/pdf_doc/Manual%20for%20Thesis%20Writing.pdf

Tuesday, 17 July 2012

SYNOPSIS REPORT format

 It must contain the elements given in the listing below:
1) Cover sheet
2) Title page
3) Certificate page (From outside and/or Institute)
4) Declaration
5)  Table of Contents
6)  Introduction
7)   Plan of work
8) Title of the proposed project
9) Aim and objectives
10) Literature survey and Research envisaged
11)  Methodology/Schedule of activities
12) Achievements till date
13) Remaining Work
14) Solution to problems (if any)
15) Bibliography

The format may vary depending on universities/ courses/ ordinance.

Pharmacy project synopsis guidelines

GUIDELINES FOR PREPARING SYNOPSIS REPORT:
1. Paper Size = A4
2. Spacing between Lines = 1.5 inch
3. Font Size = 12
4. Fonts = Times New Roman / Book Antiqua
5. Left Margin = 1.3 inch
6. Right Margin = 0.8 inch
7. Top Margin = 1.2 inch
8. Bottom Margin = 1.2 inch
9. Header Contents: Short Title of Project
10. Footer Contents: College/Institute name and page number lower right side
11. Hard Bound File


Pharmacy is the health profession that links the health sciences with the chemical sciences and it is charged with ensuring the safe and effective use of pharmaceutical drugs. The word derives from the Greek: φάρμακον (pharmakon), meaning "drug" or "medicine" (the earliest form of the word is the Mycenaean Greek pa-ma-ko, attested in Linear B syllabic script
The field of Pharmacy can generally be divided into four primary disciplines:

Project work planning
The project plan is one of the most important and useful documents in your toolkit, and should be referred to and updated throughout the project lifecycle. Its initial purpose is to kick-start the project by convincing the decision makers (usually the people who control the funds e.g. the Project Board or Steering Committee) that the project is viable and will meet their needs and timeframes, budgets, expectations. If the project plan is poorly written or contains insufficient detail, the project may not even get past this first decision gate and may never actually get off the ground. Many viable projects have floundered at this stage due to poor planning and communication. On the flip side, if you can deliver a great project plan, it establishes your credibility as a project manager, starts the project on a sound footing, and provides the team with a mandate for action and a clear direction to follow.