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Journal of Pharmacy Research
ISSN NO: 0974-6943
The Journal of Pharmacy Research is an online Journal,  publishing of correct version and document can be modified (when we/or author) get comments and any readers can give comments. The journal is devoted to the promotion of Pharmaceutical sciences and related disciplines (including Pharmacy, medical, Biotech, Botany, organic and medicinal  chemistry,  Nursing, Paramedical, prescription etc  fields).
Process of publishing research communication continues to grow with many new tools, which will help analysis of total citation count and  Impact Factor TM ( India ) of JPR. JPR Solutions is publishing, Archiving freely, and our tools to catch the data of citations, which are available from online, and JPR solutions will complete by monitoring and capturing the proper citations.
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Journal Metrics for this  Journal of Pharmacy Research (Source ID: 21100325431): 2015(SNIP) Source Normalized Impact Per Paper : 0.575; SCImago Journal Rank (SJR):0.194; Impact Per Publication : 0.575 (Top level : Life Science)
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  •    Impact Factor TM ( India ) of JPR. 2.95 as on date (02.01.2017) Authors can use these sites to for more visibility of their articles 





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  • Main Author Guideline

    The Journal publishes reviews, research articles and short communications.

    The scope of the journals is to publish clinical and Pharmaceutical Sciences which include organic, inorganic, analytical chemistry, pharmaceutics, pharmacology, phytochemistry and pharmacognosy, pharmaceutical analysis, pharmaceutical microbiology and biotechnology.

    It is essential that authors prepare their manuscripts according to established specifications. Failure to follow them may result in papers being delayed or rejected. Therefore, contributors are strongly encouraged to read these instructions carefully before preparing a manuscript for submission. The manuscripts should be checked carefully for grammatical errors. All papers are subjected to rapid peer corrections and publish in Online. Types of manuscripts Research papers: Papers should present new experimental studies in elaborate form that constitute a significant contribution to knowledge. Research Papers should not exceed 15 pages. Short communications: Papers are the one that should present new important findings in a brief form,a maximum of 10 pages including illustrations. Review articles : Papers should bring up the most important current topics or present interpretative and critical accounts, but not simple compilation, on subjects of general interest. They should be around 30 or more pages. Manuscripts are accepted on the understanding that the authors have obtained the necessary authority for publication. Manuscripts with multi-authors imply the consent of each of the authors. Submission of an article to JPR is understood to imply that it has not been either published or not being considered for publication elsewhere. Manuscripts should be neatly typed, single-spaced throughout, including tables, graphs, figures ( IN EXCEL FORMAT). Manuscript should be uniform size with at least 1.0 cm margins on all sides. We do not want any hard copy or CD of the Manuscripts. Only complete file should be submitted to the

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    Examples: Journals Author (last name) AB (initials), Author BB, Title of Article, Journal name, volume, year, page numbers.:Books: Author AB, Author BB, Author CC, Title of Book, Ed, Vol, Publisher, City, year, page numbers.

  • As part of the submission process, authors are required to check off their submission's compliance with all of the following items, and submissions may be returned to authors that do not adhere to these guidelines.

    1. Journal of Pharmacy Research ( ISSN (ONLINE ) : 0974-6943 As part of the submission process, authors are required to check off their submission's compliance with all of the following items, and submissions may be returned to authors that do not adhere to these guidelines.
    • The submission (Research or Review etc.) has not been previously published elsewhere, is original and has been written by the stated authors.
    • The article is not currently being considered for publication by any other journal and will not be submitted for such review while under review by JPR
    • The submission file is in Microsoft Word file (2003 or 2000 format).All Tables and figures in Excel format only
    • Table number ,figure number should be placed within the text at the appropriate points rather than at the end.
    • Figures should be always original. if copied then proper citation must be placed bellow the figures.
    • Corresponding authors E-mail,Mobile number and full address must be given at the first page of article.
    • Copyright must be signed by all authors and submitted along with article.
    • Do not copy of 10 words at a stretch many words or paragraph from other author published work.
    • Work should be novel and full of novel informations
    • References given in text should be superscript with numerical .
    • Article Should be arrange like the following

    Title: Development and Validation of a RP-HPLC Method for Simultaneous Densitometric Analysis ------

    Authors: A.B. Mukherjee1, S. A. Gupta*1 and K. Kumar2------------------

    Affiliations:1Asian University ,Department of Pharmaceutical Sciences, Indian College of Science, Pune – 411038,Maharastra, India. Address for corresponding author: A.B. Mukherjee Asian University ,Department of Pharmaceutical Sciences, Indian College of Science, Pune – 411038,Maharastra, India. E-mail: Phone:



    INTRODUCTION G. acid is a group of triterpenoid saponins isolated from Gymnema sylvestre which is responsible for its anti-diabetic action1. G-------- basic hydrolysis2. -------------------ene3. 18β-Glycyrrhetinic acid is ----------------------- induced diabetic rats4. Extensive literature survey ------------t few HPTLC5, 6, 7 and HPLC2 methods have been reported for estimation of gymnemagenin. HPTLC8. 9, 10 and HPLC11, 12 methods have---------------------- compounds. To the best of our knowledge no reports were found for simultaneous estimation of gymnemagenin and 18β-glycyrrhetinic acid by HPTLC method. ------------------------- in UV regions5. It is therefore necessary to develop methods for rapid, precise ----------------- and inherent quality13, 14. HPTLC is most widely used at industrial level for routine analysis of herbal medicines15. Hence the objective of this work was to develop ------------------------ herbal drug formulation.

    MATERIALS AND METHODS Solvents and chemicals Instrumentation and Chromatographic Conditions RESULTS AND DISCUSSION: HPTLC Method optimization ( table 1,2,3, and fig.1.2.3. ) legends of table and fig has to be given above the table and fig.



    REFERENCES: for Journal:

    1. Chatterjee SE, Shinha AA, Lankota A, Bpahed S, Gymnema Sylvestre: A Comprehensive Review, Drug Invention Today, 2010, 2,144-157. BOOK:

    2.ICH Harmonised Tripartite Guideline, Validation of Analytical Procedures: Text and Methodology Q2 (R1), Nov. 2005.

    3. ---- 40. ----------------------------------------------- once you will finish the preparation then submit the article


  • The Journal of Pharmacy Research 

    JPR seeks to foster multi-disciplinary research and collaboration among scientists, pharmaceutical industries and healthcare sector as well as provide a National and international forum for the communication and evaluation of data, methods and opinions in pharmaceutical sciences and related disciplines. The Editor  welcome contributions of field relevance. Although primarily devoted to original research papers, the journal particularly welcomes reviews on current topics of special interest and relevance.

    All manuscripts will be subjected to rapid peer corrections and publish. Those of high quality (not previously published and not already under consideration for publication) will be published. All published article text can also be modified with new idea ( only by corresponding authors ) and republish new article and modified article should contain the old article reference in reference section and also after KEY WORDS mentioned [Modification applied ];  in that section author has to describe what  modification done in new article. This modified article will appear in current issue. ( This Open Evaluation Type apply only when editorial will get proper justification from corresponding author to do the modification in article and as we all know the research is a continuous process so need modification with time and this process can save the time and energy and readers can get new idea from one place.

    The  Journal of Pharmacy Research  allowing online submission of manuscripts.  Author should therefore submit and monitor the status of their manuscripts online .


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    • All authors are required to sign this above copyright form. However, first author & corresponding author may sign on behalf of others in case of non-availability of other authors, after taking consent of all authors/coauthors.
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    The editorial decision is final. The editorial board reserves the right to make corrections/revisions aimed at greater clarity or conformity of style.



     Sumita Mukherjee

    Dr. B.L.R. Madhavi , [Area of Interest: Pharmaceutics] Dept. of Pharmaceutics ,Acharya & BM Reddy College of Pharmacy, (ABMRCP) Dr. Sarvepalli Radhakrishnan road, Soldevanvahalli,  Bangalore –560090,Karnataka,India.

    ·Prof. Dr. G. Babu, M. Pharm., Ph. D.,Professor & Principal, [Area of Interest: Pharmaceutical Analysis, Natural Products Chemistry] Devaki Amma Memorial College of Pharmacy,Chelembra,Malappuram dist. 673634,Kerala,India.

    ·Dr. Suvardhan Kanchi, [Area of Interest: Analytical Chemistry, Biosensors, Green Synthesis of NPs, Dye Sensitized Solar cells] Department of Chemistry,Durban University of Technology,Durban,South Africa.

    ·Dr. Zhiyong Peng,Department of CardioVascular Sciences,Heart Institute,East Carolina University,115 Heart Dr,Greenville, NC 27834,USA.

    ·Dr. Debasish Bandyopadhyay [Area of Interest:Herbal Antioxidant Drug Study, Calcutta University, Kolkata.

    ·Dr. Ryszard Amarowicz , [ Area of Interest: Phenolic Compound, antioxidants, Chromatography, food analysis, bioactive compd of plant]Institute of Animal Reproduction and Food Research of the Polish Academy of Sciences, Olsztyn, Poland.

    ·Dr. Y. K . Gupta, Professor and Head,Dept. of Chemistry,B K Birla Institute of Engineering and Technology,CEERI road,Pilani (Rajasthan), India.

    ·Dr. Bishwambhar Mishra , (Assistant Professor, Dept. of Biotechnology, Sreenidhi Institute of Science and Technology,Hyderabad, India)

    ·Dr. Sat Pal Singh Bisht, ( Professor, Dept of Zoology, Kumaun University, Nainital-263002, Uttarakhand, India )

    ·Dr.Mohamed El Houseiny El Sebeay Shams,Head of the Department of Pharmacy Practice,Oman Pharmacy Institute,Ministry of Health, PO Box 1928, Muscat 114, Oman.

    ·Dr. Smaranika Pattnaik, School of Life Sciences, Sambalpur University, Burla 768019, Odisha,India.

    ·Dr. Kondawar M. S.Prof. and Head,Department of Quality Assurance,Appasaheb Birnale college of Pharmacy,South Shivajinagar, Sangli-Miraj road,Sangli - 416416 (MS)India.

    ·Dr. Md. Amirul Islam , Pharmacy Discipline,Khulna University,Khulna-9208, Bangladesh·Prof. Vaithiamanithi Perumal,SAIMS Medical College, Indore,India·Dr. Biswa Mohan Sahoo,HOD & Associate Professor,Dept. of Medicinal Chemistry,Vikas College of Pharmacy,Putrela Road, Vissannapeta, Krishna Dist-521215 ,Andhra Pradesh, India·Dr. Popat Mohite.Associate Professor, Dapartment of Pharmaceutical Chemistry, MES's College of Pharmacy, SonaiTal- Newasa Dist-Ahmednagar, Maharashtra-414105·Dr.M.Swaroopa, UGC Post Doctoral Fellow in Biomedicine, Division of Zoology, Sri Padmavati Mahila Visvavidyalayam, Tirupati,A.P,India·Dr. Jiafeng Geng, School of Chemistry and Biochemistry, Georgia Institute of Technology, 315 Ferst Dr, Atlanta, GA 30332,  United States·Dr. M. V. Kumudhavalli., [Area of Interest: Phytochemistry and Pharmacology] Dept. of Pharmaceutical Analysis,Vinayaka Mission’s College of Pharmacy, Yercaud Main Road, Kondappanaikenpatty, Salem- 636008, T.N, India·Dr.Rajkumar Venkatadri [ area of Interest: Cancer Research, Pharmaceutical Sciences, Molecular Biology, Drug Invention], Department of Pharmaceutical Sciences, School of Pharmacy, Hampton University, 100 E Queen St, Hampt, VA 23668, USA·Dr. Pankaj  Goyal, Amity Institute of Microbial Technology, Amity University, Noida, Sec-125, India·Dr. Bao Yang, PhD, Professor, [Area of Interest: Botany, enzyme ,bioactive compounds] South China Botanical Garden (Formerly South China Institute of Botany), Chinese Academy of Sciences, Guangzhou 510650, China.Dr. Appala Raju. Nemala, [Area of Interest: Pharmaceutical Analysis] , Department of Pharmaceutical Chemistry,8-2-249, Mount Pleasant, Road#3, Banjara Hills,Sultan-ul-Uloom College of Pharmacy, Hyderabad, Telanagana State. India

    ·Dr. Goutam Kumar Jana,Department of Pharmacognosy,Gayatri College of Pharmacy,At- Gayatri Vihar, PO- Jamadarpali, Via- Sason,Dist- Sambalpur, Pin- 768200, OrissaIndia

    ·Dr. Bhushankumar Suresh Sathe ,[Area of Interest: Pharmacy,Medicinal Chemistry], Department of Pharmaceutical Chemistry, MGSM’S Smt. Sharadchandrika Suresh Patil, College of Pharmacy,Chopda-425107, M.H., India

    ·Dr. Versha Parcha,[Area of Interest: Natural products and Drug Discovery] Sardar Bhagwan Singh Post Graduate Institute of Biomedical Sciences and Research,Balawala,  Dehradun,  Uttarakhand, India

    ·Dr.Tareeka Dilip Sonawane,[Area of Interest: Biotechnology and Bioinformatics (Reproductive toxicity, Molecular Biology)] D.Y.Patil University ,School of Biotechnology and Bioinformatics Level 5 , Sector 15, Plot No. 50 ,  CBD Belapur, Navi Mumbai  400 614,Maharashtra  India

    ·Dr. Sabyasachi Maiti, [Area of Interest: Pharmaceutics (Novel Drug Delivery, Pharmacokinetics, Biopolymer Hydrogels)], Gupta College of Technological Sciences, Ashram More, GT Road, Asansol-713301, West Bengal, India

    ·Raghunath Singh,Senior Research Fellow (PhD Scholar), [Area of Interest: Nueropsychopharmacology, Ethnopharmacology, Inflammation, Neurodegenerative disorders]  University Institute of Pharmaceutical SciencesUGC-Center of Advanced Study (UGC-CAS),Panjab University,Chandigarh-160014,India

    ·Mohammed Rageeb Mohammed Usman, [Area of Interest: Pharmacognosy] ,Dept. of Pharmacognosy, Smt. Sharadchandrika Suresh Patil College of Pharmacy, Chopda 425107, Dist - Jalgaon Maharshtra, India.

    ·Dr. Durgacharan Arun Bhagwat, [Area of Interest: Pharmaceutics (Development of Novel Drug Delivery System)],  Dept of Pharmaceutics, Bharati Vidyapeeth College of Pharmacy, Kolhapur, Pin: 416 013, M.S. India.

    ·Dr.. Abhishek Laxminarayan Sharma, Q.A./ Q.C. Manager- Ayurvedic Section; Choksi Laboratories Limited; Vapi,India

    ·Dr. Agnimitra Dinda,[Area of Interest: Pharmaceutics ], Dept of Pharmaceutics, Gyana Jyothi College of Pharmacy,7-48/1, Gyana Jyothi Nagar,Uppal Bus Depot,Hyderabad-98,India

    ·Dr. A. Sai Ramesh, M.S. (by Research), Ph.D.,[Area of Interest: Medicinal Biochemistry, Natural Products, Medicinal Plants] Assistant Professor, Department of Biotechnology,Sree Sastha Institute of Engineering and Technology, Chemberambakkam, Chennai 600123, Tamil Nadu,India.

    ·Dr. Renu Sankar, Postdoctoral Researcher, [Area of Interest: Nanobiotechnology],Biomolecular Therapeutics Laboratory, Department of Chemistry, Sungkyunkwan University, Suwon, 440-746, South Korea.

    Dr. Shashikant  V. Bhandari.[Area of Interest: Drug design and development , Molecular modeling studies viz. QSAR, Anti-cancer], Professor, Head, Department of Pharmaceutical Chemistry, AISSMS College of pharmacy,  Near RTO Office , Kenedy Road, Pune-4110001 ,M.H.,India.

    Dr. Dhavalkumar V Patel, [Area of Interest: Pharmaceutics ] B K Mody Govt Pharmacy College,NR AJI DAM,Polytechnic Campus,Rajkot-360003, Gujarat,India.

    ·Mr. Mayank Sharma, Doctoral Research Fellow, [Area of Interest:  Pharmaceutics(Drug Delivery, Nanotechnology) Department of Pharmaceutics, School of Pharmacy, Devi Ahilya Vishwavidyalaya, Takshashila Campus, Khandwa Road, Indore (M.P.) – 452001, India

    Dr.Senthil Venkatachalam , Pharmaceutics [Area of Interest:Muco/Bioadhesive drug delivery system, Nanostructured Lipid carrier system], JSS College of Pharmacy, Rocklands, Ooty, Tamil Nadu 643001,India.

    Dr. M.R Jayapal, [Area of Interest:Organic chemistry,Analytical chemistry,Nanotechnology]Dept of Chemistry, National University of Cordoba,Argentina.

    Dr. Quan Wang,[ Area of Interest : fluorescence spectroscopy, single-molecule detection, biophysics, microfluidics, optics] Department of Chemistry, Stanford University, MC5080,USA.

    Advisory Board:

    ·Dr. Fengguo Xu,Dept of Epidemiology and Public Health,Yong Loo Lin School of Medicine,National University of Singapore,MD3, 16 Medical Drive, Singapore 117600.

    ·Dr. D. Nagasamy Venketash,Dept of Pharmaceutics,JSS College of Pharmacy,Ooty - 643 001. Tamil Nadu. India.

    ·Dr. G.S. Lavekar, Former DG, CCRAS – AYUSH (Govt. of India)

    ·Dr. Debasish Bandyopadhyay ( Calcutta University, Kolkata)

    ·Dr. Vijay Dhondiram Wagh, Pharmaceutical Technology, India

    ·Dr. Ramdas Bhanudas Pandhare[Area of Interest: Pharmacology], University of Pune, India

    ·Dr. Faiyaz Ahamed, India

    ·Dr. Shete R.V, India

    ·Dr. Ramesh Putheti, United States

    ·Dr. Yuanxiong Deng, China

    ·Dr. Praveen Bansal, India

    ·Dr. C. Rajasekaran, India

    ·Dr. A. K. Meena, (NIAPR, Patiala) India

    · Dr. Jongwha Chang, USA 

    · Dr. Somasekhar Penumajji, South Korea

    ·Dr. Geetha Kodali,Mexico

     [ Join the Editorial board by sending brief biodata mail OR Register  in login page : ]

Recent Manuscripts published

Journal: Journal of Pharmacy Research

Title: Studies of the role of the methanol fraction of the ethanol layer of the chloroform-ethanol leaf extract of Dacryodes edulis on diclofenac-induced gastric ulcer in rats
Section: Research Article
Category: Pharmacology
Country: India
View Article

Background and Aim: The leaves of Dacryodes edulis are used in traditional medicine for the treatment of gastric ulcer among other ailments in Nigeria. The aqueous extract, chloroform and ethanol layers of the chloroform-ethanol leaf extract of D. edulis were investigated for their qualitative and quantitative phytochemical compositions. Based on the outcomes of the preliminary investigations, the most promising of the three (ethanol layer) was further fractionated and the effects of the most desirable fraction (methanol fraction) on ulcer index, gastric juice volume, gastric juice pH and histopathology of diclofenac-ulcerated Wistar rats were determined. Methods: The qualitative and quantitative phytochemical compositions and acute toxicities of the aqueous extract, chloroform and ethanol layers as well as the effects of the methanol fraction of the ethanol layer of the chloroform-ethanol leaf extract of D. edulis on ulcer index, gastric juice volume, gastric juice pH and histopathology of diclofenac-ulcerated Wistar rats were determined using standard methods. Results:The qualitative and quantitative phytochemical analyses of the aqueous extract, chloroform and ethanol layers showed the presence and amounts of the following:  alkaloids, flavonoids, tannins, saponins and steroids. Each of the aqueous extract, chloroform and ethanol layers was found to be safe at 5000 mg/kg body weight (b.w). At the tested doses (100, 200 and 400 mg/kg b.w), the methanol fraction caused significant (p < 0.05) and dose-dependent decreases in the ulcer indices and gastric juice volumes as well as increases in the gastric juice pH of the rats in the test groups compared with those of the rats in the ulcer-untreated group. Results of the histopathological evaluation supported the gastroprotective effects of the fraction. Results of the fraction were comparable with those of the standard anti-ulcer drug, ranitidine at the dose of 150 mg/kg b.w. Conclusion: Experimental findings indicate that the leaves of D. edulis possess remarkable anti-ulcer effect probably due to their phytochemical constituents.

Journal: Journal of Pharmacy Research

Title: Diverse mechanisms of the anti-ulcer feature of the methanol fraction of the ethanol layer of the chloroform-ethanol extract of the leaves of Dacryodes edulis: Are anti-oxidant approaches and anti-lip
Section: Research Article
Category: Natural Drugs
Country: India
View Article

Background and Aim: Investigations into medicinal plants with potent anti-oxidant activity will continue to garner the attention of researchers due to the contributory role of oxidative stress in a number of disease conditions and thus, the aqueous extract, chloroform and ethanol layers of the chloroform-ethanol extract of the leaves of Dacryodes edulis were evaluated for their anti-oxidant vitamin contents. Based on the outcomes of the preliminary investigations, the most promising of the three (ethanol layer) was further fractionated and the effects of the most desirable fraction (methanol fraction) on the activity of superoxide dismutase (SOD) and concentrations of reduced glutathione (GSH) and malondealdehyde (MDA) of diclofenac-ulcerated Wistar rats were determined. Methods: The anti-oxidant vitamin contents of the aqueous extract, chloroform and ethanol layers as well as the effects of the methanol fraction of the ethanol layer of the chloroform-ethanol extract of the leaves of D. edulis on the activity of SOD and concentrations of GSH and MDA of diclofenac-ulcerated Wistar rats were examined using standard methods. Results: The ethanol layer contained the highest concentration of vitamin C (0.79 ± 0.03 mg/100 g) while the chloroform layer contained the highest concentrations of vitamins A (1.83 ± 0.08 μg/g) and E (1.17 ± 0.07 mg/100 g). The aqueous extract contained the least concentrations of vitamins A (1.34 ± 0.06 μg/g) and E (0.86 ± 0.05 mg/100 g). At the administered doses (100, 200 and 400 mg/kg b.w), the methanol fraction caused significant (p < 0.05) and dose-related increases in SOD activity and GSH concentration as well as decrease in MDA concentration of the rats in the test groups compared with those of the rats in the ulcer-untreated group. Conclusion: This study reveals that the leaves of D. edulis possess remarkable anti-oxidant feature and anti-lipid peroxidation effect which may be crucial in the amelioration of gastric ulceration.

Journal: Journal of Pharmacy Research

Title: In-vitro Antibacterial Activity of Sri Lankan Traditional Rice (Oryza sativa L.) Extracts against Bacteria Causing Skin and Soft Tissue Infections
Section: Research Article
Category: Natural Drugs
Country: India
View Article

The aim of this study was to evaluate the potential antibacterial activity of the extracts of selected parboiled and un-parboiled Sri Lankan traditional rice against bacteria causing skin and soft tissue infections. Methanolic extracts of five Sri Lankan traditional rice including Kalu Heenati, Pokkali, Rathdal, Kahawanu and Sudu Murunga were used for in vitro antibacterial analysis. Antibacterial activity was evaluated in both the parboiled and un-parboiled rice samples. Concentrations of rice extracts used for the assays were 1000 µg/mL and 2000 µg/mL from the each extract. The antibacterial activity was evaluated against common bacteria causing skin and soft tissue infections (Staphylococcus aureus (ATCC 25923), Pseudomonas aeroginosa (ATCC 27853), Escherichia coli (ATCC 25922) and three clinical isolates of Methicillin resistant staphylococcus aureus (MRSA)) by well diffusion method and viable colony count technique. According to the results, methanolic extracts of all the selected Sri Lankan traditional rice varieties exhibited a potent antibacterial activity against Staphylococcus aureus with minimum bactericidal concentrations (MBC) of 200 µg/mL (minimum incubation time (MIT); 30 min) for Rathdal, 200 µg/mL (MIT; 60 min) for  Kalu Heenati, Pokkali and Kahawanu, and 2000 µg/mL (MIT; 60 min) forSudu Murunga. The largest inhibition zones were observed in the extracts of Kalu Heenati and Rathdal. Kalu Heenati, Pokkali and Rathdal showed an efficacious inhibitory effect against MRSA (MBC; 200 µg/mL, MIT; 60 min), whereas the highest inhibitory activity was observed for Rathdal. Only the extract of Kalu Heenati was slightly active against Pseudomonas aeroginosa. None of the rice extracts studied showed an antibacterial activity against Escherichia coli.Reduction and loss of antibacterial activity was detected in rice after subjected to parboiling. In conclusion, Sri Lankan traditional rice varieties with red pericarp are good sources of antibacterial compounds mainly against Gram positive bacteria. Methanolic extract of Rathdal and Kalu Heenati showed a high efficacious inhibitory effect against skin and wound pathogens of Staphylococcus aureus and MRSA.