Drug Invention Today
ISSN NO: 0975-7619
Drug Invention Today (DIT) was first published in 2009 by JPR Solutions. It is a journal, which publishes reviews, research papers and short communications . 
• Novel Drug Delivery Systems • Nanotechnology & Nanomedicine • Biotechnology related pharmaceutical technology • Polymeric bio-conjugates • Biological macromolecules • Biomaterials • Drug Information • Drug discovery/development • Screening of drugs from natural & synthetic origins • Novel therapeutic strategies • Combinatorial chemistry and parallel synthesis • Clinical trials • Case Reports
 Impact FactorTM ( India ) = 0.897 as on date (08.05.2017)
  Scopus Indexed ( link http://www.scimagojr.com/journalsearch.php?q=21100202909&tip=sid&clean=0)
Journal Metrics for this   Drug Invention Today (Source ID: 21100202909): 2014 (SNIP) Source Normalized Impact Per Paper : 0.402; SCImago Journal Rank (SJR):0.301; Impact Per Publication : 0.517 (Top level : Life Science)
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  • 1. http://www.scimagojr.com/journalsearch.php?q=21100202909&tip=sid&clean=0
    SCImago Journal & Country Rank
    2. http://endnote.com/downloads/style/drug-invention-today
    3. http://publicationethics.org/members/drug-invention-today
    4. https://scholar.google.co.in/citations?user=DvHkMU0AAAAJ&hl=en
    5.http://www.citefactor.org/journal/index/1532/drug-invention-today#.VcYmm3 Gqqko  
    6. http://www.ncbi.nlm.nih.gov/nlmcatalog/101619441
    7. http://journaldir.petra.ac.id/browse_journal2.php?id=17101
    8. http://www.webcitation.org/archive.php (author can freely upload )
    9.http://www.citationmachine.net/drug-invention-today/cite-a-journal/manual (author can freely upload)
    10. http://en.journals.sid.ir/JournalList.aspx?ID=23338
    11. http://ores.su/en/journals/drug-invention-today/
    12. http://pubget.com/journal/0975-7619/drug-invention-today
    13. http://www.journals4free.com/link.jsp?l=17953464
    14. http://library.wur.nl/WebQuery/clc/2032712 
    15. http://trove.nla.gov.au/work/38532528?versionId=51078376
    Manuscripts must be in "Times New Roman" font-size 10, with double spacing. Please arrange the manuscript as follows: Title page, abstract, introduction, methods, results and discussion, and references, tables, figure captions and figures. Number all pages consecutively at the bottom, beginning with the title page. Figures and tables must be cited in the manuscript.
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    Introduction: State the objectives of the work and provide an adequate background, avoiding a detailed literature survey or a summary of the results.
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    Title page information
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    Submit each figure as a separate Excel file.
    Journal Articles
    1) George JN, Woolf SH, Raskob GE, Wasser JS, Aledrot LM, Ballem PJ. Idiopathic thrombocytopenic purpura: A practice guideline developed by explicit methods of the American Society of Hematology. Blood, 1996, 88, 3–40.
    2) Driessens FCM, Boltong MG, Bermudez O, Planell JA. Formulation and setting times of some calcium orthophosphate cements: A pilot study. J. Mater. Sci: Mater. Med., 1993, 4, 503–508.
    Strunk W, Jr, White EB. The Elements of Style 4th ed. Longman, New York, 2000.
    Book Chapters
    Mettam GR, Adams LB. How to prepare an electronic version of your article. In: Jones BS, Smith RZ (Eds.),Introduction to the Electronic Age. E-Publishing Inc., New York, 2009, pp. 281–304.
    Web references
    As a minimum, the full URL
  • Copyright notice & Permissions: 
    Upon acceptance of an article, authors will be asked to complete a "Copyright notice and permission letter". 
    Dear editor (Drug Invention Today),
    Sub: Submission of an original paper with copyright agreement and authorship responsibility ( submit by e-mail only)
     Topic entitled:
    I certify that I have participated sufficiently in the conception and design of this work and the analysis of the data (wherever applicable), as well as the writing of the manuscript, to take public responsibility for it. I believe the manuscript represents valid work. I have reviewed the final version of the manuscript and approve it for publication. Neither has the manuscript nor one with substantially similar content under my authorship been published or is being considered for publication elsewhere, except as described in an attachment. Furthermore I attest that I shall produce the data upon which the manuscript is based for examination by the editors or their assignees, if requested.
    Kindly find it suitable to publish in your esteemed journal.
    Thanking you
    Yours sincerely,
    Author name and address                                                             Signature
    Prof. S. Parial (Pharmacy, Pharmacognosy)
    ·Dr.M.Swaroopa, UGC Post Doctoral Fellow in Biomedicine, Division of Zoology, Sri Padmavati Mahila Visvavidyalayam, Tirupati,A.P,India
    ·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. Suvardhan Kanchi, 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. 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. Shankar Ananth,India
    ·Dr. Wei Zhang, China
    ·Dr. Goutam Kumar Jana,Department of Pharmacognosy,Gayatri College of Pharmacy,At- Gayatri Vihar, PO- Jamadarpali, Via- Sason,Dist- Sambalpur, Pin- 768200, OrissaIndia
    ·Dr. Asim Ahmad Elnour,UAE
    ·Dr. Geetha Kodali,Mexico
    ·Dr. Syed Haris Omar, Pharmacology,Qassim University,Saudi Arabia
    ·Dr. Jaykaran (Medical Sciences), India
    ·Dr. Vijay Dhondiram Wagh, Pharmaceutical Technology, India
    ·Dr. Ramdas Bhanudas Pandhare, University of Pune, India
    Advisory Board:
    ·Dr. G.S. Lavekar, Former DG, CCRAS – AYUSH (Govt. of India)
    ·Dr. Debasish Bandyopadhyay ( Calcutta University, Kolkata)
    ·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
     [ Join the Editorial board by sending brief biodata mail OR Register  in login page : info@jprsolutions.info ]

Recent Manuscripts published

Journal: Drug Invention Today

Title: Infusion of adrenomedullin22-52 antagonist causes uteroimplantation growth restriction during early gestation in rats
Section: Research Article
Category: Pharmacological Screening
Country: India
View Article

Background: The present study exploited whether antagonism of endogenous Adrenomedullin (ADM) in rats during early gestation period resulted in diminished uterus and implantation growth and explored whether this causes through induction of apoptosis. Rats on gestational day 2 were implanted subcutaneously with osmotic (ALZET) minipumps delivering 125 and 250 µg/rat/day/of ADM22-52 and were killed on gestational day 9. On gestational day 9, both in the control group rats and ADM antagonist-treated rats, 5-bromo 2´deoxyuridine labeling dye is injected in the tails of rats with a concentration of 1 ml/100 g body weight and then sacrificed the animal. We have demonstrated that the uterus growth and implantation development are seriously compromised by this modest decrease in expression and the implanted sites were shown prominently by blue-/purple-colored spots both in control and ADM-treated groups. Results: Apoptotic variations were more evident in stromal trophoblastic cells in the uteroimplantation sites of ADM22-52-treated rats when compared with vehicle control rats. Immunoreactivity to active caspase-3, Bax, Bcl2 protein was abundant in the uteroimplantation regions of the ADM22-52-treated group. Conclusion: These findings, however, show that antagonism of ADM in rats during early pregnancy caused uteroimplantation growth restriction and increased fetal resorption through the activation of mitochondrial apoptotic pathways.

Journal: Drug Invention Today

Title: Evaluation of combined wound healing activity of ethanolic extracts of leaves of Murraya koenigii and Nyctanthes arbortristis on rats
Section: Research Article
Category: Pharmacological Screening
Country: India
View Article

Objective: The present work was executed to evaluate the wound healing potency of a combined preparation of two plant extracts. The objective of this study is to induce experimental wounds using excision and incision wound model in normal albino wistar rats and to study the wound healing activity of prepared combined formulation by comparison of changes in wound healing between experimental and placebo controlled rats. Methods: The individual ethanolic extract of Murraya koenigii and Nyctanthus arbortrstis was investigated for preliminary phytochemical study. Then the effect of combined ointment formulation containing equal quantity of ethanolic extracts of leaves of Murraya koenigii and Nyctanthus arbortrstis was investigated by using excision and incision wound model in rats. Results: Both the extracts show presence of phytochemicals responsible for wound healing activity. The herbal ointment formulation 3 was found to be significantly reducing wound area, epithelization period and wound contraction rate. Similarly this formulation also shows significant increase in wound breaking strength. Conclusions: The study shows capability of both the extracts to promote accelerated wound healing activity by dose dependant manner when compared with placebo control.

Journal: Drug Invention Today

Title: In vivo antiplasmodial evaluation of syzygium jambos L. Alston by four day suppressive test
Section: Research Article
Category: Pharmacological Screening
Country: India
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Objective: The unexplored region of Western Ghats possesses natural source of noble therapeutic floras for many diseases. The present study was aimed to investigate the in vivo antiplasmodial activity of Syzygium jambos from Western Ghats. Methods: The four extracts acetone, chloroform, methanol and aqueous were explore their antiplasmodial activity by Peter’s four day test. Results: In Peter’s four day test significant parasite suppression 99.24% (P<0.001) was observed in Chloroquine (CQ 25mg/kg b.wg.) group prolonging the mean survival time of animals ≥30 days, whereas no average parasitaemia suppression (44.33±0.94) was observed in the negative control group. An effective parasite suppression (P<0.01) of 72.93% and 72.18% was identified in methanol and acetone extracts respectively at 600 mg/kg b.wt. The acetone and methanol extracts prolonged the mean survival days of mice groups up to 27.8 ± 0.68 and 26.0 ± 1.29 days respectively. Conclusion: Among the four extracts tested methanol and acetone extracts exhibited antimalarial activity. The present study report establishes, Syzygium jambos leaf extracts were effective with an assorted range of antiplasmodial activity and could be a potential source in the discovery of antimalarial drug.