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Instruction for Authors
1. Aims and scope
Archives of Pharmacal Research is an interdisciplinary journal devoted
to the publication of original scientific research papers that aim to develop
new drugs in the fields of medicinal chemistry, natural products, pharmacology,
toxicology, pharmaceutics, microbiology, and basic biomedical sciences.
The journal specifically aims to enhance scientific understanding in the fields.
Thus, technical reports that document pharmacological and toxicological observations
will not be generally accepted in the journal.
Manuscripts will be considered for publication
on the condition that the results reported are based on original research that has not been
published elsewhere in any journal.
Upon acceptance for publication of an article in Archives
of Pharmacal Research, the author tacitly agrees to make available any materials used in the
published experiments, or novel or natural products disclosed in the article that are not commercially
available, so that other researchers may confirm the observations.
In addition, natural product contribution
must meet the following specific criteria: a) any natural extract must be defined, and appropriate information provided
regarding the origin; and b) the author must be able to state that the material under study is endotoxin free.
Please note that studies with crude extract and on chemical structures will not be accepted.
2. Types of papers
Archives of Pharmacal Research considers manuscripts for
publication in the following types of papers:
Research Articles : These are full-length descriptions
of research that describe original and important pieces
of work in detail from the fields covered by the Journal.
Maximum length of manuscripts should not exceed 6,000
words (24 typescript pages) excluding figures and tables.
These manuscripts will undergo standard review and normally are not expedited.
Invited Reviews. Invited review should be a review article written on the current
topic of a specific interest within the scope of Archives of Pharmacal Research.
Authors wishing to submit a review article should send a short synopsis to
Editor-in-Chief regarding content and length prior to submission.
Please note that invited reviews will be subjected to appropriate evaluation process.
3. How to Submit Manuscripts
Submission of a manuscript to Archives of Pharmacal Research implies that the
manuscript has not been published previously and is not currently under consideration
for publication elsewhere. Manuscript must be submitted through the Springer online submission website (http://www.editorialmanager.com/arpr).
Please visit the Springer site and create your account to access to the site. Authors should submit the text, tables and
artworks in electronic form via this web-based manuscript submission system.
Authors must include a cover letter that contains the title,
authors, a brief outline of the work¡¯s originality, desired
section of publication, corresponding author¡¯s name, address,
telephone and fax numbers (including country and city codes), and e-mail address.
4. Review of Manuscripts
A panel of, at least, two independent referees
whose names are not normally disclosed to authors
will evaluate all of submitted manuscripts. Authors
will be informed of the reviewer's comments.
5. Proofs
Authors are basically responsible for the factual accuracy
of their papers. One set of proofs will be supplied for the
author to check for typesetting accuracy, to be returned to
the publisher within 3 days of receipt. No changes to the original
manuscript will be allowed at this stage. In addition, the editors
reserve the right to make any necessary correction to a paper prior to publication.
6. Transfer of Copyright
All authors must sign the ¡®Transfer of Copyright¡¯ agreement to
before the article can be published. This transfer agreement
enables the Pharmaceutical Society of Korea to protect the
copyrighted material for the authors, but does not relinquish the author¡¯s proprietary rights.
7. Page Charge
Fee of US $ 20 per printed page will be charged to the authors
upon the acceptance of the manuscript on the form accompanying
the proofs. Note that payment is not a condition of publication:
articles can be accepted or rejected on their merit alone.
8. Reprints
reprints of each accepted paper will be supplied to the corresponding
author at no cost. Additional reprints will be available by ordering on the reprint order form.
9. Preparation of Manuscripts
Manuscripts should be concisely written in English and typed double-spaced throughout
on A-4 paper with margins of at least 3.0 cm. All pages should be numbered in succession,
the title page being page 1.
Each manuscript must have a title page, which includes only the title, the authors¡¯ names
with their affiliation, a running title of not more than 50 characters including spaces,
and mailing address, which includes telephone and Fax numbers and e-mail address
of the corresponding author.
The title should be as short as is consistent with clarity.
Tables and figures should be on separate pages placed at the end of the manuscript.
Abbreviation. The excessive use of abbreviations in the text is strongly discouraged.
Authors should only use abbreviations sparingly and should always define an abbreviation
when first used by placing it in parentheses after the full term, e.g. Acetylcholinesterase (AChE).
The metric system for all measurements should be expressed in lowercase letters
without periods (ml, nm, min, etc.).
Chemical Structures. CS ChemDraw Ultra (version 5.0 or later) will be our primary
illustration software for illustration of chemical structures. Therefore, authors are strongly
recommended to use the software and to save their structures in ACS format for manuscript
submission. A detailed setting for the illustration software would be as follows; Chain angle
(120), Bond spacing (18% of length), Fixed length (0.508 cm), Bold width (0.071 cm),
Line width (0.021 cm), Margin width (0.056 cm), and Hash spacing (0.088 cm).
Drug names. Drug names should be the official or approved names;
trade names or common names may be given in brackets where the drug is first mentioned.
The manufacturer¡¯s name and address must be given. The doses of the drugs should be
given as unit weight/unit body weight, e.g. mmol/kg or mg/kg. Concentration should be
given in terms of molarity (e.g., nM or mM), or as unit weight/unit volume solution (e.g., mg/l)
stating whether the weight refers to the salt or the active component of the drug.
10. Organization of Manuscripts
Each manuscript must begin with an ABSTRACT that summarizes the results obtained
and the conclusion drawn. It should not exceed 200 words. A short list of six keywords
or phrases should be supplied following the abstract.
INTRODUCTION. An introduction should first begin with general aspect for
a non-specialist and then continue with the specific reason for undertaking the investigation.
No attempt should be made to indicate the results obtained.
MATERIALS AND METHODS. Procedures used in the work should be given
in sufficient detail to permit the repetition by other researchers. Nevertheless, published procedures
should be briefly summarized by mentioning the reference(s) and only described in detail if the
procedures have been modified.
RESULTS. In this section, only observations should be described
without discussion of their significance.
DISCUSSION. The authors¡¯ interpretations of their observations (or findings)
should be accompanied by an assessment of their significance in relation to previous work.
REFERENCES. Only papers closely related to the author¡¯s work should be cited.
References should be assembled alphabetically. Follow the Harvard format. That is, references
are referred by name and year. When referring to more than one paper from a same author from
a same year, the alphabets a, b, c, etc. should be placed next to the year of publication to distinguish the articles.
In the text, when referring to a work by sole author, the name of author should be given like (Robinson, 1998) and
(Robinson, 1999; Jeong, 2000). When referring to a work by two authors, the name of authors should be given
like (Robinson and Jeong, 2001). When referring to a work by more than three authors, the name of the first author
should be given followed by et al.
such as (Robinson et al., 2002). Literature references must consist of names and initials of all authors,
title of the paper referred to, abbreviated title of the journal and the volume, year, and first and last page numbers of the paper.
The style and punctuation of the references should confirm with the following examples:
Journals:
Lai, Y. -L., Mehta, R. C., Thacker, A. A., Yoo, S. -D., MacNamara, P. J., and DeLuca,
P. P., Sustained bron-chodilation with isoproterenol poly(glycolidecolactide) microspheres.
Arch. Pharm. Res., 10, 119-125 (1993).
Books:
Azria, M., The Calctionins: Physiology and Pharmacology. Karger, London, (1989).
Borchartdt, R. T., Hidalgo, I. J., Hillgren, K. M. and Hu., M., Pharmaceutical applications
of cell culture: An Overview, In Wilson, G., Davis, S.S., Illum,L. and Zweibaum, A. (Eds.).
Pharmaceutical Application of Cell and Tissue Culture to Drug Transport. Plenum Press, New York, pp. 1-14, (1991).
Journal names should be abbreviated in accordance with Chemical Abstracts or Biological Abstracts List of Serials.
Tables. Each table should be placed on a separate page and numbered
in one consecutive series of Roman numerals in the order cited in the text.
Tables should be formatted with horizontal lines only: vertical ruled lines are not required.
Column heading should be kept as brief as possible and should indicate units of measurements.
Any annotation to headings or to tabulated items must be identified by superscript lowercase italic
letters, a, b, c, etc. and added in sequence at the foot of the table.
Figures and Schemes. A list of figure and scheme legends must be submitted
on a separate page to accompany the figures and schemes. Each legend must give a concise
description of the figure and scheme concerned, together with any essential experimental details
not described in the text. In particular, the key to any symbols or distinctive line formats used on the figure must be given.
Note that all figures (drawings, schemes, charts and photographs) should be numbered in
one consecutive series of Arabic numerals in the order cited in the text.
Figures generated by a laser quality printer or good quality black and white photographs are acceptable.
Figures must be large enough for the necessary reduction for printing. Each figure should be numbered in order.
Essential half-tone figures, reproduced from the original, will be included at the Editors discretion.
Color photographs will be printed at the Editors discretion, on the understanding that the authors will bear the cost.
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