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ISSN 2519-4852 (online)
The manuscript can be sent to the editorial office of the journal only if the following conditions are met:
If your research is published and we find that any of these conditions have not been met, we may take action in accordance with COPE guidelines, which may result in one of the correction notices, or we may remove or revoke the article.
Dear authors, we remind you that a scientific article must be a complete scientific study. We recommend that you do not separately publish data on the acquisition and properties/standardization of new objects (plant and synthetic) and the study of their pharmacological properties. Formally, these are parts of one study. The editors of the ScienceRise: Pharmaceutical Science journal do not accept fragments of a single study for publication. Thank you for understanding.
For consideration for publication in the journal ScienceRise: Pharmaceutical Science” are accepted:
All articles must comply with the Bioethics policy.
For licensed software that was used during the study, license numbers must be indicated.
Material submitted to a “ScienceRise: Pharmaceutical Science” journal must be original and not published or submitted for publication elsewhere. This rule applies to material submitted elsewhere while the “ScienceRise: Pharmaceutical Science” journal contribution is under consideration.
If there are figures in the article, the authors must choose the main figure that reflects the results obtained. This figure will be placed at the title of the article in the archive of the journal.
Drawing requirements:
Also, electronic additional materials for the article at the request of the authors (Excel files, audio and video files) can be published.
Page format – А4, portrait
Font – Times New Roman
Font size – 14
Interval – 1.5
Paragraph indent – 1.25 mm
Alignment – Width
Margins of the document – 20 mm
Minimum number of pages – 20
Article language: English
UDC
TITLE OF THE ARTICLE IN ENGLISH
Full name, Full Name .... in English
Abstract in English (1800-1900 characters with spaces). In the abstract sections should be highlighted: aim, materials and methods, results, conclusions.
Keywords in English (10 words)
The main sections of the article:
1. Introduction
ADVICE: You can use the electronic resources of open access scientific journals around the world from Cochrane Library. The search can be performed by keyword of your subjects in English.
Aim of research. The formulation of aim of the research should be performed in such a way that it became clear how to fill in the "niche" research (i.e. to answer the question: "what needs to be done to bridge the gap of knowledge associated with the presence of pieces of total problems unidentified by other scientists?»).
The aim of research, formulated by the author, can be the formulation of Hypotheses and that the author wanted to prove or disprove.
2. Planning (methodology) of research
The section provides the scientific justification for the selection of materials (objects), research methods and the sequence of the experiment to achieve the goal.
To plan research, authors should use the basic principles of the Quality by design concept and / or risk analysis to achieve their goals.
The design of the experiment is justified by calculations, diagrams, decision tree, etc.
3. Materials and methods
This section should be structured in accordance with the following description of the results and their discussion.
Studies involving animals and humans
For research manuscripts reporting experiments on living vertebrates and / or higher invertebrates, the correspondent author must confirm that all experiments were performed in accordance with the relevant guidelines and rules. The manuscript should include a statement indicating the institutional and / or licensing committee approving the experiments, including any relevant details. Gender and other characteristics of animals that may affect results should be described. Details of housing and livestock should be included if they can affect experimental results. All animal experiments must comply with ARRIVE guidelines and be conducted in accordance with the EU Directive 2010/63/EU on the protection of animals used for scientific purposes.
For a study in which people are participants, authors must identify a committee approving the study, ensure that the work has been carried out in accordance with the Code of Ethics of the World Medical Association (Helsinki Declaration) and include in your manuscript a statement confirming that informed consent was obtained from all participants (recommendations for obtaining informed consent).
You can also read the Helsinki Declaration in Russian on the website of the Association of Clinical Research Organizations.
Clinical trial registration
Prospective clinical trials should be registered prior to the registration of patients or in a similar public store (trials in which the main purpose is to determine pharmacokinetics are excluded).
Human biological samples
To describe human biological samples, we recommend that you refer to the BRISQ reporting guidelines (reporting on biological samples to improve the quality of the study) and ensure that at least level 1 characteristics are provided (link).
Publication of images of participants in human subject research
When publishing identifiable images of study participants, authors should include a statement in the published article confirming that they have received informed consent to publish the images. All reasonable measures should be taken to protect the anonymity of the patient. Black stripes above the eyes are not an acceptable means of anonymization. In some cases, we may insist on obtaining evidence of the informed consent of the authors. Images without appropriate consent will be removed from the publication.
Studies involving human embryos, gametes, and stem cells
Manuscripts reporting experiments involving the use of human embryos and gametes, human embryonic stem cells and related materials, as well as the clinical use of stem cells, should include confirmation that all experiments have been performed in accordance with relevant guidelines and the rules.
The manuscript should include an ethical statement that identifies the institutional and / or licensing committees that approve the experiments and describe any relevant details. A statement of ethics should also confirm that informed consent has been obtained from all recipients and / or donors of cells or tissues, where necessary, and describe the conditions of donation of research materials, such as human embryos or gametes. The editors may request copies of approved and edited consent documents.
Selection of medicinal plants
Where appropriate, the species or botanical species that are selected for cultivation should correspond to those indicated in the national pharmacopoeia or recommended by other authoritative national documents of the country of the final consumer. In the absence of such national documents, the selection of species or botanical varieties should be based on the pharmacopoeia or other authoritative documents of other countries. In the case when medicinal plants are considered for the first time, samples or botanical varieties selected for cultivation should be defined and documented as raw materials used or described in traditional medicine of the country of origin.
Experimental data
Analytical data should be statistically processed using appropriate programs.
When establishing the structure of substances, the authors must provide sufficient experimental information, in particular, the available 1H and 13C NMR spectra, and X-ray crystalline structural determinations are necessary for metal complexes.
The author is responsible for presenting the correct chemical nomenclature and terminology.
An accurate description of each data set should be provided, which is shown and should include the number of biological repeats, the number of experiments performed, and a description and use of appropriate statistical methods. To verify the significance of differences in results, appropriate statistical methods should be used. The term “significant” should not be used unless a statistical analysis has been performed and the probability value used to determine significance (usually p-value) should be indicated. Manuscripts submitted without evidence of reproducibility will be rejected without formal review.
Applications and additional materials
4. Result
Results should be presented in a logical order, and it is recommended to give the results in order of importance, it is not necessary to use the order in which the experiments were conducted.
You should not duplicate the data shown in the figures, graphs and tables. A common mistake is to bring the data displayed in the figures and tables in the text of the article. Instead, the text of the article should summarize the material that the reader will find in the table or draw the reader’s attention to the main points in the figure or table. The reader, as a rule, is easier to read the data in the table than in the text of the article.
Avoid excessive figures and tables. If there is not enough data for full-fledged tables and figures, it is better to describe this information in the text.
All presented results that require repeated testing should be statistically processed. The development of analysis methods and / or technologies should be accompanied by validation characteristics.
5. Discussion
In this section of the article you need:
6. Conclusions
In this section of the article, be sure to indicate once again the main summarizing results on your work, paying particular attention to the consistency of the conclusions of the aim and objectives of research. This means that the Conclusions should reflect the specific results obtained by the author, on the basis of which it is possible to draw a conclusion about the scientific novelty and the possibility of practical application of the research results presented in the article.
Conflict of interest
It is necessary to indicate the absence or presence of a conflict of interest. If there is a conflict of interest, it must be specified.
When there is no conflict of interest, it is necessary to specify the phrase:
The authors declare that they have no conflict of interest in relation to this research, whether financial, personal, authorship or otherwise, that could affect the research and its results presented in this paper.
Financing
Sources of funding must be indicated. If there is no funding, it is necessary to indicate:
The study was performed without financial support.
Acknowledgments (if any)
List here those people/organizations that have assisted in the course of the research (for example, provided language assistance, assistance in conducting experiments, financial assistance, etc.).
References
Sources are made according to АРА standard
For each author:
The author's ORCID ID is required. ORCID provides a unique and persistent digital identifier that distinguishes researchers from every other researcher, even those who share the same name, and, through integration in key research workflows such as manuscript and grant submission, supports automated linkages between researchers and their professional activities, ensuring that their work is recognized.
Once you submit your article, it will be sent for review. Our editorial staff is practicing a double-blind peer review
*Review procedure involves checking for plagiarism, verification of compliance the article title and content, check the content of the article
If there are no corrections or all the remarks made by the reviewers are corrected, the article will be accepted for publication in the journal based on the results of double-blind review.
Only those manuscripts that meet the standards of the journal, and fit within its aims and scope, will be sent to expert reviewers.
Deadline 3–14 daysEditing procedure involves checking articles on formal grounds, according to the correctness of the requirements
Get the answer from the editors of the magazine. If there are adjustments that need to take them into account and send the article back by email pharm@entc.com.ua, sr7508990@gmail.com
If no adjustments or fixed all the comments made by the editor, you will need to prepare a package of documents