Example of Pharmaceutical Research format
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Example of Pharmaceutical Research format Example of Pharmaceutical Research format Example of Pharmaceutical Research format Example of Pharmaceutical Research format Example of Pharmaceutical Research format Example of Pharmaceutical Research format Example of Pharmaceutical Research format Example of Pharmaceutical Research format Example of Pharmaceutical Research format Example of Pharmaceutical Research format Example of Pharmaceutical Research format Example of Pharmaceutical Research format Example of Pharmaceutical Research format Example of Pharmaceutical Research format Example of Pharmaceutical Research format Example of Pharmaceutical Research format Example of Pharmaceutical Research format Example of Pharmaceutical Research format
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open access Open Access

Pharmaceutical Research — Template for authors

Publisher: Springer
Categories Rank Trend in last 3 yrs
Pharmacology (medical) #36 of 246 down down by 4 ranks
Pharmaceutical Science #27 of 166 down down by 7 ranks
Organic Chemistry #34 of 185 down down by 9 ranks
Pharmacology #63 of 297 down down by 2 ranks
Biotechnology #65 of 282 down down by 22 ranks
Molecular Medicine #52 of 167 down down by 4 ranks
journal-quality-icon Journal quality:
High
calendar-icon Last 4 years overview: 885 Published Papers | 5707 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 30/06/2020
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Related Journals

open access Open Access
recommended Recommended

American Chemical Society

Quality:  
High
CiteRatio: 6.5
SJR: 0.976
SNIP: 1.593
open access Open Access

American Chemical Society

Quality:  
High
CiteRatio: 8.1
SJR: 1.279
SNIP: 0.942
open access Open Access

Springer

Quality:  
High
CiteRatio: 2.7
SJR: 0.538
SNIP: 0.974
open access Open Access
recommended Recommended

Elsevier

Quality:  
High
CiteRatio: 7.3
SJR: 1.045
SNIP: 1.333

Journal Performance & Insights

Impact Factor

CiteRatio

Determines the importance of a journal by taking a measure of frequency with which the average article in a journal has been cited in a particular year.

A measure of average citations received per peer-reviewed paper published in the journal.

3.242

17% from 2018

Impact factor for Pharmaceutical Research from 2016 - 2019
Year Value
2019 3.242
2018 3.896
2017 3.335
2016 3.002
graph view Graph view
table view Table view

6.4

11% from 2019

CiteRatio for Pharmaceutical Research from 2016 - 2020
Year Value
2020 6.4
2019 7.2
2018 6.9
2017 6.5
2016 6.5
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has decreased by 17% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • CiteRatio of this journal has decreased by 11% in last years.
  • This journal’s CiteRatio is in the top 10 percentile category.

SCImago Journal Rank (SJR)

Source Normalized Impact per Paper (SNIP)

Measures weighted citations received by the journal. Citation weighting depends on the categories and prestige of the citing journal.

Measures actual citations received relative to citations expected for the journal's category.

0.815

11% from 2019

SJR for Pharmaceutical Research from 2016 - 2020
Year Value
2020 0.815
2019 0.913
2018 1.093
2017 1.077
2016 1.112
graph view Graph view
table view Table view

1.028

8% from 2019

SNIP for Pharmaceutical Research from 2016 - 2020
Year Value
2020 1.028
2019 1.123
2018 1.131
2017 1.066
2016 1.046
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has decreased by 11% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has decreased by 8% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Pharmaceutical Research

Guideline source: View

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Springer

Pharmaceutical Research

Approved by publishing and review experts on SciSpace, this template is built as per for Pharmaceutical Research formatting guidelines as mentioned in Springer author instructions. The current version was created on and has been used by 898 authors to write and format their manuscripts to this journal.

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Last updated on
29 Jun 2020
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ISSN
1573-904X
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Open Access
Hybrid
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Sherpa RoMEO Archiving Policy
Green faq
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Plagiarism Check
Available via Turnitin
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Endnote Style
Download Available
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Citation Type
Author Year
(Blonder et al, 1982)
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Bibliography Example
Beenakker CWJ (2006) Specular andreev reflection in graphene. Phys Rev Lett 97(6):067,007, URL 10.1103/PhysRevLett.97.067007

Top papers written in this journal

open accessOpen access Journal Article DOI: 10.1023/A:1016212804288
A Theoretical Basis for a Biopharmaceutic Drug Classification: The Correlation of in Vitro Drug Product Dissolution and in Vivo Bioavailability
Gordon L. Amidon1, Hans Lennernäs2, Vinod P. Shah, John R. Crison
01 Mar 1995 - Pharmaceutical Research

Abstract:

A biopharmaceutics drug classification scheme for correlating in vitro drug product dissolution and in vivo bioavailability is proposed based on recognizing that drug dissolution and gastrointestinal permeability are the fundamental parameters controlling rate and extent of drug absorption. This analysis uses a transport mode... A biopharmaceutics drug classification scheme for correlating in vitro drug product dissolution and in vivo bioavailability is proposed based on recognizing that drug dissolution and gastrointestinal permeability are the fundamental parameters controlling rate and extent of drug absorption. This analysis uses a transport model and human permeability results for estimating in vivo drug absorption to illustrate the primary importance of solubility and permeability on drug absorption. The fundamental parameters which define oral drug absorption in humans resulting from this analysis are discussed and used as a basis for this classification scheme. These Biopharmaceutic Drug Classes are defined as: Case 1. High solubility-high permeability drugs, Case 2. Low solubility-high permeability drugs, Case 3. High solubility-low permeability drugs, and Case 4. Low solubility-low permeability drugs. Based on this classification scheme, suggestions are made for setting standards for in vitro drug dissolution testing methodology which will correlate with the in vivo process. This methodology must be based on the physiological and physical chemical properties controlling drug absorption. This analysis points out conditions under which no in vitro-in vivo correlation may be expected e.g. rapidly dissolving low permeability drugs. Furthermore, it is suggested for example that for very rapidly dissolving high solubility drugs, e.g. 85% dissolution in less than 15 minutes, a simple one point dissolution test, is all that may be needed to insure bioavailability. For slowly dissolving drugs a dissolution profile is required with multiple time points in systems which would include low pH, physiological pH, and surfactants and the in vitro conditions should mimic the in vivo processes. This classification scheme provides a basis for establishing in vitro-in vivo correlations and for estimating the absorption of drugs based on the fundamental dissolution and permeability properties of physiologic importance. read more read less

Topics:

Dissolution testing (66%)66% related to the paper, Biopharmaceutics Classification System (61%)61% related to the paper, Drug (51%)51% related to the paper, In vivo (51%)51% related to the paper, Bioavailability (50%)50% related to the paper
View PDF
5,049 Citations
open accessOpen access Journal Article DOI: 10.1007/S11095-008-9661-9
Cancer is a Preventable Disease that Requires Major Lifestyle Changes
15 Jul 2008 - Pharmaceutical Research

Abstract:

This year, more than 1 million Americans and more than 10 million people worldwide are expected to be diagnosed with cancer, a disease commonly believed to be preventable. Only 5–10% of all cancer cases can be attributed to genetic defects, whereas the remaining 90–95% have their roots in the environment and lifestyle. The li... This year, more than 1 million Americans and more than 10 million people worldwide are expected to be diagnosed with cancer, a disease commonly believed to be preventable. Only 5–10% of all cancer cases can be attributed to genetic defects, whereas the remaining 90–95% have their roots in the environment and lifestyle. The lifestyle factors include cigarette smoking, diet (fried foods, red meat), alcohol, sun exposure, environmental pollutants, infections, stress, obesity, and physical inactivity. The evidence indicates that of all cancer-related deaths, almost 25–30% are due to tobacco, as many as 30–35% are linked to diet, about 15–20% are due to infections, and the remaining percentage are due to other factors like radiation, stress, physical activity, environmental pollutants etc. Therefore, cancer prevention requires smoking cessation, increased ingestion of fruits and vegetables, moderate use of alcohol, caloric restriction, exercise, avoidance of direct exposure to sunlight, minimal meat consumption, use of whole grains, use of vaccinations, and regular check-ups. In this review, we present evidence that inflammation is the link between the agents/factors that cause cancer and the agents that prevent it. In addition, we provide evidence that cancer is a preventable disease that requires major lifestyle changes. read more read less

Topics:

Cancer prevention (65%)65% related to the paper, Red meat (54%)54% related to the paper, Disease (50%)50% related to the paper
View PDF
1,915 Citations
Journal Article DOI: 10.1007/S11095-016-1958-5
Nanoparticle-Based Medicines: A Review of FDA-Approved Materials and Clinical Trials to Date.
14 Jun 2016 - Pharmaceutical Research

Abstract:

In this review we provide an up to date snapshot of nanomedicines either currently approved by the US FDA, or in the FDA clinical trials process. We define nanomedicines as therapeutic or imaging agents which comprise a nanoparticle in order to control the biodistribution, enhance the efficacy, or otherwise reduce toxicity of... In this review we provide an up to date snapshot of nanomedicines either currently approved by the US FDA, or in the FDA clinical trials process. We define nanomedicines as therapeutic or imaging agents which comprise a nanoparticle in order to control the biodistribution, enhance the efficacy, or otherwise reduce toxicity of a drug or biologic. We identified 51 FDA-approved nanomedicines that met this definition and 77 products in clinical trials, with ~40% of trials listed in clinicaltrials.gov started in 2014 or 2015. While FDA approved materials are heavily weighted to polymeric, liposomal, and nanocrystal formulations, there is a trend towards the development of more complex materials comprising micelles, protein-based NPs, and also the emergence of a variety of inorganic and metallic particles in clinical trials. We then provide an overview of the different material categories represented in our search, highlighting nanomedicines that have either been recently approved, or are already in clinical trials. We conclude with some comments on future perspectives for nanomedicines, which we expect to include more actively-targeted materials, multi-functional materials (“theranostics”) and more complicated materials that blur the boundaries of traditional material categories. A key challenge for researchers, industry, and regulators is how to classify new materials and what additional testing (e.g. safety and toxicity) is required before products become available. read more read less
1,837 Citations
Journal Article DOI: 10.1007/S11095-006-9132-0
Micellar nanocarriers: pharmaceutical perspectives.
Vladimir P. Torchilin1
16 Nov 2006 - Pharmaceutical Research

Abstract:

Micelles, self-assembling nanosized colloidal particles with a hydrophobic core and hydrophilic shell are currently successfully used as pharmaceutical carriers for water-insoluble drugs and demonstrate a series of attractive properties as drug carriers. Among the micelle-forming compounds, amphiphilic copolymers, i.e., polym... Micelles, self-assembling nanosized colloidal particles with a hydrophobic core and hydrophilic shell are currently successfully used as pharmaceutical carriers for water-insoluble drugs and demonstrate a series of attractive properties as drug carriers. Among the micelle-forming compounds, amphiphilic copolymers, i.e., polymers consisting of hydrophobic block and hydrophilic block, are gaining an increasing attention. Polymeric micelles possess high stability both in vitro and in vivo and good biocompatibility, and can solubilize a broad variety of poorly soluble pharmaceuticals many of these drug-loaded micelles are currently at different stages of preclinical and clinical trials. Among polymeric micelles, a special group is formed by lipid-core micelles, i.e., micelles formed by conjugates of soluble copolymers with lipids (such as polyethylene glycol-phosphatidyl ethanolamine conjugate, PEG-PE). Polymeric micelles, including lipid-core micelles, carrying various reporter (contrast) groups may become the imaging agents of choice in different imaging modalities. All these micelles can also be used as targeted drug delivery systems. The targeting can be achieved via the enhanced permeability and retention (EPR) effect (into the areas with the compromised vasculature), by making micelles of stimuli-responsive amphiphilic block-copolymers, or by attaching specific targeting ligand molecules to the micelle surface. Immunomicelles prepared by coupling monoclonal antibody molecules to p-nitrophenylcarbonyl groups on the water-exposed termini of the micelle corona-forming blocks demonstrate high binding specificity and targetability. This review will discuss some recent trends in using micelles as pharmaceutical carriers. read more read less

Topics:

Nanocarriers (61%)61% related to the paper, Micelle (61%)61% related to the paper, Drug carrier (57%)57% related to the paper, Targeted drug delivery (51%)51% related to the paper, Amphiphile (51%)51% related to the paper
1,685 Citations
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Frequently asked questions

1. Can I write Pharmaceutical Research in LaTeX?

Absolutely not! Our tool has been designed to help you focus on writing. You can write your entire paper as per the Pharmaceutical Research guidelines and auto format it.

2. Do you follow the Pharmaceutical Research guidelines?

Yes, the template is compliant with the Pharmaceutical Research guidelines. Our experts at SciSpace ensure that. If there are any changes to the journal's guidelines, we'll change our algorithm accordingly.

3. Can I cite my article in multiple styles in Pharmaceutical Research?

Of course! We support all the top citation styles, such as APA style, MLA style, Vancouver style, Harvard style, and Chicago style. For example, when you write your paper and hit autoformat, our system will automatically update your article as per the Pharmaceutical Research citation style.

4. Can I use the Pharmaceutical Research templates for free?

Sign up for our free trial, and you'll be able to use all our features for seven days. You'll see how helpful they are and how inexpensive they are compared to other options, Especially for Pharmaceutical Research.

5. Can I use a manuscript in Pharmaceutical Research that I have written in MS Word?

Yes. You can choose the right template, copy-paste the contents from the word document, and click on auto-format. Once you're done, you'll have a publish-ready paper Pharmaceutical Research that you can download at the end.

6. How long does it usually take you to format my papers in Pharmaceutical Research?

It only takes a matter of seconds to edit your manuscript. Besides that, our intuitive editor saves you from writing and formatting it in Pharmaceutical Research.

7. Where can I find the template for the Pharmaceutical Research?

It is possible to find the Word template for any journal on Google. However, why use a template when you can write your entire manuscript on SciSpace , auto format it as per Pharmaceutical Research's guidelines and download the same in Word, PDF and LaTeX formats? Give us a try!.

8. Can I reformat my paper to fit the Pharmaceutical Research's guidelines?

Of course! You can do this using our intuitive editor. It's very easy. If you need help, our support team is always ready to assist you.

9. Pharmaceutical Research an online tool or is there a desktop version?

SciSpace's Pharmaceutical Research is currently available as an online tool. We're developing a desktop version, too. You can request (or upvote) any features that you think would be helpful for you and other researchers in the "feature request" section of your account once you've signed up with us.

10. I cannot find my template in your gallery. Can you create it for me like Pharmaceutical Research?

Sure. You can request any template and we'll have it setup within a few days. You can find the request box in Journal Gallery on the right side bar under the heading, "Couldn't find the format you were looking for like Pharmaceutical Research?”

11. What is the output that I would get after using Pharmaceutical Research?

After writing your paper autoformatting in Pharmaceutical Research, you can download it in multiple formats, viz., PDF, Docx, and LaTeX.

12. Is Pharmaceutical Research's impact factor high enough that I should try publishing my article there?

To be honest, the answer is no. The impact factor is one of the many elements that determine the quality of a journal. Few of these factors include review board, rejection rates, frequency of inclusion in indexes, and Eigenfactor. You need to assess all these factors before you make your final call.

13. What is Sherpa RoMEO Archiving Policy for Pharmaceutical Research?

SHERPA/RoMEO Database

We extracted this data from Sherpa Romeo to help researchers understand the access level of this journal in accordance with the Sherpa Romeo Archiving Policy for Pharmaceutical Research. The table below indicates the level of access a journal has as per Sherpa Romeo's archiving policy.

RoMEO Colour Archiving policy
Green Can archive pre-print and post-print or publisher's version/PDF
Blue Can archive post-print (ie final draft post-refereeing) or publisher's version/PDF
Yellow Can archive pre-print (ie pre-refereeing)
White Archiving not formally supported
FYI:
  1. Pre-prints as being the version of the paper before peer review and
  2. Post-prints as being the version of the paper after peer-review, with revisions having been made.

14. What are the most common citation types In Pharmaceutical Research?

The 5 most common citation types in order of usage for Pharmaceutical Research are:.

S. No. Citation Style Type
1. Author Year
2. Numbered
3. Numbered (Superscripted)
4. Author Year (Cited Pages)
5. Footnote

15. How do I submit my article to the Pharmaceutical Research?

It is possible to find the Word template for any journal on Google. However, why use a template when you can write your entire manuscript on SciSpace , auto format it as per Pharmaceutical Research's guidelines and download the same in Word, PDF and LaTeX formats? Give us a try!.

16. Can I download Pharmaceutical Research in Endnote format?

Yes, SciSpace provides this functionality. After signing up, you would need to import your existing references from Word or Bib file to SciSpace. Then SciSpace would allow you to download your references in Pharmaceutical Research Endnote style according to Elsevier guidelines.

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I spent hours with MS word for reformatting. It was frustrating - plain and simple. With SciSpace, I can draft my manuscripts and once it is finished I can just submit. In case, I have to submit to another journal it is really just a button click instead of an afternoon of reformatting.

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