Example of Current Pharmaceutical Analysis format
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Example of Current Pharmaceutical Analysis format Example of Current Pharmaceutical Analysis format Example of Current Pharmaceutical Analysis format Example of Current Pharmaceutical Analysis format Example of Current Pharmaceutical Analysis format Example of Current Pharmaceutical Analysis format Example of Current Pharmaceutical Analysis format Example of Current Pharmaceutical Analysis format
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Example of Current Pharmaceutical Analysis format Example of Current Pharmaceutical Analysis format Example of Current Pharmaceutical Analysis format Example of Current Pharmaceutical Analysis format Example of Current Pharmaceutical Analysis format Example of Current Pharmaceutical Analysis format Example of Current Pharmaceutical Analysis format Example of Current Pharmaceutical Analysis format
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This content is only for preview purposes. The original open access content can be found here.
open access Open Access

Current Pharmaceutical Analysis — Template for authors

Publisher: Bentham Science
Categories Rank Trend in last 3 yrs
Pharmaceutical Science #98 of 166 -
Biophysics #105 of 131 down down by 10 ranks
Biochemistry #362 of 415 down down by 14 ranks
Molecular Medicine #146 of 167 down down by 1 rank
journal-quality-icon Journal quality:
Medium
calendar-icon Last 4 years overview: 373 Published Papers | 455 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 29/06/2020
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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
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American Chemical Society

Quality:  
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CiteRatio: 8.1
SJR: 1.13
SNIP: 1.113
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American Chemical Society

Quality:  
High
CiteRatio: 7.6
SJR: 1.899
SNIP: 1.107
open access Open Access

The Royal Society

Quality:  
High
CiteRatio: 6.6
SJR: 1.655
SNIP: 1.709

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.

0.923

11% from 2018

Impact factor for Current Pharmaceutical Analysis from 2016 - 2019
Year Value
2019 0.923
2018 0.829
2017 0.859
2016 0.75
graph view Graph view
table view Table view

1.2

8% from 2019

CiteRatio for Current Pharmaceutical Analysis from 2016 - 2020
Year Value
2020 1.2
2019 1.3
2018 1.1
2017 1.2
2016 1.4
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has increased by 11% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • CiteRatio of this journal has decreased by 8% 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.

0.21

27% from 2019

SJR for Current Pharmaceutical Analysis from 2016 - 2020
Year Value
2020 0.21
2019 0.286
2018 0.218
2017 0.224
2016 0.242
graph view Graph view
table view Table view

0.481

4% from 2019

SNIP for Current Pharmaceutical Analysis from 2016 - 2020
Year Value
2020 0.481
2019 0.461
2018 0.415
2017 0.457
2016 0.638
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has decreased by 27% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has increased by 4% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

Current Pharmaceutical Analysis

Guideline source: View

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Bentham Science

Current Pharmaceutical Analysis

Current Pharmaceutical Analysis publishes expert reviews and original research articles on all the most recent advances in pharmaceutical and biomedical analysis. All aspects of the field are represented including drug analysis, analytical methodology and instrumentation. The ...... Read More

Pharmaceutical Science

Biophysics

Biochemistry

Molecular Medicine

Pharmacology, Toxicology and Pharmaceutics

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Last updated on
29 Jun 2020
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ISSN
1573-4129
i
Impact Factor
Medium - 0.687
i
Open Access
No
i
Sherpa RoMEO Archiving Policy
Yellow faq
i
Plagiarism Check
Available via Turnitin
i
Endnote Style
Download Available
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Bibliography Name
Vancouver
i
Citation Type
Numbered
[25]
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Bibliography Example
Blonder, G E, Tinkham, M, & Klapwijk, T M. Transition from metallic to tunnel- ing regimes in superconducting microconstrictions: Excess current, charge imbalance, and supercurrent conversion. Phys. Rev. B. 2013;87(10):100510.

Top papers written in this journal

Journal Article DOI: 10.2174/157341209787314936
Noteworthy Secondary Metabolites Naphthoquinones – their Occurrence, Pharmacological Properties and Analysis
Babula Petr, Adam Vojtech, Havel Ladislav, Kizek René1

Abstract:

Chemical investigation of many bacterial and fungal, as well as plant species has revealed the presence of in- teresting compounds derived from naphthalene - 1,4-naphthoquinones and rarely also 1,2-naphthoquinones. They were detected in many species of families Bignoniaceae, Droseraceae, Plumbaginace, Boraginaceae, Juglandace... Chemical investigation of many bacterial and fungal, as well as plant species has revealed the presence of in- teresting compounds derived from naphthalene - 1,4-naphthoquinones and rarely also 1,2-naphthoquinones. They were detected in many species of families Bignoniaceae, Droseraceae, Plumbaginace, Boraginaceae, Juglandaceae as well as in species of small families, such as Dioncophyllaceae or Acanthaceae. Naphthoquinones have very interesting spectrum of biological actions, including antibiotic, antiviral, anti-inflammatory, antipyretic, antiproliferative and cytotoxic effects. Because of these properties the plants containing them are used in folk medicines, mainly by natives in Asia, where espe- cially Chinese medicine uses aerial as well as subterranean parts of these plants for hundreds years, and South America. The utilizing of naphthoquinones for medicinal purposes and their occurrence in nature is reviewed and discussed. Moreover, we review analytical techniques using for their analysis. read more read less
219 Citations
Journal Article DOI: 10.2174/157341207779802386
Lipid Disorders in Diabetes Mellitus and Current Management

Abstract:

Lipid disorders are common in diabetes mellitus (DM), and play crucial roles in the development of diabetic cardiovascular complications. Diabetic dyslipidemia is characterized by hypertriglyceridemia, increased levels of very low density lipoproteins (VLDL), small dense low density lipoprotein (LDL), and decreased levels of ... Lipid disorders are common in diabetes mellitus (DM), and play crucial roles in the development of diabetic cardiovascular complications. Diabetic dyslipidemia is characterized by hypertriglyceridemia, increased levels of very low density lipoproteins (VLDL), small dense low density lipoprotein (LDL), and decreased levels of high density lipoprotein (HDL)-cholesterol. The activity of lipoprotein lipase is reduced in diabetic patients, which attenuates the lipolysis of triglyceride-rich lipoproteins and the uptake of free fatty acids. The increased uptake of triglycerides in liver promotes the production of VLDL. Hypertriglyceridemia promotes the exchange of cholesteryl ester from HDL to VLDL or LDL for triglycerides. Obesity or nephropathy deteriorates the dyslipidemia in DM patients. The initial management of lipid disorders in diabetic patients without cardiovascular disease is lifestyle intervention and glucose control. The abnormalities in the metabolism of LDL or HDL in diabetic patients often require pharmacological intervention. Target of LDL-cholesterol (LDL-c) is more restrict in diabetic patients than in non-diabetic subjects. Treatment with HMG-CoA reductase inhibitors (statins) effectively reduces LDL-c and cardiac events, and that was associated with moderately increases in HDL-c. The combination of ezetimibe with a statin helps to achieve LDL-c target in patients with unsatisfactory cholesterol lowering by statin alone. Fibrates (PPAR-α agonists) or PPAR-γ agonists reduce the levels of triglycerides and moderately elevate HDL-c. PPAR-γ agonists also improve insulin sensitivity. Cholesteryl ester transfer protein inhibitors may dramatically increase HDL-c. Lipid management has been considered as an effective approach to reduce cardiovascular risk in diabetes. read more read less

Topics:

Cholesterylester transfer protein (63%)63% related to the paper, Very low-density lipoprotein (62%)62% related to the paper, Hypertriglyceridemia (60%)60% related to the paper, High-density lipoprotein (59%)59% related to the paper, Statin (59%)59% related to the paper
107 Citations
Journal Article DOI: 10.2174/1573412052953328
Enantioselective Toxicity and Carcinogenesis

Abstract:

In a non-chiral environment, the enantiomers of a racemate possess the same physico-chemical properties but in the biological systems they possess different activities. One of the enantiomers may be more toxic or carcinogenic, and, therefore, the present data available on the toxicity and carcinogenesis of the racemic mixture... In a non-chiral environment, the enantiomers of a racemate possess the same physico-chemical properties but in the biological systems they possess different activities. One of the enantiomers may be more toxic or carcinogenic, and, therefore, the present data available on the toxicity and carcinogenesis of the racemic mixtures of these chiral pollutants are not reliable and need modification in terms of the enantioselective toxicity and carcinogenesis. It is essential to explore the enantioselective toxicity and carcinogenesis due to the different enantiomers of the chiral pollutants. The knowledge of the stereoselective metabolisms of the chiral pollutants may be useful for the treatment of cancer and other diseases. The enantioselective toxicity and carcinogenesis due to the chiral pesticides, pollutants and some drugs have been discussed in this review article. read more read less
107 Citations
Journal Article DOI: 10.2174/1573412052953346
Critical Review of Development, Validation, and Transfer for High Throughput Bioanalytical LC-MS/MS Methods
Shaolian Zhou, Qi Song, Yong Tang, Weng Naidong

Abstract:

Swift growth in the use of LC-MS/MS for the analysis of drugs in biological matrices has been compelled by the need for timely and high-quality data at many stages in drug discovery and development process: from high throughput screening of drug candidates and rapid data generation for pre-clinical studies to almost 'real-tim... Swift growth in the use of LC-MS/MS for the analysis of drugs in biological matrices has been compelled by the need for timely and high-quality data at many stages in drug discovery and development process: from high throughput screening of drug candidates and rapid data generation for pre-clinical studies to almost 'real-time' analysis of clinical samples. Prompt and rational method development, validation, and transfer play a pivotal role in achieving the goals of "faster, better, and cheaper" for pharmacokinetic studies since this could easily account for more than 50% of the time and labor resources for a moderate-sized project. Strategy for rational method development, validation and transfer has been largely kept as institutional knowledge but rarely appeared in literature. In this review article, strategies for developing and validating robust high throughput LC-MS/MS methods will be critically reviewed and discussed. Automated sample preparation, fast chromatography, minimization of matrix effects, and strategy of narrowing the gap between validation and incurred sample analysis are just a few topics covered in this review. Other interesting approaches for improving method efficiency and ruggedness such as direct injection SPE and liquid/liquid extracts as well as multiplexing of LC columns will also be discussed. Potential pitfalls during method development and validation are pointed out. At the end, the question "how fast is fast enough and how fast is too fast?" will be answered after considering all aspects of the method development and validation. read more read less
86 Citations
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Current Pharmaceutical Analysis format uses Vancouver citation style.

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Frequently asked questions

1. Can I write Current Pharmaceutical Analysis in LaTeX?

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

2. Do you follow the Current Pharmaceutical Analysis guidelines?

Yes, the template is compliant with the Current Pharmaceutical Analysis 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 Current Pharmaceutical Analysis?

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 Current Pharmaceutical Analysis citation style.

4. Can I use the Current Pharmaceutical Analysis 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 Current Pharmaceutical Analysis.

5. Can I use a manuscript in Current Pharmaceutical Analysis 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 Current Pharmaceutical Analysis that you can download at the end.

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

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

7. Where can I find the template for the Current Pharmaceutical Analysis?

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 Current Pharmaceutical Analysis'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 Current Pharmaceutical Analysis'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. Current Pharmaceutical Analysis an online tool or is there a desktop version?

SciSpace's Current Pharmaceutical Analysis 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 Current Pharmaceutical Analysis?

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 Current Pharmaceutical Analysis?”

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

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

12. Is Current Pharmaceutical Analysis'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 Current Pharmaceutical Analysis?

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 Current Pharmaceutical Analysis. 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 Current Pharmaceutical Analysis?

The 5 most common citation types in order of usage for Current Pharmaceutical Analysis 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 Current Pharmaceutical Analysis?

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 Current Pharmaceutical Analysis's guidelines and download the same in Word, PDF and LaTeX formats? Give us a try!.

16. Can I download Current Pharmaceutical Analysis 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 Current Pharmaceutical Analysis 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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