Example of International Journal of Peptide Research and Therapeutics format
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Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format
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Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format Example of International Journal of Peptide Research and Therapeutics format
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open access Open Access

International Journal of Peptide Research and Therapeutics — Template for authors

Publisher: Springer
Categories Rank Trend in last 3 yrs
Analytical Chemistry #88 of 122 down down by 16 ranks
Drug Discovery #108 of 145 down down by 1 rank
Bioengineering #113 of 148 down down by 21 ranks
Biochemistry #328 of 415 down down by 13 ranks
Molecular Medicine #137 of 167 down down by 4 ranks
journal-quality-icon Journal quality:
Medium
calendar-icon Last 4 years overview: 511 Published Papers | 1001 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 02/07/2020
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General info
Top papers
Popular templates
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FAQ

Related Journals

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open access Open Access

Springer

Quality:  
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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.

1.5

23% from 2018

Impact factor for International Journal of Peptide Research and Therapeutics from 2016 - 2019
Year Value
2019 1.5
2018 1.219
2017 1.132
2016 0.904
graph view Graph view
table view Table view

2.0

25% from 2019

CiteRatio for International Journal of Peptide Research and Therapeutics from 2016 - 2020
Year Value
2020 2.0
2019 1.6
2018 1.9
2017 2.0
2016 1.7
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has increased by 23% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

insights Insights

  • CiteRatio of this journal has increased by 25% 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.

0.304

15% from 2019

SJR for International Journal of Peptide Research and Therapeutics from 2016 - 2020
Year Value
2020 0.304
2019 0.264
2018 0.284
2017 0.333
2016 0.334
graph view Graph view
table view Table view

0.571

3% from 2019

SNIP for International Journal of Peptide Research and Therapeutics from 2016 - 2020
Year Value
2020 0.571
2019 0.555
2018 0.431
2017 0.422
2016 0.424
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has increased by 15% in last years.
  • This journal’s SJR is in the top 10 percentile category.

insights Insights

  • SNIP of this journal has increased by 3% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

International Journal of Peptide Research and Therapeutics

Guideline source: View

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Springer

International Journal of Peptide Research and Therapeutics

The International Journal for Peptide Research & Therapeutics is an international, peer-reviewed journal focusing on issues, research, and integration of knowledge on the latest developments in peptide therapeutics. The Journal brings together in a single source the most excit...... Read More

Bioengineering

Analytical Chemistry

Drug Discovery

Biochemistry

Molecular Medicine

Chemical Engineering

i
Last updated on
02 Jul 2020
i
ISSN
1573-3904
i
Impact Factor
Medium - 0.904
i
Acceptance Rate
Not provided
i
Frequency
Not provided
i
Open Access
Yes
i
Sherpa RoMEO Archiving Policy
Green faq
i
Plagiarism Check
Available via Turnitin
i
Endnote Style
Download Available
i
Bibliography Name
SPBASIC
i
Citation Type
Author Year
(Blonder et al, 1982)
i
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

Journal Article DOI: 10.1007/S10989-006-9059-7
In Situ Neutralization in Boc-chemistry Solid Phase Peptide Synthesis
Martina Schnölzer1, Paul F. Alewood2, Alun Jones1, Dianne Alewood2, Stephen B. H. Kent1

Abstract:

Simple, effective protocols have been developed for manual and machine-assisted Boc-chemistry solid phase peptide synthesis on polystyrene resins. These use in situ neutralization [i.e. neutralization simultaneous with coupling], high concentrations (>0.2 m) of Boc-amino acid-OBt esters plus base for rapid coupling, 100% TFA ... Simple, effective protocols have been developed for manual and machine-assisted Boc-chemistry solid phase peptide synthesis on polystyrene resins. These use in situ neutralization [i.e. neutralization simultaneous with coupling], high concentrations (>0.2 m) of Boc-amino acid-OBt esters plus base for rapid coupling, 100% TFA for rapid Boc group removal, and a single short (30 s) DMF flow wash between deprotection/coupling and between coupling/deprotection. Single 10 min coupling times were used throughout. Overall cycle times were 15 min for manual and 19 min for machine-assisted synthesis (75 residues per day). No racemization was detected in the .base-catalyzed coupling step. Several side reactions were studied, and eliminated. These included: pyrrolidonecarboxylic acid formation from Gln in hot TFA-DMF; chain-termination by reaction with excess HBTU; and, chain termination by acetylation (from HOAc in commercial Boc-amino acids). The in situ neutralization protocols gave a significant increase in the efficiency of chain assembly, especially for “difficult” sequences arising from sequence-dependent peptide chain aggregation in standard (neutralization prior to coupling) Boc-chemistry SPPS protocols or in Fmoc-chemistry SPPS. Reported syntheses include HIV-1 protease(1–50,Cys.amide), HIV-1 protease(53–99), and the full length HIV-l protease(1–99). read more read less

Topics:

Peptide synthesis (53%)53% related to the paper, Chain termination (50%)50% related to the paper
175 Citations
open accessOpen access Journal Article DOI: 10.1007/S10989-005-9010-3
Development and Comparison of Different Nanoparticulate Polyelectrolyte Complexes as Insulin Carriers

Abstract:

The overall objective of our research is to produce polyanion/chitosan nanoparticulate oral delivery systems for insulin. Specific objectives of the present study were to study dextran sulfate or alginate complexation with chitosan on mean particle size, insulin association efficiency, loading capacity and release profile. Na... The overall objective of our research is to produce polyanion/chitosan nanoparticulate oral delivery systems for insulin. Specific objectives of the present study were to study dextran sulfate or alginate complexation with chitosan on mean particle size, insulin association efficiency, loading capacity and release profile. Nanoparticles were formed by ionotropic complexation and coacervation between polyanions (dextran sulfate and alginate) and chitosan. Diameter was evaluated with photon correlation spectroscopy, polymer interaction was confirmed by DSC and FTIR and particle morphology was assessed by SEM and TEM. Mean nanoparticle diameter ranged from 423 to 850 nm, insulin association efficiency from 63 to 94% and loading capacity from 5 to 13%. Dextran sulfate provided highest insulin association efficiency and retention of insulin in gastric simulated conditions. These nanoparticle systems show promise as insulin and potentially other therapeutic polypeptides carriers. read more read less

Topics:

Chitosan (50%)50% related to the paper
View PDF
152 Citations
Journal Article DOI: 10.1007/S10989-019-09823-5
A Review on Bioactive Peptides: Physiological Functions, Bioavailability and Safety
Divya Bhandari1, Shafiya Rafiq1, Yogesh Gat1, Punam Gat1, Roji Waghmare, Vikas Kumar1

Abstract:

Bioactive peptides can be defined as isolated small fragments of proteins which provide some physiological health benefits. They act as potential modifiers reducing the risk of many chronic diseases. To the best of our knowledge, limited literature is available for the methods of isolation of these peptides from different pro... Bioactive peptides can be defined as isolated small fragments of proteins which provide some physiological health benefits. They act as potential modifiers reducing the risk of many chronic diseases. To the best of our knowledge, limited literature is available for the methods of isolation of these peptides from different protein sources with their in vitro and vivo physiological effects. Also, there is a need to adopt healthy lifestyle choices for prevention of diseases, to counter increase in consumption of functional foods and nutraceuticals day-by-day. Thus, these peptides play a major role in the development of various functional foods. In the present study, attempts are made to review different physiological effects from peptides. Also, effects of processing on the peptides are discussed with special emphasis on its bioavailability, safety and future application for further development. read more read less
120 Citations
open accessOpen access Journal Article DOI: 10.1007/S10989-005-9393-1
Prediction of Cell-Penetrating Peptides

Abstract:

Cell-penetrating peptides, CPPs, are used as delivery vectors for pharmacologically interesting substances, such as antisense oligonucleotides, proteins and peptides. We present a general principle for designing cell-penetrating peptides derived from naturally occurring proteins as well as from randomly generated polyamino ac... Cell-penetrating peptides, CPPs, are used as delivery vectors for pharmacologically interesting substances, such as antisense oligonucleotides, proteins and peptides. We present a general principle for designing cell-penetrating peptides derived from naturally occurring proteins as well as from randomly generated polyamino acid sequences. Thereby, we introduce a novel pharmacological principle for identification of cell-penetrating peptides for which the applications can be numerous, including cellular transduction vectors and mimics of intracellular protein–protein interactions. The methods of identifying a CPP comprises assessing the averaged bulk property values of the defined sequence, and ensuring that they fall within the bulk property value interval obtained from the training set. Despite this simplistic approach, the search criteria proved useful for finding CPP properties in either proteins or random sequences. We have experimentally verified cell-penetrating properties of 10–20-mer peptides derived from naturally occurring proteins as well as from random poly-amino acids. We note that since CPPs can be found in part of the protein sequences that may govern protein interactions, it is possible to produce cell-penetrating protein agonists or antagonists. read more read less
View PDF
98 Citations
open accessOpen access Journal Article DOI: 10.1007/S10989-014-9413-0
The Evaluation of Dipeptidyl Peptidase (DPP)-IV, α-Glucosidase and Angiotensin Converting Enzyme (ACE) Inhibitory Activities of Whey Proteins Hydrolyzed with Serine Protease Isolated from Asian Pumpkin (Cucurbita ficifolia)

Abstract:

In the present study, whey protein concentrate (WPC-80) and β-lactoglobulin were hydrolyzed with a noncommercial serine protease isolated from Asian pumpkin (Cucurbita ficifolia) Hydrolysates were further fractionated by ultrafiltration using membranes with cut-offs equal 3 and 10 kDa Peptide fractions of molecular weight low... In the present study, whey protein concentrate (WPC-80) and β-lactoglobulin were hydrolyzed with a noncommercial serine protease isolated from Asian pumpkin (Cucurbita ficifolia) Hydrolysates were further fractionated by ultrafiltration using membranes with cut-offs equal 3 and 10 kDa Peptide fractions of molecular weight lower than 3 and 3–10 kDa were further subjected to the RP-HPLC Separated preparations were investigated for their potential as the natural inhibitors of dipeptidyl peptidase (DPP-IV), α-glucosidase and angiotensin converting enzyme (ACE) WPC-80 hydrolysate showed higher inhibitory activities against the three tested enzymes than β-lactoglobulin hydrolysate Especially high biological activities were exhibited by peptide fractions of molecular weight lower than 3 kDa, with ACE IC50 <064 mg/mL and DPP-IV IC50 <055 mg/mL This study suggests that peptides generated from whey proteins may support postprandial glycemia regulation and blood pressure maintenance, and could be used as functional food ingredients in the diet of patients with type 2 diabetes read more read less

Topics:

Dipeptidyl peptidase (59%)59% related to the paper, Whey protein (55%)55% related to the paper, Hydrolysate (55%)55% related to the paper, Angiotensin-converting enzyme (54%)54% related to the paper, Serine protease (52%)52% related to the paper
View PDF
98 Citations
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Frequently asked questions

1. Can I write International Journal of Peptide Research and Therapeutics in LaTeX?

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3. Can I cite my article in multiple styles in International Journal of Peptide Research and Therapeutics?

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 International Journal of Peptide Research and Therapeutics citation style.

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12. Is International Journal of Peptide Research and Therapeutics'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 International Journal of Peptide Research and Therapeutics?

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 International Journal of Peptide Research and Therapeutics. 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 International Journal of Peptide Research and Therapeutics?

The 5 most common citation types in order of usage for International Journal of Peptide Research and Therapeutics are:.

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

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16. Can I download International Journal of Peptide Research and Therapeutics 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 International Journal of Peptide Research and Therapeutics Endnote style according to Elsevier guidelines.

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