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Journal of Pharmacy and Pharmacology — Template for authors

Publisher: Wiley

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Guideline source

Categories	Rank	Trend in last 3 yrs
Pharmaceutical Science	#45 of 166	down by 2 ranks
Pharmacology	#109 of 297	up by 14 ranks

Journal quality:

Good

Last 4 years overview: 662 Published Papers | 3298 Citations

Indexed in: Scopus

Last updated: 08/07/2020

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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.

2.571

8% from 2018

Impact factor for Journal of Pharmacy and Pharmacology from 2016 - 2019
Year	Value
2019	2.571
2018	2.39
2017	2.309
2016	2.405

Graph view

5.0

14% from 2019

CiteRatio for Journal of Pharmacy and Pharmacology from 2016 - 2020
Year	Value
2020	5.0
2019	4.4
2018	4.1
2017	4.2
2016	4.7

Graph view

Insights

Impact factor of this journal has increased by 8% in last year.
This journal’s impact factor is in the top 10 percentile category.

Insights

CiteRatio of this journal has increased by 14% 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.

0.745

28% from 2019

SJR for Journal of Pharmacy and Pharmacology from 2016 - 2020
Year	Value
2020	0.745
2019	0.58
2018	0.568
2017	0.657
2016	0.74

Graph view

0.999

10% from 2019

SNIP for Journal of Pharmacy and Pharmacology from 2016 - 2020
Year	Value
2020	0.999
2019	0.909
2018	0.789
2017	0.83
2016	0.938

Graph view

Insights

SJR of this journal has increased by 28% in last years.
This journal’s SJR is in the top 10 percentile category.

Insights

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

Guideline source: View

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Wiley

Journal of Pharmacy and Pharmacology

Journal of Pharmacy and Pharmacology, one of the leading pharmaceutical sciences journals has been published continuously since 1870 and monthly since 1949. The Journal publishes original research papers, critical reviews and rapid communications on the latest developments in the pharmaceutical sciences. JPP keeps pace with new research on how drug action may be optimized by new technologies, and attention is given to understanding and improving drug interactions in the body. At the same time, the journal maintains its established and well-respected core strengths in areas such as pharmaceutics and drug delivery, experimental and clinical pharmacology, biopharmaceutics and drug disposition, and drugs from natural sources. JPP publishes at least one special issue on a topical theme each year. Read Less

Pharmaceutical Science

Pharmacology

Pharmacology, Toxicology and Pharmaceutics

Last updated on	08 Jul 2020
ISSN	0022-3573
Impact Factor	High - 1.05
Open Access	Yes
Sherpa RoMEO Archiving Policy	Yellow
Plagiarism Check	Available via Turnitin
Endnote Style	Download Available
Bibliography Name	apa
Citation Type	Numbered [25]
Bibliography Example	Beenakker, C.W.J. (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: 10.1111/J.2042-7158.2012.01567.X •

Doxorubicin: an update on anticancer molecular action, toxicity and novel drug delivery systems

Oktay Tacar¹, Pornsak Sriamornsak², •

02 Aug 2012 - Journal of Pharmacy and Pharmacology

Abstract:

Objectives The frontline drug doxorubicin has been used for treating cancer for over 30 years. While providing a cure in select cases, doxorubicin causes toxicity to most major organs, especially life-threatening cardiotoxicity, which forces the treatment to become dose-limiting. Key findings Doxorubicin is known to bind ... Objectives The frontline drug doxorubicin has been used for treating cancer for over 30 years. While providing a cure in select cases, doxorubicin causes toxicity to most major organs, especially life-threatening cardiotoxicity, which forces the treatment to become dose-limiting. Key findings Doxorubicin is known to bind to DNA-associated enzymes, intercalate with DNA base pairs, and target multiple molecular targets to produce a range of cytotoxic effects. For instance, it causes the activation of various molecular signals from AMPK (AMP-activated protein kinase inducing apoptosis) to influence the Bcl-2/Bax apoptosis pathway. By altering the Bcl-2/Bax ratio, downstream activation of different caspases can occur resulting in apoptosis. Doxorubicin also induces apoptosis and necrosis in healthy tissue causing toxicity in the brain, liver, kidney and heart. Over the years, many studies have been conducted to devise a drug delivery system that would eliminate these adverse affects including liposomes, hydrogel and nanoparticulate systems, and we highlight the pros and cons of these drug delivery systems. Summary Overall the future for the continued use of doxorubicin clinically against cancer looks set to be prolonged, provided certain enhancements as listed above are made to its chemistry, delivery and toxicity. Increased efficacy depends on these three aims being met satisfactorily as discussed in turn in this review. read more

Topics:

Drug delivery (54%)54% related to the paper, Doxorubicin (53%)53% related to the paper

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1,876 Citations

Journal Article • DOI: 10.1111/J.2042-7158.1997.TB06761.X •

Nitric Oxide Scavenging by Curcuminoids

Sreejayan¹, M. N. A. Rao¹ •

12 Apr 2011 - Journal of Pharmacy and Pharmacology

Abstract:

Because curcumin, a compound with anti-inflammatory and anticancer activity, inhibits induction of nitric oxide synthase in activated macrophages and has been shown to be a potent scavenger of free radicals we have investigated whether it can scavenge nitric oxide directly. Curcumin reduced the amount of nitrite formed by the... Because curcumin, a compound with anti-inflammatory and anticancer activity, inhibits induction of nitric oxide synthase in activated macrophages and has been shown to be a potent scavenger of free radicals we have investigated whether it can scavenge nitric oxide directly. Curcumin reduced the amount of nitrite formed by the reaction between oxygen and nitric oxide generated from sodium nitroprusside. Other related compounds, e.g. demethoxycurcumin, bisdemethoxycurcumin and diacetylcurcumin were as active as curcumin, indicating that the methoxy and the phenolic groups are not essential for the scavenging activity. The results indicate curcumin to be a scavenger of nitric oxide. Because this compound is implicated in inflammation and cancer, the therapeutic properties of curcumin against these conditions might be at least partly explained by its free-radical scavenging properties, including those toward nitric oxide. read more

Topics:

Nitric oxide (60%)60% related to the paper, Nitric oxide synthase (56%)56% related to the paper, Curcumin (54%)54% related to the paper,

1,080 Citations

Journal Article • DOI: 10.1111/J.2042-7158.1975.TB09378.X •

The concept of dissolution efficiency.

K A Khan

12 Apr 2011 - Journal of Pharmacy and Pharmacology

Abstract:

The recent interest in drug availability has resulted in a proliferation of in vitro dissolution testing, now standard for many dosage forms. The usual method of evaluation is the comparison of the time taken for given proportions of the active drug to be released into solution and figures such as the t20, t50 and t90 % times... The recent interest in drug availability has resulted in a proliferation of in vitro dissolution testing, now standard for many dosage forms. The usual method of evaluation is the comparison of the time taken for given proportions of the active drug to be released into solution and figures such as the t20, t50 and t90 % times are often quoted. Alternatively the fraction of drug in solution after a given time is used for comparison, i.e. 60% release in 30 min. A further parameter suitable for the evaluation of in vitro dissolution has been suggested by Khan & Rhodes (1972), who introduced the idea of Dissolution Efficiency. This is defined as the area under the dissolution curve up to a certain time, t, expressed as a percentage of the area of the rectangle described by 100% dissolutionin the sametime. The simplest case, shown in Fig. 1 where, dissolution of a tableted drug, is read more

Topics:

Pharmaceutic Aids (57%)57% related to the paper

928 Citations

Journal Article • DOI: 10.1111/J.2042-7158.1967.TB09604.X •

Evidence for dopamine receptor stimulation by apomorphine

Nils-Erik Andén, Allan Rubenson, •

12 Apr 2011 - Journal of Pharmacy and Pharmacology

Abstract:

Sm,-Recently, Ernst (1967) has reported that the apomorphine-induced compulsive gnawing in rats is not mediated via the release of catecholamines, since it is not reduced by the catecholamine synthesis inhibitors a-methyl-3,4dihydroxyphenylalanine and a-methyltyrosine. On the other hand, the gnawing seen after treatment with ... Sm,-Recently, Ernst (1967) has reported that the apomorphine-induced compulsive gnawing in rats is not mediated via the release of catecholamines, since it is not reduced by the catecholamine synthesis inhibitors a-methyl-3,4dihydroxyphenylalanine and a-methyltyrosine. On the other hand, the gnawing seen after treatment with (+)-amphetamine is blocked by these synthesis inhibitors. Since the apomorphine-induced gnawing requires an intact corpus striatum and gnawing can also be produced by the catecholamine precursor dihydroxyphenylalanine, Ernst (1967) suggested that apomorphine acts on the dopamine receptors whereas amphetamine acts by releasing dopamine. In the present paper supporting evidence for this view is given by further functional, biochemical and histochemical studies. The functional influence of apomorphine on dopamine neurotransmission in the corpus striatum was examined after unilateral removal of the corpus striatum of adult hooded rats weighing about 200 g (And& Dahlstrom & others, 1966a). A possible action of apomorphine on the noradrenaline receptors of the spinal cord was tested in acutely spinalized adult hooded rats by evaluating the changes in the flexor reflex evoked by pinching the hind limbs. The effect of apomorphine on the dopamine and noradrenaline levels of the brain and spinal cord was determined biochemically (Bertler, Carlsson & Rosengren, 1958; Carlsson & Waldeck, 1958) and histochemically (Falck, Hillarp & others, 1962; Dahlstrom & Fuxe, 1964; Hamberger, Malmfors & Sachs, 1965). Function. These studies were made mainly on rats which had been pretreated with reserpine (10 mg/kg i.p., 3 hr) plus a-methyltyrosine methylester (H 44/68, 500mg/kg, i.p., 2 hr) after removal of the left corpus striatum by suction. After this treatment all the operated animals turned towards the unoperated side (cf. And6n & others, 1966a). After injection of apomorphine (1-25 mg/kg s.c.) these rats changed their position and turned or rotated towards the operated side. This effect began about 5 min after the injection and was evident for about 45-60 min. If apomorphine was given to operated rats not pretreated with reserpineH 44/68 combination, this action of apomorphine, like the gnawing, seemed to be less pronounced. If haloperidol (5 mg/kg i.p.) was given 15-20 min after apomorphine all the rats turned from the operated towards the unoperated side in about 15 min and the gnawing ceased. (+)-Amphetamine (0.5-25 mg/kg s.c.), like apomorphine, made the rats turn or rotate towards the operated side. In contrast to apomorphine, however, this action of amphetamine was not seen after pretreatment with reserpine plus H 44/68 (cf. Weissman, Koe & Tenen, 1966; Hanson, 1967; Ernst, 1967). Apomorphine (25 mg/kg s.c.), in contrast to (+)-amphetamine (05-25 mg/kg s.c.) and ~-3,4-dihydroxyphenylalanine (50-75 mg/kg i.v. 2 hr after nialamide 50 mg/kg i.p.), did not cause a definite increase of the flexor reflex in spinalized rats. Chemistry. The biochemical results obtained in unoperated adult hooded rats are presented in Table 1. Apomorphine caused a retardation of the depletion in brain dopamine produced by H 44/68. The difference between the dopamine levels in the apomorphine-H 44/68 group and in the H 44/68 group is statistically significant (P < 0.001, Student’s r-test). This action of apomorphine on the brain dopamine was blocked by haloperidol. The disappearance of noradrenaline from the brain and the spinal cord after H 44/68 did not seem to be influenced by apomorphine. (+)-Amphetamine did not cause any significant retardation of the dopamine and noradrenaline loss after H 44/68. read more

Topics:

Dopamine receptor D2 (76%)76% related to the paper, Dopamine receptor D1 (73%)73% related to the paper, Apomorphine Hydrochloride (67%)67% related to the paper,

894 Citations

Journal Article • DOI: 10.1111/J.2042-7158.1990.TB07033.X •

Nanoparticle uptake by the rat gastrointestinal mucosa : quantitation and particle size dependency

P.U. Jani¹, Gavin Halbert², •

12 Apr 2011 - Journal of Pharmacy and Pharmacology

Abstract:

Polystyrene microspheres in the size range 50 nm to 3 microns were fed by gavage to female Sprague Dawley rats daily for 10 days at a dose of 1.25 mg/kg-1. Previous histological evidence of the uptake of these particles and their absorption across the gastrointestinal tract and passage via the mesentery lymph supply and lymph... Polystyrene microspheres in the size range 50 nm to 3 microns were fed by gavage to female Sprague Dawley rats daily for 10 days at a dose of 1.25 mg/kg-1. Previous histological evidence of the uptake of these particles and their absorption across the gastrointestinal tract and passage via the mesentery lymph supply and lymph nodes to the liver and spleen was confirmed by analysis of tissues for the presence of polystyrene by gel permeation chromatography. Measurement of radioactivity of tissues following administration of 100 nm and 1 micron I125-labelled polystyrene latex particles for 8 days was corroborative although less secure because of the potential lability of the labelled particles. The extent of absorption of 50 nm particles under the conditions of these experiments was 34% and of the 100 nm particles 26% (as measured by determination of polystyrene content), of which total, about 7% (50 nm) and 4% (100 nm), was in the liver, spleen, blood and bone marrow. Particles larger than 100 nm did not reach the bone marrow, and those larger than 300 nm were absent from blood. No particles were detected in heart or lung tissue. read more

Topics:

Particle size (52%)52% related to the paper, Intestinal absorption (51%)51% related to the paper

861 Citations

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12. Is Journal of Pharmacy and Pharmacology'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 Journal of Pharmacy and Pharmacology?

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 Journal of Pharmacy and Pharmacology. 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:

Pre-prints as being the version of the paper before peer review and
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 Journal of Pharmacy and Pharmacology?

The 5 most common citation types in order of usage for Journal of Pharmacy and Pharmacology 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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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 Journal of Pharmacy and Pharmacology Endnote style according to Elsevier guidelines.

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Journal of Pharmacy and Pharmacology — Template for authors

Related Journals

Journal Performance & Insights

Impact Factor

CiteRatio

2.571

5.0

Insights

Insights

SCImago Journal Rank (SJR)

Source Normalized Impact per Paper (SNIP)

0.745

0.999

Insights

Insights

Journal of Pharmacy and Pharmacology

Top papers written in this journal

Abstract:

Topics:

Abstract:

Topics:

Abstract:

Topics:

Abstract:

Topics:

Abstract:

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What to expect from SciSpace?

Speed and accuracy over MS Word

Plagiarism Reports via Turnitin

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Frequently asked questions

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No word template required

Verifed journal formats

Trusted by academicians

Fast and reliable,
built for complaince.