Example of Current Drug Delivery format
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Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format
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Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format Example of Current Drug Delivery format
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open access Open Access ISSN: 15672018

Current Drug Delivery — Template for authors

Publisher: Bentham Science
Categories Rank Trend in last 3 yrs
Pharmaceutical Science #67 of 166 up up by 6 ranks
journal-quality-icon Journal quality:
Good
calendar-icon Last 4 years overview: 375 Published Papers | 1352 Citations
indexed-in-icon Indexed in: Scopus
last-updated-icon Last updated: 25/06/2020
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FAQ

Journal Performance & Insights

  • Impact Factor
  • CiteRatio
  • SJR
  • SNIP

Impact factor 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.

1.582

4% from 2018

Impact factor for Current Drug Delivery from 2016 - 2019
Year Value
2019 1.582
2018 1.645
2017 2.078
2016 2.516
graph view Graph view
table view Table view

insights Insights

  • Impact factor of this journal has decreased by 4% in last year.
  • This journal’s impact factor is in the top 10 percentile category.

CiteRatio is a measure of average citations received per peer-reviewed paper published in the journal.

3.6

13% from 2019

CiteRatio for Current Drug Delivery from 2016 - 2020
Year Value
2020 3.6
2019 3.2
2018 2.7
2017 2.8
2016 2.5
graph view Graph view
table view Table view

insights Insights

  • CiteRatio of this journal has increased by 13% in last years.
  • This journal’s CiteRatio is in the top 10 percentile category.

SCImago Journal Rank (SJR) measures weighted citations received by the journal. Citation weighting depends on the categories and prestige of the citing journal.

0.449

25% from 2019

SJR for Current Drug Delivery from 2016 - 2020
Year Value
2020 0.449
2019 0.359
2018 0.402
2017 0.443
2016 0.504
graph view Graph view
table view Table view

insights Insights

  • SJR of this journal has increased by 25% in last years.
  • This journal’s SJR is in the top 10 percentile category.

Source Normalized Impact per Paper (SNIP) measures actual citations received relative to citations expected for the journal's category.

0.611

22% from 2019

SNIP for Current Drug Delivery from 2016 - 2020
Year Value
2020 0.611
2019 0.499
2018 0.557
2017 0.622
2016 0.747
graph view Graph view
table view Table view

insights Insights

  • SNIP of this journal has increased by 22% in last years.
  • This journal’s SNIP is in the top 10 percentile category.

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CiteRatio: 6.5 | SJR: 0.976 | SNIP: 1.593
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CiteRatio: 8.1 | SJR: 1.13 | SNIP: 1.113
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Current Drug Delivery

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Bentham Science

Current Drug Delivery

Current Drug Delivery aims to publish peer-reviewed articles, research articles, short and in-depth reviews, and drug clinical trials studies in the rapidly developing field of drug delivery. Modern drug research aims to build delivery properties of a drug at the design phase,...... Read More

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Last updated on
25 Jun 2020
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ISSN
1875-5704
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Impact Factor
High - 2.516
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Acceptance Rate
Not provided
i
Frequency
Not provided
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Open Access
No
i
Sherpa RoMEO Archiving Policy
Yellow faq
i
Plagiarism Check
Available via Turnitin
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Endnote Style
Download Available
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Bibliography Name
Vancouver
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Citation Type
Numbered
[25]
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Bibliography Example
Blonder, G.E.; Tinkham, M.; Klapwijk, T.M. Transition from metallic to tunneling regimes in superconducting microconstrictions: Excess current, charge imbalance, and supercurrent conversion. Phys. Rev. B 1982, 25, 4515–4532.

Top papers written in this journal

Journal Article DOI: 10.2174/156720107782151269
Liposomal Drug Delivery Systems: An Update Review
Abdus Samad1, Yasmin Sultana, Mohd. Aqil
30 Sep 2007 - Current Drug Delivery

Abstract:

The discovery of liposome or lipid vesicle emerged from self forming enclosed lipid bi-layer upon hydration; liposome drug delivery systems have played a significant role in formulation of potent drug to improve therapeutics. Recently the liposome formulations are targeted to reduce toxicity and increase accumulation at the t... The discovery of liposome or lipid vesicle emerged from self forming enclosed lipid bi-layer upon hydration; liposome drug delivery systems have played a significant role in formulation of potent drug to improve therapeutics. Recently the liposome formulations are targeted to reduce toxicity and increase accumulation at the target site. There are several new methods of liposome preparation based on lipid drug interaction and liposome disposition mechanism including the inhibition of rapid clearance of liposome by controlling particle size, charge and surface hydration. Most clinical applications of liposomal drug delivery are targeting to tissue with or without expression of target recognition molecules on lipid membrane. The liposomes are characterized with respect to physical, chemical and biological parameters. The sizing of liposome is also critical parameter which helps characterize the liposome which is usually performed by sequential extrusion at relatively low pressure through polycarbonate membrane (PCM). This mode of drug delivery lends more safety and efficacy to administration of several classes of drugs like antiviral, antifungal, antimicrobial, vaccines, anti-tubercular drugs and gene therapeutics. Present applications of the liposomes are in the immunology, dermatology, vaccine adjuvant, eye disorders, brain targeting, infective disease and in tumour therapy. The new developments in this field are the specific binding properties of a drug-carrying liposome to a target cell such as a tumor cell and specific molecules in the body (antibodies, proteins, peptides etc.); stealth liposomes which are especially being used as carriers for hydrophilic (water soluble) anticancer drugs like doxorubicin, mitoxantrone; and bisphosphonate- liposome mediated depletion of macrophages. This review would be a help to the researchers working in the area of liposomal drug delivery. read more read less

Topics:

Liposome (68%)68% related to the paper, Targeted drug delivery (64%)64% related to the paper, Cationic liposome (63%)63% related to the paper, Drug delivery (60%)60% related to the paper, Eye disorder (51%)51% related to the paper
719 Citations
Journal Article DOI: 10.2174/1567201052772915
Transdermal drug delivery: penetration enhancement techniques.
Heather A. E. Benson1
01 Jan 2005 - Current Drug Delivery

Abstract:

There is considerable interest in the skin as a site of drug application both for local and systemic effect. However, the skin, in particular the stratum corneum, poses a formidable barrier to drug penetration thereby limiting topical and transdermal bioavailability. Skin penetration enhancement techniques have been developed... There is considerable interest in the skin as a site of drug application both for local and systemic effect. However, the skin, in particular the stratum corneum, poses a formidable barrier to drug penetration thereby limiting topical and transdermal bioavailability. Skin penetration enhancement techniques have been developed to improve bioavailability and increase the range of drugs for which topical and transdermal delivery is a viable option. This review describes enhancement techniques based on drug/vehicle optimisation such as drug selection, prodrugs and ion-pairs, supersaturated drug solutions, eutectic systems, complexation, liposomes, vesicles and particles. Enhancement via modification of the stratum corneum by hydration, chemical enhancers acting on the structure of the stratum corneum lipids and keratin, partitioning and solubility effects are also discussed. The mechanism of action of penetration enhancers and retarders and their potential for clinical application is described. read more read less

Topics:

Transdermal (65%)65% related to the paper, Stratum corneum (60%)60% related to the paper
592 Citations
Journal Article DOI: 10.2174/1567201043480036
The role of ABC transporters in drug resistance, metabolism and toxicity.
01 Jan 2004 - Current Drug Delivery

Abstract:

ATP Binding Cassette (ABC) transporters form a special family of membrane proteins, characterized by homologous ATP-binding, and large, multispanning transmembrane domains. Several members of this family are primary active transporters, which significantly modulate the absorption, metabolism, cellular effectivity and toxicity... ATP Binding Cassette (ABC) transporters form a special family of membrane proteins, characterized by homologous ATP-binding, and large, multispanning transmembrane domains. Several members of this family are primary active transporters, which significantly modulate the absorption, metabolism, cellular effectivity and toxicity of pharmacological agents. This review provides a general overview of the human ABC transporters, their expression, localization and basic mechanism of action. Then we shortly deal with the human ABC transporters as targets of therapeutic interventions in medicine, including cancer drug resistance, lipid and other metabolic disorders, and even gene therapy applications. We place a special emphasis on the three major groups of ABC transporters involved in cancer multidrug resistance (MDR). These are the classical P-glycoprotein (MDR1, ABCB1), the multidrug resistance associated proteins (MRPs, in the ABCC subfamily), and the ABCG2 protein, an ABC half-transporter. All these proteins catalyze an ATP-dependent active transport of chemically unrelated compounds, including anticancer drugs. MDR1 (Pglycoprotein) and ABCG2 preferentially extrude large hydrophobic, positively charged molecules, while the members of the MRP family can extrude both hydrophobic uncharged molecules and water-soluble anionic compounds. Based on the physiological expression and role of these transporters, we provide examples for their role in Absorption-Distribution- Metabolism-Excretion (ADME) and toxicology, and describe several basic assays which can be applied for screening drug interactions with ABC transporters in the course of drug research and development. read more read less

Topics:

ATP-binding domain of ABC transporters (77%)77% related to the paper, Multidrug Resistance-Associated Proteins (66%)66% related to the paper, ATP-binding cassette transporter (61%)61% related to the paper
517 Citations
Journal Article DOI: 10.2174/1567201043334605
Pegylated poly(lactide) and poly(lactide-co-glycolide) nanoparticles: preparation, properties and possible applications in drug delivery.
Konstantinos Avgoustakis1
30 Sep 2004 - Current Drug Delivery

Abstract:

The preparation, properties and potential applications in drug delivery of biocompatible and biodegradable PLA-PEG and PLGA-PEG nanoparticles are discussed. PLA-PEG and PLGA-PEG nanoparticles have been produced by emulsification-solvent evaporation, solvent displacement and salting out methods. The nanoparticles can be stored... The preparation, properties and potential applications in drug delivery of biocompatible and biodegradable PLA-PEG and PLGA-PEG nanoparticles are discussed. PLA-PEG and PLGA-PEG nanoparticles have been produced by emulsification-solvent evaporation, solvent displacement and salting out methods. The nanoparticles can be stored as freeze-dried powders, but an adequate amount of a suitable lyoprotectant should be added prior lyophilisation to prevent nanoparticle aggregation and retain nanoparticle redispersibility. The nanoparticles have a core-shell structure with a PLA core and a PEG coating. Their basic colloidal properties and degradation depend on copolymer composition. The PLA-PEG and PLGA-PEG nanoparticles exhibit prolonged blood circulation following intravenous administration to animals. The composition of the nanoparticles determine their biodistribution properties, probably through its effects on the effectiveness of the PEG steric barrier and the size of the nanoparticles. The ability of the PLA-PEG and PLGA-PEG nanoparticles to evade rapid phagocytocis has extended the range of sites within the body that the nanoparticles can reach, which has significant implications with regard to their application in controlled drug delivery and targeting. The PLA-PEG and PLGA-PEG nanoparticles can be loaded with a variety of bioactive agents achieving satisfactory loading, especially in the case of hydrophobic drugs. The nanoparticles have been investigated for the treatment of infectious diseases and cancer, the intravenous and mucosal delivery of proteins, and oligonucleotide and gene delivery. The results have been encouraging and PLA-PEG and PLGA-PEG nanoparticle formulations, improving the therapeutic potential of both established and new drugs, may be expected to be available in the near future. read more read less

Topics:

Drug delivery (57%)57% related to the paper, Nanoparticle (51%)51% related to the paper
421 Citations
Journal Article DOI: 10.2174/1567201052772906
Mathematical modelling and controlled drug delivery: matrix systems.
Mario Grassi1, Gabriele Grassi
01 Jan 2005 - Current Drug Delivery

Abstract:

This paper deals with the physical and mathematical modelling description of drug release from matrix systems. In the introduction, matrix systems are considered in the wide frame of the controlled release systems and the concept of mathematical model is briefly discussed. Then, matrix structure and topology are matched, anal... This paper deals with the physical and mathematical modelling description of drug release from matrix systems. In the introduction, matrix systems are considered in the wide frame of the controlled release systems and the concept of mathematical model is briefly discussed. Then, matrix structure and topology are matched, analysing the characteristics of the three-dimensional network constituting them. In this context, drug release mechanisms are considered with particular emphasis on the key factors ruling the release kinetics, such as matrix swelling, erosion, drug dissolution (re-crystallisation), drug diffusion, drug - polymer interaction, initial drug distribution and particle size distribution (for powdered matrix systems). The mathematical modelling section firstly considers the empirical and semi-empirical models that have the great advantage of showing analytical solutions. Then, the attention is focused on theoretical approaches regarding matrix swelling equilibrium and kinetics, drug dissolution, drug diffusion, drug - polymer interaction, initial drug distribution and matrix erosion. Finally, release kinetics from polydispersed spherical particles is studied. This review points out the fact that the comprehension of the phenomena ruling drug release from matrix systems is appropriate from both the physical and modelling point of view, although further improvements are always possible and desirable. read more read less

Topics:

Dissolution testing (53%)53% related to the paper, Controlled release (52%)52% related to the paper
313 Citations
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Current Drug Delivery format uses Vancouver citation style.

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One little Google search can get you the Word template for any journal. However, why do you need a Word template when you can write your entire manuscript on SciSpace, autoformat it as per Current Drug Delivery's guidelines and download the same in Word, PDF and LaTeX formats? Try us out!.

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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 those factors the review board, rejection rates, frequency of inclusion in indexes, Eigenfactor, etc. You must assess all the factors and then take the final call.

SHERPA/RoMEO Database

We have extracted this data from Sherpa Romeo to help our researchers understand the access level of this journal. The following table indicates the level of access a journal has as per Sherpa Romeo 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.

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