JOURNAL OF PHARMACEUTICAL SCIENCES

JOURNAL OF PHARMACEUTICAL SCIENCES(英文缩写 J PHARM SCI-US),ISSN 0022-3549,eISSN 1520-6017 是一本学术期刊。本页汇总该期刊的最新影响因子、分区信息以及最新收录于 PubMed 的文献,帮助您快速了解期刊全貌。

2026 年数据 · 影响因子
3.900
JCR 分区
Q2
CAS 分区
B3
近一年发文量
0

指标来源:jcr_cas_ifqb

ISSN: 0022-3549 · eISSN: 1520-6017 · 缩写: J PHARM SCI-US

期刊简介

暂无简介。

历年影响因子趋势

年份影响因子JCR 分区
-Q2
-Q2
-Q2
-Q2
-Q2

JOURNAL OF PHARMACEUTICAL SCIENCES 最新收录文献

  1. Desolvation kinetics of sulfameter solvates.

    Solvates are often encountered in pharmaceutical solids and knowledge of their physical stability is necessary for their effective formulation. This work investigates the solid-state stability of five…

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  2. Conformation and side chains environments of recombinant human interleukin-1 receptor antagonist (rh-IL-1ra) probed by raman, raman optical activity, and UV-resonance Raman spectroscopy.

    The conformation and local environments of the side chains cysteines and aromatics of recombinant human interleukin-1 receptor antagonist (rh-IL-1ra) have been studied by visible Raman, Raman optical …

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  3. Echogenic liposome compositions for increased retention of ultrasound reflectivity at physiologic temperature.

    Targetable echogenic liposomes (ELIP) for ultrasound enhancement of atheroma have recently been developed; however, their retention of echogenicity at physiological temperature is less than desirable.…

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  4. Data mining of fractured experimental data using neurofuzzy logic-discovering and integrating knowledge hidden in multiple formulation databases for a fluid-bed granulation process.

    In the pharmaceutical field, current practice in gaining process understanding by data analysis or knowledge discovery has generally focused on dealing with single experimental databases. This limits …

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  5. Formulation and statistical optimization of a novel crosslinked polymeric anti-tuberculosis drug delivery system.

    The crux of this research was the pragmatic investigation into the formulation of a reconstitutable multiparticulate anti-tuberculosis drug delivery system for facilitated administration for the attai…

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  6. Stabilization of low glass transition temperature indomethacin formulations: impact of polymer-type and its concentration.

    The objectives of this study were to formulate and stabilize amorphous formulation of low T(g) drug (Indomethacin, INM) with selected polymers and compare these formulations based on solubility and di…

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  7. Stable-form screening: overcoming trace impurities that inhibit solution-mediated phase transformation to the stable polymorph of sulfamerazine.

    Solution-mediated phase transformation (SMPT) has been used as a focused technique to rapidly identify the stable polymorph of a given substance. Despite ample precedence for acetonitrile being a good…

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  8. Enhanced oral bioavailability of doxorubicin in a dendrimer drug delivery system.

    PAMAM dendrimers can permeate across intestinal epithelial barriers suggesting their potential as oral drug carriers. In the present study, we have developed a drug-PAMAM complex for oral administrati…

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  9. Combination particles containing salmeterol xinafoate and fluticasone propionate: Formulation and aerodynamic assessment.

    A precipitation process is used to produce combined particles consisting of two antiasthmatic drugs: salmeterol xinafoate and fluticasone propionate. To control the crystallisation of these particles,…

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  10. Rapid throughput screening of apparent KSP values for weakly basic drugs using 96-well format.

    A rapid-throughput screening assay was developed to estimate the salt solubility parameter, K(SP), with a minimal quantity of drug. This assay allows for early evaluation of salt limited solubility wi…

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