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British Journal of Pharmacy最新文献

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The distinct role of kappa opioid receptor in attenuating relapse to morphine/methamphetamine (polydrug) dependence in mice 阿片受体在减轻小鼠吗啡/甲基苯丙胺(多种药物)依赖复发中的独特作用
Pub Date : 2018-07-17 DOI: 10.5920/bjpharm.2017.20
I. E. Ridzwan, Maryam Saadah Suhaimi, Nur Syafinaz Wasli, A. Kasmuri, Marwan Saad Azzubaidi, R. Hashim, Q. Ahmed, L. Ming, Nornisah Mohamed, Syed Mohd Syhami
A Combination of 0.3mg/kg buprenorphine and 1.0 mg/kg naltrexone treatment shows a promising result due to its ability to attenuate reinstatement (relapse) in morphine/methamphetamine (polydrug)-dependent mice in a conditioned place preference (CPP) model. This prompted us to identify which opioid receptor that contributes to its anti-relapse activity. Using the same CPP model, 10 mg/kg nor- BNI (a selective kappa opioid receptor [KOR] antagonist) was used to evaluate the involvement of KOR in mediating relapse to polydrug dependence. By applying the immunohistochemistry (IHC) technique, the investigation was extended to the mice brain using KOR antibody (EPR18881), focusing on the brain regions that are abundant in KOR density. The results showed that nor-BNI alone failed to attenuate relapse to polydrug dependence. However, the IHC results proved that the number of KOR significantly increased in the striatum during reinstatement compared to post-conditioning (p <0.05). The KOR was significantly suppressed in the treatment group which strengthens the findings from previous studies proving that the KOR plays an important role in mediating relapse to polydrug dependence.
在条件位置偏好(CPP)模型中,0.3mg/kg丁丙诺啡和1.0 mg/kg纳曲酮联合治疗能够减轻吗啡/甲基苯丙胺(多种药物)依赖小鼠的恢复(复发),显示出良好的效果。这促使我们确定哪些阿片受体有助于其抗复发活性。使用相同的CPP模型,使用10 mg/kg nor- BNI(一种选择性kappa阿片受体[KOR]拮抗剂)来评估KOR在介导多种药物依赖复发中的作用。应用免疫组织化学(IHC)技术,利用KOR抗体(EPR18881)将研究扩展到小鼠大脑,重点关注KOR密度丰富的大脑区域。结果表明,单独使用非bni不能减轻对多种药物依赖的复发。然而,IHC结果证明,恢复期间纹状体中KOR的数量明显增加(p <0.05)。在治疗组中,KOR被显著抑制,这加强了先前的研究结果,证明KOR在介导多种药物依赖复发中起重要作用。
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引用次数: 1
Microencapsulation: A taste and odour masking approach for garlic (Allium sativum) powder 微胶囊化:大蒜(Allium sativum)粉末的味道和气味掩盖方法
Pub Date : 2018-07-17 DOI: 10.5920/BJPHARM.2017.19
S. Gondal, N. Abbas, A. Hussain
The purpose of this study was to prepare a convenient formulation of garlic powder which has enhanced user compliance by suppressing its characteristic odour and masking the taste. Microcapsules of garlic powder were formulated by solvent evaporation method. Results show >80% yield, >70% drug loading efficiency and slow release profile (promising sustained action for more than 2hrs) and a significant reduction in the aromatic smell and taste evaluated through a single blind cross-over study conducted using ten healthy human volunteers.
本研究的目的是制备一种方便的大蒜粉配方,通过抑制其特征气味和掩盖味道来提高用户的依从性。采用溶剂蒸发法制备大蒜粉微胶囊。通过对10名健康人体志愿者进行的单盲交叉研究,结果显示出>80%的产率,>70%的载药效率和缓释特性(有望持续作用超过2小时),并显着降低了芳香气味和味觉。
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引用次数: 1
Physicochemical characterisation of biosynthetic bacterial cellulose as a potential wound dressing material 生物合成细菌纤维素作为潜在创面敷料的理化特性研究
Pub Date : 2018-07-17 DOI: 10.5920/BJPHARM.2017.27
Abhishek Gupta, W. Low, S. Britland, I. Radecka, Claire Martin
The aim of this study was to characterise the physicochemical and biocompatibility properties of biosynthetic bacterial cellulose (BC) as a potential wound dressing material. The moisture content, water vapour transmission rate (WVTR), thermal stability, cyto- and haemo-compatibility of BC were investigated. Results indicated that the physicochemical properties of biosynthetic BC allow an optimum WVTR to be maintained for improved localised wound moisture levels, good thermal stability and excellent water imbibing capabilities. In vitro cytotoxicity and haemocompatibility confirmed the biocompatibility of BC and hence suitability of this material for further exploration into its’ application as a wound dressing material.
本研究的目的是表征生物合成细菌纤维素(BC)作为潜在伤口敷料的物理化学和生物相容性。研究了BC的含水量、水蒸气透过率(WVTR)、热稳定性、细胞和血液相容性。结果表明,生物合成BC的物理化学性质允许维持最佳的WVTR,以改善局部伤口水分水平,良好的热稳定性和优异的吸水能力。体外细胞毒性和血液相容性证实了BC的生物相容性,因此该材料适合进一步探索其作为伤口敷料的应用。
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引用次数: 8
Twin-screw granulation – a systematic analysis of process parameters 双螺杆造粒工艺参数系统分析
Pub Date : 2018-07-17 DOI: 10.5920/bjpharm.2017.26
M. Richter, W. Kaialy, H. Bello
Twin-screw granulation has a significant advantage over traditional granulation methods leading to the possibility of continuous manufacturing. Although this technology has drawn attention in recent years, the general understanding of the process is limited. This study gives a brief overview of the most important process parameters and their influence on product quality. Experimental results from a benchtop granulator and an in-line particle size measurement have been analysed. From this basic study conclusions can be drawn how to tailor the particle size distribution in twin-screw granulation. The most crucial parameters are the liquid-to-solid ratio and the filling level of the screws.
与传统造粒方法相比,双螺杆造粒具有显著的优势,可以实现连续制造。尽管近年来该技术引起了人们的关注,但对该工艺的一般理解是有限的。本文简要介绍了最重要的工艺参数及其对产品质量的影响。对台式造粒机和在线粒度测量的实验结果进行了分析。通过这一基础研究,可以得出如何调整双螺杆造粒粒度分布的结论。最关键的参数是液固比和螺杆的填充水平。
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引用次数: 1
Micro-photogrammetry as a tool for characterisation of dissolution behaviour of pharmaceutical dosage forms 微摄影测量作为表征药物剂型溶出行为的工具
Pub Date : 2018-07-17 DOI: 10.5920/bjpharm.2017.22
A. D’Angelo, M. Reading, Milan D Antonjievic
The aim of this project is to develop an innovative analytical technique for the 3D chemical mapping of pharmaceutical dosage forms, via simultaneous topographic characterisation and dissolution analysis of solid drug delivery systems. The developed apparatus was optimised using the results obtained from the application of micro-photogrammetry to the analysis of commercial solid drug delivery systems. Results of the application of the developed method on the dissolution of a sugarcoated tablet sample are here presented.
该项目的目的是开发一种创新的分析技术,用于药物剂型的三维化学制图,通过同时的地形特征和固体药物输送系统的溶解分析。利用微摄影测量学在商业固体给药系统分析中的应用结果,对所开发的仪器进行了优化。本文给出了该方法在糖衣片溶出度测定中的应用结果。
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引用次数: 0
Title Pending 1414 1414未决所有权
Pub Date : 1900-01-01 DOI: 10.5920/bjpharm.1414
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引用次数: 0
Title Pending 965 965未决标题
Pub Date : 1900-01-01 DOI: 10.5920/bjpharm.965
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引用次数: 0
Title Pending 1385 1385未决产权
Pub Date : 1900-01-01 DOI: 10.5920/bjpharm.1385
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引用次数: 0
Title Pending 899 待定所有权899
Pub Date : 1900-01-01 DOI: 10.5920/bjpharm.899
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引用次数: 0
Title Pending 1046 1046未决标题
Pub Date : 1900-01-01 DOI: 10.5920/bjpharm.1046
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引用次数: 0
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British Journal of Pharmacy
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