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Journal of Research in Pharmacy最新文献

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Effects of Cornus mas L. on lipid peroxidation and anti-oxidative enzyme activity in high fat diet fed rats 山茱萸对高脂日粮大鼠脂质过氧化和抗氧化酶活性的影响
IF 0.8 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-01-01 DOI: 10.29228/jrp.325
D. Kargın, Şule Aktaç, A. Yavuz, M. Cam
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引用次数: 0
Identification of major phenolic compounds of Aloe vera and its protective effect on ovaries under oxidative stress in diabetic rats 芦荟主要酚类化合物的鉴定及其对糖尿病大鼠卵巢氧化应激的保护作用
IF 0.8 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-01-01 DOI: 10.29228/jrp.348
S. Kurt, U. Şeker, M. Yazlık, Engin Er, M. Hürkul, S. Soker
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引用次数: 1
Investigation of the anticancer effects of some plant seed oils with medicinal uses 几种药用植物籽油抗癌作用的研究
IF 0.8 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-01-01 DOI: 10.29228/jrp.444
Yener Kurman, Görkem Dülger, Ö. Pasin
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引用次数: 0
QbD based approach to RP-HPLC method development and validation of Bupivacaine hydrochloride in bulk and in-house developed nanostructured lipid carriers 基于QbD的反相高效液相色谱法开发和验证盐酸布比卡因散装和自主开发的纳米结构脂质载体
IF 0.8 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-01-01 DOI: 10.29228/jrp.475
Sarfaraz Khan, F. Khan
: The present study describes the principles of systematic Quality by design (QbD) approach for the development of RP-HPLC method for the quantification of Bupivacaine hydrochloride (BUP) in bulk and in-house developed nanostructured lipid carriers (NLCs). Initially analytical target profile (ATP), and critical analytical attributes (CAAs) were identified. Primary assessment studies were checked using Plackett-Burman Design. Further optimization studies were performed by applying Box-Behnken design. The Shimadzu C-18 column (250mm x 4.6mm i.d., 5µm particle size) was utilized for reversed-phase chromatographic separation with a mobile phase comprising a mixture of acetonitrile (ACN) and 0.1% ortho phosphoric acid (OPA) (pH 2.04) in 69.45:30.55 (% v/v). The flow rate was 0.805mL/min at a λ max of 214 nm and an injection volume of 12µL. The new developed method was validated according to the guidelines given by International Conference on Harmonization which revealed linearity between 25 to 80µg/ml and r 2 = 0.999. The result of % RSD was 0.38 and 0.44 respectively for high degree of intraday and interday precision. As per the new method the LOD and LOQ is 0.900µg/ml and 2.72µg/ml, respectively. Further the validated method was also applied for the estimation of BUP in NLCs formulation, which showed no interference of any formulation excipients. The studies demonstrated that the new method is rapid, simple, selective, and reproducible for the estimation of pure drug and in-house developed NLCs.
本研究描述了系统质量设计(QbD)方法的原理,用于开发RP-HPLC法定量散装盐酸布比卡因(BUP)和自主开发的纳米结构脂质载体(nlc)。初步确定了分析目标轮廓(ATP)和关键分析属性(CAAs)。使用Plackett-Burman设计检查初步评估研究。采用Box-Behnken设计进行进一步优化研究。采用Shimadzu C-18色谱柱(250mm × 4.6mm,粒径5µm)进行反相色谱分离,流动相为乙腈(ACN)和0.1%邻位磷酸(OPA) (pH 2.04)的混合物,浓度为69.45:30.55 (% v/v)。流速为0.805mL/min, λ max为214 nm,进样量为12µL。根据国际协调会议给出的准则对新方法进行了验证,结果表明,该方法在25 ~ 80µg/ml之间呈线性,r2 = 0.999。日内、日间精密度较高,% RSD分别为0.38和0.44。新方法的定量限和定量限分别为0.900µg/ml和2.72µg/ml。并将该方法应用于nclc制剂中BUP的估计,结果表明该方法不受任何辅料的干扰。研究结果表明,该方法具有快速、简便、选择性好、可重复性好等优点,可用于纯药物和自主研发的NLCs的检测。
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引用次数: 0
In silico evaluation of potential murine M49 DNA aptamer on ORF7a of SARS-COV-2: A similar target 在SARS-COV-2的ORF7a上潜在的小鼠M49 DNA适体的计算机评价:一个类似的靶标
IF 0.8 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-01-01 DOI: 10.29228/jrp.306
Nor Azlina AHMAD, R. M. Zulkifli, H. Hussin, S. Amran, M. Nadri, Saiful Izwan Abd Razak, Sabrina Adam, F. M. Yusof
DNA aptamers are short nucleotides with a high affinity for their target. However, the process of isolating aptamers via the systematic evolution of ligands by exponential enrichment (SELEX) procedure is laborious. Therefore, an in silico approach is used to screen potential DNA aptamer candidates as a kickstart specifically for ORF7a of SARSCOV-2. By applying the TM-align program, the murine receptor (CD200R) protein was found to have structural similarities with ORF7a. Based on the literature, this CD200R protein is successfully bound by M49 DNA aptamers experimentally. Herein, the 3D structure of the M49 DNA aptamer was generated using Mfold, RNA Composer webserver, Discovery Studio Visualizer, and UCSF Chimera software, and the docking simulation was predicted using the HDOCK webserver. The binding energy scores for the M49-CD200R complex were slightly higher than those for the M49-ORF7a complex with-233.78 and-220.11, respectively. The molecular interaction in the complexes was contributed by the hydrogen bond. In conclusion, the M49 aptamer of CD200R protein can bind to the other similar target, the ORF7a protein of SARS-COV-2. Even though CD200R and ORF7a proteins share structural similarities, the binding sites of the individual complex are distinct. The current study shows that two different proteins with structural similarities may have a possibility to share the same DNA aptamer. This strategy may result in efficient aptamer discovery using an in silico method as a first step. © 2022 Marmara University Press.
DNA适体是一种短核苷酸,对目标具有高亲和力。然而,通过配体的系统进化通过指数富集(SELEX)程序分离适体的过程是费力的。因此,采用一种计算机方法筛选潜在的DNA适体候选体,作为SARSCOV-2的ORF7a特异性启动。通过应用TM-align程序,发现小鼠受体(CD200R)蛋白与ORF7a具有结构相似性。根据文献,该CD200R蛋白通过实验成功地与M49 DNA适配体结合。本文使用Mfold、RNA Composer webserver、Discovery Studio Visualizer和UCSF Chimera软件生成M49 DNA适配体的三维结构,并使用HDOCK webserver进行对接模拟预测。M49-CD200R配合物的结合能得分略高于M49-ORF7a配合物,分别为-233.78和-220.11。配合物中的分子相互作用是由氢键促成的。综上所述,CD200R蛋白的M49适体可以与SARS-COV-2的另一个类似靶点ORF7a蛋白结合。尽管CD200R和ORF7a蛋白具有结构上的相似性,但单个复合物的结合位点是不同的。目前的研究表明,两种结构相似的不同蛋白质可能有可能共享相同的DNA适体。这一策略可能导致使用计算机方法作为第一步有效的适体发现。©2022马尔马拉大学出版社。
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引用次数: 0
Intranasal Oleic acid-based nanoemulsion of Diazepam: design, formulation and in-vitro evaluation 地西泮鼻内油酸纳米乳:设计、配方及体外评价
IF 0.8 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-01-01 DOI: 10.29228/jrp.335
Yousif K. YOUNIS, S. N. A. Alhammid
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引用次数: 0
Formulation of an anti-aging cream containing Alteromonas ferment extract and evaluation of the effect on collagen concentration 含异单胞菌发酵提取物的抗衰老乳霜的配方及对胶原蛋白浓度的影响
IF 0.8 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-01-01 DOI: 10.29228/jrp.370
G. Gedik
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引用次数: 0
NANOBIOMATERIALS FOR DRUG DELIVERY 用于药物递送的纳米生物材料
Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-01-01 DOI: 10.29228/jrp.503
Gulsah GEDIK
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引用次数: 0
Origanum minutiflorum O. Schwarz et P. H. Davis essential oil: enzyme inhibitory activities and chemical composition. 荆芥精油:酶抑制活性及化学成分。
Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-01-01 DOI: 10.29228/jrp.498
Gülsüm YILDIZ, Betül DEMİRCİ, Halide Edip TEMEL, Neşe KIRIMER
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引用次数: 0
Antiepileptic Effect of Musa paradisiaca Stem Juice on Pentylenetetrazole (PTZ)-induced Seizures in Albino Rats 天麻茎汁对戊四唑(PTZ)致白化大鼠癫痫发作的抗癫痫作用
Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-01-01 DOI: 10.29228/jrp.398
Sabastine Chinweike UGWUOKE, Valentine Odirachukwumma NWANELO, Martins Obinna OGUGOFOR, Obiora Celestine UGWU, Chioma Assumpta ANOSIKE
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引用次数: 1
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Journal of Research in Pharmacy
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