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Protective effect of Enicostemma axillare - Swertiamarin on oxidative stress against nicotine-induced liver damage in SD rats 箭毒-獐牙菜苷对尼古丁诱导的 sd 大鼠肝损伤的氧化应激的保护作用
IF 1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2024-09-01 DOI: 10.1016/j.pharma.2024.03.009
<div><h3>Objective</h3><p>The current investigation was aimed to determine the hepatoprotective benefits of Swertiamarin (ST) administration against nicotine-induced hepatotoxicity in SD rats.</p></div><div><h3>Material and methods</h3><p>A total of 48 adult male SD rats were allocated into six groups using a fully randomised approach. As a control, group I was given oral (PO) normal saline. For 65 days, the animals in groups II, III, IV, V and VI received 2.5<!--> <!-->mg/kg/day of nicotine intraperitoneally (IP), 100<!--> <!-->mg/kg/day of ST orally (PO), 200<!--> <!-->mg/kg/day of ST orally (PO), 2.5<!--> <!-->mg/kg/day of nicotine (IP)<!--> <!-->+<!--> <!-->100<!--> <!-->mg/kg/day of ST (PO), and 2.5<!--> <!-->mg/kg/day of nicotine (IP)<!--> <!-->+<!--> <!-->200<!--> <!-->mg/kg/day of ST (PO), respectively. Animals were killed on 66<sup>th</sup>day, liver tissue was removed and used for histopathological analysis as well as biochemical testing (oxidative stress parameters and liver function enzymes).</p></div><div><h3>Results</h3><p>When compared to control animals, the animals in group II showed a substantial rise in their aspartate aminotransferase (AST), alanine aminotransferase (ALT), urea, and creatinine levels (<em>P</em> <!-->˂<!--> <!-->0.001). Furthermore, compared to control animals, these animals displayed enhanced hepatic oxidative stress as indicated by significantly higher Malondialdehyde (MDA) levels (<em>P</em> <!-->˂<!--> <!-->0.001) and lower levels of Catalase (CAT), Glutathione (GSH), Glutathione peroxidase (GSH-Px) and Superoxide dismutase (SOD) (<em>P</em> <!-->˂<!--> <!-->0.001). Further, more histological anomalies were seen in the liver of nicotine-treated rats compared to control rats, including significant vacuolization, poor tissue architecture, the growth of pycnotic nuclei, and dilated sinusoids. Contrary to nicotine-treated rats, the co-administration of ST and nicotine was observed to prevent the abnormalities caused by nicotine (groups V and VI).</p></div><div><h3>Conclusion</h3><p>The results of the current study show that nicotine can seriously harm liver tissue and that swertiamarin can prevent the harmful effects of nicotine on rat liver. Future research is necessary to delve deeply into the mechanisms behind swertiamarin protective impact against nicotine-induced hepatotoxicity.</p></div><div><h3>Objectif</h3><p>La présente enquête visait à déterminer les bénéfices hépatoprotecteurs de l’administration de Swertiamarine (ST) contre l’hépatotoxicité induite par la nicotine chez les rats SD.</p></div><div><h3>Matériel et méthodes</h3><p>Au total, 48 rats SD mâles adultes ont été répartis en six groupes en utilisant une approche entièrement randomisée. À titre de contrôle, le groupe I a reçu une solution saline normale par voie orale (PO). Pendant 65<!--> <!-->jours, les animaux des groupes II, III, IV, V et VI ont reçu 2,5<!--> <!-->mg/kg/j de nicotine par voie intrapéritonéale (IP), 100<!--> <!-->mg/kg/j de
材料和方法采用完全随机的方法将 48 只成年雄性 SD 大鼠分为六组。作为对照,I 组口服(PO)生理盐水。第 65 天,II、III、IV、V 和 VI 组动物分别腹腔注射尼古丁 2.5 毫克/千克/天(IP)、口服 ST 100 毫克/千克/天(PO)、口服 ST 200 毫克/千克/天(PO)、尼古丁 2.5 毫克/千克/天(IP)+ ST 100 毫克/千克/天(PO)和尼古丁 2.5 毫克/千克/天(IP)+ ST 200 毫克/千克/天(PO)。结果与对照组动物相比,第二组动物的天门冬氨酸氨基转移酶(AST)、丙氨酸氨基转移酶(ALT)、尿素和肌酐水平大幅上升(P ˂0.001)。此外,与对照组动物相比,这些动物的肝脏氧化应激能力增强,表现为丙二醛(MDA)水平显著升高(P ˂ 0.001),过氧化氢酶(CAT)、谷胱甘肽(GSH)、谷胱甘肽过氧化物酶(GSH-Px)和超氧化物歧化酶(SOD)水平降低(P ˂ 0.001)。此外,与对照组大鼠相比,尼古丁处理过的大鼠肝脏出现了更多的组织学异常,包括明显的空泡化、组织结构不良、细胞核增生和窦道扩张。与尼古丁处理的大鼠相反,同时服用 ST 和尼古丁可防止尼古丁引起的异常(第五组和第六组)。本研究旨在确定服用獐牙菜苷 (ST) 对 SD 大鼠尼古丁诱导的肝脏毒性的保护作用。作为对照,I 组口服生理盐水(ORS)。第 65 天,II、III、IV、V 和 VI 组动物分别腹腔注射尼古丁 2.5 毫克/千克/天(IP)、口服 ST 100 毫克/千克/天(PO)、口服 ST 200 毫克/千克/天(PO)、尼古丁 2.5 毫克/千克/天(IP)+ ST 100 毫克/千克/天(PO)和尼古丁 2.5 毫克/千克/天(IP)+ ST 200 毫克/千克/天(PO)。结果与对照组动物相比,II 组动物的天门冬氨酸氨基转移酶(AST)、丙氨酸氨基转移酶(ALT)、尿素和肌酐水平显著升高(p ˂0.001)。此外,与对照组动物相比,这些动物的肝脏氧化应激增加,表现为丙二醛(MDA)水平显著升高(p ˂ 0.001),过氧化氢酶(CAT)、谷胱甘肽(GSH)、谷胱甘肽过氧化物酶(GSH-Px)和超氧化物歧化酶(SOD)水平降低(p ˂ 0.001)。此外,与对照组大鼠相比,尼古丁处理的大鼠肝脏出现了更多的组织学异常,包括广泛的空泡化、组织结构不良、脓核增生和窦道扩张。结论本研究结果表明,尼古丁会严重破坏肝脏组织,而獐牙菜素能防止尼古丁对大鼠肝脏的有害影响。今后的研究还需要进一步探讨獐牙菜红素对尼古丁诱导的肝毒性具有保护作用的机制。
{"title":"Protective effect of Enicostemma axillare - Swertiamarin on oxidative stress against nicotine-induced liver damage in SD rats","authors":"","doi":"10.1016/j.pharma.2024.03.009","DOIUrl":"10.1016/j.pharma.2024.03.009","url":null,"abstract":"&lt;div&gt;&lt;h3&gt;Objective&lt;/h3&gt;&lt;p&gt;The current investigation was aimed to determine the hepatoprotective benefits of Swertiamarin (ST) administration against nicotine-induced hepatotoxicity in SD rats.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Material and methods&lt;/h3&gt;&lt;p&gt;A total of 48 adult male SD rats were allocated into six groups using a fully randomised approach. As a control, group I was given oral (PO) normal saline. For 65 days, the animals in groups II, III, IV, V and VI received 2.5&lt;!--&gt; &lt;!--&gt;mg/kg/day of nicotine intraperitoneally (IP), 100&lt;!--&gt; &lt;!--&gt;mg/kg/day of ST orally (PO), 200&lt;!--&gt; &lt;!--&gt;mg/kg/day of ST orally (PO), 2.5&lt;!--&gt; &lt;!--&gt;mg/kg/day of nicotine (IP)&lt;!--&gt; &lt;!--&gt;+&lt;!--&gt; &lt;!--&gt;100&lt;!--&gt; &lt;!--&gt;mg/kg/day of ST (PO), and 2.5&lt;!--&gt; &lt;!--&gt;mg/kg/day of nicotine (IP)&lt;!--&gt; &lt;!--&gt;+&lt;!--&gt; &lt;!--&gt;200&lt;!--&gt; &lt;!--&gt;mg/kg/day of ST (PO), respectively. Animals were killed on 66&lt;sup&gt;th&lt;/sup&gt;day, liver tissue was removed and used for histopathological analysis as well as biochemical testing (oxidative stress parameters and liver function enzymes).&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Results&lt;/h3&gt;&lt;p&gt;When compared to control animals, the animals in group II showed a substantial rise in their aspartate aminotransferase (AST), alanine aminotransferase (ALT), urea, and creatinine levels (&lt;em&gt;P&lt;/em&gt; &lt;!--&gt;˂&lt;!--&gt; &lt;!--&gt;0.001). Furthermore, compared to control animals, these animals displayed enhanced hepatic oxidative stress as indicated by significantly higher Malondialdehyde (MDA) levels (&lt;em&gt;P&lt;/em&gt; &lt;!--&gt;˂&lt;!--&gt; &lt;!--&gt;0.001) and lower levels of Catalase (CAT), Glutathione (GSH), Glutathione peroxidase (GSH-Px) and Superoxide dismutase (SOD) (&lt;em&gt;P&lt;/em&gt; &lt;!--&gt;˂&lt;!--&gt; &lt;!--&gt;0.001). Further, more histological anomalies were seen in the liver of nicotine-treated rats compared to control rats, including significant vacuolization, poor tissue architecture, the growth of pycnotic nuclei, and dilated sinusoids. Contrary to nicotine-treated rats, the co-administration of ST and nicotine was observed to prevent the abnormalities caused by nicotine (groups V and VI).&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Conclusion&lt;/h3&gt;&lt;p&gt;The results of the current study show that nicotine can seriously harm liver tissue and that swertiamarin can prevent the harmful effects of nicotine on rat liver. Future research is necessary to delve deeply into the mechanisms behind swertiamarin protective impact against nicotine-induced hepatotoxicity.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Objectif&lt;/h3&gt;&lt;p&gt;La présente enquête visait à déterminer les bénéfices hépatoprotecteurs de l’administration de Swertiamarine (ST) contre l’hépatotoxicité induite par la nicotine chez les rats SD.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Matériel et méthodes&lt;/h3&gt;&lt;p&gt;Au total, 48 rats SD mâles adultes ont été répartis en six groupes en utilisant une approche entièrement randomisée. À titre de contrôle, le groupe I a reçu une solution saline normale par voie orale (PO). Pendant 65&lt;!--&gt; &lt;!--&gt;jours, les animaux des groupes II, III, IV, V et VI ont reçu 2,5&lt;!--&gt; &lt;!--&gt;mg/kg/j de nicotine par voie intrapéritonéale (IP), 100&lt;!--&gt; &lt;!--&gt;mg/kg/j de","PeriodicalId":8332,"journal":{"name":"Annales pharmaceutiques francaises","volume":"82 5","pages":"Pages 792-799"},"PeriodicalIF":1.0,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140760073","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Design of quetiapine fumarate loaded polyethylene glycol decorated graphene oxide nanosheets: In vitro-ex vivo characterization 富马酸喹硫平负载聚乙二醇装饰氧化石墨烯纳米片的设计:体内外表征
IF 1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2024-09-01 DOI: 10.1016/j.pharma.2024.04.009
<div><p><span><span>Quetiapine Fumarate (QF) is an atypical antipsychotic with poor oral bioavailability (9%) due to its low permeability and pH-dependent solubility. Therefore, this study aims to design QF-loaded polyethylene glycol (PEG) functionalized </span>graphene oxide<span> nanosheets (GON) for nasal delivery of QF. In brief, GO was synthesized using a modified Hummers process, followed by ultra-sonication to produce GON. Subsequently, PEG-functionalized GON was prepared using carbodiimide chemistry (PEG-GON). QF was then decorated onto the cage of PEG-GON using the π–π stacking phenomenon (QF@PEG-GON). The QF@PEG-GON nanocomposite underwent several spectral characterizations, </span></span><em>in vitro</em> drug release, mucoadhesion study, <em>ex vivo</em> diffusion study, etc. The surface morphology of QF@PEG-GON nanocomposite validates the cracked nature of the nanocomposite, whereas the diffractograms and thermogram of nanocomposite confirm the conversion of QF into an amorphous form with uniform distribution in PEG-GON. Moreover, an <em>ex vivo</em> study of PEG-GON demonstrates superior mucoadhesion capacity due to its surface functional groups and hydrophilicity. The percent drug loading content and percent entrapment efficiency of the nanocomposite were found to be 9.2<!--> <!-->±<!--> <!-->0.62% and 92.3<!--> <!-->±<!--> <!-->1.02%, respectively. The developed nanocomposite exhibited 43.82<!--> <!-->±<!--> <!-->1.65% drug release within 24<!--> <!-->h, with the Korsemeyer-Peppas model providing the best-fit release kinetics (<em>R</em><sup>2</sup>: 0.8614). Here, the interlayer spacing of PEG-GON prevented prompt diffusion of the buffer, leading to a delayed release pattern. In conclusion, the anticipated QF@PEG-GON nanocomposite shows promise as a nanocarrier platform for nasal delivery of QF.</p></div><div><p>Le fumarate de quétiapine (QF) est un antipsychotique atypique avec une faible biodisponibilité orale (9 %) en raison de sa faible perméabilité et de sa solubilité dépendante du pH. Par conséquent, cette étude vise à concevoir des nanofeuilles d’oxyde de graphène (GON) fonctionnalisées en polyéthylène glycol (PEG) chargées de QF pour l’administration nasale de QF. En bref, GO a été synthétisé à l’aide d’un procédé Hummers modifié, suivi d’une ultra-sonication pour produire du GON. Par la suite, du GON fonctionnalisé par PEG a été préparé en utilisant la chimie du carbodiimide (PEG-GON). QF a ensuite été décoré sur la cage de PEG-GON en utilisant le phénomène d’empilement π–π (QF@PEG-GON). Le nanocomposite QF@PEG-GON a subi plusieurs caractérisations spectrales, libération de médicaments in vitro, étude de mucoadhésion, étude de diffusion ex vivo, etc. La morphologie de surface du nanocomposite QF@PEG-GON valide la nature fissurée du nanocomposite, alors que les diffractogrammes et le thermogramme de nanocomposite confirment la conversion du QF en une forme amorphe à distribution uniforme dans le PEG-GON. De plus, une étud
富马酸喹硫平(QF)是一种非典型抗精神病药物,由于其低渗透性和依赖于 pH 值的溶解度,其口服生物利用度较低(9%)。因此,本研究旨在设计负载 QF 的聚乙二醇(PEG)功能化氧化石墨烯纳米片(GON),用于 QF 的鼻腔给药。简而言之,GO 的合成采用改良的 Hummers 工艺,然后用超声波法制备 GON。随后,利用碳二亚胺化学方法制备了 PEG 功能化 GON(PEG-GON)。然后利用 π-π 堆叠现象将 QF 装饰到 PEG-GON 的笼子上(QF@PEG-GON)。QF@PEG-GON纳米复合材料进行了多项光谱表征、体外药物释放、粘附性研究和体内外扩散研究等。QF@PEG-GON纳米复合材料的表面形貌验证了纳米复合材料的裂解性质,而纳米复合材料的衍射图和热图则证实了QF在PEG-GON中转化为分布均匀的无定形形式。此外,对 PEG-GON 的体内外研究表明,由于其表面官能团和亲水性,它具有优异的粘附能力。纳米复合材料的载药百分含量和夹带效率分别为 9.2 ± 0.62% 和 92.3 ± 1.02%。所开发的纳米复合材料在 24 小时内的药物释放率为 43.82 ± 1.65%,Korsemeyer-Peppas 模型提供了最佳拟合释放动力学(R2:0.8614)。在这种情况下,PEG-GON 的层间间隔阻碍了缓冲剂的快速扩散,从而导致了延迟释放模式。总之,预期的 QF@PEG-GON 纳米复合材料有望成为鼻腔输送 QF 的纳米载体平台。
{"title":"Design of quetiapine fumarate loaded polyethylene glycol decorated graphene oxide nanosheets: In vitro-ex vivo characterization","authors":"","doi":"10.1016/j.pharma.2024.04.009","DOIUrl":"10.1016/j.pharma.2024.04.009","url":null,"abstract":"&lt;div&gt;&lt;p&gt;&lt;span&gt;&lt;span&gt;Quetiapine Fumarate (QF) is an atypical antipsychotic with poor oral bioavailability (9%) due to its low permeability and pH-dependent solubility. Therefore, this study aims to design QF-loaded polyethylene glycol (PEG) functionalized &lt;/span&gt;graphene oxide&lt;span&gt; nanosheets (GON) for nasal delivery of QF. In brief, GO was synthesized using a modified Hummers process, followed by ultra-sonication to produce GON. Subsequently, PEG-functionalized GON was prepared using carbodiimide chemistry (PEG-GON). QF was then decorated onto the cage of PEG-GON using the π–π stacking phenomenon (QF@PEG-GON). The QF@PEG-GON nanocomposite underwent several spectral characterizations, &lt;/span&gt;&lt;/span&gt;&lt;em&gt;in vitro&lt;/em&gt; drug release, mucoadhesion study, &lt;em&gt;ex vivo&lt;/em&gt; diffusion study, etc. The surface morphology of QF@PEG-GON nanocomposite validates the cracked nature of the nanocomposite, whereas the diffractograms and thermogram of nanocomposite confirm the conversion of QF into an amorphous form with uniform distribution in PEG-GON. Moreover, an &lt;em&gt;ex vivo&lt;/em&gt; study of PEG-GON demonstrates superior mucoadhesion capacity due to its surface functional groups and hydrophilicity. The percent drug loading content and percent entrapment efficiency of the nanocomposite were found to be 9.2&lt;!--&gt; &lt;!--&gt;±&lt;!--&gt; &lt;!--&gt;0.62% and 92.3&lt;!--&gt; &lt;!--&gt;±&lt;!--&gt; &lt;!--&gt;1.02%, respectively. The developed nanocomposite exhibited 43.82&lt;!--&gt; &lt;!--&gt;±&lt;!--&gt; &lt;!--&gt;1.65% drug release within 24&lt;!--&gt; &lt;!--&gt;h, with the Korsemeyer-Peppas model providing the best-fit release kinetics (&lt;em&gt;R&lt;/em&gt;&lt;sup&gt;2&lt;/sup&gt;: 0.8614). Here, the interlayer spacing of PEG-GON prevented prompt diffusion of the buffer, leading to a delayed release pattern. In conclusion, the anticipated QF@PEG-GON nanocomposite shows promise as a nanocarrier platform for nasal delivery of QF.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;p&gt;Le fumarate de quétiapine (QF) est un antipsychotique atypique avec une faible biodisponibilité orale (9 %) en raison de sa faible perméabilité et de sa solubilité dépendante du pH. Par conséquent, cette étude vise à concevoir des nanofeuilles d’oxyde de graphène (GON) fonctionnalisées en polyéthylène glycol (PEG) chargées de QF pour l’administration nasale de QF. En bref, GO a été synthétisé à l’aide d’un procédé Hummers modifié, suivi d’une ultra-sonication pour produire du GON. Par la suite, du GON fonctionnalisé par PEG a été préparé en utilisant la chimie du carbodiimide (PEG-GON). QF a ensuite été décoré sur la cage de PEG-GON en utilisant le phénomène d’empilement π–π (QF@PEG-GON). Le nanocomposite QF@PEG-GON a subi plusieurs caractérisations spectrales, libération de médicaments in vitro, étude de mucoadhésion, étude de diffusion ex vivo, etc. La morphologie de surface du nanocomposite QF@PEG-GON valide la nature fissurée du nanocomposite, alors que les diffractogrammes et le thermogramme de nanocomposite confirment la conversion du QF en une forme amorphe à distribution uniforme dans le PEG-GON. De plus, une étud","PeriodicalId":8332,"journal":{"name":"Annales pharmaceutiques francaises","volume":"82 5","pages":"Pages 848-864"},"PeriodicalIF":1.0,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140847204","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
HIV rapid tests immunological internal control can be misleading 艾滋病毒快速检测 免疫学内部控制可能会产生误导。
IF 1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2024-09-01 DOI: 10.1016/j.pharma.2024.05.009
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引用次数: 0
Base de données Enthalpies : évidence et théorie appliquée à la pratique en stérilisation [焓:应用于消毒实践的证据和理论]。
IF 1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2024-09-01 DOI: 10.1016/j.pharma.2024.04.002
<div><h3>Objectifs</h3><p>Afin de partager leurs connaissances, les responsables d’unités de stérilisation publient les résultats de leurs travaux dans des revues ou lors de congrès scientifiques. Enthalpies a pour objectif de répertorier l’ensemble de ces travaux dans une base de données unique. Le travail présenté décrit la construction de cette base et l’évaluation de la faisabilité de sa mise en place pour l’étape du lavage.</p></div><div><h3>Méthodes</h3><p>La première étape a consisté à réaliser une revue de la littérature. Seuls les articles publiés sur 10<!--> <!-->ans (2013–2023) en lien avec l’étape de lavage ont été inclus. Ensuite, chaque publication a été catégorisée, codée, gradée et résumée par un binôme pharmacien-interne. L’ensemble de ces données a été colligé dans un tableur Excel® puis à partir de la catégorisation des données, une arborescence a été créée permettant d’appréhender l’interface entre l’utilisateur et la plateforme devant héberger Enthalpies.</p></div><div><h3>Résultats</h3><p>Quatre-vingt et une publications ont été identifiées. Celles-ci ont été catégorisées en 6 thèmes et 27 sous-thèmes. Pour chaque publication, une grille de lecture a été rédigée. Genially®, plateforme en ligne, a été choisi pour héberger notre base de données.</p></div><div><h3>Conclusion</h3><p>Enthalpies n’a pas été conçu pour émettre des recommandations de bonne pratique. Cependant, cet outil permet en colligeant les données scientifiques publiées d’aider à la prise de décision. Il représente une solution innovante pour mettre à disposition une revue de la littérature dans le domaine de la stérilisation hospitalière.</p></div><div><h3>Objectives</h3><p>In order to share their knowledge, sterilization unit managers publish the results of their work in journals or at scientific conferences. The aim of Enthalpies is to list all such work in a single database. The work presented describes the construction of this database and the assessment of its feasibility for the washing step.</p></div><div><h3>Methods</h3><p>The first step was to carry out a literature review. Only articles published over 10<!--> <!-->years (2013–2023) in connection with the ten-year washing stage were included. Then, each publication was categorized, coded, graded and summarized by a pharmacist-internal pair. All this data was collated in an Excel® spreadsheet, and from the data categorization a tree structure was created, enabling the interface between the user and the platform hosting Enthalpies to be understood.</p></div><div><h3>Results</h3><p>Eighty-one publications were identified. These were categorized into 6 themes and 27 sub-themes. A reading grid was drawn up for each publication. Genially®, an online platform, was chosen to host our database.</p></div><div><h3>Conclusion</h3><p>Enthalpies was not designed to issue recommendations for best practice. However, by collating published scientific data, this tool can be used to assist decision-making. It represents
目标为了分享知识,灭菌装置的管理人员会在期刊或科学会议上发表他们的工作成果。Enthalpies 的目的是在一个数据库中列出所有这些工作成果。本文介绍的工作描述了该数据库的构建过程,以及为清洗阶段建立该数据库的可行性评估。只有在 10 年内(2013-2023 年)发表的与洗涤阶段有关的文章才被纳入其中。然后,由一名实习药剂师对每篇文章进行分类、编码、分级和总结。所有数据均整理在 Excel® 电子表格中,并根据数据分类创建了一个树形结构,为用户和 Enthalpies 托管平台之间提供了一个界面。这些出版物被分为 6 个主题和 27 个子主题。为每份出版物绘制了阅读网格。我们选择了在线平台 Genially® 作为数据库的主机。然而,通过整理已发表的科学数据,该工具可以帮助决策。目的为了分享知识,消毒单位管理人员会在期刊或科学会议上发表他们的工作成果。Enthalpies的目的是在一个数据库中列出所有此类工作。本文介绍了该数据库的构建过程以及对其在清洗步骤中可行性的评估。只有在 10 年内(2013-2023 年)发表的与 10 年洗涤阶段相关的文章才被纳入其中。然后,由一对药剂师内部人员对每篇出版物进行分类、编码、分级和汇总。所有这些数据都整理在 Excel® 电子表格中,并根据数据分类创建了树形结构,以便了解用户与 Enthalpies 托管平台之间的界面。这些出版物被分为 6 个主题和 27 个子主题。为每份出版物绘制了阅读网格。结论 "焓 "并不是为了提出最佳实践建议而设计的。不过,通过整理已发表的科学数据,该工具可用于协助决策。它是提供医院消毒领域文献综述的创新解决方案。
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引用次数: 0
Covid-19 psychological distress: Analysis of antipsychotic drugs’ use in an Italian population sample Covid-19心理困扰:意大利人口样本中抗精神病药物使用情况分析。
IF 1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2024-09-01 DOI: 10.1016/j.pharma.2024.04.007
<div><h3>Background</h3><p>The current pandemic, in addition to putting a strain on healthcare systems and global economies, has exacerbated psychiatric problems and undermined the mental health of many individuals. In an Italian cohort, this phenomenon has been assessed through a retrospective study aimed at evaluating the consumption and costs of antipsychotic drugs between 2020 and 2022.</p></div><div><h3>Methods</h3><p>All dispensations made in local pharmacies accessible to the public have been extracted from a database called ‘Sistema Tessera Sanitaria’, which covers a population of approximately one million people residents in the ASL Napoli 3 Sud. Consumption data expressed in defined daily dose (DDD) and expenditure data expressed in Euro have been extrapolated.</p></div><div><h3>Results</h3><p>The results in the years 2020–2021 were relatively consistent, with consumption and expenditure decreasing slightly from 2020 to 2021. In 2022, the results showed a decrease in consumption and expenditure (2,706,951.07 DDD and €1,700,897.47) representing the reduced accessibility of patients to the healthcare facilities due to the pandemic. However, it should be noted that the antipsychotic drug aripiprazole showed an upward trend, registering an increase in consumption.</p></div><div><h3>Conclusion</h3><p>Despite expectations of increased consumption of antipsychotic medications, real-world evidence indicated a different phenomenon, with the pandemic seemingly not affecting the consumption of these drugs. The difficulty in accessing care and medical appointments has probably influenced this data, masking the therapeutic needs of citizens. It will be necessary to assess in the coming years, as normal clinical activity resumes, whether there will be a growing consumption of these medications, which represent one of the main expenditure categories for the National Healthcare System.</p></div><div><h3>Contexte</h3><p>La pandémie actuelle, en plus de mettre à rude épreuve les systèmes de santé et les économies mondiales, a exacerbé les problèmes psychiatriques et miné la santé mentale de nombreux individus. Il est bien connu que les événements épidémiques, en particulier les périodes de confinement, augmentent le risque de développer des troubles anxieux, des dépressions et des comportements agressifs.</p></div><div><h3>Méthodes</h3><p>Dans une cohorte italienne, ce phénomène a été évalué par le biais d’une étude rétrospective visant à évaluer la consommation et les coûts des médicaments antipsychotiques pendant et après la pandémie de Covid-19 dans les années 2020–2022. Toutes les ordonnances délivrées dans les pharmacies locales accessibles au public ont été extraites d’une base de données appelée Health Card System, couvrant une population d’environ un million de personnes.</p></div><div><h3>Résultats</h3><p>Les résultats pour les années 2020 à 2021 sont relativement cohérents, la consommation et les dépenses ayant légèrement diminué entre 2020 et
背景当前的大流行病除了给医疗系统和全球经济造成压力外,还加剧了精神问题,损害了许多人的心理健康。方法从名为 "Sistema Tessera Sanitaria "的数据库中提取了公众可访问的当地药房的所有配药情况,该数据库涵盖了ASL Napoli 3 Sud地区约100万居民。结果2020-2021 年的结果相对一致,2020-2021 年的消费和支出略有下降。2022 年的结果显示,消费和支出均有所减少(2 706 951.07DD 和 1 700 897.47 欧元),这表明由于大流行病,病人使用医疗设施的机会减少。结论尽管预期抗精神病药物的消费量会增加,但实际情况却显示出不同的现象,大流行似乎并没有影响这些药物的消费。难以获得护理和就诊可能影响了这一数据,掩盖了公民的治疗需求。有必要在未来几年内,随着正常临床活动的恢复,评估这些药物的消耗量是否会增长,因为这些药物是国家医疗保健系统的主要支出类别之一。 背景当前的大流行病不仅给医疗保健系统和全球经济造成了压力,还加剧了精神问题,损害了许多人的心理健康。众所周知,流行病事件,尤其是囚禁期间,会增加患焦虑症、抑郁症和攻击行为的风险。方法在意大利的一个队列中,通过一项回顾性研究对这一现象进行了评估,以评价 2020-2022 年科维德-19 大流行期间和之后抗精神病药物的消耗量和成本。研究人员从一个名为健康卡系统的数据库中提取了公众可访问的当地药房开具的所有处方,该数据库覆盖了约一百万人口。结果2020年至2021年的结果相对一致,消费和支出在2020年至2021年期间略有下降。结论尽管预期抗精神病药物的消费量会增加,但实际数据却显示出不同的现象,大流行似乎并没有影响这些药物的消费量。难以获得护理和就诊可能影响了这些数据,掩盖了人们的治疗需求。今后几年,当临床活动恢复正常时,有必要评估这些药物的消费是否会增加,因为这些药物是国家医疗保健系统的主要支出类别之一。
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引用次数: 0
Glycemic and lipid control in patients with diabetes at time of myocardial infarction 心肌梗死时糖尿病患者的血糖和血脂控制。
IF 1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2024-09-01 DOI: 10.1016/j.pharma.2024.04.010
<div><h3>Objective</h3><p>Cardiovascular risk is increased in patients with diabetes. Little is known about glycemic and lipid control in patients with diabetes. We aimed to assess glycemic and lipid controls in patients with diabetes at time of their myocardial infarction.</p></div><div><h3>Method</h3><p>All known patients with type 2 diabetes consecutively admitted for a myocardial infarction in our coronary care unit between March 1<sup>st</sup> and December 31<sup>st</sup>, 2021 were included in this retrospective study. Glycemic and lipid control was assessed through individualized target of glycated haemoglobin (HbA<sub>1c</sub>) and low-density lipoprotein cholesterol (LDL-c), respectively. At admission, the comprehensive list of chronic medications was obtained through medication reconciliation.</p></div><div><h3>Results</h3><p>This study included 112 patients with a median age of 72 years. Most of patients had an individualized target of HbA<sub>1c</sub> and LDL-c of 7.0% (67%) and 0.55<!--> <!-->g/L (96%), respectively. The rate of uncontrolled patients for HbA<sub>1c</sub> and LDL-c and both was 46%, 90%, and 42% respectively. The rate of patients with non-optimal glucose- and lipid-lowering medications in uncontrolled patients was 63% and 87%, respectively. The rate of inappropriate glucose- and lipid-lowering medications was 73% and 91%, respectively.</p></div><div><h3>Conclusion</h3><p>We highlighted the poor glycemic and lipid control in high-risk CV patients. There is an urgent need to develop multidisciplinary approaches to optimize CV risk factors control to reduce myocardial infarction and strokes.</p></div><div><h3>Objectif</h3><p>Les patients diabétiques présentent un haut risqué cardiovasculaire. Peu de données existent sur le contrôle glycémique et lipidique des patients diabétiques en vie réelle. Notre objectif était d’évaluer le contrôle glycémique et lipidique des patients diabétiques au moment de leu infarctus du myocarde.</p></div><div><h3>Méthode</h3><p>Tous les patients diabétiques connus admis dans notre unité de soins intensifs de cardiologie pour un infarctus du myocarde entre mars et décembre 2021 ont été inclus dans notre analyse rétrospective. Le contrôle glycémique et lipidique a été évalué à l’aide des valeurs cibles individualisées d’hémoglobine glyquée (HbA<sub>1c</sub>) et du cholestérol lipoprotéine de faible densité (LDL-c). À l’admission, un bilan médicamenteux optimisé a été effectué par le pharmacien.</p></div><div><h3>Résultats</h3><p>L’étude a inclus 112 patients d’âge médian 72 ans. La plupart des patients avait des valeurs de HbA<sub>1c</sub> et LDL-c cibles de 7,0 % (67 %) et 0,55 g/L (96 %), respectivement. Le taux de patients non contrôlés pour HbA<sub>1c</sub>, LDL-c et les deux était 46 %, 90 % et 42 %, respectivement. Le taux de patients avec un traitement antidiabétique et hypolipémiant non optimal était 63 % et 87 %, respectivement. Le taux de médicaments antidiabétiques et hypolipémiants
目的:糖尿病患者的心血管风险增加。人们对糖尿病患者的血糖和血脂控制知之甚少。我们旨在评估糖尿病患者心肌梗死时的血糖和血脂控制情况:这项回顾性研究纳入了 2021 年 3 月 1 日至 12 月 31 日期间在我院冠心病监护病房连续收治的所有已知 2 型糖尿病心肌梗死患者。血糖和血脂控制分别通过糖化血红蛋白(HbA1c)和低密度脂蛋白胆固醇(LDL-c)的个体化目标进行评估。入院时,通过药物对账获得慢性药物的综合清单:本研究共纳入 112 名患者,中位年龄为 72 岁。大多数患者的个体化 HbA1c 和 LDL-c 目标值分别为 7.0% (67%)和 0.55g/L (96%)。HbA1c 和 LDL-c 未受控制的患者比例分别为 46%、90% 和 42%。在血糖和血脂未受控制的患者中,使用非最佳降糖和降脂药物的比例分别为 63% 和 87%。降糖和降脂药物使用不当的比例分别为 73% 和 91%:我们强调了高危冠心病患者血糖和血脂控制不佳的问题。当务之急是制定多学科方法,优化对心血管风险因素的控制,以减少心肌梗死和脑卒中的发生。
{"title":"Glycemic and lipid control in patients with diabetes at time of myocardial infarction","authors":"","doi":"10.1016/j.pharma.2024.04.010","DOIUrl":"10.1016/j.pharma.2024.04.010","url":null,"abstract":"&lt;div&gt;&lt;h3&gt;Objective&lt;/h3&gt;&lt;p&gt;Cardiovascular risk is increased in patients with diabetes. Little is known about glycemic and lipid control in patients with diabetes. We aimed to assess glycemic and lipid controls in patients with diabetes at time of their myocardial infarction.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Method&lt;/h3&gt;&lt;p&gt;All known patients with type 2 diabetes consecutively admitted for a myocardial infarction in our coronary care unit between March 1&lt;sup&gt;st&lt;/sup&gt; and December 31&lt;sup&gt;st&lt;/sup&gt;, 2021 were included in this retrospective study. Glycemic and lipid control was assessed through individualized target of glycated haemoglobin (HbA&lt;sub&gt;1c&lt;/sub&gt;) and low-density lipoprotein cholesterol (LDL-c), respectively. At admission, the comprehensive list of chronic medications was obtained through medication reconciliation.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Results&lt;/h3&gt;&lt;p&gt;This study included 112 patients with a median age of 72 years. Most of patients had an individualized target of HbA&lt;sub&gt;1c&lt;/sub&gt; and LDL-c of 7.0% (67%) and 0.55&lt;!--&gt; &lt;!--&gt;g/L (96%), respectively. The rate of uncontrolled patients for HbA&lt;sub&gt;1c&lt;/sub&gt; and LDL-c and both was 46%, 90%, and 42% respectively. The rate of patients with non-optimal glucose- and lipid-lowering medications in uncontrolled patients was 63% and 87%, respectively. The rate of inappropriate glucose- and lipid-lowering medications was 73% and 91%, respectively.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Conclusion&lt;/h3&gt;&lt;p&gt;We highlighted the poor glycemic and lipid control in high-risk CV patients. There is an urgent need to develop multidisciplinary approaches to optimize CV risk factors control to reduce myocardial infarction and strokes.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Objectif&lt;/h3&gt;&lt;p&gt;Les patients diabétiques présentent un haut risqué cardiovasculaire. Peu de données existent sur le contrôle glycémique et lipidique des patients diabétiques en vie réelle. Notre objectif était d’évaluer le contrôle glycémique et lipidique des patients diabétiques au moment de leu infarctus du myocarde.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Méthode&lt;/h3&gt;&lt;p&gt;Tous les patients diabétiques connus admis dans notre unité de soins intensifs de cardiologie pour un infarctus du myocarde entre mars et décembre 2021 ont été inclus dans notre analyse rétrospective. Le contrôle glycémique et lipidique a été évalué à l’aide des valeurs cibles individualisées d’hémoglobine glyquée (HbA&lt;sub&gt;1c&lt;/sub&gt;) et du cholestérol lipoprotéine de faible densité (LDL-c). À l’admission, un bilan médicamenteux optimisé a été effectué par le pharmacien.&lt;/p&gt;&lt;/div&gt;&lt;div&gt;&lt;h3&gt;Résultats&lt;/h3&gt;&lt;p&gt;L’étude a inclus 112 patients d’âge médian 72 ans. La plupart des patients avait des valeurs de HbA&lt;sub&gt;1c&lt;/sub&gt; et LDL-c cibles de 7,0 % (67 %) et 0,55 g/L (96 %), respectivement. Le taux de patients non contrôlés pour HbA&lt;sub&gt;1c&lt;/sub&gt;, LDL-c et les deux était 46 %, 90 % et 42 %, respectivement. Le taux de patients avec un traitement antidiabétique et hypolipémiant non optimal était 63 % et 87 %, respectivement. Le taux de médicaments antidiabétiques et hypolipémiants ","PeriodicalId":8332,"journal":{"name":"Annales pharmaceutiques francaises","volume":"82 5","pages":"Pages 865-872"},"PeriodicalIF":1.0,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140849298","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Development of mucoadhesive microspheres for intranasal delivery of fluconazole as an alternative treatment of cryptococcal meningitis infection in patients with acquired immunodeficiency 开发用于鼻内给药氟康唑的黏附性微球,作为获得性免疫缺陷患者隐球菌脑膜炎感染的替代治疗方法。
IF 1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2024-09-01 DOI: 10.1016/j.pharma.2024.04.001
<div><h3>Introduction</h3><p>Cryptococcal meningitis is a deadly disease with few treatment options. Its incidence is still high and closely linked to the HIV/AIDS epidemic. This study aimed to develop a mucoadhesive microsphere delivery system for fluconazole for the intranasal route.</p></div><div><h3>Method</h3><p>Microspheres of mucoadhesive fluconazole formulation variables such as different amounts of drug concentration and polymer concentration were prepared by a simple emulsion-crosslinking method. The prepared microspheres’ surface was characterised by SEM (Scanning electron microscopy) and evaluated for particle size, entrapment efficiency, production yield, infrared spectroscopic study, in-vitro muco-adhesion, and in-vitro drug release.</p></div><div><h3>Results</h3><p>The results showed that formula 1 is the optimal mucoadhesive microsphere preparation, with a particle size of 56.375<!--> <!-->m, a spherical surface shape, an entrapment efficiency of 99.96%, and a greater mucoadhesive capability during 6-hour evaluation. Furthermore, wash-off examination revealed that the mucoadhesive ability of this delivery system has a long duration and may release the active material at the right time.</p></div><div><h3>Conclusion</h3><p>The result of the researches suggesting that the formulation of mucoadhesive microspheres of fluconazole could be used to treat cryptococcal meningitis infection in HIV/AIDS patients.</p></div><div><h3>Introduction</h3><p>La méningite à cryptocoque est une maladie mortelle avec peu d’options de traitement. Son incidence est encore élevée et étroitement liée à l’épidémie de VIH/sida. Cette étude visait à développer un système d’administration de microsphère muco-adhésif pour le fluconazole par voie intranasale.</p></div><div><h3>Méthode</h3><p>Des microsphères de variables de formulation de fluconazole mucoadhesives telles que différentes quantités de concentration de médicament et de concentration de polymère ont été préparées par une méthode simple de réticulation d’émulsion. La surface des microsphères préparées a été caractérisée par SEM (microscopie électronique à balayage) et évaluée pour la taille des particules, l’efficacité du piégeage, le rendement de la production, l’étude spectroscopique infrarouge, la muco-adhésion in vitro et la libération de médicaments in vitro.</p></div><div><h3>Résultats</h3><p>Les résultats ont montré que la formule (1) est la préparation optimale de la microsphère muco-adhésive, avec une taille de particule de 56,375<!--> <!-->m, une forme de surface sphérique, une efficacité de piégeage de 99,96 % et une plus grande capacité de muco-adhésive pendant 6<!--> <!-->h d’évaluation. De plus, l’examen de lavage a révélé que la capacité muco-adhésive de ce système d’administration a une longue durée et peut libérer le matériau actif au bon moment.</p></div><div><h3>Conclusion</h3><p>Le résultat des recherches suggère que la formulation de microsphères muco-adhésives du fluconazole pour
导言加密球菌脑膜炎是一种致命疾病,治疗方法很少。其发病率仍然很高,与艾滋病毒/艾滋病的流行密切相关。本研究旨在开发一种用于鼻内给药途径的氟康唑粘附性微球给药系统。方法采用简单的乳液交联法制备粘附性氟康唑配方变量(如不同的药物浓度和聚合物浓度)的微球。结果结果表明,配方 1 是最佳的黏附性微球制剂,其粒径为 56.375 m,表面呈球形,黏附效率为 99.96%,在 6 小时评估中具有更强的黏附能力。研究结果表明,氟康唑粘附微球制剂可用于治疗艾滋病毒/艾滋病患者的隐球菌脑膜炎感染。隐球菌性脑膜炎是一种致命疾病,治疗方法很少,发病率仍然很高,与艾滋病毒/艾滋病的流行密切相关。本研究旨在开发一种用于鼻内注射氟康唑的粘附性微球给药系统。方法采用简单的乳液交联法制备粘附性氟康唑制剂变体微球,如不同量的药物浓度和聚合物浓度。用 SEM(扫描电子显微镜)对制备的微球表面进行了表征,并对粒度、包埋效率、产量、红外光谱研究、体外粘附性和体外药物释放进行了评估。结果结果表明,式(1)是粘附性微球的最佳制备方法,其粒径为 56.375 m,表面呈球形,夹持效率为 99.96%,在 6 小时评估期间具有更强的粘附能力。结论 研究结果表明,氟康唑的粘附微球制剂可用于治疗艾滋病毒/艾滋病患者的隐球菌脑膜炎感染。
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引用次数: 0
Urinary cytomegalovirus excretion: The unresolved issues 尿液巨细胞病毒排泄:悬而未决的问题。
IF 1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2024-09-01 DOI: 10.1016/j.pharma.2024.03.004

Cytomegalovirus (CMV) excretion in urine is frequently observed in clinical practice. However, the specific circumstances and pathophysiological mechanisms underlying this shedding remain largely unknown. Here, we address some of the key questions regarding urinary CMV excretion, focusing on new hypotheses raised by recent advances in the field. Cellular origins of CMV shedding, clinical contexts of occurrence, systemic spread of the virus versus compartmentalization in the urinary tract, and clinical impact are successively discussed.

Le cytomégalovirus (CMV) est fréquemment détecté dans l’urine mais les circonstances cliniques et les mécanismes physiopathologiques qui sous-tendent cette virurie restent mal compris. Dans cette revue, nous cherchons à répondre aux principales questions soulevées par cette excrétion urinaire de CMV, en appréhendant successivement: l’origine cellulaire de l’excrétion virale au sein de l’arbre urinaire, le contexte clinique sous-jacent, la distinction entre diffusion systémique du virus et compartimentation et l’impact clinique de ces viruries à CMV.

临床上经常观察到巨细胞病毒(CMV)从尿液中排出。然而,这种脱落的具体情况和病理生理机制在很大程度上仍不为人所知。在此,我们将探讨有关尿液中 CMV 排泄的一些关键问题,重点关注该领域最新进展提出的新假设。我们将依次讨论 CMV 脱落的细胞起源、发生的临床背景、病毒在全身的传播与在泌尿道的分隔以及临床影响。
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引用次数: 0
Validated green and white RP-HPLC method for the estimation of Zolmitriptan in marketed dosage form. 经验证的绿色和白色 RP-HPLC 法,用于估算市售剂型中的佐米曲普坦。
IF 1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2024-08-31 DOI: 10.1016/j.pharma.2024.08.010
Channabasavaiah Naveenaradhya, Veeresh Prabhakar Veerapur, Ranganatha Puttaraju, Kodigenahalli Balarajagupta Ajaykumar, DeviReddy Prashanthi, Varsha D Savanth, Mathud Shivamurthaiah Chaithanya, Bychapur Siddaiah Gowrishankar

Objective: To develop and validate a rapid, accurate, economical, effective and greenery RP-HPLC method for the determination of Zolmitriptan in tablet dosage form.

Material and method: RP-HPLC method was developed using Luna (C18) (4.6×250mm, 5μm) column and Sodium phosphate buffer (pH 4.7): Methanol [75: 25, v/v] was used as mobile phase at a flow rate of 1.0mL/min. The detection was carried out at 227nm. Further, eco-friendliness, productivity and performance of the optimized analytical method were assessed by green and white tools.

Results: The retention time of Zolmitriptan was found to be 3.25min with acceptable chromatographic parameters. The optimized RP-HPLC method was more eco-friendly, efficient, throughput and practicable than the reported methods as confirmed by AES, AGREE, GAPI and RGB tools. Further, the proposed analytical method showed all the validation parameters within the acceptance limit of ICH Q2 R1 guidelines. The linear regression analysis indicated a good linear response in the 10 to 120μg/mL concentration range with R2 of 0.99998. The percentage content and percentage assay of Zolmitriptan in Zomig-5mg tablet was found to be 103.36±0.356% and 97.86±0.693%.

Conclusion: The developed and validated method has several advantages compared to the reported HPLC methods and is useful in the systematic analysis of Zolmitriptan in its dosage form.

材料和方法: - 采用 Luna (C18) (4.6 x 250 mm, 5 µm)色谱柱和磷酸钠缓冲液(pH 4.7),以甲醇[75:25, v/v]为流动相,流速为 1.0 mL/min:流动相为甲醇[75: 25, v/v],流速为 1.0 mL/min。检测波长为 227 纳米。此外,还通过绿色和白色工具对优化分析方法的环保性、生产率和性能进行了评估:- 佐米曲普坦的保留时间为 3.25 分钟,色谱参数可接受。经AES、AGREE、GAPI和RGB工具确认,优化后的RP-HPLC方法比已报道的方法更环保、高效、通量大且实用。此外,该分析方法的所有验证参数均在 ICH Q2 R1 指南的接受范围内。线性回归分析表明,在 10 至 120 μg/mL 浓度范围内线性响应良好,R2 为 0.99998。佐米格-5 毫克片剂中佐米曲普坦的含量百分比和测定百分比分别为 103.36 ± 0.356 % 和 97.86 ± 0.693 %。
{"title":"Validated green and white RP-HPLC method for the estimation of Zolmitriptan in marketed dosage form.","authors":"Channabasavaiah Naveenaradhya, Veeresh Prabhakar Veerapur, Ranganatha Puttaraju, Kodigenahalli Balarajagupta Ajaykumar, DeviReddy Prashanthi, Varsha D Savanth, Mathud Shivamurthaiah Chaithanya, Bychapur Siddaiah Gowrishankar","doi":"10.1016/j.pharma.2024.08.010","DOIUrl":"10.1016/j.pharma.2024.08.010","url":null,"abstract":"<p><strong>Objective: </strong>To develop and validate a rapid, accurate, economical, effective and greenery RP-HPLC method for the determination of Zolmitriptan in tablet dosage form.</p><p><strong>Material and method: </strong>RP-HPLC method was developed using Luna (C<sub>18</sub>) (4.6×250mm, 5μm) column and Sodium phosphate buffer (pH 4.7): Methanol [75: 25, v/v] was used as mobile phase at a flow rate of 1.0mL/min. The detection was carried out at 227nm. Further, eco-friendliness, productivity and performance of the optimized analytical method were assessed by green and white tools.</p><p><strong>Results: </strong>The retention time of Zolmitriptan was found to be 3.25min with acceptable chromatographic parameters. The optimized RP-HPLC method was more eco-friendly, efficient, throughput and practicable than the reported methods as confirmed by AES, AGREE, GAPI and RGB tools. Further, the proposed analytical method showed all the validation parameters within the acceptance limit of ICH Q<sub>2</sub> R<sub>1</sub> guidelines. The linear regression analysis indicated a good linear response in the 10 to 120μg/mL concentration range with R<sup>2</sup> of 0.99998. The percentage content and percentage assay of Zolmitriptan in Zomig-5mg tablet was found to be 103.36±0.356% and 97.86±0.693%.</p><p><strong>Conclusion: </strong>The developed and validated method has several advantages compared to the reported HPLC methods and is useful in the systematic analysis of Zolmitriptan in its dosage form.</p>","PeriodicalId":8332,"journal":{"name":"Annales pharmaceutiques francaises","volume":" ","pages":""},"PeriodicalIF":1.0,"publicationDate":"2024-08-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142118883","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Application progress of nanomaterials in the treatment of prostate cancer. 纳米材料在前列腺癌治疗中的应用进展。
IF 1 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2024-08-24 DOI: 10.1016/j.pharma.2024.08.009
Xuewu Wu, Longtu Ma, Yang Zhang, Shuai Liu, Long Cheng, Chengyu You, Zhilong Dong

Prostate cancer is one of the most common malignant tumors in men, which seriously threatens the survival and quality of life of patients. At present, there are serious limitations in the treatment of prostate cancer, such as drug tolerance, drug resistance and easy recurrence. Sonodynamic therapy and chemodynamic therapy are two emerging tumor treatment methods, which activate specific drugs or sonosensitizers through sound waves or chemicals to produce reactive oxygen species and kill tumor cells. Nanomaterials are a kind of nanoscale materials with many excellent physical properties such as high targeting, drug release regulation and therapeutic monitoring. Sonodynamic therapy and chemodynamic therapy combined with the application of nanomaterials can improve the therapeutic effect of prostate cancer, reduce side effects and enhance tumor immune response. This article reviews the application progress of nanomaterials in the treatment of prostate cancer, especially the mechanism, advantages and challenges of nanomaterials in sonodynamic therapy and chemodynamic therapy, which provides new ideas and prospects for research in this field.

前列腺癌是男性最常见的恶性肿瘤之一,严重威胁着患者的生存和生活质量。目前,前列腺癌的治疗存在耐药性、抗药性、易复发等严重局限性。声动力疗法和化学动力疗法是两种新兴的肿瘤治疗方法,通过声波或化学物质激活特定药物或声敏剂,产生活性氧,杀死肿瘤细胞。纳米材料是一种纳米尺度的材料,具有高靶向性、药物释放调控和治疗监测等多种优异的物理特性。声动力学治疗和化学动力学治疗结合纳米材料的应用,可以提高前列腺癌的治疗效果,减少副作用,增强肿瘤免疫反应。本文综述了纳米材料在前列腺癌治疗中的应用进展,尤其是纳米材料在声动力治疗和化学动力治疗中的作用机制、优势和挑战,为该领域的研究提供了新的思路和展望。
{"title":"Application progress of nanomaterials in the treatment of prostate cancer.","authors":"Xuewu Wu, Longtu Ma, Yang Zhang, Shuai Liu, Long Cheng, Chengyu You, Zhilong Dong","doi":"10.1016/j.pharma.2024.08.009","DOIUrl":"10.1016/j.pharma.2024.08.009","url":null,"abstract":"<p><p>Prostate cancer is one of the most common malignant tumors in men, which seriously threatens the survival and quality of life of patients. At present, there are serious limitations in the treatment of prostate cancer, such as drug tolerance, drug resistance and easy recurrence. Sonodynamic therapy and chemodynamic therapy are two emerging tumor treatment methods, which activate specific drugs or sonosensitizers through sound waves or chemicals to produce reactive oxygen species and kill tumor cells. Nanomaterials are a kind of nanoscale materials with many excellent physical properties such as high targeting, drug release regulation and therapeutic monitoring. Sonodynamic therapy and chemodynamic therapy combined with the application of nanomaterials can improve the therapeutic effect of prostate cancer, reduce side effects and enhance tumor immune response. This article reviews the application progress of nanomaterials in the treatment of prostate cancer, especially the mechanism, advantages and challenges of nanomaterials in sonodynamic therapy and chemodynamic therapy, which provides new ideas and prospects for research in this field.</p>","PeriodicalId":8332,"journal":{"name":"Annales pharmaceutiques francaises","volume":" ","pages":""},"PeriodicalIF":1.0,"publicationDate":"2024-08-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142071888","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Annales pharmaceutiques francaises
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