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Bioactivity-guided isolation and estimation of hepatoprotective marker compounds from Onosma bracteata; a species of the controversial drug ‘Gojihva’ 小苞草肝保护标志化合物的生物活性指导分离与评价一种有争议的药物“Gojihva”
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-10-18 DOI: 10.1007/s13596-024-00795-6
Udaykumar G. Vegad, Jigna Vadalia, Nira Kalwani, Bhavinkumar Gayakvad, Riya A. Desai, Vaibhav Bhatt, Sanjay P. Chauhan, Devang J. Pandya

Gojihva or Gaozaban, an Ayurvedic and Unani medicinal plant, is a commercially important drug with a controversial botanical origin. Onosma bracteata, officially considered Gojihva in India, has very few scientific validations of traditional claims, and few attempts have been made to standardise the plant. The successive extracts were screened for in vitro DPPH assay and hepatoprotective activities (HepG2 cells) to evaluate the traditional claim of vishaghna - antitoxic. The methanol extract has the highest antioxidant capacity of 88.48 ± 0.00% at a concentration of 62.5 µg/mL. The methanol extract at a concentration of 125 µg/mL and above exhibited significant protection against paracetamol and carbon tetrachloride-induced toxicity compared to the control group and other extracts. The caffeic acid and β-sitosterol were isolated from methanol extract, with the latter being reported for the first time. A high-performance thin layer chromatography method was developed for estimating two compounds. The content of caffeic acid and β-sitosterol was found to be 19.06 mg/100 g and 40.42 mg/100 g of the plant material, respectively. Our studies have validated the hepatoprotective property and established quality parameters that are useful for standardisation of O. bracteata and distinguishing it from the other species of Gojihva.

Graphical Abstract

Gojihva或Gaozaban,一种阿育吠陀和乌纳尼药用植物,是一种具有争议的植物起源的重要商业药物。印度官方将其称为Gojihva的Onosma bracteata,其传统说法很少得到科学验证,也很少有人尝试将这种植物标准化。通过体外DPPH测定和肝保护活性(HepG2细胞)的筛选,对传统说法的抗毒性进行评价。甲醇提取物在浓度为62.5µg/mL时抗氧化能力最高,为88.48±0.00%。与对照组和其他提取物相比,浓度为125µg/mL及以上的甲醇提取物对扑热息痛和四氯化碳诱导的毒性具有显著的保护作用。从甲醇提取物中分离得到咖啡酸和β-谷甾醇,其中β-谷甾醇为首次报道。建立了高效薄层色谱法测定两种化合物的含量。咖啡酸和β-谷甾醇的含量分别为19.06 mg/100 g和40.42 mg/100 g。本研究验证了其保肝作用,并建立了相应的质量参数,为其标准化和与其它品种的鉴别提供了依据。图形抽象
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引用次数: 0
Chemical components, antioxidant activity and antidiabetic activity (in vitro, in silico and in vivo, streptozotocin-induced diabetic rats) of extracts from Pathum Thani fragrant rice 丹参香米提取物的化学成分、抗氧化活性和抗糖尿病活性(体外、体内、硅内、链脲霉素诱导的糖尿病大鼠)
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-10-17 DOI: 10.1007/s13596-024-00794-7
Sompong Sansenya, Nopparat Buddhakala, Apirak Payaka, Orathai Sarakul, Moragote Buddhakala, Manatchanok Kongdin, Sasiprapha Asawawibul

Rice has been reported to possess a variety of biological activities and non-colored rice demonstrates the activities less potent than colored rice. Pathum Thani fragrant rice is new strain non-colored Thai rice that become highly consumed rice. Due to less potent activity, an increase in activity of the non-colored rice is needed to perform. Cereals are rich in active compounds and exhibit a number of activities. To verify whether combination with cereals could enhance the activities of the non colored rice, therefore this study was carried out to determine chemical components, antioxidant and antidiabetic activities of ethanol extracts from Pathum Thani fragrant rice both individual and combination with cereals, compared to those from Black rice. GC-MS analysis revealed the presence of 32, 48, 63, and 66 chemicals in the ethanol extracts from Pathum Thani fragrant rice extract (PTRE), Pathum Thani fragrant rice extract combined with cereals (PTRCE), Black rice extract (BRE), and Black rice extract combined with cereals (BRCE), respectively. The docking study showed that 9-Octadecadienoic acid (Z, Z)-, one of the predominant chemicals in the extracts interacted in the active site pocket of α-glucosidase and α-amylase. PTRE exhibited antioxidant activity by DPPH scavenging activity and antidiabetic activity by inhibiting α-glucosidase activity, increasing body weight and serum insulin levels and reducing blood glucose levels in STZ diabetic rats. Interestingly, PTRCE exerted higher affective activities higher compared to PTRE. The results indicate that Pathum Thani fragrant rice can be enhanced the activities and developed as a therapeutic agent for management of free radical-related diseases and diabetes mellitus, by combination with cereals.

据报道,水稻具有多种生物活性,而非有色水稻的活性不如有色水稻。巴吞他尼香米是一种新的非彩色泰国大米,成为高度消费的大米。由于活性较弱,需要增加非有色米的活性来发挥作用。谷类富含活性化合物,并表现出许多活性。为了验证与谷物组合是否能增强非有色米的活性,本研究对单独和与谷物组合的巴塔姆香米乙醇提取物与黑米乙醇提取物的化学成分、抗氧化和抗糖尿病活性进行了比较。气相色谱-质谱分析显示,巴塔尼香米提取物(PTRE)、巴塔尼香米与谷物结合提取物(PTRCE)、黑米提取物(BRE)和黑米与谷物结合提取物(BRCE)的乙醇提取物中分别含有32、48、63和66种化学物质。对接研究表明,在α-葡萄糖苷酶和α-淀粉酶的活性位点口袋中,9-十八烯二烯酸(Z, Z)-是提取物中的优势化学物质之一。PTRE通过清除DPPH和抑制α-葡萄糖苷酶活性,提高STZ糖尿病大鼠的体重和血清胰岛素水平,降低血糖水平,显示抗氧化活性。有趣的是,与PTRE相比,PTRCE表现出更高的情感活动。结果表明,与杂粮配伍可提高其活性,并可作为治疗自由基相关疾病和糖尿病的药物。
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引用次数: 0
Anti-diarrhoea properties of ethanol extract of Citrullus colocynthis fruit pulp: in vivo and in silico studies 瓜泥果肉乙醇提取物的抗腹泻特性:体内和计算机研究
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-10-16 DOI: 10.1007/s13596-024-00783-w
Asiat Na’Allah, Simbiat Bashir, Mutiu Alabi, Fatai A. Kareem, Gabriel O. Olaifa, Femi J. Afolabi, Sesan Abiodun Aransiola, Chandra Shekhar Seth, Naga Raju Maddela, Ram Prasad

This study aimed to establish anti-diarrhoea agents, through in vivo and in silico molecular modelling from the phytoconstituents of Citrullus colocynthis ethanol fruit pulp extract (CCEFPE). The crystal structure of µ (mu) opioid and aquaporin 4 (AQP4) receptors were retrieved from the RCSB database, while the identified compounds from C. colocynthis ethanol fruit pulp extract were sequentially docked via Schrödinger suite. In CCEFPE in vivo anti-diarrhoea studies, control received distilled water (2 mL/kg, p.o.), diarrhoea was administered with castor oil or MgSO4 (2 mL/kg, p.o.), standard drug was administered 2 mg/kg, p.o. loperamide, while CCEFPE (50, 100 and 150 mg/kg, p.o.) was administered to the treated groups. Seven hit compounds out of which 54 displayed relatively higher free binding energy for mu opioid and AQP4. Swiss ADME predicted compounds 54 to be blood–brain impermeant, have low gastrointestinal absorption, strong druglike-ness, and safety profile among the hits. In the in vivo study, the onset of diarrhoea was significantly (p < 0.05) delayed by CCEFPE. A significant reduction (p < 0.05) in gastrointestinal motility, enteropooling and PGE2 in diarrhoea-induced groups was also observed after CCEFPE administration. Compound 54, even though it has drug-like properties, displayed a weak interaction with the receptor and hence can be structurally modified to an analogue of loperamide for a better ligand-receptor interaction while the in vivo studies confirmed the anti-diarrhoea activities of C. colocynthis ethanol fruit pulp extract.

本研究旨在通过体内和硅分子模拟的方法,从甜瓜乙醇果肉提取物(CCEFPE)的植物成分中提取抗腹泻药物。从RCSB数据库中检索µ(mu)阿片样物质和水通道蛋白4 (AQP4)受体的晶体结构,并通过Schrödinger suite对巨藻醇浆提取物中鉴定的化合物进行顺序对接。在CCEFPE体内抗腹泻研究中,对照组给予蒸馏水(2 mL/kg, p.o.),腹泻组给予蓖麻油或MgSO4 (2 mL/kg, p.o.),标准药物2 mg/kg, p.o.洛哌丁胺,治疗组给予CCEFPE(50、100和150 mg/kg, p.o.)。7个被击中的化合物中有54个对mu阿片样物质和AQP4表现出较高的自由结合能。瑞士ADME预测化合物54是不含血脑的,具有低胃肠道吸收,强药物性和安全性。在体内研究中,CCEFPE显著延迟了腹泻的发生(p < 0.05)。服用CCEFPE后,腹泻诱导组的胃肠蠕动、肠蠕动和PGE2也显著降低(p < 0.05)。化合物54虽然具有药物性质,但与受体的相互作用较弱,因此可以在结构上修饰为类似洛哌丁胺的物,以获得更好的配体-受体相互作用,而体内研究证实了colocynthis乙醇果肉提取物的抗腹泻活性。
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引用次数: 0
Herbal medicine: a potent booster for stem cell therapy in cardiovascular diseases 草药:心血管疾病干细胞治疗的有力助推器
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-10-14 DOI: 10.1007/s13596-024-00793-8
Amir Hossein Kheirkhah, Maria Kavianpour, Shima Ababzadeh

The fact that cardiovascular diseases have continued to be the top cause of death across the world over the course of many years hammers home the crucial need of discovering breakthrough therapeutic approaches. Stem cell therapy has emerged as a potentially beneficial method due to the fact that it has the ability to boost functional improvement and facilitate the regeneration of tissue. This has led to the application of stem cell therapy by the medical community. On the other hand, its therapeutic efficacy has been impeded by a variety of obstacles, including insufficient engraftment and survival of transplanted cells. These difficulties have made it difficult for it to be effective. In this context, herbal medicine, which has been utilised for a very long time and has a wide variety of bioactive components, presents itself as a powerful instrument that has the potential to enhance stem cell therapy for cardiovascular diseases.

多年来,心血管疾病一直是世界各地的头号死亡原因,这一事实再次表明,迫切需要发现突破性的治疗方法。干细胞疗法已经成为一种潜在的有益方法,因为它具有促进功能改善和促进组织再生的能力。这导致了医学界对干细胞疗法的应用。另一方面,其治疗效果一直受到各种障碍的阻碍,包括移植细胞的植入不足和存活。这些困难使它难以发挥作用。在这种情况下,草药已经被使用了很长时间,具有各种各样的生物活性成分,它是一种强有力的工具,有可能加强心血管疾病的干细胞治疗。
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引用次数: 0
Biosynthesis of silver nanoparticles using Pterorhachis zenkeri: characterization and evaluation of antioxidant, anti-apoptotic, and androgenic properties in TM3 leydig cells exposed to cyclophosphamide 在环磷酰胺暴露的TM3 leydig细胞中,利用翼黄芪生物合成纳米银:抗氧化、抗凋亡和雄激素特性的表征和评价
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-10-09 DOI: 10.1007/s13596-024-00792-9
Patrick Brice Defo Deeh, Nagabhishek Sirpu Natesh, Karthik Alagarsamy, Madan Kumar Arumugam, Ramachandran Dasnamoorthy, Tharunkumar Sivaji, Vinita Vishwakarma

We fabricated silver nanoparticles (AgNPs) using Pterorhachis zenkeri, characterized by Atomic Force Microscopy (AFM) and determined their antioxidant potentials in vitro. Results confirmed the fabrication of AgNPs by using P. zenkeri as a bioreducing agent for the first time. AgNPs possessed potent antioxidant activity in vitro. Furthermore, the TM3 cells were treated for 24 h with AgNPs, vitamin E and cyclophosphamide (CP) at different concentrations (25, 50, 100, 250 and 500 µg/ml). The cells morphology, apoptosis, mitochondrial membrane depolarisation (MMD), Reactive Oxygen Species (ROS), caspase 3/9, oxidative stress-related enzymes, testosterone, and the mRNA expression of steroidogenic acute regulatory protein (StAR) were measured. Results revealed that AgNPs, vitamin E and CP decreased the cell viability in a dose-dependent manner, but did not affect the TM3 cells morphology after treatment. The cytotoxicity of CP in TM3 cells was alleviated after AgNPs application. For instance, AgNPs significantly (p < 0.001–0.05) reduced the MMD, ROS production, and caspase 3/9 activities, but increased the activities of superoxide dismutase, catalase and glutathione peroxidase in the TM3 cells. Moreover, AgNPs improved testosterone production by activating StAR machineries. These results indicate that AgNPs/P. zenkeri could be a potential alternative drug in the management of oxidative stress and androgen deficit associated with CP chemotherapy.

本研究以紫蕨为原料制备银纳米粒子,利用原子力显微镜(AFM)对其进行表征,并测定其体外抗氧化能力。实验结果首次证实了以紫藻为生物还原剂制备AgNPs的可行性。AgNPs具有较强的体外抗氧化活性。将AgNPs、维生素E和不同浓度(25、50、100、250和500µg/ml)的环磷酰胺(CP)分别作用于TM3细胞24 h。测定各组细胞形态、凋亡、线粒体膜去极化(MMD)、活性氧(ROS)、caspase 3/9、氧化应激相关酶、睾酮、类固醇急性调节蛋白(StAR) mRNA表达量。结果显示,AgNPs、维生素E和CP均呈剂量依赖性降低细胞活力,但对TM3细胞形态无影响。应用AgNPs后,CP对TM3细胞的毒性明显减轻。例如,AgNPs显著(p < 0.001-0.05)降低了TM3细胞的MMD、ROS生成和caspase 3/9活性,但增加了超氧化物歧化酶、过氧化氢酶和谷胱甘肽过氧化物酶的活性。此外,AgNPs通过激活StAR机制来改善睾酮的产生。这些结果表明AgNPs/P。zenkeri可能是一种潜在的替代药物,用于管理与CP化疗相关的氧化应激和雄激素缺陷。
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引用次数: 0
Therapeutic potential of freeze-dried Kaempferia galanga herbal formulation in alleviating hyperglycemia in diabetic mice: an in-vivo and in-silico investigation 冻干山柰高良姜中药制剂缓解糖尿病小鼠高血糖的治疗潜力:体内和计算机研究
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-09-27 DOI: 10.1007/s13596-024-00784-9
Flavius Phrangsngi Nonglang, Revelbornstar Snaitang, Dhritiman Roy, Shankupar Rynjah, Surya Bhan

A never-ending search is being made for a natural remedy to cure diabetes, which is one of the biggest worldwide health concerns. Kaempferia galanga (K. galanga), an important medicinal herb, is reported to have various pharmacological effects. This study aims to conduct in-depth research on the antihyperglycemic activity of K galanga in streptozotocin (STZ)-induced diabetic mice and the mechanism by which it elicits its response. For 21 days, various dosages of freeze-dried K. galanga ethanolic extract (KGE) therapy were given intraperitoneally in STZ-induced diabetic mice. KGE at 350 mg/kg b.w. was selected as the ideal dose. Acute toxicology studies have shown that KGE is non-toxic. Protein and gene expression studies targeting various metabolic pathways show that in the diabetic mice treated with KGE, there was stimulation of AKT, inhibition of glycogen synthase kinase-3, stimulation of glucokinase (GK), and inhibition of phosphoenolpyruvate carboxykinase (PEPCK) expression. Histopathological studies show the protective effect of herbal KGE on the integrity of the mice's pancreas. Molecular docking studies was performed in which the bio-active compound ethyl-p-methoxy cinnamate (EPMC) found in KGE shows good binding energy with the target protein AKT, GSK3, insulin receptor (IR), protein-tyrosine phosphatase 1B (PTB1B), GK, and PEPCK, indicating a good binding interaction. ADMET studies also revealed that EPMC has desirable physicochemical and pharmacokinetic properties and very low toxicity (LD 50 7900 mg/kg) compared to standard metformin (LD50 680 mg/kg). Herbal KGE and EPMC show a pleiotropic therapeutic effect and may be a potent adjunct and drug, respectively, in attenuating diabetes.

Graphical Abstract

人们一直在寻找治疗糖尿病的自然疗法,糖尿病是世界上最大的健康问题之一。山柰属高良姜(kk . galanga)是一种重要的中药,具有多种药理作用。本研究旨在深入研究高良姜对链脲佐菌素(STZ)诱导的糖尿病小鼠的降糖作用及其作用机制。以冻干高良姜乙醇提取物(KGE)治疗stz诱导的糖尿病小鼠21 d。选择350 mg/kg b.w.的KGE为理想剂量。急性毒理学研究表明KGE是无毒的。针对多种代谢途径的蛋白和基因表达研究表明,在KGE治疗的糖尿病小鼠中,AKT受到刺激,糖原合成酶激酶-3受到抑制,葡萄糖激酶(GK)受到刺激,磷酸烯醇丙酮酸羧激酶(PEPCK)的表达受到抑制。组织病理学研究表明,草药KGE对小鼠胰腺的完整性有保护作用。分子对接研究发现,在KGE中发现的生物活性化合物乙基-对甲氧基肉桂酸乙酯(EPMC)与靶蛋白AKT、GSK3、胰岛素受体(IR)、蛋白酪氨酸磷酸酶1B (PTB1B)、GK和PEPCK具有良好的结合能,表明其具有良好的结合相互作用。ADMET研究还表明,与标准二甲双胍(LD50 680 mg/kg)相比,EPMC具有理想的物理化学和药代动力学特性,毒性非常低(LD50 7900 mg/kg)。中药KGE和EPMC具有多效性的治疗效果,可能分别作为一种有效的辅助治疗和药物治疗糖尿病。图形抽象
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引用次数: 0
Investigation of biological activities of in vitro grown Sesamum orientale plant extract on the cell cultures: wound healing and antiproliferation 芝麻植物提取物体外培养细胞的生物活性研究:伤口愈合和抗增殖
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-09-22 DOI: 10.1007/s13596-024-00791-w
Sevil Yeniocak, Selin Galatalı, İrem Demir, Aysel Uğur, Nurdan Saraç, Ergun Kaya

Sesame has gained significant attention in the pharmaceutical industry for its antifungal, antiproliferative, antioxidant, and antiproliferative properties, as well as its use as a nutritional supplement. Additionally, sesame is a good source of vitamins B and E and has shown potential as a food that can lower serum cholesterol, balance blood pressure, and aid wound healing. In vitro grown Sesamum orientale L. cv. "Gökova" are presently undergoing tests to determine their cytotoxic, wound-healing, and antiproliferative properties using L929 fibroblasts, A549 lung epithelial, and MCF-7 breast cell lines. The IC50 values for A549 were 922.73 g ml−1 (extract) and 33.09 g ml−1 (cisplatin), 1837.07 g ml−1 (extract) and 19.27 g ml−1 (cisplatin), and for L929 they were 154.70 g ml−1 (extract). The subcytotoxic dosages of the extract demonstrated wound healing in L929 fibroblast cell cultures within 48 h. The transcripts of the BCL-XL gene, which exhibit an inverse correlation with the apoptotic pathway, and the transcripts of the Cas3 and Cas9, which show a positive correlation with the apoptotic pathway, were scrutinized to ascertain the anti-cancer properties. The study revealed a significant increase in gene expression in A549 and MCF-7 lines after exposure to plant extract or cisplatin. The findings suggest that sesame extract can promote wound healing at lower doses and exhibit antiproliferative activity at higher doses. The study provides a promising foundation for the development of a pharmacological drug that offers wound-healing and/or antiproliferative effects. The product has potential applications across a range of future projects and can be utilised with numerous cell lines.

芝麻因其抗真菌、抗增殖、抗氧化和抗增殖的特性以及作为营养补充剂的用途而在制药行业获得了极大的关注。此外,芝麻是维生素B和E的良好来源,已经显示出作为一种食物的潜力,可以降低血清胆固醇,平衡血压,帮助伤口愈合。离体培养芝麻的研究。“Gökova”目前正在接受使用L929成纤维细胞、A549肺上皮细胞和MCF-7乳腺细胞系的细胞毒性、伤口愈合和抗增殖特性的测试。A549的IC50值分别为922.73 g ml−1(提取物)和33.09 g ml−1(顺铂),1837.07 g ml−1(提取物)和19.27 g ml−1(顺铂),L929的IC50值分别为154.70 g ml−1(提取物)。亚细胞毒性剂量的提取物在L929成纤维细胞培养中显示伤口在48小时内愈合。BCL-XL基因的转录本与凋亡途径呈负相关,Cas3和Cas9的转录本与凋亡途径呈正相关,我们仔细检查了它们的抗癌特性。该研究显示,暴露于植物提取物或顺铂后,A549和MCF-7系的基因表达显著增加。研究结果表明,芝麻提取物在低剂量下可以促进伤口愈合,在高剂量下具有抗增殖活性。该研究为开发具有伤口愈合和/或抗增殖作用的药理学药物提供了有希望的基础。该产品在未来的一系列项目中有潜在的应用,可以与许多细胞系一起使用。
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引用次数: 0
The synthesis, application and therapeutic perspectives of medicinal plants-based solid lipid nanoparticles: a comprehensive review 药用植物固体脂质纳米颗粒的合成、应用及治疗前景综述
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-09-21 DOI: 10.1007/s13596-024-00787-6
MohammadSadeq Mottaqi, Mohammad Amin Langarizadeh, Neda Molaali, Masoud Rezaei, Alieh Ameri, Hamid Forootanfar

Lipid-based drug carriers have gained massive amounts of interest in the last two-decade period as a way to deliver drugs that are not particularly water-soluble. Pharmaceutical uses of lipid nanocarriers include carrying and administering a wide range of therapeutic ingredients. Solid lipid nanoparticles (SLNs) were designed and formulated to rise above the disadvantages of existing colloidal systems, including microemulsions, liposomes and polymeric nanoparticles, by offering benefits such as a favorable release profile and targeted medication distribution while having great physical integrity. We sought to evaluate the recent findings on the current issue to provide a comprehensive perspective of the subject utilizing an extensive literature search to pinpoint the latest scientific reports on this subject. The focus of this paper is on the research employing SLNs for delivery of medicinal plants and testing them in vitro and in vivo. There are a number various standard variables affecting the release of compounds from SLNs throughout all administration routes. Further, the current paper comprehensively elucidates assorted prospects of SLNs. Next, the investigated SLNs encapsulating herbal compounds in scientific articles are reviewed in details. As many herbal compounds are hydrophobic substances, the SLNs encapsulating them can be beneficial in various therapeutic applications. The most studies herbal compounds are Curcumin, followed by Silibinin and Artemisinin.

在过去的二十年里,基于脂质的药物载体作为一种非水溶性药物的递送方式获得了极大的兴趣。脂质纳米载体的医药用途包括携带和施用广泛的治疗成分。固体脂质纳米颗粒(sln)的设计和配方克服了现有胶体系统(包括微乳液、脂质体和聚合物纳米颗粒)的缺点,具有良好的释放特性和靶向药物分布等优点,同时具有良好的物理完整性。我们试图对当前问题的最新发现进行评估,利用广泛的文献检索来确定有关该主题的最新科学报告,以提供该主题的全面视角。本文的重点是利用sln作为药用植物的体外和体内给药方法的研究。在所有给药途径中,有许多不同的标准变量影响sln中化合物的释放。此外,本文还全面阐述了sln的各种前景。接下来,详细回顾了科学文章中所研究的包封草药化合物的sln。由于许多草药化合物是疏水物质,包裹它们的sln在各种治疗应用中是有益的。研究最多的草药化合物是姜黄素,其次是水飞蓟宾和青蒿素。
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引用次数: 0
Chemical, elemental, morphological and toxicological characteristics of traditional Indian Siddha formulation: Kasthuri Karuppu 传统印度悉达配方的化学、元素、形态和毒理学特征:Kasthuri Karuppu
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-09-18 DOI: 10.1007/s13596-024-00790-x
N. Kannan, Anil Kumar NV, S. Balaji

The chemical, elemental, morphological and toxicological characteristics of organometallic formulation (Kasthuri Karuppu) were assessed using UV-spectrophotometer, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, ICP-OES, Energy dispersive X-ray, XRD and Zeta potential. The physical properties such as size (10–80 nm), surface area (3.1 m2/g), surface charge (-36mV), and bandgap energy (3.6 eV) were correlated with reactivity. Based on the elemental distribution of Hg, As and S, the proportion favours HgS that is less toxic and reactive. There were no toxic effects of the tested formulation at concentration 60 µg/mL against normal and cancer cells (observed during 24 h). However, the increase in time duration (72 h) had lethal effects in both the cells. The developmental toxicity of the organometallic formulation was assessed in Zebrafish embryos. The safe dosage was found to be 100 µg/mL. The toxicity of the formulation in vitro and in vivo is based on the exposure time and dosage.

采用紫外分光光度计、x射线光电子能谱、傅里叶变换红外光谱、ICP-OES、能量色散x射线、XRD和Zeta电位对有机金属制剂(Kasthuri Karuppu)的化学、元素、形态和毒理学特性进行了评价。尺寸(10-80 nm)、表面积(3.1 m2/g)、表面电荷(-36mV)和带隙能(3.6 eV)等物理性质与反应性相关。从Hg、As和S的元素分布来看,毒性和活性较弱的HgS占比更大。浓度为60µg/mL的试验制剂对正常细胞和癌细胞均无毒性作用(24 h观察),但时间延长(72 h)对两种细胞均有致死作用。在斑马鱼胚胎中评估了有机金属制剂的发育毒性。安全剂量为100µg/mL。制剂在体内和体外的毒性取决于暴露时间和剂量。
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引用次数: 0
Predictors of high phytotherapy usage among women with cancer: the impact of cancer duration, symptoms, and psychosocial factors 癌症女性患者植物疗法使用率高的预测因素:癌症病程、症状和社会心理因素的影响
IF 1.8 Q3 PHARMACOLOGY & PHARMACY Pub Date : 2024-09-11 DOI: 10.1007/s13596-024-00789-4
Nadia Ouzennou , Mohamed Aboufaras, Rajae Najib, Asmaa Lakhdissi, Karima Selmaoui

Objective: Gynecological and Breast Cancers (GCBC) are extremely common worldwide, including in Morocco. Patients suffering from these forms of cancer often turn to complementary and alternative medicine (CAM), particularly phytotherapy. However, there has been no research on Moroccan patients using this medicine. We aim to assess the frequency and factors involved in the use of phytotherapy. Methods: This was a cross-sectional analytical study. We interviewed 317 patients in an oncology unit. We calculated the 12-month prevalence of herbal medicine use and identified predictors of herbal medicine use by multivariate analysis using SPSS software. Results: The prevalence of patients using phytotherapy was 40.7%. Patients used 48 plant species. The most commonly used plants were Marrubium vulgare L., Allium cepa L. and Retama monosperma (L.) Boiss. This use was associated with a cancer duration greater than one year (p < 0.05; OR = 0.414), pain (p < 0.01; OR = 2.711), anorexia (p < 0.05; OR = 2.079), the social impact of the disease (p < 0.01; OR = 4.140), the expected benefits of C&CM (p < 0.000; OR = 3.453), and the social norms of relatives (p < 0.000; OR = 3.502). Conclusion: The use of herbal medicine as CAM among women with is highly prevalent. The user profile identified in this study deviates from the patterns observed in the international literature. Further research is warranted in different regions of Morocco, exploring various CAM modalities, and employing alternative methodological approaches. The use of herbal medicine as CAM in women with GCBC is widespread. The profile of users identified in this study deviates from patterns observed in the international literature. Further research is warranted in different regions of Morocco, exploring different CAM modalities and using other methodological approaches.

目的:妇科和乳腺癌(GCBC)在世界范围内极为常见,包括在摩洛哥。患有这些类型癌症的患者往往转向补充和替代医学(CAM),特别是植物疗法。然而,没有关于摩洛哥患者使用这种药物的研究。我们的目的是评估使用植物疗法的频率和因素。方法:采用横断面分析研究。我们在一个肿瘤科采访了317名患者。我们计算了12个月草药使用的流行率,并通过SPSS软件进行多变量分析,确定了草药使用的预测因素。结果:采用植物疗法治疗的患者占40.7%。患者使用了48种植物。最常使用的植物是野豌豆(Marrubium vulgare L.)、葱属植物(Allium cepa L.)和单子母草(remama monosperma)。木香。这种使用与癌症持续时间大于1年相关(p < 0.05;OR = 0.414),疼痛(p < 0.01;OR = 2.711)、厌食症(p < 0.05;OR = 2.079),疾病的社会影响(p < 0.01;OR = 4.140), CM的预期收益(p < 0.000;OR = 3.453),亲属社会规范(p < 0.000;or = 3.502)。结论:中草药作为替代药物在老年妇女中应用较为普遍。本研究中确定的用户概况偏离了国际文献中观察到的模式。有必要在摩洛哥不同地区进行进一步研究,探索各种CAM模式,并采用替代的方法方法。在GCBC妇女中广泛使用草药作为辅助治疗。本研究中确定的用户概况与国际文献中观察到的模式不同。有必要在摩洛哥不同地区进行进一步研究,探索不同的CAM模式和使用其他方法方法。
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引用次数: 0
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Advances in Traditional Medicine
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