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Pharmacological Investigation of Anticonvulsant Effect of ArtemisiaVulgaris on Pentylenetetrazole-Induced Epileptic Seizures in ZebrafishExperimental Model 青蒿对戊四唑诱导斑马鱼癫痫发作实验模型抗惊厥作用的药理研究
IF 0.6 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2024-01-08 DOI: 10.2174/0115748855268042231130041958
M. Sharma, G. V. N. Kumar, Pankaj Gupta
Epilepsy is the most common neurological disorder, characterized by abnormal,unpredictable, and recurrent seizures. In the alternative medicine system, Artemisia vulgaris hasbeen used to treat epileptic symptoms since its inception. However, scientific evidence concerningits effect on the treatment of epileptic seizures is not available.The objective of the study is to evaluate the anti-convulsant potential of Artemisia vulgarisin zebrafish experimental models.Zebrafish larvae and adult zebrafish were used as experimental models. Briefly, larvae andadult zebrafish were exposed to 0.5% of the test medicine Artemisia vulgaris mother tincture (ϕ) andits potencies (6CH, 30CH), and valproic acid for 1 hour. After 1 hour of exposure, they were exposedto pentylenetetrazole to record different seizure scores from 1 to 5 using ANY maze video trackingsoftware.Artemisia vulgaris 30CH in zebrafish larvae and Artemisia vulgaris 6CH and 30CH in adultzebrafish delayed the latency score from score 1 to score 5 and were found effective against PTZinducedlocomotor activity and seizure duration and intensity.In conclusion, Artemisia vulgaris (6CH and 30CH) has the potential to be a novel treatmentfor symptomatic epileptic seizures and could be a potential alternative drug candidate for symptomatictreatment of epilepsy.
癫痫是最常见的神经系统疾病,其特点是异常、不可预测和反复发作。在替代医学体系中,青蒿自诞生以来一直被用于治疗癫痫症状。本研究的目的是评估青蒿在斑马鱼实验模型中的抗惊厥潜力。简单地说,将斑马鱼幼体和成体暴露于 0.5% 的试验药物青蒿母酊剂(j)及其效力(6CH、30CH)和丙戊酸中 1 小时。斑马鱼幼鱼服用 30CH 青蒿,成年斑马鱼服用 6CH 和 30CH 青蒿后,潜伏期从 1 分延迟到 5 分,对 PTZ 诱导的运动活动、癫痫发作持续时间和强度有效。总之,青蒿(6CH 和 30CH)具有治疗症状性癫痫发作的新潜力,可作为治疗症状性癫痫的潜在替代药物。
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引用次数: 0
Evaluation of Phytochemicals, Antioxidants, and Antidiabetic Activity ofNitophyllum marginale by Using Analytical Approaches 用分析方法评估叶枯素的植物化学成分、抗氧化剂和抗糖尿病活性
IF 0.6 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2024-01-03 DOI: 10.2174/0115748855270408230925073813
Rohit Malhotra, Louis Cojandaraj
Nitophyllum marginale holds potential for medical applications due to itsbioactive compounds, making it promising for developing new therapeutic interventions. Our studyaims to evaluate the bioactivity of Nitophyllum marginale extracts obtained using methanol andchloroform solvents. We focus on analyzing the phytochemical profile, antioxidant activity, and antidiabeticpotential of seaweed extract in this study. By examining the medicinal propertiesof Nitophyllum marginale, we aim to explore the therapeutic bioactivity potentiality and its primerole in improvising and searching for potential alternatives for seizing Diabetes mellitus.The antioxidant activity of Nitophyllum marginale was evaluated using ABTS,DPPH, nitric oxide, lipid peroxidation, and hydrogen peroxide assays. Additionally, alphaglucosidaseinhibition tests were conducted to evaluate the potential as an antidiabetic agent.The study revealed that extracts from Nitophyllum marginale contain antioxidants that protectcells from oxidative stress. These extracts also contain bioactive compounds like alkaloids, flavonoids,phenols, saponins, and carbohydrates. These compounds work together to provide antioxidantbenefits. Additionally, the extracts showed activity against alpha-glucosidase, which is vital formanaging blood sugar levels.These results emphasize the existence of bioactive metabolites exhibiting phytochemicals,antioxidants, and antidiabetic activities obtained from the extract using chloroform and methanolsolvents. These findings suggest the potential of Nitophyllum marginale extracts as a naturalreservoir of antioxidants and antidiabetic agents.
Nitophyllum marginale 因其生物活性化合物而具有医疗应用潜力,使其有望开发出新的治疗干预措施。我们的研究旨在评估使用甲醇和氯仿溶剂提取的边缘叶菜提取物的生物活性。本研究的重点是分析海藻提取物的植物化学成分、抗氧化活性和抗糖尿病潜力。通过研究 Nitophyllum marginale 的药用特性,我们旨在探索其治疗生物活性潜力及其在改善和寻找治疗糖尿病的潜在替代品方面的作用。此外,还进行了α-葡萄糖苷酶抑制试验,以评估其作为抗糖尿病剂的潜力。研究表明,边茶提取物含有抗氧化剂,可保护细胞免受氧化应激。这些提取物还含有生物活性化合物,如生物碱、黄酮类、酚类、皂苷和碳水化合物。这些化合物共同发挥抗氧化作用。此外,提取物还显示出对α-葡萄糖苷酶的活性,而α-葡萄糖苷酶对控制血糖水平至关重要。这些结果表明,使用氯仿和甲醇溶剂从提取物中提取的生物活性代谢物具有植物化学、抗氧化和抗糖尿病活性。这些研究结果表明,叶绿素提取物具有作为天然抗氧化剂和抗糖尿病药物宝库的潜力。
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引用次数: 0
Evaluation of Clozapine-induced Toxicities in Psychic Patients in MentalHealth Care Hospitals in the Southern Region of the Saudi ArabiaKingdom 对沙特阿拉伯王国南部地区精神保健医院精神疾病患者氯氮平所致毒性的评估
IF 0.6 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2024-01-01 DOI: 10.2174/0115748855281044231206042618
Ali Ali Eissa Qhtani, Mohammed Zayed Alassiry, Yazeed Hussein Al-Jmaai, Mohammed Ayed Almushafi, Hassan Saeed Hassan
Clozapine is a psychiatric medication that may cause various side effects,some of them may be serious and fatal adverse effects, such as severe neutropenia, agranulocytosis,lymphocytopenia, myocarditis, and orthostatic hypotension, that have been associated to an increasedrisk of death.This study aimed to evaluate the serious and potentially fatal adverse effects of clozapinetoxicity in psychic patients at mental health care hospitals in the Southern region of the Kingdom ofSaudi Arabia.By using a survey, data were retrospectively collected from 193 adult psychic patient reportswho have been administrated clozapine with regular follow-ups, in mental health hospitals inthe Southern region of Saudi Arabia between 2019 and 2021. Then, these data are recorded and analyzedStatistically using SPSS software, with suitable tests, and predetermined statistical significance(p-value) of less than 0.001.The occurrence of agranulocytosis, neutropenia, hypotension, and seizures showed a highlysignificant correlation with higher doses of clozapine administration (i.e. p<0.001). Similarly, agranulocytosisand neutropenia were significantly associated with the occurrence of both hypotension andseizures (i.e. p<0.001).The collected data in this study showed an increased incidence of agranulocytosis andneutropenia associated with clozapine-treated psychic patients in the Southern region of the Kingdomof Saudi Arabia which warrants further clinical studies to find this correlation.
氯氮平是一种精神科药物,可能会引起各种副作用,其中一些可能是严重和致命的不良反应,如严重的中性粒细胞减少症、粒细胞减少症、淋巴细胞减少症、心肌炎和正性低血压,这些不良反应与死亡风险增加有关。本研究旨在评估沙特阿拉伯王国南部地区精神卫生保健医院的精神疾病患者因氯氮平中毒而产生的严重且可能致命的不良反应。研究人员通过调查的方式,回顾性地收集了沙特阿拉伯南部地区精神卫生保健医院在 2019 年至 2021 年期间接受氯氮平治疗并定期随访的 193 名成年精神疾病患者的报告数据。然后,使用 SPSS 软件对这些数据进行记录和统计分析,并进行适当的检验,预设统计显著性(P 值)小于 0.001。粒细胞减少症、中性粒细胞减少症、低血压和癫痫发作的发生与氯氮平用药剂量的增加呈高度显著相关性(即 P<0.001)。本研究收集的数据显示,在沙特阿拉伯王国南部地区,接受氯氮平治疗的精神病患者粒细胞减少和中性粒细胞减少的发生率增加,因此有必要开展进一步的临床研究,以发现这种相关性。
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引用次数: 0
Investigation of Nosocomial Urinary Tract Infections Post Transplantation, Main Pathogens, and Sensitivity Tests 器官移植后尿路感染调查、主要病原体和敏感性测试
IF 0.6 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-11-28 DOI: 10.2174/0115748855271275231115064229
Z. Ghamari
Regarding end-stage organ disease, transplantation is recommended as the best therapeutic management. After organ transplantation, the incidence of nosocomial urinary tract infections (NUTIs) due to multidrug-resistant Gram-negative bacilli increases. Regarding end-stage organ disease organ transplantation recommended as the best therapeutic management. After organ transplantation the incidence of urinary tract infections (UTIs) due to multidrug-resistant Gram-negative bacilli is increasing The study aimed to investigate NUTIs post-transplantation, the main pathogens involved, and sensitivity tests conducted in a tertiary hospital in Isfahan, Iran. A retrospective survey on patients admitted to a tertiary hospital in Isfahan (Alzahra), Iran, was performed between 27 March, 2017, and 9 February, 2022. The information recorded included the date of infection, date of hospitalization, gender, age, type of pathogens, and resistance or sensitivity to antibiotics. 73 kidney transplant recipients (61% females) with a mean age of 43. 2 ± 15.1 years were included. Within this population involving both genders, the main pathogens involved in NUTIs were as follows: Escherichia coli (30%), Klebsiella pneumonia (19%), Candida albicans and non-albicans (14%), Enterococcus faecalis (12%), Enterobacteriaceae (8%), Pseudomonas aeruginosa (6%), Staphylococcus spp. (6%), Acinetobacter baumannii (4%), and Streptococcus spp. (4%). Antibiotic susceptibility testing showed the most sensitivity of isolates against amikacin (n=29; 66%), meropenem (n= 28; 64%), piperacillin/tazobactam (n=26; 54%), cefepime (n= 25; 40%), ceftazidime (n= 27; 30%), ciprofloxacin (n= 40; 18%), and co-trimoxazole (n= 29; 10%). 72 kidney transplant recipients (61 Escherichia coli, Klebsiella pneumonia, and Candida spp. are the major causes of NUTIs within organ-transplanted recipients. Amikacin, meropenem, and piperacillin/tazobactam have shown more than 50% sensitivity against isolates. Further evidence-based management associated with the different spectrum antibiotics and overall antimicrobial success rate is recommended to be advantageous.
对于终末期器官疾病,移植被推荐为最佳治疗方法。器官移植后,耐多药革兰氏阴性杆菌引起的院内尿路感染(NUTIs)发病率增加。 对于终末期器官疾病,建议将器官移植作为最佳治疗方法。这项研究旨在调查器官移植后的尿路感染、主要病原体以及在伊朗伊斯法罕一家三级医院进行的药敏试验。 研究于 2017 年 3 月 27 日至 2022 年 2 月 9 日期间对伊朗伊斯法罕(Alzahra)一家三级医院的住院患者进行了回顾性调查。所记录的信息包括感染日期、住院日期、性别、年龄、病原体类型以及对抗生素的耐药性或敏感性。 研究对象包括 73 名肾移植受者(61% 为女性),平均年龄为 43.2 ± 15.1 岁。在这一涉及男女的人群中,NUTIs 所涉及的主要病原体如下:大肠埃希菌(30%)、肺炎克雷伯菌(19%)、白色念珠菌和非白色念珠菌(14%)、粪肠球菌(12%)、肠杆菌科(8%)、铜绿假单胞菌(6%)、葡萄球菌属(6%)、鲍曼不动杆菌(4%)和链球菌属(4%)。抗生素药敏试验显示,分离菌株对阿米卡星(n=29;66%)、美罗培南(n=28;64%)、哌拉西林/他唑巴坦(n=26;54%)、头孢吡肟(n=25;40%)、头孢他啶(n=27;30%)、环丙沙星(n=40;18%)和联合曲唑(n=29;10%)最敏感。 72 名肾移植受者(61 例)大肠埃希菌、克雷伯氏肺炎和念珠菌属是器官移植受者发生 NUTI 的主要原因。阿米卡星、美罗培南和哌拉西林/他唑巴坦对分离菌株的敏感性超过 50%。建议对不同谱系的抗生素和总体抗菌成功率进行进一步的循证管理。
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引用次数: 0
Inclusive Exploration of Harmonizing and Alternative Treatments for Hypothyroidism 对甲状腺功能减退症的协调疗法和替代疗法的包容性探索
IF 0.6 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-11-28 DOI: 10.2174/0115748855276876231114074145
Jaspreet Lagah, R. Pal, M. Chaitanya, Y. Pal, Sonia Morya
A clinical syndrome known as hypothyroidism occurs due to a shortage of thyroid hormone as a result of decreased production, abnormal distribution, or no action of thyroid hormones. The most typical clinical symptoms included are dry skin, hair loss, weight gain, painful-prolonged periods, infertility, balance problems, slow speech, bradycardia, hypothermia, fatigue, anxiety & depression, joint pain, and indigestion. Basically, age, gender, the severity of the ailment, and a few other factors affect the various signs and symptoms of hypothyroidism. The limitations of allopathic modalities necessitate the investigation of alternative treatment options. Future healthcare initiatives for the poor world will increasingly depend on CAM approaches to these concerns because lifestyle, diet, obesity, lack of exercise, and stress are significant contributing factors to the development of hypothyroidism. This review's objective is to provide information on herbs as well as complementary and alternative medications which are grouped into five major domains: Biologically Based therapies, Manipulative body-based therapies, Mind body-based therapies, and the whole Medical system. These have traditionally been used to treat thyroid dysfunction. The distribution of diseases in emerging nations is altering as a result of globalization. Hence the existing and potential roles of CAM techniques in the general practice of medicine are illustrated in these approaches. Scientists are being compelled to consider traditional herbal medical treatments and CAM therapy in order to combat adverse medication occurrences, high treatment costs, and compliance problems thus described in this review paper.
由于甲状腺激素分泌减少、分布异常或无作用,导致甲状腺激素不足,从而引发临床综合征,即甲状腺功能减退症。最典型的临床症状包括皮肤干燥、脱发、体重增加、痛经、不孕不育、平衡问题、语速缓慢、心动过缓、体温过低、疲劳、焦虑和抑郁、关节疼痛和消化不良。基本上,年龄、性别、疾病的严重程度以及其他一些因素都会影响甲状腺功能减退症的各种体征和症状。由于对抗疗法的局限性,有必要研究替代治疗方案。由于生活方式、饮食、肥胖、缺乏锻炼和压力是甲状腺功能减退症的重要诱因,因此未来针对贫困人口的医疗保健措施将越来越多地依赖于CAM方法来解决这些问题。本综述旨在提供有关草药以及补充和替代药物的信息,这些药物分为五大领域:以生物为基础的疗法、以操纵身体为基础的疗法、以精神身体为基础的疗法以及整个医疗系统。这些疗法历来被用于治疗甲状腺功能障碍。随着全球化的发展,新兴国家的疾病分布正在发生变化。因此,这些方法说明了CAM技术在一般医疗实践中的现有和潜在作用。科学家们不得不考虑传统草药疗法和CAM疗法,以应对药物不良反应、高昂的治疗费用和依从性问题。
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引用次数: 0
Optogenetics: A New Era of Novel Drug Delivery-Based Approach for Neurodegeneration 光遗传学:基于新型给药方法治疗神经退行性病变的新时代
IF 0.6 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-11-27 DOI: 10.2174/0115748855274992231114051324
Dilpreet Singh
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引用次数: 0
Improved Transdermal Delivery of Anti-hypertensive Drug Loaded Nanostructured Lipid Carriers: Statistical Design, Optimization, Depiction and Pharmacokinetic Assessment 纳米结构脂质载体改善了抗高血压药物的透皮给药:统计设计、优化、描述和药代动力学评估
IF 0.6 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-11-27 DOI: 10.2174/0115748855267831231113112445
A. Chettupalli, Purnachandra Rao Avula, Vivek Chauhan
The vasoselective calcium-channel blocker lercanidipine hydrochloride (LCH) is poorly absorbed orally (only 10% bioavailability) owing to its low solubility and hepatic metabolism. Because of the LCH's poor solubility and permeability, bioavailability is low and very variable, stable aqueous liquid formulations are challenging to create, and a uniform distribution of the medication is almost impossible to produce. The purpose of this research was to see whether an approach involving the development of nanostructured lipid carriers (NLCs) might be used to create an effective, innovative oral formulation of LCH. The efficacy of several synthetic and natural liquid lipids was compared using a hot homogenization-ultrasonication strategy. Following initial improvements with hot homogenization and ultrasonication, the LCHloaded NLCs formulation was fine-tuned by Box-Behnken statistical analysis. The optimal LCHNLCs composition includes the lipid phase (2-4% w/v) of stearic acid and oleic acid, the surfactants poloxamer 188 (1%) and Tween 80(1%), and other ingredients. The optimized NLCs formulation was found to have mean vesicle sizes of 128.72±1.59 nm, polydispersity indices of 0.169±0.06, zeta potentials of -36.81±0.42 mV, and entrapment efficiencies of 79.84±0.11%. The optimized NLCs formulation released much more LCH (88.74±4.62) than the LCH-suspension (36.84±0.37%) in in-vitro drug release experiments lasting up to 24 hours. Ex vivo studies on the ability of LCH-NLCs to pass through the gut showed that drug permeation was much better than it was with plain LCH-solution. The in vivo pharmacodynamic analysis demonstrated that, compared to conventional LCH-suspension, NLCs released LCH more slowly and steadily over a longer time period. These findings provide additional evidence that NLCs have great promise as a drug delivery technology for the treatment of hypertension, just as they show promise as a controlled release formulation for the treatment of LCH.
血管选择性钙通道阻滞剂盐酸氯卡尼平(LCH)由于溶解度低和肝脏代谢,口服吸收率很低(生物利用度仅为 10%)。由于 LCH 的溶解度和渗透性较差,因此生物利用度很低且变化很大,稳定的水性液体制剂很难制造,药物的均匀分布几乎不可能实现。 本研究的目的是探讨是否可以采用开发纳米结构脂质载体(NLCs)的方法来创造一种有效、创新的 LCH 口服制剂。研究人员采用热均质-超声策略比较了几种合成和天然液态脂质的疗效。 通过热均质化和超声波处理进行初步改进后,利用方框-贝肯统计分析对LCH负载NLCs配方进行了微调。最佳的 LCHNLCs 成分包括硬脂酸和油酸脂相(2-4% w/v)、表面活性剂 poloxamer 188(1%)和 Tween 80(1%)以及其他成分。 优化后的 NLCs 配方的平均囊泡大小为 128.72±1.59 nm,多分散指数为 0.169±0.06,zeta 电位为 -36.81±0.42 mV,夹带效率为 79.84±0.11%。在长达 24 小时的体外药物释放实验中,优化的 NLCs 制剂释放的 LCH(88.74±4.62)远高于 LCH 悬浮液(36.84±0.37%)。对 LCH-NLCs 通过肠道能力的体内外研究表明,药物渗透性比普通 LCH 溶液好得多。体内药效学分析表明,与传统的 LCH 悬浮液相比,NLCs 释放 LCH 的速度更慢,且释放时间更长。 这些研究结果进一步证明,NLCs 作为一种治疗高血压的给药技术大有可为,正如它们作为一种治疗 LCH 的控释制剂大有可为一样。
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引用次数: 0
Challenges in Immunomodulation for Psoriasis: Recent Advancements and Need of Therapies 银屑病免疫调节疗法面临的挑战:最新进展和治疗需求
IF 0.6 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-11-24 DOI: 10.2174/0115748855274998231113110529
Dilpreet Singh
Psoriasis is a chronic immune-mediated skin disorder affecting millions worldwide. The pathogenesis of psoriasis involves dysregulated immune responses characterized by aberrant activation of T cells and proinflammatory cytokines. Immunomodulation has emerged as a promising therapeutic approach for managing psoriasis, aiming to restore immune homeostasis. However, despite significant advancements, challenges persist in developing effective immunomodulatory therapies. This abstract reviews recent developments in psoriasis immunomodulation, encompassing novel targets and therapeutic modalities. Advances in biologics targeting interleukins (IL) and their receptors, such as IL-17, IL-23, and IL-12/23, have demonstrated substantial clinical efficacy. Additionally, small molecules that inhibit Janus kinases (JAK) and phosphodiesterase 4 (PDE4) have shown promise in regulating immune responses. Despite these advancements, certain limitations hinder the success of immunomodulatory therapies. Treatment resistance, safety concerns, and high costs remain critical challenges. Furthermore, a deeper understanding of the complex immunopathogenesis of psoriasis is essential for developing targeted and personalized therapies. In conclusion, immunomodulation has revolutionized the management of psoriasis, offering remarkable improvements in patient outcomes. Continued research and innovative therapeutic strategies are needed to overcome current challenges and pave the way for more efficient, safe, and accessible treatments for psoriasis.
银屑病是一种由免疫介导的慢性皮肤病,影响着全球数百万人。银屑病的发病机制涉及以 T 细胞异常激活和促炎细胞因子为特征的免疫反应失调。免疫调节已成为治疗银屑病的一种很有前景的方法,其目的是恢复免疫平衡。然而,尽管取得了重大进展,但开发有效的免疫调节疗法仍面临挑战。本摘要回顾了银屑病免疫调节的最新进展,包括新的靶点和治疗模式。以白细胞介素(IL)及其受体(如IL-17、IL-23和IL-12/23)为靶点的生物制剂取得的进展已显示出巨大的临床疗效。此外,抑制 Janus 激酶 (JAK) 和磷酸二酯酶 4 (PDE4) 的小分子药物也显示出调节免疫反应的前景。尽管取得了这些进展,但某些局限性阻碍了免疫调节疗法的成功。耐药性、安全性问题和高昂的成本仍然是严峻的挑战。此外,深入了解银屑病复杂的免疫发病机制对于开发靶向和个性化疗法至关重要。总之,免疫调节已彻底改变了银屑病的治疗方法,显著改善了患者的治疗效果。我们需要继续研究和创新治疗策略,以克服当前的挑战,并为银屑病的更高效、更安全和更易获得的治疗铺平道路。
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引用次数: 0
Discerning the Multi-dimensional Role of Salicin: Bioactive Glycoside Beyond Analgesic: Different Perspectives 辨析水杨酸的多维作用:止痛之外的生物活性苷:不同视角
IF 0.6 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-11-22 DOI: 10.2174/0115748855272391231114042540
R. Pal, Y. Pal, M. Chaitanya, Avijit Mazumder, N. Khurana, Prabin Kumar Tharu
Salicin is a glycoside that can be found in several Salix and Populus species. Salicin is also connected to the glycoside populin, commonly known as benzoyl Salicin, in the Salicaceae tree barks. D-glucose is a component of the alcoholic glycoside Salicin (C13H18O7). The willow tree, as well as other trees like poplar and aspen, contains the natural chemical Salicin, which is a member of the salicylate family. Salicin is an anti-inflammatory and analgesic used in conventional medicine, and it served as the inspiration for the creation of aspirin. This molecule may have important human pharmacological actions that need to be considered in determining the efficacy and safety of willow herbal medicines. The extracts obtained from the bark of the tree, belonging to the Saliceae family in different solvents have been known for possessing many important medicinal values by potent pharmacological actions. The current effort deals with exquisite detailed aspects and concerns related to Salicin, which will be fruitful for the futuristic approaches to Salicin.
水杨苷是一种苷类化合物,存在于多种柳树和杨树中。水杨苷还与水杨科树皮中的苷类杨梅素(通常称为苯甲酰基水杨苷)有关。D-葡萄糖是醇苷水杨酸(C13H18O7)的成分之一。柳树以及杨树和杨树等其他树木都含有天然化学物质水杨素,它属于水杨酸盐家族。水杨素是传统医学中的一种消炎镇痛药,阿司匹林就是受它的启发而诞生的。这种分子可能具有重要的人体药理作用,在确定柳叶菜草药的有效性和安全性时需要加以考虑。从属于水杨科的柳树树皮中以不同溶剂提取的萃取物因其强大的药理作用而具有许多重要的药用价值。目前的研究涉及与水杨梅素有关的精致的细节方面和关注点,这将对水杨梅素的未来研究方法大有裨益。
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引用次数: 0
Unlocking the Potential of Drug Delivery Systems: A Comprehensive Review of Formulation Strategies and Technologies in the Field of Pharmaceutics 释放给药系统的潜能:全面回顾制药学领域的制剂策略和技术
IF 0.6 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2023-11-22 DOI: 10.2174/0115748855262877231114050949
Nitin Rajan, Shubham Kanaujiya
The creation of innovative drug delivery systems to enhance therapeutic effectiveness, safety, and patient compliance has resulted in considerable developments in pharmaceutics in recent years. The most recent formulation techniques and technologies are reviewed in this article to improve medication distribution and accomplish specific therapeutic goals. This article thoroughly summarizes the most recent formulation techniques and technologies used to enhance medication delivery and provide specific therapeutic effects. It discusses the variety of medication delivery methods, including nanoparticles, liposomes, micelles, and dendrimers, and explores the application of nanotechnology and biotechnology in drug delivery. Additionally, the paper emphasizes the significance of targeted drug delivery systems and their capacity to cross biological barriers including the blood-brain barrier and tumor microenvironment. The review also addresses the challenges faced in developing and commercializing drug delivery systems and suggests potential solutions to overcome them. Furthermore, the article emphasizes the role of computational modeling and simulation in designing and optimizing drug delivery systems. Overall, this review paper offers insightful information for pharmaceutics researchers, scientists, and practitioners that will help in the creation of novel drug delivery systems that improve patient outcomes and quality of life.
近年来,为提高治疗效果、安全性和患者依从性而开发的创新给药系统在制药学领域取得了长足的发展。本文综述了最新的制剂技术和工艺,以改善药物分布并实现特定的治疗目标。本文全面总结了用于改善给药和提供特定治疗效果的最新制剂技术。文章讨论了各种给药方法,包括纳米颗粒、脂质体、胶束和树枝状分子,并探讨了纳米技术和生物技术在给药方面的应用。此外,论文还强调了靶向给药系统的重要性及其穿越生物屏障(包括血脑屏障和肿瘤微环境)的能力。这篇综述还探讨了药物递送系统的开发和商业化所面临的挑战,并提出了克服这些挑战的潜在解决方案。此外,文章还强调了计算建模和模拟在设计和优化给药系统中的作用。总之,这篇综述论文为制药学研究人员、科学家和从业人员提供了具有洞察力的信息,有助于创造新型给药系统,改善患者的治疗效果和生活质量。
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Current Drug Therapy
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