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Role of Artificial Intelligence in Drug Discovery to Revolutionizethe Pharmaceutical Industry: Resources, Methods and Applications 人工智能在药物发现中的作用将彻底改变制药业:资源、方法和应用
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-03-21 DOI: 10.2174/0118722083297406240313090140
P. Singh, Kapil Sachan, Vishal Khandelwal, Sumita Singh, Smita Singh
Traditional drug discovery methods such as wet-lab testing, validations, andsynthetic techniques are time-consuming and expensive. Artificial Intelligence (AI) approacheshave progressed to the point where they can have a significant impact on thedrug discovery process. Using massive volumes of open data, artificial intelligencemethods are revolutionizing the pharmaceutical industry. In the last few decades, manyAI-based models have been developed and implemented in many areas of the drug developmentprocess. These models have been used as a supplement to conventional researchto uncover superior pharmaceuticals expeditiously. Drug research and developmentto repurposing and productivity benefits in the pharmaceutical business throughclinical trials. AI is studied in this article for its numerous potential uses. We have discussedhow AI can be put to use in the pharmaceutical sector, specifically for predicting adrug's toxicity, bioactivity, and physicochemical characteristics, among other things. Inthis review article, we have discussed its application to a variety of problems, includingde novo drug discovery, target structure prediction, interaction prediction, and binding affinityprediction. AI for predicting drug interactions and nanomedicines were also considered.
传统的药物发现方法,如湿实验室测试、验证和合成技术,既耗时又昂贵。人工智能(AI)方法已经发展到可以对药物发现过程产生重大影响的地步。利用海量开放数据,人工智能方法正在彻底改变制药行业。在过去的几十年里,许多基于人工智能的模型已经被开发出来,并在药物开发过程的许多领域得到了应用。这些模型被用作传统研究的补充,以迅速发现优质药品。从药物研发到再利用,再到通过临床试验为制药企业带来生产效益。本文研究了人工智能的众多潜在用途。我们讨论了如何将人工智能用于制药领域,特别是用于预测药物的毒性、生物活性和理化特性等。在这篇综述文章中,我们讨论了人工智能在各种问题上的应用,包括新药发现、靶点结构预测、相互作用预测和结合亲和力预测。此外,还考虑了用于预测药物相互作用和纳米药物的人工智能。
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引用次数: 0
Development of a Novel Peptide with RGD Tumor Homing Motif: Evaluation of its Anticancer Potential in Hepatocellular Carcinoma and Colon Cancer Cells 开发具有 RGD 肿瘤归巢基团的新型多肽:评估其在肝细胞癌和结肠癌细胞中的抗癌潜力
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-03-20 DOI: 10.2174/0118722083300452240315035722
Reda Abdallah Mohamed, Ohoud M. Marie, Dahlia I. Badran, O. Hammam, Hend Okasha
Peptide-based therapy has emerged as a promising avenue fortreating various disorders, and recent research has highlighted the potential of anti-cancerpeptides (ACPs) in cancer treatment. In this context, this study aimed to design a novelpeptide incorporating a tumor-homing peptide (RGD) and C-amidation to enhance its anticanceractivity, particularly against liver (HepG2) and colon (HCT-116) cancer cell lines.The primary objective was to design a peptide with improved anticancerproperties by leveraging the tumor-homing capabilities of RGD and enhancing its activitythrough C-amidation. The study sought to evaluate the cytotoxicity of the designedpeptide against red blood cells (RBCs) and normal Vero cells. Furthermore, the anticancerefficacy of the peptide was assessed in hepatocellular carcinoma (HepG2) and coloncancer (HCT-116) cell lines. The specific objectives included examining the apoptoticinduction and morphological changes in treated cells compared to untreated cells.The peptide was designed using the ACPred-FL bioinformatics tool, and itscytotoxicity was assessed through hemolysis assays against RBCs and normal Vero cells.Anticancer activity was evaluated against HepG2 and HCT-116 cell lines. The analysisof apoptotic induction involved measuring the relative gene expression of oncogenicmarker BCL2 and apoptotic markers (BAX, BID, CAS-8). Additionally, Cytopathologicalexamination and Western Blot analysis were employed to study morphologicalchanges and confirm the quantification of relevant markers.The designed peptide, consisting of twelve amino acids with a molecular massof 1230.6233 Da and an isoelectric point of 9.81, exhibited low erythrocyte lysis andminimal toxicity to normal cells. The IC50 values demonstrated significant anticanceractivity against both HepG2 (36.49±2.6 μg/mL) and HCT-116 (11.03±2.5 μg/mL) celllines. Treated cells exhibited a significant decrease in the oncogenic marker BCL2 and anupregulation of apoptotic markers (BAX, BID, CAS-8). Western Blot analysis confirmedthese findings, and Cytopathological examination revealed scattered apoptotic and degenerativechanges.The designed peptide displayed remarkable anticancer activity againsthepatocellular carcinoma and colon cancer cell lines, effectively modulating apoptoticand oncogenic markers. These findings highlight the potential of the peptide as a therapeuticagent for cancer treatment, emphasizing its clinical significance in combating liverand colon cancers. Nonetheless, further research and development are warranted to explorethe translational potential of this peptide in clinical settings.
基于肽的疗法已成为治疗各种疾病的一种前景广阔的途径,最近的研究强调了抗癌肽(ACPs)在癌症治疗中的潜力。在此背景下,本研究旨在设计一种新型多肽,该多肽结合了肿瘤定位肽(RGD)和C-酰胺化,以增强其抗癌活性,尤其是针对肝癌(HepG2)和结肠癌(HCT-116)细胞系的抗癌活性。研究试图评估所设计的多肽对红细胞(RBC)和正常 Vero 细胞的细胞毒性。此外,还评估了该肽在肝癌(HepG2)和结肠癌(HCT-116)细胞系中的抗癌功效。该多肽是利用 ACPred-FL 生物信息学工具设计的,其毒性通过针对红细胞和正常 Vero 细胞的溶血试验进行评估。凋亡诱导分析包括测量致癌标记物 BCL2 和凋亡标记物(BAX、BID、CAS-8)的相对基因表达。所设计的肽由 12 个氨基酸组成,分子质量为 1230.6233 Da,等电点为 9.81,红细胞裂解率低,对正常细胞的毒性极小。其 IC50 值显示了对 HepG2(36.49±2.6 μg/mL)和 HCT-116 (11.03±2.5 μg/mL)细胞系的显著抗癌活性。经处理的细胞表现出致癌标记物 BCL2 的显著下降和凋亡标记物(BAX、BID、CAS-8)的上调。所设计的多肽对肝细胞癌和结肠癌细胞系具有显著的抗癌活性,能有效调节细胞凋亡和致癌标志物。这些发现凸显了多肽作为癌症治疗剂的潜力,强调了它在抗击肝癌和结肠癌方面的临床意义。尽管如此,仍需进一步研究和开发,以挖掘该肽在临床中的转化潜力。
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引用次数: 0
Patents Selections 专利选择
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-03-01 DOI: 10.2174/187220831801231013004218
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引用次数: 0
Meet the Editorial Board Member 认识编辑委员会成员
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-03-01 DOI: 10.2174/187220831801231012235532
Younes Ghasemi
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引用次数: 0
Construction of Camelus dromedaries Immune Single Domain Antibodies Library for Development of Schistosoma mansoni Specific Nanobodies Using Phage Display Strategy 利用噬菌体展示策略构建用于开发曼氏血吸虫特异性纳米抗体的骆驼免疫单域抗体库
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-01-29 DOI: 10.2174/0118722083275669231227063413
Hadeer Adel El-Kalamawy, Mohamed Awwad, Tarek Diab, Hend Okasha, Amal M. Abdel-Kareim, M. Marawan, Salma A. Shoulah, E. El-Dabaa
Schistosoma mansoni poses a considerable global public healthchallenge. In Egypt, approximately 60% of the inhabitants in the Northern and Easternareas of the Nile Delta are affected by this parasite, whereas the Southern region experiencesa significantly lower infection rate of 6%.Schistosoma (S.) mansoni infect 60% of the population in the Northern and Eastern parts of the Nile Delta and only 6% in the Southern part. Therefore, seeking for cost effective, sensitive and specific diagnostic tool for rapid detection of S. mansoni is necessary. Variable domains of camelid heavy-chain antibodies (VHHs) which are known as nanobodies (Nb) are approximately 15 kDa in size with high affinity to their antigens. Phage display technology was used in construction of Nbs library based on the camelid VHH framework for selection of S. mansoni specific NbsConstruction of an immune phage display Nbs library based on the VHH frameworkfor selecting S. mansoni-specific Nbs for seeking cost-effective, sensitive, and specificdiagnostic tools for rapidly detecting Schistosoma mansoni.Camel was immunized using soluble adult worm antigens (SAWP) for the productionof Variable domains of heavy chains of camelid heavy-chain only antibodies(VHHs), which are known as nanobodies (Nb). The PBMCs repertoires VHH sequenceslibrary have been constructed with a high percentage of insertion and right orientation usingpADL-23c phagmid and M13 phage followed by three rounds of bio-panning againstSAWP using phage display technique. Evaluations using polyclonal phage ELISA andother techniques have been carried out to reveal the successful enrichment of anti-SAWPNbs (VHH) clones. Evaluation of the diagnostic potentiality of these Nbs was carried outusing ELISA on human serum samples confirmed for S. mansoni infection. Receiver Operatorof Characteristics (ROC) curve analysis was used for discrimination between S.mansoni infection and both negative controls and the Fasciola hepatica group.Using monoclonal ELISA, Nbs of 22 clones out of 24 selected clones showedbinding affinity to SAWP. The cutoff values of the produced anti-S. mansoni Nbs was >0.19, leading to 80% sensitivity, 95% specificity, and 90% accuracy. Sequence analysis ofthree of these Nbs with high binding affinities showed diversity in their targets, consideringtheir CDR3 aa sequences.Using monoclonal ELISA, Nbs of 22 clones out of 24 selected clones showed binding affinity to SAWP. Sequence analysis of three of these Nbs with high binding affinities showed diversity in their targets considering their CDR3 aa sequences.This study successfully produced high diversity, anti-S.mansoni VHHs enrichedphage library and the generated nanobodies have high diagnostic potential for S.mansoni infection in human patients.We had successfully constructed high diversity VHH immune library against S. mansoni SAWP which can be efficiently used to develop anti-S. mansoni Nbs for diagnosis.
曼氏血吸虫对全球公共卫生构成了巨大挑战。在埃及,尼罗河三角洲北部和东部地区约有 60% 的居民受到这种寄生虫的影响,而南部地区的感染率要低得多,仅为 6%。因此,有必要寻找成本效益高、灵敏且特异的诊断工具来快速检测曼氏血吸虫。驼科动物重链抗体(VHHs)的可变结构域被称为纳米抗体(Nb),大小约为 15 kDa,对其抗原具有高亲和力。噬菌体展示技术被用于构建基于驼科动物 VHH 框架的 Nbs 库,以筛选曼森氏杆菌特异性 Nbs。使用可溶性成虫抗原(SAWP)对骆驼进行免疫,以生产驼科动物重链唯一抗体(VHHs)重链的可变域,这种抗体被称为纳米抗体(Nb)。利用pADL-23c噬菌体和M13噬菌体构建了具有高插入率和正确方向的PBMCs Reppertoires VHH序列库,然后利用噬菌体展示技术针对SAWP进行了三轮生物筛选。使用多克隆噬菌体酶联免疫吸附试验(ELISA)和其他技术进行了评估,结果显示成功地富集了抗SAWPNbs(VHH)克隆。对这些 Nbs 的诊断潜力的评估是在确认感染曼森氏杆菌的人类血清样本上使用 ELISA 进行的。利用单克隆酶联免疫吸附法,在筛选出的 24 个克隆中,有 22 个克隆的 Nbs 显示出与 SAWP 的结合亲和力。通过单克隆酶联免疫吸附试验(ELISA),24 个克隆中有 22 个克隆的 Nbs 与 SAWP 有亲和力,所产生的抗 S. mansoni Nbs 的临界值大于 0.19,灵敏度为 80%,特异度为 95%,准确度为 90%。通过单克隆酶联免疫吸附试验(ELISA),在筛选出的24个克隆中,有22个克隆的Nbs显示出与SAWP的结合亲和力。这项研究成功地建立了高分辨率的抗曼氏沙门氏菌VHHs富集噬菌体文库,所产生的纳米抗体对人类患者的曼氏沙门氏菌感染具有很高的诊断潜力。
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引用次数: 0
Designing a Secretory form of RTX-A as an Anticancer Toxin: AnIn Silico Approach 设计一种分泌型 RTX-A 作为抗癌毒素:硅学方法
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-01-08 DOI: 10.2174/0118722083267796231210060150
Mortaza Taheri‐Anganeh, Navid Nezafat, S. Gharibi, S. H. Khatami, Farzaneh Vahedi, Zahra Shabaninejad, Marzieh Asadi, A. Savardashtaki, A. Movahedpour, Hassan Ghasemi
Cancer is a leading cause of death and a significant public healthissue worldwide. Standard treatment methods such as chemotherapy, radiotherapy, andsurgery are only sometimes effective. Therefore, new therapeutic approaches are neededfor cancer treatment. Sea anemone actinoporins are pore-forming toxins (PFTs) withmembranolytic activities. RTX-A is a type of PFT that interacts with membrane phospholipids, resulting in pore formation. The synthesis of recombinant proteins in a secretoryform has several advantages, including protein solubility and easy purification. In thisstudy, we aimed to discover suitable signal peptides for producing RTX-A in Bacillussubtilis in a secretory form.Signal peptides were selected from the Signal Peptide Web Server. The probability and secretion pathways of the selected signal peptides were evaluated using theSignalP server. ProtParam and Protein-sol were used to predict the physico-chemicalproperties and solubility. AlgPred was used to predict the allergenicity of RTX-A linkedto suitable signal peptides. Non-allergenic, stable, and soluble signal peptides fused toproteins were chosen, and their secondary and tertiary structures were predicted usingGOR IV and I-TASSER, respectively. The PROCHECK server performed the validationof 3D structures.According to bioinformatics analysis, the fusion forms of OSMY_ECOLI andMALE_ECOLI linked to RTX-A were identified as suitable signal peptides. The finalproteins with signal peptides were stable, soluble, and non-allergenic for the human body.Moreover, they had appropriate secondary and tertiary structures.The signal above peptides appears ideal for rationalizing secretory and soluble RTX-A. Therefore, the signal peptides found in this study should be further investigated through experimental research.
癌症是导致死亡的主要原因之一,也是全球重要的公共卫生问题。标准的治疗方法,如化疗、放疗和手术,只是有时有效。因此,癌症治疗需要新的治疗方法。海葵肌动蛋白是一种具有膜溶解活性的孔形成毒素(PFTs)。RTX-A 是一种与膜磷脂相互作用导致孔隙形成的 PFT。以分泌物形式合成重组蛋白具有多种优势,包括蛋白可溶性和易于纯化。在这项研究中,我们的目标是发现适合于在芽孢杆菌中以分泌形式生产 RTX-A 的信号肽。从信号肽网络服务器上选择信号肽,使用信号肽服务器(SignalP)评估所选信号肽的可能性和分泌途径。ProtParam 和 Protein-sol 用于预测信号肽的物理化学性质和溶解度。AlgPred 用于预测 RTX-A 与合适信号肽连接后的过敏性。选择了与蛋白质融合的非过敏性、稳定和可溶性信号肽,并分别使用 GOR IV 和 I-TASSER 预测了它们的二级和三级结构。根据生物信息学分析,OSMY_ECOLI和MALE_ECOLI与RTX-A的融合形式被确定为合适的信号肽。带有信号肽的最终蛋白质稳定、可溶、对人体无过敏性,而且具有适当的二级和三级结构。因此,本研究发现的信号肽应通过实验研究进行进一步研究。
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引用次数: 0
Exploring Trachyspermum ammi and Foeniculum vulgare in Hydroponic System and Compare its Chemical Constituents with Soil-Based Method: A Prospective in Agriculture. 水培系统中羊草和小茴香的研究及其化学成分与土壤法的比较研究:农业应用前景
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-01-01 DOI: 10.2174/1872208317666230601104843
Shilpa Debnath, Alok Sharma

Background: The forthcoming problems will be of food, and soil due to environmental alteration, growing populations, pollution, and exhaustion of natural resources among other factors. Hydroponic farming has the capacity to alleviate the intimidation of these con-cerned issues in the agricultural system. Hydroponics is recommended as an alternative way to enhance product yield compared to conventional agriculture.

Objective: The present study aimed to determine the different growth parameters and constituents of soil-grown and hydroponically grown Trachyspermum ammi and Foeniculum vulgare for the first time, which could be a patentable in future.

Methods: In this study, extraction was carried out by maceration method using methanol as a solvent whereas, growth parameters were performed by the leaves number, plant height, and leaf area. Chlorophyll content was also performed in both sources. Further, a comparison of chemical constituents from different sources was analyzed by GC-MS.

Results: The bioactive components in hydroponically grown T. ammi were found more as compared to soil-grown T. ammi. The GC-MS analysis revealed the presence of various compounds in the methanolic extract of plant materials.

Conclusion: Hence, hydroponics could be an alternative in agriculture and this system is now accepted globally. This method provides diverse perspectives for farmers to harvest high-yield, better quality, and enhanced bioactive compounds.

由于环境变化、人口增长、污染和自然资源枯竭等因素,即将出现的问题将与粮食和土壤有关。水培农业有能力减轻农业系统中这些相关问题的威胁。与传统农业相比,水培是提高产品产量的一种替代方式。本研究首次测定了土栽和水培Trachyspermum amm和Foeniculum vulgare的不同生长参数和成分。在本研究中,以甲醇为溶剂,通过浸渍法进行提取,而生长参数则通过叶数、株高和叶面积进行。两种来源的叶绿素含量也进行了测定。此外,通过GC-MS对不同来源的化学成分进行了比较分析。水培T.ammi中的生物活性成分比土壤种植T.ammi更多。GC-MS分析揭示了植物材料的甲醇提取物中存在各种化合物。因此,水培可能是农业的一种替代方案,这种系统现在已被全球接受。这种方法为农民收获高产、优质和增强生物活性的化合物提供了不同的视角。
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引用次数: 0
Nano Lipid Carriers as a Promising Drug Delivery Carrier for Neurodegenerative Disorders - An Overview of Recent Advances. 纳米脂质载体作为神经退行性疾病的一种有前途的药物递送载体-最新进展综述
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-01-01 DOI: 10.2174/1872208317666230320164219
Vishal Kumar, Sreeja C Nair

The last few decades have seen a rise in the number of deaths caused by neurological disorders. The blood-brain barrier (BBB), which is very complex and has multiple mechanisms, makes drug delivery to the brain challenging for many scientists. Lipid nanoparticles (LNPs) such as nanoemulsions, solid-lipid nanoparticles, liposomes, and nano lipid carriers (NLCs) exhibit enhanced bioavailability and flexibility among these nanocarriers. NLCs are found to be very effective. In the last few decades, they have been a center of attraction for controlled drug delivery. According to the current global status of specific neurological disorders, out of all LNPs, NLC significantly reduces the cross-permeability of drugs through the BBB due to their peculiar properties. They offer a host of advantages over other carriers because of their biocompatibility, safety, non-toxicity, non-irritating behavior, stability, high encapsulation efficiency, high drug loading, high drug targeting, control of drug release, and ease in manufacturing. The biocompatible lipid matrix is ideally suited as a drug carrier system due to the nano-size range. For certain neurological conditions such as Parkinsonism, Alzheimer's, Epilepsy, Multiple sclerosis, and Brain cancer, we examined recent advances in NLCs to improve brain targeting of bioactive with special attention to formulation aspects and pharmacokinetic characteristics. This article also provides a brief overview of a critical approach for brain targeting, i.e., direct nose-to-brain drug delivery and some recent patents published on NLC".

在过去的几十年里,由神经系统疾病引起的死亡人数有所上升。血脑屏障(BBB)非常复杂,具有多种机制,使药物输送到大脑对许多科学家来说具有挑战性。脂质纳米颗粒(LNPs),如纳米乳液、固体脂质纳米颗粒、脂质体和纳米脂质载体(nlc)在这些纳米载体中表现出更高的生物利用度和灵活性。研究发现,非NLCs非常有效。在过去的几十年里,它们一直是控制药物输送的中心。根据目前全球特定神经系统疾病的现状,在所有LNPs中,NLC由于其特殊的性质,显著降低了药物通过血脑屏障的交叉通透性。与其他载体相比,它们具有生物相容性、安全性、无毒性、无刺激性、稳定性、高包封效率、高载药量、高靶向性、药物释放控制和易于制造等优点。由于纳米尺寸范围,生物相容性脂质基质非常适合作为药物载体系统。对于某些神经系统疾病,如帕金森病、阿尔茨海默病、癫痫、多发性硬化症和脑癌,我们研究了NLCs的最新进展,以改善生物活性的脑靶向性,并特别关注配方方面和药代动力学特征。本文还简要介绍了脑靶向治疗的一种关键方法,即直接从鼻子到大脑给药。
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引用次数: 0
Role of Algal-derived Bioactive Compounds in Human Health. 藻类生物活性化合物在人类健康中的作用。
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-01-01 DOI: 10.2174/1872208317666230623141740
Gyanendra Tripathi, Priyanka Dubey, Suhail Ahmad, Alvina Farooqui, Vishal Mishra

Algae is emerging as a bioresource with high biological potential. Various algal strains have been used in traditional medicines and human diets worldwide. They are a rich source of bioactive compounds like ascorbic acid, riboflavin, pantothenate, biotin, folic acid, nicotinic acid, phycocyanins, gamma-linolenic acid (GLA), adrenic acid (ARA), docosahexaenoic acid (DHA), eicosapentaenoic acid (EPA), etc. Beta-carotene, astaxanthin, and phycobiliproteins are different classes of pigments that are found in algae. They possess antioxidant, anti-inflammatory and anticancer properties. The sulfur-coated polysaccharides in algae have been used as an anticancer, antibacterial, and antiviral agent. Scientists have exploited algal-derived bioactive compounds for developing lead molecules against several diseases. Due to the surge in research on bioactive molecules from algae, industries have started showing interest in patenting for the large-scale production of bioactive compounds having applications in sectors like pharmaceuticals, food, and beverage. In the food industry, algae are used as a thickening, gelling, and stabilizing agent. Due to their gelling and thickening characteristics, the most valuable algae products are macroalgal polysaccharides such as agar, alginates, and carrageenan. The high protein, lipid, and nutrient content in microalgae makes it a superfood for aquaculture. The present review aims at describing various non-energy-based applications of algae in pharmaceuticals, food and beverage, cosmetics, and nutraceuticals. This review attempts to analyze information on algal-derived drugs that have shown better potential and reached clinical trials.

藻类是一种新兴的生物资源,具有很高的生物潜力。各种藻类菌株已被用于世界各地的传统医药和人类饮食中。它们是抗坏血酸、核黄素、泛酸、生物素、叶酸、烟酸、藻蓝蛋白、γ-亚麻酸(GLA)、肾上腺酸(ARA)、二十二碳六烯酸(DHA)、二十碳五烯酸(EPA)等生物活性化合物的丰富来源。β-胡萝卜素、虾青素和藻蓝蛋白是藻类中不同种类的色素。它们具有抗氧化、抗炎和抗癌特性。藻类中的硫涂层多糖已被用作抗癌、抗菌和抗病毒剂。科学家们利用从藻类中提取的生物活性化合物来开发抗多种疾病的先导分子。由于对藻类生物活性分子的研究激增,各行业开始对大规模生产生物活性化合物的专利表现出兴趣,这些化合物可应用于制药、食品和饮料等行业。在食品行业,藻类被用作增稠剂、胶凝剂和稳定剂。由于其胶凝和增稠特性,最有价值的藻类产品是大型藻类多糖,如琼脂、海藻酸盐和卡拉胶。微藻中的高蛋白、高脂和高营养成分使其成为水产养殖的超级食品。本综述旨在介绍藻类在制药、食品饮料、化妆品和营养保健品方面的各种非能源应用。本综述试图分析有关藻类衍生药物的信息,这些药物已显示出较好的潜力并已进入临床试验阶段。
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引用次数: 0
Potentials of Stem Cell Therapy in Patients Infected with COVID- 19: A Systematic Review. 干细胞疗法在 COVID- 19 感染者中的应用潜力:系统综述。
Q3 Biochemistry, Genetics and Molecular Biology Pub Date : 2024-01-01 DOI: 10.2174/1872208317666230818092522
Zahra Tamis, Fatemeh Sadeghi, Aigin Heydari, Saima Shahzad Mirza, Mohammad Hossein Morowvat

Introduction: In the present study, we have examined different aspects and potentials of stem cells for the management of patients infected with COVID-19.

Background: The novel coronavirus disease (COVID-19) has been reported in most of the countries and territories (>230) of the world with .686 million confirmed cases (as of Apr. 22, 2023). While the scientific community is working to develop vaccines and develop drugs against the COVID-19 pandemic, novel alternative therapies may reduce the mortality rate. Recently, the application of stem cells for critically ill COVID-19 patients in a small group of patients has been examined.

Methods: We searched PubMed, Web of Science, and Google Scholar up to July 2022. Those studies that reviewed COVID-19 and cell therapy potentials were entered into the study. Moreover, some recently published patents were exploited and reviewed. Patentscope, USPTO, Espacenet, Free Patents Online, and Google Patents were used for patent searches.

Results: Cell-based therapy as a modality of regenerative medicine is considered one of the most promising disciplines in the fields of modern science and medicine. Such an advanced technology offers endless possibilities for transformative and potentially curative treatments for some of the most life-threatening diseases. This therapeutic tool can be useful to reduce the rate of mortality. There have been several published patents for different stem cell therapy platforms in recent years.

Conclusion: Stem cell therapy could be considered a safe and effective therapeutic strategy to reduce death cases in patients infected with COVID-19. Besides, stem cell therapy might increase the pulmonary functions in the patients, it suppresses the occurring inflammations and ameliorates the symptoms.

简介在本研究中,我们研究了干细胞治疗COVID-19感染者的不同方面和潜力:新型冠状病毒病(COVID-19)已在全球大多数国家和地区(超过230个)报告,确诊病例达6.86亿例(截至2023年4月22日)。尽管科学界正在努力开发疫苗和药物来应对 COVID-19 大流行,但新型替代疗法可能会降低死亡率。最近,研究人员对一小部分 COVID-19 重症患者应用干细胞进行了研究:我们搜索了截至 2022 年 7 月的 PubMed、Web of Science 和 Google Scholar。方法:我们检索了截至 2022 年 7 月的 PubM、Web Science 和谷歌学术,其中包括对 COVID-19 和细胞疗法潜力进行了综述的研究。此外,我们还利用并审查了一些近期发表的专利。专利检索使用了Patentscope、美国专利商标局、Espacenet、免费专利在线和谷歌专利:结果:细胞疗法作为一种再生医学模式,被认为是现代科学和医学领域最有前途的学科之一。这种先进的技术为治疗一些威胁生命的疾病提供了无限的可能性。这种治疗工具可以有效降低死亡率。近年来,不同的干细胞疗法平台已公布了多项专利:结论:干细胞疗法可被视为一种安全有效的治疗策略,可减少COVID-19感染者的死亡病例。此外,干细胞疗法可增强患者的肺功能,抑制炎症,改善症状。
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Recent patents on biotechnology
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