International Journal of Drug Delivery Technology最新文献

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Chemometric Assisted UV-Spectrophotometric Quantification of Tigecycline in Parenteral Dosage Form 化学计量辅助紫外分光光度法测定替加环素非肠外剂型的含量
International Journal of Drug Delivery Technology Pub Date : 2023-09-25 DOI: 10.25258/ijddt.13.3.33
Kirtimaya Mishra, A Dash, A Jabeen, S Vegesna, SK Sahoo, V Gupta, D Jena
{"title":"Chemometric Assisted UV-Spectrophotometric Quantification of Tigecycline in Parenteral Dosage Form","authors":"Kirtimaya Mishra, A Dash, A Jabeen, S Vegesna, SK Sahoo, V Gupta, D Jena","doi":"10.25258/ijddt.13.3.33","DOIUrl":"https://doi.org/10.25258/ijddt.13.3.33","url":null,"abstract":"Relating to the current study, the quality by design (QbD) concept is used for creating and validating an unique, resilient, accurate, and reliable spectrophotometric approach to quantify Tigecycline (TIG) in injections. Fractional factorial design (FFD) was a design implemented to screen the initial parameters. Moreover, the variables went through the central composite design (CCD) to assess the dependency and optimize the design. Several measures were analyzed statistically to determine the appropriateness of the data obtained from the experiments. At 250 nm, by the use of ethanol, TIG displays an absorption maximum. Variables like screening, slit-width, and sampling interval were recognized as critical method and again, evaluation was done by a CCD. A good linearity was produced for TIG within a range of 2 to 12 μg/mL, with R2 less than 0.999. The process was determined to be perfect, having a good average percent recovery (greater than 100%). According to ICH guidelines, validation of the developed method was performed. By the implementation of QbD principles, spectrophotometric techniques were created and planned to, integrate the qualities into the methods. These processes were manifested for being flexible and pertinent for identifying TIG in pharmaceutical dose regimens.","PeriodicalId":13851,"journal":{"name":"International Journal of Drug Delivery Technology","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135866586","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
Antioxidant Role of Methionine: As an Essential Sulfur-containing Amino Acids 蛋氨酸的抗氧化作用:作为必需的含硫氨基酸
International Journal of Drug Delivery Technology Pub Date : 2023-09-25 DOI: 10.25258/ijddt.13.3.38
Samera M Alkatib, Ahmed M Zaki, May Kh Ismail, Raghad Kh Alsarraf
{"title":"Antioxidant Role of Methionine: As an Essential Sulfur-containing Amino Acids","authors":"Samera M Alkatib, Ahmed M Zaki, May Kh Ismail, Raghad Kh Alsarraf","doi":"10.25258/ijddt.13.3.38","DOIUrl":"https://doi.org/10.25258/ijddt.13.3.38","url":null,"abstract":"Methionine is one of the essential sulfur-containing amino acids that are used in building proteins. In the body, methionine condenses with ATP to form S-adenosylmethionine (SAM), which acts as a methylation donor in various biological pathways. Methionine is characterized by its antioxidant activity and its ability to modify tissue sensitivity against oxidizing agents. Therefore, this study’s aim included using hydrogen peroxide 0.5% in drinking water to induce oxidative stress in the male rats and testing the ability of different concentrations of methionine for protection or prevention the oxidative stress during 10, 20 and 30 days. Forty male rats with the age of 3-4 months and of weights ranging between 300 to 400 gm were divided into 4 groups: Group (1): control group received drinking tap water, group (2): treated with H2O2 0.5% in drinking water, group (3): treated with H2O2 and methionine 0.3%, group (4): treated with H2O2 and methionine 0.6%. The following parameters in the serum were measured: Vit. C, Vit. E, peroxynitrite, albumin, selenium, zinc, and copper. Treatment with 0.3% methionine produced clear effects on the vit C, peroxynitrite, Zn and Cu levels in the serum, while the treatment with 0.6% methionine produced clear effects on the serum vit E, albumin, and Se levels","PeriodicalId":13851,"journal":{"name":"International Journal of Drug Delivery Technology","volume":"14 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135866870","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
Organic Extraction, Purification and Evaluation of Long Chain Fatty Alcohol from Saccharum officinarum of Sugar Refinery Waste for Human Wellness 制糖厂废糖中长链脂肪醇的有机提取、纯化及对人体健康的评价
International Journal of Drug Delivery Technology Pub Date : 2023-09-25 DOI: 10.25258/ijddt.13.3.14
Singh A.K, Kharb R, Kandpal J.B
{"title":"Organic Extraction, Purification and Evaluation of Long Chain Fatty Alcohol from Saccharum officinarum of Sugar Refinery Waste for Human Wellness","authors":"Singh A.K, Kharb R, Kandpal J.B","doi":"10.25258/ijddt.13.3.14","DOIUrl":"https://doi.org/10.25258/ijddt.13.3.14","url":null,"abstract":"The current study has explored an extraction and purification method for 1-octacosanol from sugarcane waste, commonly known as press mud, through the application of SCFE by the unique concept of solid-solid and liquid-liquid extraction which increases content and decreases impurity which is an extra advantage at purification stage by help of green solvent instead any carcinogenic solvent, which reduce process time, increase content and environment friendly. The isolated compounds were characterized by gas chromatography-flame ionization detection, which shows 50% content of octacosanol in the final product. Novel refinement technique through hot ethanolic reflux method has substantially increased the octacosanol assay to ≥ 50% with more than 67% purity from the crude wax assay of 26% obtained by the current method of extraction. The identity of said compound was further authenticated by X-ray diffraction (XRD), Diffraction scanning calorimetry (DSC) and FTIR studies. The purity of the octacosanol obtained was ≤70% and the conversion recovery of octacosanol was 80.04% by the reflux method, thereby representing the simplicity of the above process for industrial feasibility. The current process represents a value addition liquid-liquid supercritical extraction with a time-saving, cost-effective, reproducible, newer, green, safe, and sustainable technology valorizing sugarcane waste for a high-end nutraceutical","PeriodicalId":13851,"journal":{"name":"International Journal of Drug Delivery Technology","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135866873","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
Novel Synthesis, Physicochemical Characterization of 1,3,4-Oxadiazinoindole Derivatives for the Purpose of Antidepressant Activity 以抗抑郁活性为目的的1,3,4-恶二嗪吲哚衍生物的新合成及理化表征
International Journal of Drug Delivery Technology Pub Date : 2023-09-25 DOI: 10.25258/ijddt.13.3.26
Mahadev Agarwal, Neelam Singla, S.K Singh
{"title":"Novel Synthesis, Physicochemical Characterization of 1,3,4-Oxadiazinoindole Derivatives for the Purpose of Antidepressant Activity","authors":"Mahadev Agarwal, Neelam Singla, S.K Singh","doi":"10.25258/ijddt.13.3.26","DOIUrl":"https://doi.org/10.25258/ijddt.13.3.26","url":null,"abstract":"The present study synthesized a series of 1,3,4-oxadiazinoindole moiety-containing compounds by combining MAOI’s hydrazide moiety and tricyclic moiety having antidepressant activity. The formation of amino acid chloride from amino acids started the synthesis. Further, they were converted into amino acid hydrazide, and then amino acid hydrazones were prepared by reaction of amino acid hydrazide with isatin. Finally, cyclization was acted on hydrazone-containing compounds in the presence of cold H2SO4. Synthesized compounds are characterized and confirmed via mass spectroscopy, 1H-nuclear magnetic resonance strategies, fourier transform infrared spectroscopy, thin layer chromatography, and melting point. The compounds were evaluated for antidepressant activity.","PeriodicalId":13851,"journal":{"name":"International Journal of Drug Delivery Technology","volume":"53 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135867686","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
Synthesis and Molecular Docking Studies of New Pyrimidinone ring Containing 1,2,3-Triazole Derivatives 含1,2,3-三唑类新型嘧啶环的合成及分子对接研究
International Journal of Drug Delivery Technology Pub Date : 2023-09-25 DOI: 10.25258/ijddt.13.3.39
Ahmed A Kozan, Riyadh J Nahi
{"title":"Synthesis and Molecular Docking Studies of New Pyrimidinone ring Containing 1,2,3-Triazole Derivatives","authors":"Ahmed A Kozan, Riyadh J Nahi","doi":"10.25258/ijddt.13.3.39","DOIUrl":"https://doi.org/10.25258/ijddt.13.3.39","url":null,"abstract":"The current work describes the design, synthesis and molecular mocking studies of a series of new 1,4-disubstituted-1,2,3-triazole linked 2-pyrimidinone derivatives. Firstly, 4-(4-acetyl-5-methyl-1H-1,2,3-triazol-1-yl)benzene sulfonic acid 1 was synthesized as a key starting material. This compound was reacted with a series of aromatic aldehydes under-investigated conditions to give a new series of chalcones 2a-f. Reaction of compounds 2a-f with urea in the presence of an aqueous solution of sodium hydroxide led to the construct 2-pyrimidinone ring system to obtain a series of new compounds containing 1,2,3-triaozle ring and pyrimidinone ring 3a-f. The newly synthesized compounds 2a-f and 3a-f were characterized by FT-IR, 1H-NMR and 13C-NMR spectra. In-silico molecular docking simulations, compounds 3a-f and their precursors 2a-f were conducted on two selected proteins: 7dpp and 8cx9. The results revealed that all of the newly synthesized compounds 2a-f and 3a-f displayed have a good binding affinity with the target proteins and higher than values recorded for the selected three standard antiviral drugs.","PeriodicalId":13851,"journal":{"name":"International Journal of Drug Delivery Technology","volume":"42 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135867829","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
In-silico Assessment of Potent Immunomodulators from Pimpinella anisum and its Antioxidant Potential 茴香草有效免疫调节剂及其抗氧化潜力的计算机评价
International Journal of Drug Delivery Technology Pub Date : 2023-09-25 DOI: 10.25258/ijddt.13.3.15
Snehal Kashid, Ashish Suttee, Prasad Kadam, Ramesh Kasarla
{"title":"In-silico Assessment of Potent Immunomodulators from Pimpinella anisum and its Antioxidant Potential","authors":"Snehal Kashid, Ashish Suttee, Prasad Kadam, Ramesh Kasarla","doi":"10.25258/ijddt.13.3.15","DOIUrl":"https://doi.org/10.25258/ijddt.13.3.15","url":null,"abstract":"New targets, effective substances, and safety in pharmacological models are highlighted by recent drug development. The study’s primary goal is to use an in-silico technique to determine the immunomodulatory potential of phytoconstituents from Pimpinella anisum. Several computer aided tool were utilized for in-silico. autodock vina is major free tool utilized to examine a drug discovery strategy based on the atomic-level screening of small compounds and proteins and protein-ligand interactions. Basic docking phases include ligand position, orientation, and binding affinities. The current methodology includes ligand choice, protein prep, target, ligand optimisation, target active binding site analysis, and binding affinity. SwissADME was used to assess the pharmacokinetic parameters, and Lipinski’s “rules” were used to assess drug similarity. In the current research paper six ligands such as P-anisaldehyde, trans-anethole, cis-anethole, estragole, and linalool were dock against two proteins 1M48 and 1P9M. Molecular docking studies suggest strong binding affinity between -6.9 to -4.2 in case on 1M48 and -6.2 to -4.7 in case of 1P9M. Further antioxidant potential of P. anisum using several solvents was determined. In-vitro antioxidant study and in-silico screening suggested that P. anisum ethanolic extract can be contributed in immunomodulation","PeriodicalId":13851,"journal":{"name":"International Journal of Drug Delivery Technology","volume":"2014 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135866584","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
Synthesis and Characterization of Colloidally Stable Self-crosslinking Water-based Anticorrosive Polymer at Room Temperature 室温稳定自交联水性防腐聚合物的合成与表征
International Journal of Drug Delivery Technology Pub Date : 2023-09-25 DOI: 10.25258/ijddt.13.3.25
Khalida A Omran
{"title":"Synthesis and Characterization of Colloidally Stable Self-crosslinking Water-based Anticorrosive Polymer at Room Temperature","authors":"Khalida A Omran","doi":"10.25258/ijddt.13.3.25","DOIUrl":"https://doi.org/10.25258/ijddt.13.3.25","url":null,"abstract":"The emulsion polymerization of butyl acrylate (BuA), styrene (St), and 3-isopropenyl-α,α-dimethylbenzyl isocyanate (IPMBI) is presented in this work. Obtain colloidally stable latexes for the poly (BuA/St/IPMBI) system during polymerization and storage for use in a water-based coating formulation. A series of semicontinuous polymerizations were also performed to investigate the effect of comonomer composition (w/w) in the feed (BuA/St) on conversion. The particle diameter (Dp), particle number (Np), hydrolysis of the IPMBI’s isocyanate groups, stability and storage properties. Films were created in which the effect of comonomer composition was also investigated, the glass transition temperature (Tg) was determined, the gel content was selected, and the mechanical properties and capacity as a barrier to water vapour and oxygen were assessed. Another series of reactions, on the other hand, was carried out in which the effect of the IPMBI content (1.5, 3.5, and 5.5%) was studied using a constant composition BuA/St=60/40. The studies conducted are the same as those mentioned for the effect of comonomer composition in feed. With increasing IPMBI percentage, slight differences in conversion, Dp, and Np were observed; the latices undergo hydrolysis during polymerization and storage. Colloidal stability, on the other hand, was preserved. The mechanical properties of the films improved as the percentage of IPMBI increased, while the boundary characteristics to moisture and oxygen improved when compared to the white film (0% of IPMBI). Finally, the formulation of a self-crosslinking water-based coating at room temperature using the previously obtained latex as a binder is reported; the coating demonstrated excellent adhesion, scratch hardness, and gloss regardless of the type of latex used.","PeriodicalId":13851,"journal":{"name":"International Journal of Drug Delivery Technology","volume":"34 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135867448","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
Formulation and Evaluation of Moxifloxacin Dry Powder Inhaler Combined with Mucolytic Agent for Pulmonary Diseases 莫西沙星干粉吸入剂联合黏液剂治疗肺部疾病的处方及疗效评价
International Journal of Drug Delivery Technology Pub Date : 2023-09-25 DOI: 10.25258/ijddt.13.3.07
Ratnaparkhi M.P, Kamble O.V, Salvankar S.S, Shinde S.R, Kulkarni G.M, Shewale A.B, Kadam D.D, Shaikh A.J
{"title":"Formulation and Evaluation of Moxifloxacin Dry Powder Inhaler Combined with Mucolytic Agent for Pulmonary Diseases","authors":"Ratnaparkhi M.P, Kamble O.V, Salvankar S.S, Shinde S.R, Kulkarni G.M, Shewale A.B, Kadam D.D, Shaikh A.J","doi":"10.25258/ijddt.13.3.07","DOIUrl":"https://doi.org/10.25258/ijddt.13.3.07","url":null,"abstract":"The DPI is the device that administers the drug through the dry powder to the lungs. People with Multi-drug resistant tuberculosis or other lung diseases frequently use such devices to take their prescribed medicines. Numerous approaches have been used to formulate dry powder inhalation formulation and enhance the delivery performance of dry powder inhaler preparation. In the case of multi-drug resistance tuberculosis, a high dose of combination therapy was delivered, resulting in resistance to the anti-TB medications in the majority of patients. Moxifloxacin and levofloxacin are being used to minimize the need for a high-dose treatment regimen. This study aimed to achieve local lung administration of tumor-targeting Moxifloxacin, by administering microspheres that can be inhaled as a dry powder inhaler for targeting Phagocytes of alveoli via pulmonary passage. Spray drying had been used to formulate MXN-DPI formulations, afterward optimized with the 23-factorial design model. Two different amounts of lactose, leucine, and medication were used to make the eight batches. The developed formulation was studied for physicochemical properties like morphology and particle size. The particle dimensions of the MXN-DPI compositions have been confirmed to be in the range of 1.4 to 4.1 μm. The prepared formulations effectively showed drug release up to 93% in 5 hours, which was observed through in-vitro diffusion studies.","PeriodicalId":13851,"journal":{"name":"International Journal of Drug Delivery Technology","volume":"23 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135867451","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
Synthesis and Characterization of Co3O4 Spinel Nanoparticles with Antibacterial Activity 具有抗菌活性的Co3O4尖晶石纳米颗粒的合成与表征
International Journal of Drug Delivery Technology Pub Date : 2023-09-25 DOI: 10.25258/ijddt.13.3.37
Mustafa Hammadi, Rulla Sabah, Esam H Hummadi
{"title":"Synthesis and Characterization of Co3O4 Spinel Nanoparticles with Antibacterial Activity","authors":"Mustafa Hammadi, Rulla Sabah, Esam H Hummadi","doi":"10.25258/ijddt.13.3.37","DOIUrl":"https://doi.org/10.25258/ijddt.13.3.37","url":null,"abstract":"Nanoparticles are abundant and usable in the medical field as an antibiotic. It has been found that metal oxide nanoparticles, such as Co3O4, are efficient against bacteria that are resistant to antibiotics. Escherichia and Staphylococcus bring on enteric sickness and other illnesses. This study used co-precipitation to create Co3O4 nanoparticles. SEM, X-ray diffraction (XRD), and Fourier-transform infrared (FTIR) spectroscopy were used to analyze these oxide nanoparticles. The XRD pattern validated the Co3O4 crystalline match. SEM also showed the morphology of Co3O4 nanoparticles. As determined by X-rays, Co3O4 has an average diameter of around 37.08 nm. The Co3O4 nanoparticles were highly pure, showed by an energy-dispersive EDX pattern. Both on their own and in conjunction with cephalexin, these metal oxide nanoparticles demonstrated antibacterial efficacy against S. aureus and E. coli. These Co3O4 nanoparticles showed high growth inhibition compared with using cephalexin individually. These conclusions found that the presence of cephalexin with Co3O4 showed high growth inhibition. The antibacterial activity of Co3O4 nanoparticles should be subjected for further studies.","PeriodicalId":13851,"journal":{"name":"International Journal of Drug Delivery Technology","volume":"30 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135867471","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
Virtual Screening, Molecular Docking, and ADMET Analysis of Flavonoids as a Potential Pi3k Inhibitor for Cancer Treatment 类黄酮作为Pi3k抑制剂的虚拟筛选、分子对接和ADMET分析
International Journal of Drug Delivery Technology Pub Date : 2023-09-25 DOI: 10.25258/ijddt.13.3.31
Khushabu Patil, Mahesh Nemade, Anjali Bedse, Piyush Bedse, Rakesh Ranjan, Harshal Tare, Manish Bedse
{"title":"Virtual Screening, Molecular Docking, and ADMET Analysis of Flavonoids as a Potential Pi3k Inhibitor for Cancer Treatment","authors":"Khushabu Patil, Mahesh Nemade, Anjali Bedse, Piyush Bedse, Rakesh Ranjan, Harshal Tare, Manish Bedse","doi":"10.25258/ijddt.13.3.31","DOIUrl":"https://doi.org/10.25258/ijddt.13.3.31","url":null,"abstract":"Cancer continues to be a global health burden, necessitating the exploration of innovative anti-cancer therapeutics. This study leverages computational biology tools such as molecular docking, ligand-based virtual screening, and ADMET to evaluate quercetin flavonoids as potential PI3K inhibitors for cancer treatment. Using Swiss Similarity and CB-Dock tools, 51 compounds were identified that showed promising interactions with PI3K. DB01645 exhibited the highest binding affinity among these, with a Vina score of -8.6. ADMET analysis revealed that this compound has favorable physicochemical properties, moderate lipophilicity, and good water solubility. The study adds to the growing evidence that Quercetin flavonoids have significant potential as next-generation anti-cancer agents targeting the PI3K pathway.","PeriodicalId":13851,"journal":{"name":"International Journal of Drug Delivery Technology","volume":"26 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2023-09-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"135867706","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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