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  1. Article: Yifei sanjie

    Wu, Yingchao / Pi, Dajin / Chen, Yiliu / Zuo, Qian / Lin, Lizhu / Ouyang, Mingzi

    Evidence-based complementary and alternative medicine : eCAM

    2022  Volume 2022, Page(s) 2357616

    Abstract: Chemotherapy-related fatigue (CRF), one of the most severe adverse effects observed in cancer patients, has been theoretically related to oxidative stress, and antioxidant treatment might be one of the most valuable therapeutic approaches. However, there ...

    Abstract Chemotherapy-related fatigue (CRF), one of the most severe adverse effects observed in cancer patients, has been theoretically related to oxidative stress, and antioxidant treatment might be one of the most valuable therapeutic approaches. However, there are still few effective pharmacological therapies.
    Language English
    Publishing date 2022-08-22
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2171158-6
    ISSN 1741-4288 ; 1741-427X
    ISSN (online) 1741-4288
    ISSN 1741-427X
    DOI 10.1155/2022/2357616
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Deciphering the Molecular Mechanism of Yifei-Sanjie Pill in Cancer-Related Fatigue.

    Wu, Yingchao / Zhou, Shuyao / Pi, Dajin / Dong, Yangyang / Wang, Wuhong / Ye, Huan / Yi, Zhongjia / Chen, Yiliu / Lin, Lizhu / Ouyang, Mingzi

    Journal of oncology

    2023  Volume 2023, Page(s) 5486017

    Abstract: ... of the Yifei-Sanjie pill (YFSJ). The active components of YFSJ were found by LC/MS, the in vitro inflammatory ...

    Abstract Background: The incidence of cancer-related fatigue (CRF) is increasing, but its lack of clear pathogenesis makes its prevention and treatment difficult. Therefore, it is of great significance to clarify the pathogenesis of CRF and find effective methods to treat it.
    Methods: The CRF model was established by intraperitoneal injection of LLC cells in ICR mice to explore the pathogenesis of CRF and verify the therapeutic effect of the Yifei-Sanjie pill (YFSJ). The active components of YFSJ were found by LC/MS, the in vitro inflammatory infiltration model of skeletal muscle was constructed by TNF-
    Results: Behavioral analysis results showed that YFSJ alleviated CRF; histological examination results showed that YFSJ could reverse the tumor microenvironment leading to skeletal muscle injury; ELISA and RNA-seq results showed that the occurrence of CRF and the therapeutic effect of YFSJ were closely related to the tumor inflammatory microenvironment; IHC and WB results showed that the occurrence of CRF and the therapeutic effect of YFSJ were closely related to the Stat3-related signaling pathway and autophagy.
    Conclusions: YFSJ can reduce the level of inflammation in the tumor microenvironment in vivo, inhibit the abnormal activation of the Stat3/HIF-1
    Language English
    Publishing date 2023-02-13
    Publishing country Egypt
    Document type Journal Article
    ZDB-ID 2461349-6
    ISSN 1687-8469 ; 1687-8450
    ISSN (online) 1687-8469
    ISSN 1687-8450
    DOI 10.1155/2023/5486017
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Yifei Sanjie formula alleviates lung cancer progression via regulating PRMT6-YBX1-CDC25A axis.

    Tang, Jie / Yin, Chenyan / Chen, Meiyun / Dong, Mengjia / Xu, Youqi

    Environmental toxicology

    2024  Volume 39, Issue 5, Page(s) 3225–3237

    Abstract: ... Yifei Sanjie (YFSJ), a well-applicated traditional Chinese medicine formula, is widely used to treat ...

    Abstract Lung cancer (LC) is the most prevalent cancer type, with a high mortality rate worldwide. The current treatment options for LC have not been particularly successful in improving patient outcomes. Yifei Sanjie (YFSJ), a well-applicated traditional Chinese medicine formula, is widely used to treat pulmonary diseases, especially LC, yet little is known about its molecular mechanisms. This study was conducted to explore the molecular mechanism by which YFSJ ameliorated LC progression. The A549, NCI-H1975, and Calu-3 cells were treated with the YFSJ formula and observed for colony number, apoptosis, migration, and invasion properties recorded via corresponding assays. The PRMT6-YBX1-CDC25A axis was tested and verified through luciferase reporter, RNA immunoprecipitation, and chromatin immunoprecipitation assays and rescue experiments. Our results demonstrated that YFSJ ameliorated LC cell malignant behaviors by increasing apoptosis and suppressing proliferation, migration, and invasion processes. We also noticed that the xenograft mouse model treated with YFSJ significantly reduced tumor growth compared with the control untreated group in vivo. Mechanistically, it was found that YFSJ suppressed the expression of PRMT6, YBX1, and CDC25A, while the knockdown of these proteins significantly inhibited colony growth, migration, and invasion, and boosted apoptosis in LC cells. In summary, our results suggest that YFSJ alleviates LC progression via the PRMT6-YBX1-CDC25A axis, confirming its efficacy in clinical use. The findings of our study provide a new regulatory network for LC growth and metastasis, which could shed new insights into pulmonary medical research.
    MeSH term(s) Humans ; Animals ; Mice ; Lung Neoplasms/pathology ; Cell Proliferation/genetics ; Cell Movement/genetics ; Lung/pathology ; Cell Line, Tumor ; Gene Expression Regulation, Neoplastic ; MicroRNAs/genetics ; Y-Box-Binding Protein 1/genetics ; Y-Box-Binding Protein 1/metabolism ; Nuclear Proteins/genetics ; Protein-Arginine N-Methyltransferases/genetics ; Protein-Arginine N-Methyltransferases/metabolism ; Protein-Arginine N-Methyltransferases/therapeutic use ; cdc25 Phosphatases/genetics ; cdc25 Phosphatases/metabolism
    Chemical Substances MicroRNAs ; YBX1 protein, human ; Y-Box-Binding Protein 1 ; PRMT6 protein, human (EC 2.1.1.319) ; Nuclear Proteins ; Protein-Arginine N-Methyltransferases (EC 2.1.1.319) ; CDC25A protein, human (EC 3.1.3.48) ; cdc25 Phosphatases (EC 3.1.3.48)
    Language English
    Publishing date 2024-02-15
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1463449-1
    ISSN 1522-7278 ; 1520-4081
    ISSN (online) 1522-7278
    ISSN 1520-4081
    DOI 10.1002/tox.24160
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Mechanism of Yifei Decoction Combined with MitoQ on Inhibition of TGF

    Chen, Lijuan / Lan, Chengzhong / Xiao, Hong / Zhang, Xiaoli / Qi, Xiangrong / Ouyang, Li / Yang, Yanbin / Wang, Fengying / Jin, Qihua / Sun, Yi

    Evidence-based complementary and alternative medicine : eCAM

    2021  Volume 2021, Page(s) 6615615

    Abstract: ... fibrogenic factor-PDGF play a critical role in collagen deposition in rat lung tissue. Yifei decoction (YFT ...

    Abstract Background: Rho-related coiled helix forming protein kinase (Rho-ROCK) and another important fibrogenic factor-PDGF play a critical role in collagen deposition in rat lung tissue. Yifei decoction (YFT), a Chinese herbal decoction, has been used to treat idiopathic pulmonary fibrosis (IPF) in clinical practice and has produced positive outcomes; however, convincing evidence is currently lacking. The present study aimed to investigate the effects of YFT combined with MitoQ in rats with IPF and to explore the underlying mechanism.
    Methods: Rat IPF model was established by endotracheal injection of 5 mg/kg BleomycinA5 into the specific pathogen-free SD rats. MitoQ (6.5 
    Results: After 4 weeks of drug treatment, comparison of the MitoQ + YFT group with the IPF group showed that lung injury scores, W/D, lung tissue hydroxyproline, fibronectin, collagen IV content, and IL-6, IL-1
    Conclusion: MitoQ combined with YFT can improve lung injury in rats with pulmonary fibrosis by reducing the secretion of proinflammatory cytokines and inhibiting TGF
    Language English
    Publishing date 2021-05-28
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2171158-6
    ISSN 1741-4288 ; 1741-427X
    ISSN (online) 1741-4288
    ISSN 1741-427X
    DOI 10.1155/2021/6615615
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Network pharmacology and transcriptomics to determine Danggui Yifei Decoction mechanism of action for the treatment of chronic lung injury.

    Guo, Jianning / Liang, Junming / Guo, Ziyi / Bai, Xue / Zhang, Hongxian / Zhang, Ning / Wang, Handong / Chen, Qian / Li, Wei / Dong, Ruijuan / Ge, Dongyu / Yu, Xue / Cui, Xia

    Journal of ethnopharmacology

    2023  Volume 318, Issue Pt A, Page(s) 116873

    Abstract: ... which eventually results in chronic lung injury. Danggui yifei Decoction (DGYFD), a traditional Chinese formula ...

    Abstract Ethnopharmacological relevance: Several children with pneumonia (especially severe cases) have symptoms of cough and expectoration during the recovery stage after standard symptomatic treatment, which eventually results in chronic lung injury. Danggui yifei Decoction (DGYFD), a traditional Chinese formula, has shown clinical promise for the treatment of chronic lung injury during the recovery stage of pneumonia, however, its mechanism of action is yet to be deciphered.
    Aim of this study: To investigate the therapeutic mechanism of DGYFD for the treatment of chronic lung injury by integrating network pharmacology and transcriptomics.
    Materials and methods: BALB/c mice were used to establish the chronic lung injury mouse model by intratracheal instillation of lipopolysaccharide (LPS). Pathological analysis of lung tissue, lung injury histological score, lung index, protein levels in bronchoalveolar lavage fluid (BALF), immunohistochemical staining, blood rheology, inflammatory cytokines, and oxidative stress levels were used to evaluate the pharmacological effects of DGYFD. Chemical components of DGYFD were identified using ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). Integrated network pharmacology together with transcriptomics was used to predict potential biological targets. Western blot analysis was used to verify the results.
    Results: In this study, we demonstrated that DGYFD could improve lung injury pathological changes, decreases lung index, down-regulate NO and IL-6 levels, and regulate blood rheology. In addition, DGYFD was able to reduce the protein levels in BALF, up-regulate the expression levels of occludin and ZO-1, improve the ultrastructure of lung tissues, and reverse the imbalance of AT I and AT II cells to repair the alveolar-capillary permeability barrier. Twenty-nine active ingredients of DGYFD and 389 potential targets were identified by UPLC-MS/MS and network pharmacology, and 64 differentially expressed genes (DEGs) were identified using transcriptomics. GO and KEGG analysis revealed that the MAPK pathway may be the molecular target. Further, we found that DGYFD inhibits phosphorylation levels of p38 MAPK and JNK in chronic lung injury mouse models.
    Conclusions: DGYFD could regulate the imbalance between the excessive release of inflammatory cytokines and oxidative stress, repair the alveolar-capillary permeability barrier and improve the pathological changes during chronic lung injury by regulating the MAPK signaling pathway.
    MeSH term(s) Animals ; Mice ; Lung Injury ; Chromatography, Liquid ; Network Pharmacology ; Transcriptome ; Tandem Mass Spectrometry ; Cytokines/genetics ; Disease Models, Animal ; Mice, Inbred BALB C ; Drugs, Chinese Herbal/pharmacology ; Drugs, Chinese Herbal/therapeutic use
    Chemical Substances Cytokines ; Drugs, Chinese Herbal
    Language English
    Publishing date 2023-07-05
    Publishing country Ireland
    Document type Journal Article
    ZDB-ID 134511-4
    ISSN 1872-7573 ; 0378-8741
    ISSN (online) 1872-7573
    ISSN 0378-8741
    DOI 10.1016/j.jep.2023.116873
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Yifei Sanjie Formula or Placebo With Anlotinib as Second-Line or Above Treatment for Metastatic Non-Small-Cell Lung Cancer: Study Protocol for a Double-Blind, Placebo-Controlled Randomized Pilot Study.

    Chen, Wenmin / Lin, Jietao / Yang, Ting / Xin Zhang, Ze / Tao, Lanting / Xiao, Zhiwei / Chen, Hanrui / Qi, Xiangjun / Sun, Lingling / Cao, Yang / Lin, Lizhu

    Integrative cancer therapies

    2023  Volume 22, Page(s) 15347354221151147

    Abstract: ... of the Chinese herbal medicine Yifei Sanjie formula (YFSJF) to anlotinib can improve ...

    Abstract Background: Anlotinib is used as a third-line treatment for advanced non-small-cell lung cancer (NSCLC), but has limited clinical benefits and several side effects, such as diarrhea and acneiform skin rash. Traditional Chinese Medicine (TCM) is commonly used to treat cancers in China. Chinese herbal medicines may have the potential as adjuvant therapies to reduce toxicity and improve the efficacy of treatments for NSCLC. Given the positive outcomes of basic research, we plan to evaluate whether the addition of the Chinese herbal medicine Yifei Sanjie formula (YFSJF) to anlotinib can improve the progression-free survival (PFS) of advanced NSCLC patients.
    Methods: A multicenter, randomized, double-blind, placebo-controlled parallel-group controlled pilot trial will be performed. Forty eligible patients will be randomized in a ratio of 1:1 to the intervention (YFSJF + anlotinib) and control (placebo + anlotinib) groups. Participants will be advised to take 12 mg/day of anlotinib on days 1 to 14 of each 21-day cycle. YFSJF or placebo will be administered (15 g twice daily) during each cycle until progression of disease (PD). The primary outcome will be progression-free survival (PFS), and the secondary outcomes will be overall survival (OS), the objective response rate (ORR), and patient-reported outcomes (PRO). Tumors will be assessed based on RECIST v. 1.1 after every 2 cycles of treatment. The M. D. Anderson Symptom Inventory-Lung Cancer (MDASI-LC) will be used to evaluate PRO at baseline and weekly thereafter until PD.
    Discussion: This will be the first trial to evaluate the effectiveness and safety of TCM combined with anlotinib for the treatment of NSCLC. The results of this randomized controlled trial will fill a gap in the research by showing whether YFSJF combined with anlotinib can improve PFS in NSCLC patients.
    Trial registration: The study was registered on June 8th, 2021 on Chinese Clinical Registry; registration number ChiCTR2100047143. (https://www.chictr.org.cn/index.aspx).
    Ethics and dissemination: The Ethics Committee of the First Affiliated Hospital of Guangzhou University of Traditional Chinese Medicine approved the study protocol (approval no.: K2020151, 2021/08/19). The study will also be supervised and managed by the Ethics Committee.
    MeSH term(s) Humans ; Carcinoma, Non-Small-Cell Lung/drug therapy ; Carcinoma, Non-Small-Cell Lung/pathology ; Pilot Projects ; Lung Neoplasms/pathology ; Treatment Outcome ; Double-Blind Method ; Randomized Controlled Trials as Topic ; Multicenter Studies as Topic
    Chemical Substances anlotinib
    Language English
    Publishing date 2023-03-27
    Publishing country United States
    Document type Clinical Trial Protocol ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2182320-0
    ISSN 1552-695X ; 1534-7354
    ISSN (online) 1552-695X
    ISSN 1534-7354
    DOI 10.1177/15347354221151147
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article: Yifei Xuanfei Jiangzhuo Chinese bioformulation improves cognitive function in a murine model of vascular dementia - the implication of PI3K/AKT and Erk signalling pathway.

    Chen, W / Wu, L / Jiang, L F / Hu, Y Q / Zhai, Y / Li, J H / Wu, Y / Tang, N

    Journal of biological regulators and homeostatic agents

    2020  Volume 34, Issue 6, Page(s) 2177–2183

    MeSH term(s) Animals ; Asian Continental Ancestry Group ; Cognition ; Dementia, Vascular/drug therapy ; Disease Models, Animal ; Drugs, Chinese Herbal ; Humans ; MAP Kinase Signaling System ; Mice ; Phosphatidylinositol 3-Kinases/genetics ; Proto-Oncogene Proteins c-akt/genetics
    Chemical Substances Drugs, Chinese Herbal ; yifei xuanfei jiangzhuo ; Proto-Oncogene Proteins c-akt (EC 2.7.11.1)
    Language English
    Publishing date 2020-11-12
    Publishing country Italy
    Document type Letter
    ZDB-ID 639196-5
    ISSN 1724-6083 ; 0393-974X
    ISSN (online) 1724-6083
    ISSN 0393-974X
    DOI 10.23812/20-310-L
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Mechanism of Yifei Decoction Combined with MitoQ on Inhibition of TGFβ1/NOX4 and PDGF/ROCK Signal Pathway in Idiopathic Pulmonary Fibrosis

    Lijuan Chen / Chengzhong Lan / Hong Xiao / Xiaoli Zhang / Xiangrong Qi / Li Ouyang / Yanbin Yang / Fengying Wang / Qihua Jin / Yi Sun

    Evidence-Based Complementary and Alternative Medicine, Vol

    2021  Volume 2021

    Abstract: ... fibrogenic factor-PDGF play a critical role in collagen deposition in rat lung tissue. Yifei decoction (YFT ...

    Abstract Background. Rho-related coiled helix forming protein kinase (Rho-ROCK) and another important fibrogenic factor-PDGF play a critical role in collagen deposition in rat lung tissue. Yifei decoction (YFT), a Chinese herbal decoction, has been used to treat idiopathic pulmonary fibrosis (IPF) in clinical practice and has produced positive outcomes; however, convincing evidence is currently lacking. The present study aimed to investigate the effects of YFT combined with MitoQ in rats with IPF and to explore the underlying mechanism. Methods. Rat IPF model was established by endotracheal injection of 5 mg/kg BleomycinA5 into the specific pathogen-free SD rats. MitoQ (6.5 μmol/kg once daily), YFT (10 ml/kg once daily), and MitoQ + YFT (6.5 μmol/kg + 10 ml/kg once daily) were used to treat the rat model for 4 weeks, respectively. The normal rats without IPF were used as the controls. After 4 weeks of drug treatment, lung histopathology was assessed. Immunohistochemistry was used to detect the expression of fibronectin and collagen IV in lung tissue. The expression of IL-6, IL-1β, TNF-α, GSH-Px, SOD, MDA, and hydroxyproline was determined by enzyme-linked immunosorbent assay. The expressions of TGFβ1, NOX4, PDGFR-β, and ROCK1 were determined using real-time quantitative PCR and Western blot. Results. After 4 weeks of drug treatment, comparison of the MitoQ + YFT group with the IPF group showed that lung injury scores, W/D, lung tissue hydroxyproline, fibronectin, collagen IV content, and IL-6, IL-1β, TNF-α, and MDA levels were significantly lower (P<0.05), as well as the expression of TGFβ1, NOX4, PDGFR-β, and ROCK1, but the activity of GSH-Px and SOD was higher (P<0.05). Conclusion. MitoQ combined with YFT can improve lung injury in rats with pulmonary fibrosis by reducing the secretion of proinflammatory cytokines and inhibiting TGFβ1/NOX4 and PDGF/ROCK signaling pathways. It may provide a new method for the treatment of pulmonary fibrosis.
    Keywords Other systems of medicine ; RZ201-999
    Subject code 610
    Language English
    Publishing date 2021-01-01T00:00:00Z
    Publisher Hindawi Limited
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  9. Article ; Online: Antifibrotic action of Yifei Sanjie formula enhanced autophagy via PI3K-AKT-mTOR signaling pathway in mouse model of pulmonary fibrosis.

    Yu, Jing-Ze / Ying, Yi / Liu, Yang / Sun, Chun-Bin / Dai, Chen / Zhao, Shan / Tian, Shou-Zheng / Peng, Jing / Han, Ni-Ping / Yuan, Jia-Li / Yan, Jin-Yuan / Yang, Zhong-Shan

    Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie

    2019  Volume 118, Page(s) 109293

    Abstract: ... with a high mortality rate, but its origin is unknown and there is no effective treatment. Yifei Sanjie ...

    Abstract Pulmonary fibrosis (PF) is a crippling disease characterized by progressive dyspnea and associated with a high mortality rate, but its origin is unknown and there is no effective treatment. Yifei Sanjie formula (YFSJF) is a Chinese medicine that is widely used for treatment of respiratory systems disease. However, the molecular basis for the function of YFSJF has not been determined. Here we investigate the contribution of YFSJF in BLM-induced PF mice. Administration with YFSJF significantly alleviated the degree of BLM-induced collagen I and III deposition and the inflammatory injuring in the lungs and suppressed hydroxyproline release in PF animals. The active components of YFSJF are comprised with flavonoid, amino acids, saponins, oligosaccharide, organic acid, vitamin, esters, purine nucleosides. Additionally, there was a significant increase in autophagosomes, after treatment with YFSJF in PF animals. Interestingly, autophagy dysfunction by the blocker chloroquine (CQ) resulted in collagen deposition and inducing the expression of fibrosis-related genes. In addition, YFSJF-induced autophagy is mediated by the PI3K-AKT-mTOR pathway, and knockdown of PI3K by siRNA up-regulated the expression of autophagy-related genes and down-regulated the expression of collagen in human lung fibroblasts (HLF). Our findings provide a detailed understanding that YFSJF-antifibrotic effects are mainly mediated by triggering autophagy, and suppressing phosphorylation of the PI3K-AKT-mTOR pathway is required for YFSJF-curative effect.
    MeSH term(s) Animals ; Autophagosomes/metabolism ; Autophagosomes/ultrastructure ; Autophagy/drug effects ; Collagen/metabolism ; Disease Models, Animal ; Drugs, Chinese Herbal ; Humans ; Inflammation/complications ; Inflammation/pathology ; Lung/pathology ; Male ; Phosphatidylinositol 3-Kinases/metabolism ; Phosphorylation/drug effects ; Proto-Oncogene Proteins c-akt/metabolism ; Pulmonary Fibrosis/complications ; Pulmonary Fibrosis/drug therapy ; Pulmonary Fibrosis/metabolism ; Pulmonary Fibrosis/pathology ; Signal Transduction ; TOR Serine-Threonine Kinases/metabolism ; Transforming Growth Factor beta1/metabolism
    Chemical Substances Drugs, Chinese Herbal ; Transforming Growth Factor beta1 ; Collagen (9007-34-5) ; TOR Serine-Threonine Kinases (EC 2.7.1.1) ; Proto-Oncogene Proteins c-akt (EC 2.7.11.1)
    Language English
    Publishing date 2019-08-08
    Publishing country France
    Document type Journal Article
    ZDB-ID 392415-4
    ISSN 1950-6007 ; 0753-3322 ; 0300-0893
    ISSN (online) 1950-6007
    ISSN 0753-3322 ; 0300-0893
    DOI 10.1016/j.biopha.2019.109293
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Book ; Online: Fractal and Fractional in Geomaterials

    Sun, Yifei / Chen, Cheng / Goudarzy, Meisam / Chen, Cheng

    2023  

    Keywords Technology: general issues ; History of engineering & technology ; nuclear magnetic resonance ; pore size distribution ; fractal dimension ; grain size ; calcareous sand ; quartz sand ; deformation conditions ; relative permeability coefficient ; air-entry value ; void ratio ; model ; saturated permeability coefficient ; maximum pore ; comprehensive proportionality constant ; fractional derivative ; fractional diffusion equation ; fractional advection-dispersion equation ; solute transport ; porous media ; soil-structure interaction ; fractional plasticity ; cyclic loads ; soil-rock mixture ; fractal theory ; particle distribution ; scale effect ; discrete element model ; particle size distribution ; critical state ; shear characteristic ; frozen-thawed soft clay ; fractal characteristics ; NMR ; pore structure ; artificial ground freezing ; laterally loaded piles ; cyclic loading ; unsaturated soil ; pile-soil interaction ; model tests ; particle image velocimetry ; anisotropic stress ; Hostun sand ; resonant column ; maximum shear modulus ; fines content ; equivalent granular void ratio ; hydraulic gradient ; random field ; hydraulic conductivity ; porosity ; concrete-rock ITZ ; permeability ; granular materials ; particle breakage ; relative density ; grading curve ; discrete element method ; ballast ; PSD evolution ; soft soil ; SEM ; microstructure ; cumulative strain ; effective particle diameter ; fractal entropy ; abstract interval ; hydraulic coefficient ; n/a
    Language English
    Size 1 electronic resource (262 pages)
    Publisher MDPI - Multidisciplinary Digital Publishing Institute
    Publishing place Basel
    Document type Book ; Online
    Note English
    HBZ-ID HT030377080
    ISBN 9783036570556 ; 3036570551
    Database ZB MED Catalogue: Medicine, Health, Nutrition, Environment, Agriculture

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