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m8407 5 fluorouracil 5 fu sigma aldrich  (MedChemExpress)


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    Structured Review

    MedChemExpress m8407 5 fluorouracil 5 fu sigma aldrich
    M8407 5 Fluorouracil 5 Fu Sigma Aldrich, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 98/100, based on 162 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/fluorouracil+5+fu/5-Fluorouracil/pm42594868-228-55-63
    Average 98 stars, based on 162 article reviews
    m8407 5 fluorouracil 5 fu sigma aldrich - by Bioz Stars, 2026-10
    98/100 stars

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    Article Title: Exploring the effect of Huangqi Fuling Decoction on gastric cancer based on UPLC-MS, network pharmacology and experiments in vitro.
    Article Snippet: Fluorouracil (5-FU) was purchased from MedChemExpress (HY-90006, MedChemExpress, United States), dissolved in DMSO.

    Article Title: Gancao Xiexin decoction alleviates 5-fluorouracil-induced intestinal mucositis by inhibiting ACSL4 and activating Keap1-Nrf2 pathway.
    Article Snippet: 5-Fluorouracil (5-Fu) is a commonly used chemotherapy drug, but it frequently induces toxic side effects such as intestinal mucositis and is closely associated with ferroptosis.. Gancao Xiexin (GCXX) decoction, a renowned formula in traditional Chinese medicine, is widely employed for treating gastrointestinal inflammatory diseases.. However, the therapeutic effects and underlying mechanisms of GCXX on 5-Fu-induced intestinal mucositis remain unclear.

    Article Title: Triggering mitotic catastrophe by podophyllotoxin induces apoptosis in oral squamous cell carcinoma.
    Article Snippet: Objective: This study investigated the relationship between mitotic catastrophe (MC) and apoptosis in oral squamous cell carcinoma (OSCC) using podophyllotoxin (PPT), a natural compound with antimitotic properties.. Design: We evaluated the concentration-dependent effects of PPT on cell proliferation (CCK-8 and soft agar assays) and morphology (transmission electron microscopy).. Mechanistic insights were obtained by assessing DNA damage (western blotting), cell cycle progression (sub-G1 analysis), and apoptosis-related protein activation in both 2D and 3D spheroid models of HSC-3 oral squamous carcinoma cells.

    Article Title: PLGA-based herb Toosendanin delivery system for efficient therapy of oral squamous cell carcinoma
    Article Snippet: TSN and 5-fluorouracil (5-FU) were purchased from Med Chem Express (Shanghai, China).

    Article Title: The Study of the Antitumor Effects and Molecular Mechanisms of Byakangelicol on HepG2 Cells.
    Article Snippet: Byakangelicol (BYA) belongs to coumarins, which have anti‐inflammatory and anti‐tumor pharmacological properties, but its inhibitory effect on liver cancer and its mechanism are still indistinct.. This study explored the mechanism of action by which BYA affects hepatocellular carcinoma (HCC).. Cell cytotoxic and apoptosis assay results showed that BYA effectively killed three kinds of HCC cells and induced mitochondrial pathway apoptosis of HepG2 cells.

    Article Title: PLGA-based herb Toosendanin delivery system for efficient therapy of oral squamous cell carcinoma.
    Article Snippet: TSN and 5-fluorouracil (5-FU) were purchased from Med Chem Express (Shanghai, China).

    Article Title: Exploring the effect of Huangqi Fuling Decoction on gastric cancer based on UPLC-MS, network pharmacology and experiments in vitro
    Article Snippet: Fluorouracil (5-FU) was purchased from MedChemExpress (HY-90006, MedChemExpress, United States), dissolved in DMSO.

    Article Title: Arenobufagin Induces Ferroptosis in Gastric Cancer Stem Cells via the HCAR1-GPX4/SLC7A11 Antioxidant Axis.
    Article Snippet: 30 Arenobufagin (ARBU), a steroid compound extracted from the venom of Bufo 31 gargarizans, exhibits multi-target pharmacological activities, yet its role in regulating 32 ferroptosis in gastric cancer stem cells (GCSCs) remains unclear.. This study 33 systematically evaluated the antitumor effects and mechanisms of ARBU using in 34 vitro sphere culture, organoid models, and xenografts.. ARBU inhibited GCSC 35 proliferation and sphere formation in a concentration-dependent manner, reduced EdU 36 incorporation and SOX2 expression in organoids, and markedly suppressed tumor 37 growth in vivo while downregulating SOX2 and Nanog, with favorable biosafety.



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    HeB108 and its ribavirin-associated mutants were inoculated into Marc-145 cells that were pre-treated with ribavirin (A) <t>or</t> <t>5-FU</t> (B) at an MOI of 0.01 for 72 h. HuN4 and its ribavirin-associated mutants were inoculated into Marc-145 cells that were pre-treated with ribavirin (C) or 5-FU (D) . Cells without ribavirin or 5-FU treatment served as a control to evaluate the virus titers. Viral genomic RNA level was determined by RT-qPCR. *, P < 0.05; **, P < 0.01; ***, P < 0.001; ****, P < 0.0001.
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    HeB108 and its ribavirin-associated mutants were inoculated into Marc-145 cells that were pre-treated with ribavirin (A) <t>or</t> <t>5-FU</t> (B) at an MOI of 0.01 for 72 h. HuN4 and its ribavirin-associated mutants were inoculated into Marc-145 cells that were pre-treated with ribavirin (C) or 5-FU (D) . Cells without ribavirin or 5-FU treatment served as a control to evaluate the virus titers. Viral genomic RNA level was determined by RT-qPCR. *, P < 0.05; **, P < 0.01; ***, P < 0.001; ****, P < 0.0001.
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    HeB108 and its ribavirin-associated mutants were inoculated into Marc-145 cells that were pre-treated with ribavirin (A) <t>or</t> <t>5-FU</t> (B) at an MOI of 0.01 for 72 h. HuN4 and its ribavirin-associated mutants were inoculated into Marc-145 cells that were pre-treated with ribavirin (C) or 5-FU (D) . Cells without ribavirin or 5-FU treatment served as a control to evaluate the virus titers. Viral genomic RNA level was determined by RT-qPCR. *, P < 0.05; **, P < 0.01; ***, P < 0.001; ****, P < 0.0001.
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    HeB108 and its ribavirin-associated mutants were inoculated into Marc-145 cells that were pre-treated with ribavirin (A) <t>or</t> <t>5-FU</t> (B) at an MOI of 0.01 for 72 h. HuN4 and its ribavirin-associated mutants were inoculated into Marc-145 cells that were pre-treated with ribavirin (C) or 5-FU (D) . Cells without ribavirin or 5-FU treatment served as a control to evaluate the virus titers. Viral genomic RNA level was determined by RT-qPCR. *, P < 0.05; **, P < 0.01; ***, P < 0.001; ****, P < 0.0001.
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    Macklin Inc 5 fluorouracil 5 fu
    Effect of <t>Luteolin/5-Fu</t> on apoptosis-related genes in A431 cells. ( a ) Bcl-2 ; ( b ) BAX ; ( c ) EGFR ; ( d ) PI3K ; ( e ) AKT mRNA levels. n = 3. * p < 0.05, ** p < 0.01 vs. control group.
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    Shanghai Macklin Biochemical fluorouracil 5 fu
    (a) Synthesis of <t>β-CD@5-Fu;</t> (b) preparation process of β-CD@5-Fu/CMCS/CMCNa/SA hydrogel beads; (c) in vitro release mechanism of β-CD@5-Fu/CMCS/CMCNa/SA hydrogel beads.
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    Image Search Results


    HeB108 and its ribavirin-associated mutants were inoculated into Marc-145 cells that were pre-treated with ribavirin (A) or 5-FU (B) at an MOI of 0.01 for 72 h. HuN4 and its ribavirin-associated mutants were inoculated into Marc-145 cells that were pre-treated with ribavirin (C) or 5-FU (D) . Cells without ribavirin or 5-FU treatment served as a control to evaluate the virus titers. Viral genomic RNA level was determined by RT-qPCR. *, P < 0.05; **, P < 0.01; ***, P < 0.001; ****, P < 0.0001.

    Journal: PLOS Pathogens

    Article Title: Single amino acid substitution in RdRp reduces viral recombination frequency of NADC30-like porcine reproductive and respiratory syndrome virus type 2

    doi: 10.1371/journal.ppat.1014500

    Figure Lengend Snippet: HeB108 and its ribavirin-associated mutants were inoculated into Marc-145 cells that were pre-treated with ribavirin (A) or 5-FU (B) at an MOI of 0.01 for 72 h. HuN4 and its ribavirin-associated mutants were inoculated into Marc-145 cells that were pre-treated with ribavirin (C) or 5-FU (D) . Cells without ribavirin or 5-FU treatment served as a control to evaluate the virus titers. Viral genomic RNA level was determined by RT-qPCR. *, P < 0.05; **, P < 0.01; ***, P < 0.001; ****, P < 0.0001.

    Article Snippet: Monolayers of Marc-145 cells were pre-treated with 100, 200, 300, and 350 μM ribavirin, or 400 and 600 μM 5-fluorouracil (5-FU) (MCE, China) for 2 h. The cells were infected with site-directed mutated or parental virus at an MOI of 0.01 for 2 h. The infected cells were washed three times with PBS.

    Techniques: Control, Virus, Quantitative RT-PCR

    Effect of Luteolin/5-Fu on apoptosis-related genes in A431 cells. ( a ) Bcl-2 ; ( b ) BAX ; ( c ) EGFR ; ( d ) PI3K ; ( e ) AKT mRNA levels. n = 3. * p < 0.05, ** p < 0.01 vs. control group.

    Journal: Biomolecules

    Article Title: Potential Efficacy of Luteolin in Cutaneous Squamous Cell Carcinoma: A Combined In Vitro and In Vivo Study

    doi: 10.3390/biom16050737

    Figure Lengend Snippet: Effect of Luteolin/5-Fu on apoptosis-related genes in A431 cells. ( a ) Bcl-2 ; ( b ) BAX ; ( c ) EGFR ; ( d ) PI3K ; ( e ) AKT mRNA levels. n = 3. * p < 0.05, ** p < 0.01 vs. control group.

    Article Snippet: The chemicals and materials used in this experiment are as follows: 5-Fluorouracil (5-Fu) (99.9%, CAS: 51-21-8, C13964619, Macklin, Shanghai, China); Luteolin (≥98%, RP210105, Madsen, Chengdu, China); 7,12-Dimethylbenz[a]anthracene (DMBA) (98%, A807576, Alphabio, Tianjin, China); Croton oil (≥95%, C865142, Macklin, Shanghai, China); high-glucose DMEM (2383696, Gibco, Waltham, MA, USA); fetal bovine serum (220315JF, Alphabio, Tianjin, China); DMSO (>99.9%, 20220301, Tianjin Hengxing, Tianjin, China); 4% paraformaldehyde tissue fixative (23039118, Beijing Lanjieke, Beijing, China); CCK-8 kit (101824133EF5E, Apexbio, Houston, TX, USA); Annexin V-FITC/PI apoptosis kit (2306001, Solarbio, Beijing, China); RIPA lysis buffer (IN-WB001, Invent Biotechnologies, Eden Prairie, MN, USA); Protease and Phosphatase Inhibitor Cocktail (051823230704, Beyotime, Shanghai, China); BCA protein assay kit (BL521A, Beyotime, Shanghai, China); DAB chromogenic kit (FL-6001, Changdao Biotech, Shanghai, China); Trizol reagent (1B14KA7304; Sangon Biotech, Shanghai, China); HiFiScript cDNA Synthesis Kit (26323, CWBio, Taizhou, China); anti-PI3K (1:1000, bs-2067R, Bioss, Beijing, China); anti-p-PI3K (1:1000, bs-5570R, Bioss, Beijing, China); anti-AKT (1:1000, bsm-33278M, Bioss, Beijing, China); anti-p-AKT (1:1000, bs-2720R, Bioss, Beijing, China); anti-EGFR (1:1000, bsm-33050M, Bioss, Beijing, China); anti-p-EGFR (1:1000, bsm-52149R, Bioss, Beijing, China); anti-BAX (1:1000, #2772, CST, Danvers, MA, USA); anti-Bcl-2 (1:1000, RO62O1556, Shenyang Wanyu, Shenyang, China); anti-β-actin (1:2000, AF2811, Beyotime, Shanghai, China); HRP-conjugated goat anti-rabbit IgG (1:8000, 234750818, ZSGB-BIO, Beijing, China); HRP-conjugated goat anti-mouse IgG (1:8000, 235680828, ZSGB-BIO, Beijing, China).

    Techniques: Control

    Effect of luteolin/5-Fu on apoptosis-related proteins of A431 cell. ( a ) Bcl-2 and Bax protein expression (luteolin/5-Fu treatment); ( b ) Bcl-2/β-actin ratio; ( c ) Bax/β-actin ratio; ( d ) EGFR, PI3K, AKT, and phosphorylated protein levels; ( e ) p-EGFR/EGFR ratio; ( f ) p-PI3K/PI3K ratio; ( g ) p-AKT/AKT ratio. * p < 0.05, ** p < 0.01 vs. control group.

    Journal: Biomolecules

    Article Title: Potential Efficacy of Luteolin in Cutaneous Squamous Cell Carcinoma: A Combined In Vitro and In Vivo Study

    doi: 10.3390/biom16050737

    Figure Lengend Snippet: Effect of luteolin/5-Fu on apoptosis-related proteins of A431 cell. ( a ) Bcl-2 and Bax protein expression (luteolin/5-Fu treatment); ( b ) Bcl-2/β-actin ratio; ( c ) Bax/β-actin ratio; ( d ) EGFR, PI3K, AKT, and phosphorylated protein levels; ( e ) p-EGFR/EGFR ratio; ( f ) p-PI3K/PI3K ratio; ( g ) p-AKT/AKT ratio. * p < 0.05, ** p < 0.01 vs. control group.

    Article Snippet: The chemicals and materials used in this experiment are as follows: 5-Fluorouracil (5-Fu) (99.9%, CAS: 51-21-8, C13964619, Macklin, Shanghai, China); Luteolin (≥98%, RP210105, Madsen, Chengdu, China); 7,12-Dimethylbenz[a]anthracene (DMBA) (98%, A807576, Alphabio, Tianjin, China); Croton oil (≥95%, C865142, Macklin, Shanghai, China); high-glucose DMEM (2383696, Gibco, Waltham, MA, USA); fetal bovine serum (220315JF, Alphabio, Tianjin, China); DMSO (>99.9%, 20220301, Tianjin Hengxing, Tianjin, China); 4% paraformaldehyde tissue fixative (23039118, Beijing Lanjieke, Beijing, China); CCK-8 kit (101824133EF5E, Apexbio, Houston, TX, USA); Annexin V-FITC/PI apoptosis kit (2306001, Solarbio, Beijing, China); RIPA lysis buffer (IN-WB001, Invent Biotechnologies, Eden Prairie, MN, USA); Protease and Phosphatase Inhibitor Cocktail (051823230704, Beyotime, Shanghai, China); BCA protein assay kit (BL521A, Beyotime, Shanghai, China); DAB chromogenic kit (FL-6001, Changdao Biotech, Shanghai, China); Trizol reagent (1B14KA7304; Sangon Biotech, Shanghai, China); HiFiScript cDNA Synthesis Kit (26323, CWBio, Taizhou, China); anti-PI3K (1:1000, bs-2067R, Bioss, Beijing, China); anti-p-PI3K (1:1000, bs-5570R, Bioss, Beijing, China); anti-AKT (1:1000, bsm-33278M, Bioss, Beijing, China); anti-p-AKT (1:1000, bs-2720R, Bioss, Beijing, China); anti-EGFR (1:1000, bsm-33050M, Bioss, Beijing, China); anti-p-EGFR (1:1000, bsm-52149R, Bioss, Beijing, China); anti-BAX (1:1000, #2772, CST, Danvers, MA, USA); anti-Bcl-2 (1:1000, RO62O1556, Shenyang Wanyu, Shenyang, China); anti-β-actin (1:2000, AF2811, Beyotime, Shanghai, China); HRP-conjugated goat anti-rabbit IgG (1:8000, 234750818, ZSGB-BIO, Beijing, China); HRP-conjugated goat anti-mouse IgG (1:8000, 235680828, ZSGB-BIO, Beijing, China).

    Techniques: Expressing, Control

    (a) Synthesis of β-CD@5-Fu; (b) preparation process of β-CD@5-Fu/CMCS/CMCNa/SA hydrogel beads; (c) in vitro release mechanism of β-CD@5-Fu/CMCS/CMCNa/SA hydrogel beads.

    Journal: RSC Advances

    Article Title: pH-responsive sodium alginate/CMCS/CMCNa composite hydrogel beads for sustained delivery of 5-fluorouracil-β-cyclodextrin inclusion complexes

    doi: 10.1039/d6ra00194g

    Figure Lengend Snippet: (a) Synthesis of β-CD@5-Fu; (b) preparation process of β-CD@5-Fu/CMCS/CMCNa/SA hydrogel beads; (c) in vitro release mechanism of β-CD@5-Fu/CMCS/CMCNa/SA hydrogel beads.

    Article Snippet: β-Cyclodextrin (β-CD) and sodium alginate (SA) were purchased from Shanghai Aladdin Biochemical Technology, Carboxymethyl chitosan (CMCS), carboxymethyl cellulose sodium (CMCNa), calcium chloride (CaCl 2 ), and sodium chloride (NaCl) were obtained from Sinopharm Chemical Reagent, 5-fluorouracil (5-Fu) was acquired from Shanghai Macklin Biochemical Technology.

    Techniques: In Vitro

    Characterization of β-CD@5-Fu inclusion complex and drug-loaded hydrogels: (a) UV-Vis spectra of 5-Fu, β-CD, and β-CD@5-Fu; (b) FTIR spectra of 5-Fu, β-CD, and β-CD@5-Fu; (c) XRD patterns of 5-Fu, β-CD, and β-CD@5-Fu; (d) UV-Vis calibration curves of 5-Fu at different concentrations; (e) linear regression of 5-Fu concentration versus absorbance; (f) encapsulation efficiency (EE) and drug loading (DL) capacity of β-CD@5-Fu; (g) absorbance comparison of β-CD@5-Fu in water versus PBS; (h and i) EE and DL of hydrogel beads with different drug-carrier ratios (w/w).

    Journal: RSC Advances

    Article Title: pH-responsive sodium alginate/CMCS/CMCNa composite hydrogel beads for sustained delivery of 5-fluorouracil-β-cyclodextrin inclusion complexes

    doi: 10.1039/d6ra00194g

    Figure Lengend Snippet: Characterization of β-CD@5-Fu inclusion complex and drug-loaded hydrogels: (a) UV-Vis spectra of 5-Fu, β-CD, and β-CD@5-Fu; (b) FTIR spectra of 5-Fu, β-CD, and β-CD@5-Fu; (c) XRD patterns of 5-Fu, β-CD, and β-CD@5-Fu; (d) UV-Vis calibration curves of 5-Fu at different concentrations; (e) linear regression of 5-Fu concentration versus absorbance; (f) encapsulation efficiency (EE) and drug loading (DL) capacity of β-CD@5-Fu; (g) absorbance comparison of β-CD@5-Fu in water versus PBS; (h and i) EE and DL of hydrogel beads with different drug-carrier ratios (w/w).

    Article Snippet: β-Cyclodextrin (β-CD) and sodium alginate (SA) were purchased from Shanghai Aladdin Biochemical Technology, Carboxymethyl chitosan (CMCS), carboxymethyl cellulose sodium (CMCNa), calcium chloride (CaCl 2 ), and sodium chloride (NaCl) were obtained from Sinopharm Chemical Reagent, 5-fluorouracil (5-Fu) was acquired from Shanghai Macklin Biochemical Technology.

    Techniques: Concentration Assay, Encapsulation, Comparison

    Simultaneous thermogravimetry-differential scanning calorimetry (TG-DSC) curves of 5-Fu (a), β-CD (b), physical mixture of 5-Fu and β-CD (c), β-CD@5-Fu inclusion complex (d), CMCS/CMCNa/SA hydrogel beads (e), and β-CD@5-Fu/CMCS/CMCNa/SA (f).

    Journal: RSC Advances

    Article Title: pH-responsive sodium alginate/CMCS/CMCNa composite hydrogel beads for sustained delivery of 5-fluorouracil-β-cyclodextrin inclusion complexes

    doi: 10.1039/d6ra00194g

    Figure Lengend Snippet: Simultaneous thermogravimetry-differential scanning calorimetry (TG-DSC) curves of 5-Fu (a), β-CD (b), physical mixture of 5-Fu and β-CD (c), β-CD@5-Fu inclusion complex (d), CMCS/CMCNa/SA hydrogel beads (e), and β-CD@5-Fu/CMCS/CMCNa/SA (f).

    Article Snippet: β-Cyclodextrin (β-CD) and sodium alginate (SA) were purchased from Shanghai Aladdin Biochemical Technology, Carboxymethyl chitosan (CMCS), carboxymethyl cellulose sodium (CMCNa), calcium chloride (CaCl 2 ), and sodium chloride (NaCl) were obtained from Sinopharm Chemical Reagent, 5-fluorouracil (5-Fu) was acquired from Shanghai Macklin Biochemical Technology.

    Techniques: Differential Scanning Calorimetry

    (a) FTIR spectra of raw materials; (b) FTIR spectra of six hydrogel bead formulations; swelling ratio of β-CD@5-Fu/CMCS/CMCNa/SA hydrogel dried beads (c) and swollen beads (d) in purified water and under different pH conditions (pH 1.2; pH 6.8 with and without phosphate; pH 7.4 with and without phosphate) at 37 °C for 24 h.

    Journal: RSC Advances

    Article Title: pH-responsive sodium alginate/CMCS/CMCNa composite hydrogel beads for sustained delivery of 5-fluorouracil-β-cyclodextrin inclusion complexes

    doi: 10.1039/d6ra00194g

    Figure Lengend Snippet: (a) FTIR spectra of raw materials; (b) FTIR spectra of six hydrogel bead formulations; swelling ratio of β-CD@5-Fu/CMCS/CMCNa/SA hydrogel dried beads (c) and swollen beads (d) in purified water and under different pH conditions (pH 1.2; pH 6.8 with and without phosphate; pH 7.4 with and without phosphate) at 37 °C for 24 h.

    Article Snippet: β-Cyclodextrin (β-CD) and sodium alginate (SA) were purchased from Shanghai Aladdin Biochemical Technology, Carboxymethyl chitosan (CMCS), carboxymethyl cellulose sodium (CMCNa), calcium chloride (CaCl 2 ), and sodium chloride (NaCl) were obtained from Sinopharm Chemical Reagent, 5-fluorouracil (5-Fu) was acquired from Shanghai Macklin Biochemical Technology.

    Techniques: Purification

    Scanning electron microscopy (SEM) images of hydrogel beads with different formulations: (a–f) β-CD@5-Fu-loaded hydrogel beads with varying mass ratios of β-CD@5-Fu to CCS: (a and b) 20 : 30, (c and d) 15 : 35, and (e and f) 10 : 40. (g–l) 5-Fu-incorporated hydrogel beads (without β-CD) at corresponding ratios: (g and h) 20 : 30, (i and j) 15 : 35, and (k and l) 10 : 40. (m–p) Control groups: (m and n) pure SA hydrogel beads and (o and p) CMCS/CMC-Na/SA ternary hydrogel beads (without drugs).

    Journal: RSC Advances

    Article Title: pH-responsive sodium alginate/CMCS/CMCNa composite hydrogel beads for sustained delivery of 5-fluorouracil-β-cyclodextrin inclusion complexes

    doi: 10.1039/d6ra00194g

    Figure Lengend Snippet: Scanning electron microscopy (SEM) images of hydrogel beads with different formulations: (a–f) β-CD@5-Fu-loaded hydrogel beads with varying mass ratios of β-CD@5-Fu to CCS: (a and b) 20 : 30, (c and d) 15 : 35, and (e and f) 10 : 40. (g–l) 5-Fu-incorporated hydrogel beads (without β-CD) at corresponding ratios: (g and h) 20 : 30, (i and j) 15 : 35, and (k and l) 10 : 40. (m–p) Control groups: (m and n) pure SA hydrogel beads and (o and p) CMCS/CMC-Na/SA ternary hydrogel beads (without drugs).

    Article Snippet: β-Cyclodextrin (β-CD) and sodium alginate (SA) were purchased from Shanghai Aladdin Biochemical Technology, Carboxymethyl chitosan (CMCS), carboxymethyl cellulose sodium (CMCNa), calcium chloride (CaCl 2 ), and sodium chloride (NaCl) were obtained from Sinopharm Chemical Reagent, 5-fluorouracil (5-Fu) was acquired from Shanghai Macklin Biochemical Technology.

    Techniques: Electron Microscopy, Control

    Drug release performance: (a) release kinetics; (b) shows the comparison results of the cumulative release rate (CFR) of six different hydrogel beads; (c and d) in vitro release of β-CD@5-Fu and 5-Fu loaded hydrogels at different ratios (the error bars represent the standard deviation of three replicate experiments); (e) structural stability in SGF (0–2 h) and SIF (0–12 h); (f) schematic diagram of the drug release mechanism from hydrogel beads.

    Journal: RSC Advances

    Article Title: pH-responsive sodium alginate/CMCS/CMCNa composite hydrogel beads for sustained delivery of 5-fluorouracil-β-cyclodextrin inclusion complexes

    doi: 10.1039/d6ra00194g

    Figure Lengend Snippet: Drug release performance: (a) release kinetics; (b) shows the comparison results of the cumulative release rate (CFR) of six different hydrogel beads; (c and d) in vitro release of β-CD@5-Fu and 5-Fu loaded hydrogels at different ratios (the error bars represent the standard deviation of three replicate experiments); (e) structural stability in SGF (0–2 h) and SIF (0–12 h); (f) schematic diagram of the drug release mechanism from hydrogel beads.

    Article Snippet: β-Cyclodextrin (β-CD) and sodium alginate (SA) were purchased from Shanghai Aladdin Biochemical Technology, Carboxymethyl chitosan (CMCS), carboxymethyl cellulose sodium (CMCNa), calcium chloride (CaCl 2 ), and sodium chloride (NaCl) were obtained from Sinopharm Chemical Reagent, 5-fluorouracil (5-Fu) was acquired from Shanghai Macklin Biochemical Technology.

    Techniques: Comparison, In Vitro, Standard Deviation