Return to study ST001467 main page

MB Sample ID: SA124428

Local Sample ID:BST200_5m_2
Subject ID:SU001541
Subject Type:Mammal
Subject Species:Mus musculus
Taxonomy ID:10090

Select appropriate tab below to view additional metadata details:


Subject:

Subject ID:SU001541
Subject Type:Mammal
Subject Species:Mus musculus
Taxonomy ID:10090

Factors:

Local Sample IDMB Sample IDFactor Level IDLevel ValueFactor Name
BST200_5m_2SA124428FL015055batch2Group
BST200_5m_2SA124428FL015055BST204Treatment
BST200_5m_2SA124428FL015055muscleSample Source

Collection:

Collection ID:CO001536
Collection Summary:Mice were randomized into five groups (n = 10 each): untreated, non-tumor-bearing mice (NTB group); untreated, tumor-bearing mice (TB group); tumor-bearing mice receiving 5-FU (5-FU group); tumor-bearing mice receiving 5-FU and 100-mg/kg BST204 (BST204100 group); and tumor-bearing mice receiving 5-FU and 200-mg/kg BST204 (BST204200 group). CT26 murine colon carcinoma cells (1 × 106) (Korean Cell Line Bank, Seoul, Korea) resuspended in 100 μL of phosphate-buffered saline were subcutaneously implanted in the right flank of 8-week-old BALB/c mice (Orient Bio, Seongnam, Korea). When tumor volumes reached 100–200 mm3 (approximately 10 days after tumor cell injection), day 0 was assigned and drug administration started for 5-FU and BST204 groups. BST204 (batch number 31037/H1) was obtained from Green Cross Wellbeing (Seongnam, South Korea), and 5-FU was purchased from Sigma-Aldrich (St. Louis, MO, USA). 5-FU (50 mg/kg) was injected intraperitoneally in 3-day cycles (1st cycle: days 0–2; 2nd cycle: days 6–8), in doses that did not exceed the clinically acceptable. BST204 (100 or 200 mg/kg) was orally administered in 5-day cycles (1st cycle: days 0–4; 2nd cycle: days 6–10). The BST204 doses were determined according to its effects on chemotherapy-related fatigue and toxicity. The endpoint of our study was determined according to IACUC guidelines, which recommend euthanasia with a maximum tumor volume of 1,500 mm3 and a BW loss of 20%. Therefore, our study period was limited to day 11. At this point, the change in tumor volumes was up to 810%, and significant cachexia was observed.
Sample Type:Blood (plasma)
Collection Location:muscle
Storage Conditions:-20℃

Treatment:

Treatment ID:TR001556
Treatment Summary:Mice were randomized into five groups (n = 10 each): untreated, non-tumor-bearing mice (NTB group); untreated, tumor-bearing mice (TB group); tumor-bearing mice receiving 5-FU (5-FU group); tumor-bearing mice receiving 5-FU and 100-mg/kg BST204 (BST204100 group); and tumor-bearing mice receiving 5-FU and 200-mg/kg BST204 (BST204200 group). CT26 murine colon carcinoma cells (1 × 106) (Korean Cell Line Bank, Seoul, Korea) resuspended in 100 μL of phosphate-buffered saline were subcutaneously implanted in the right flank of 8-week-old BALB/c mice (Orient Bio, Seongnam, Korea). When tumor volumes reached 100–200 mm3 (approximately 10 days after tumor cell injection), day 0 was assigned and drug administration started for 5-FU and BST204 groups. BST204 (batch number 31037/H1) was obtained from Green Cross Wellbeing (Seongnam, South Korea), and 5-FU was purchased from Sigma-Aldrich (St. Louis, MO, USA). 5-FU (50 mg/kg) was injected intraperitoneally in 3-day cycles (1st cycle: days 0–2; 2nd cycle: days 6–8), in doses that did not exceed the clinically acceptable. BST204 (100 or 200 mg/kg) was orally administered in 5-day cycles (1st cycle: days 0–4; 2nd cycle: days 6–10). The BST204 doses were determined according to its effects on chemotherapy-related fatigue and toxicity. The endpoint of our study was determined according to IACUC guidelines, which recommend euthanasia with a maximum tumor volume of 1,500 mm3 and a BW loss of 20%. Therefore, our study period was limited to day 11. At this point, the change in tumor volumes was up to 810%, and significant cachexia was observed.
Treatment:5-FU was injected intraperitoneally in 3-day cycles. BST204 was orally administerd in 5-day cycles.
Treatment Compound:5-FU, BST204
Treatment Dose:5-FU (50 mg/kg), BST204 (100 or 200 mg/kg)
Animal Endp Euthanasia:study period was limited by day 11

Sample Preparation:

Sampleprep ID:SP001549
Sampleprep Summary:Metabolites related to glucose-mediated energy metabolism were extracted using LLE. Amino acids and bioamines were also extracted using LLE and underwent chemical derivatization with phenylisothiocyante.
Processing Storage Conditions:4℃
Extraction Method:Liquid Liquid Extraction (LLE)

Combined analysis:

Analysis ID AN002443
Analysis type MS
Chromatography type Reversed phase
Chromatography system Agilent 1290
Column Zorbax Eclipse XDB-C18 (100 x 2mm)
MS Type ESI
MS instrument type Triple quadrupole
MS instrument name ABI Sciex 5500 QTrap
Ion Mode POSITIVE
Units area ratio

Chromatography:

Chromatography ID:CH001788
Chromatography Summary:Metabolites related to glucose-mediated metabolites were analyzed with LC-MS/MS (MRM)
Instrument Name:Agilent 1290
Column Name:Synergi fusion RP (50 x 2mm)
Column Temperature:23
Flow Gradient:0% B for 5 min, 0% to 90% B for 2 min, hold at 90% B for 8 min, 90% to 0% B for 1 min, and then hold at 0% B for 9 min
Flow Rate:70 μL/min except for minutes 7 to 15, when it was 140 µL/min
Internal Standard:13C5-glutamine
Sample Injection:3 uL
Solvent A:100% water; 5 mM ammonium acetate
Solvent B:100% acetonitrile; 5 mM ammonium acetate
Chromatography Type:Reversed phase
  
Chromatography ID:CH001789
Chromatography Summary:Amino acids and bioamines were analyzed with LC-MS/MS (MRM)
Instrument Name:Agilent 1290
Column Name:Zorbax Eclipse XDB-C18 (100 x 2mm)
Column Temperature:50
Flow Gradient:0% B for 0.5 min, 0% to 95% B for 5 min, hold at 95% B for 1 min, 95% to 0% B for 0.5 min, then hold at 0% B for 2.5 min
Flow Rate:500 μL/min
Internal Standard:13C5-glutamine, serotonine-d4, dopamine-d4, tryptophan-d5, serine-d3, and lysine-d8
Sample Injection:3 uL
Solvent A:100% water; 0.2% formic acid
Solvent B:100% acetonitrile; 0.2% formic acid
Chromatography Type:Reversed phase

MS:

MS ID:MS002267
Analysis ID:AN002443
Instrument Name:ABI Sciex 5500 QTrap
Instrument Type:Triple quadrupole
MS Type:ESI
MS Comments:Amino acids and bioamines MRM mode Analyst 1.52
Ion Mode:POSITIVE
  logo