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Table 1 Urinary excretion concentration of the anticancer drug and dripping concentration

From: Development and evaluation of adsorption sheet (HD safe sheet-U) using active carbon for the purpose of the preventing the contamination diffusion of urinary excreted anticancer drug

  Anticancer drug Dosagea (min ~ max) Urinary unchanged drug excretion rate (% of dosage/24h)b Urinary unchanged drug concentrationc (μg/mL) Dripping concentration (μg/mL)
Alkylating drug CPA 500mg/m2 – 60mg/kg 10.0 50.0 – 201.2 2,000
IFM 0.8 – 3g/m2 6.0 48.0 – 180.0 1,000
Platinum drug CBDCA 300 – 635mg/m2 57.0 – 82.0 171.0 – 520.7 5,000
CDDP 10 – 100mg/m2 14.0 – 54.0 1.4 – 54.0 100
Antimetabolite drug MTX 10mg/body – 300mg/kg 75.0 – 98.0(72h) 1.4 – 3285.5 6,000
5-FU 5mg/kg – 2600mg/m2 10.0 16.8 – 260 1,000
Ara-C 0.8mg/kg – 3,000mg/m2 7.1 – 7.8 1.9 – 234 1,000
GEM 1,000 – 1,250mg/m2 5.3 53.0 – 66.3 300
Anthracycline drug ADR 0.2mg/kg – 80mg/m2 11.5 0.8 – 9.2 1,000
Epi-ADR 15 – 100mg/m2 6.2 (48h) 0.5 – 3.0 1,000
Taxane drug PTX 80 – 210mg/m2 7.3 – 11.3(72h) 1.9 – 7.9 200
DTX 60 – 75mg/m2 1.7 – 4.2 (48h) 0.5 – 1.6 200
Topoisomerase inhibitor VP-16 60 – 500mg/m2 10.3 – 35.2 6.2 – 176.0 500
CPT-11 20 – 180mg/m2 16.3 – 21.1 3.3 – 38.0 1,500
  1. a; Insurance application dose in Japan, b; Report value in each pharmaceutical products IF, c;Dosege × Japanease standard body surface area (1.73m2) or body weight (58kg) × urinary unchanged drug excretion rate ÷standard urine volume (1,730mL/day)